The two primary types of cells that make up Nervous Tissue are: AAA and D O Sensory and Motor Central and Peripheral Axons and Dendrites Neurons and Glial Afferent and Efferent

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Answer 1

The correct answer is Neurons and Glial cells.

AAA and D O Sensory and Motor Central and Peripheral Axons and Dendrites Neurons and Glial Afferent and Efferent. Neurons are the primary functional cells of the nervous system and are responsible for transmitting and processing information through electrical and chemical signals.

Glial cells are on the other hand, provide support and protection to neurons. They play important roles in maintaining the structural integrity of the nervous tissue, regulating the chemical environment around neurons, and assisting in neuronal communication.

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Related Questions

5. Based on the results of the female with iron deficiency anemia and the male with polcythemia, can you conclude that the number of red blood cells is an indication of hemoglobin amount? Why or why n

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Yes, the number of red blood cells can be an indication of the hemoglobin amount in the blood.

Hemoglobin is the protein responsible for carrying oxygen from the lungs to the tissues and removing carbon dioxide from the tissues. Red blood cells contain hemoglobin, and their main function is to transport oxygen.

In the case of iron deficiency anemia, there is a decrease in the number of red blood cells (red blood cell count) as well as a decrease in the hemoglobin concentration. Iron is essential for the production of hemoglobin, and a deficiency in iron leads to reduced hemoglobin synthesis, resulting in decreased red blood cell production.

On the other hand, in polycythemia, there is an increase in the number of red blood cells (red blood cell count) and an elevated hemoglobin level. Polycythemia can be primary (a disorder of the bone marrow) or secondary (a response to certain conditions such as chronic hypoxia or excessive production of erythropoietin). In both cases, the increased red blood cell count is accompanied by an elevated hemoglobin level.

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You are curious whether cardiomyocytes contribute to regenerated tissue after heart attack or if resident stem cell populations contribute to regenerated tissue after heart attack in mice. You take the Myh6 CreER MEEG mice and inject maximum doses of tamoxifen. You wait for the tamoxifen to clear out of the circulating blood. Then you create a brief heart attack in these mice, wait for the regeneration process to occur, and then look at the % of cardiomyocytes that express dsRED or GFP in the heart. Given the results above in the bar graphs, which cell population contributes to the regeneration after heart attack? (A) Cardiomycytes (B) Resident stem cells (C) Cannot tell

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Based on the results shown in the bar graphs, it can be concluded that the resident stem cell population, rather than cardiomyocytes, contributes to tissue regeneration after a heart attack in mice.

The experiment involves using Myh6 CreER MEEG mice and injecting them with maximum doses of tamoxifen to label and activate specific cell populations. After allowing the tamoxifen to clear from the blood, a brief heart attack is induced in these mice, and the regeneration process is observed.

The bar graphs display the percentage of cardiomyocytes expressing dsRED or GFP in the heart after regeneration. From the given results, if there is a significant increase in the expression of dsRED or GFP in the cardiomyocytes, it would suggest that cardiomyocytes themselves contribute to the regeneration.

However, if the expression is primarily observed in non-cardiomyocytes, such as resident stem cells, it indicates that the resident stem cell population is involved in the regeneration process.

Therefore, based on the results shown in the bar graphs, it can be concluded that the resident stem cell population contributes to tissue regeneration after a heart attack in mice.

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Which of the following is NOT an explanation for fat that can yield more energy than glucose?
A. Fat contains more carbon atoms than glucose.
B. Fatty acids can convert to pyruvate.
C. Fat can release more hydrogen to coenzymes.
D. Fat can be oxidized more easily.

Answers

The explanation for fat that cannot yield more energy than glucose is Fatty acids can convert to pyruvate. Pyruvate is an important molecule that is produced during the process of glycolysis.

The pyruvate is then converted to acetyl-CoA and enters the citric acid cycle. Pyruvate is a crucial molecule because it is the end product of glycolysis and is used as a starting point for many other metabolic pathways. The other explanations are as follows: Fat contains more carbon atoms than glucose: Fat molecules contain more carbon atoms than glucose molecules.

This means that fat molecules have more chemical energy stored in their bonds than glucose molecules. When fat molecules are broken down, more energy is released than when glucose molecules are broken down.Fat can release more hydrogen to coenzymes: During the process of cellular respiration, coenzymes like NADH and FADH2 carry hydrogen atoms to the electron transport chain. The hydrogen atoms are used to generate ATP.

Fat molecules can release more hydrogen atoms than glucose molecules, which means that they can generate more ATP per molecule. Fat can be oxidized more easily: The bonds between carbon atoms in fat molecules are less stable than the bonds between carbon atoms in glucose molecules.

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An ORF is a continuous stretch of codons that begins with a start codon (usually AUG) and ends at a stop codon (usually UAA, UAG or UGA). The gene x has 920 codons. In a particular tissue, the base ‘C’ of 440th codon CAA (codes for glutamine) of gene x is edited to the base ‘U’. Answer the following question? Enter only a number in the provided space.
How many amino acids will be in the protein X from the un-edited mRNA Answer
How many amino acids will be in the protein Xedit from the edited mRNA? Answer
How many nucleotides will be in the open reading frame of gene Xedit from the edited mRNA?

Answers

An ORF is defined as a continuous sequence of codons that starts with a start codon and terminates at a stop codon. Gene X has 920 codons, and in a specific tissue, the C base of the 440th codon (CAA) of Gene X was replaced with a U base.

The number of amino acids in a protein is directly linked to the number of codons in the mRNA; since Gene X has 920 codons, Protein X will have 920/3 = 306 amino acids (since each codon codes for one amino acid, and there are three nucleotides in each codon).Therefore, the number of amino acids present in protein X from the unedited mRNA is 306 amino acids.

When the 440th codon (CAA) is edited by replacing the C base with a U base, the resulting codon becomes CUA, which codes for leucine rather than glutamine. The edited mRNA encodes a different protein, and the number of amino acids present in this protein is determined by the number of codons in the edited mRNA.

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13) Which of the following has a lower concentration outside of the cell compared to inside of the cell.
A) Ca++
B) K+
C) Cl-
D) Na+
14) Which of the following is an antiport transporter?
A) The Glucose/Sodium Pump
B) The acetylcholine ion transporter.
C) The Calcium Pump
D) The Sodium/Potassium pump

Answers

13) Of the following, Na+ has a lower concentration outside of the cell compared to inside of the cell. Na+ ion is less concentrated outside of the cell in comparison to inside of the cell.

14) The antiport transporters transport two or more molecules in opposite directions across the cell membrane. In the exchange process, one molecule enters the cell while the other molecule exits the cell.

13) Of the following, Na+ has a lower concentration outside of the cell compared to inside of the cell. Na+ ion is less concentrated outside of the cell in comparison to inside of the cell. The difference in the concentration of ions inside and outside of the cell forms an electrochemical gradient that regulates the transport of ions and other molecules across the cell membrane. Na+ ions are an essential component of many cellular processes, including the maintenance of osmotic pressure and the regulation of cellular pH. The concentration of Na+ ions is generally higher inside the cell than outside the cell.

14) The antiport transporters transport two or more molecules in opposite directions across the cell membrane. In the exchange process, one molecule enters the cell while the other molecule exits the cell. The Na+/K+ pump is an antiport transporter. Na+/K+ pump functions by transporting three Na+ ions from inside the cell to the outside of the cell and two K+ ions from the outside of the cell to the inside of the cell. The pump helps to establish an electrochemical gradient across the cell membrane. The other options, Glucose/Sodium pump, acetylcholine ion transporter, and calcium pump are not antiport transporters.

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You are conducting a research project on bacteriophages and have been culturing a bacterial host in the presence of its targeting phage. After exposing the host to a phage for several generations you plate the culture and isolate a bacterial colony. You then culture this colony, make a lawn with this culture, and spot your phage stock on the surface. The next day, you observe that there are no plaques on the lawn. What would you conclude from this result? The phage has mutated to be ineffective on the bacterial host O The phage is temperate/lysogenic The bacterial isolate is a phage resistant mutant The top agar is interfering with phage absorption The bacterial isolate is susceptible to antibiotics

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From the observation of the researcher where no plaques have been observed on the lawn, we can conclude that the bacterial isolate is a phage resistant mutant . What are bacteriophages? Bacteriophages are viruses that affect bacteria . They are specific to a particular type of bacteria.

Phages attach themselves to the bacteria and inject their genetic material into it. This can lead to the death of the bacterium. Bacteriophages have a wide range of potential uses, including the treatment of bacterial infections. In a research project on bacteriophages, if after exposing the host to a phage for several generations, no plaques are observed on the lawn, it means that the bacterial isolate is a phage resistant mutant.

Option 1: If the phage had mutated to be ineffective on the bacterial host, then no colonies of bacterial host would have grown in the culture.Option 2: If the phage were temperate/lysogenic, the phage would have integrated its genome into the bacterial chromosome, and the bacterial colony would have displayed turbidity or changed its colony morphology, but no plaques would have been seen on the lawn.Option 3: The bacterial isolate being a phage-resistant mutant is the correct answer.Option 4: The top agar is interfering with phage absorption, which may cause a problem in seeing the plaques in the lawn.Option 5: The susceptibility of bacteria to antibiotics is unrelated to the bacteriophages. Therefore, it is not an answer to this question.

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Cell wall inhibiting antibiotics impair ______ Multiple Cholce
a. binary fission
b. cellular respiration c. feranentation

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Cell wall inhibiting antibiotics impair binary fission in bacterial cells. Cell wall inhibiting antibiotics, such as penicillin and cephalosporins, target and interfere with the synthesis of peptidoglycan, a crucial component of the bacterial cell wall.

The cell wall provides structural support and protection to the bacterial cell. Binary fission is the process of bacterial cell division where one parent cell divides into two identical daughter cells. During binary fission, the bacterial cell elongates, replicates its DNA, and then forms a septum dividing the cell into two separate cells. The formation of a new cell wall is a critical step in the binary fission process.

By inhibiting the synthesis of peptidoglycan and disrupting cell wall formation, cell wall inhibiting antibiotics impair the process of binary fission in bacterial cells. This hinders the ability of bacterial cells to divide and multiply, ultimately inhibiting their growth and causing the bacteria to be more susceptible to immune responses or other antimicrobial treatments.

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1. Which biological science is the one that I told you is a complex subject ke immunology? & biochemistry A. microbiology B. biochemistry
D. biophysics C. neuroscience E. cell biology 2. Mucous membranes are a part of the_____________
A. adaptive immune system B. lymph node C. physical barrier D. bone marrow E. Ethymus

Answers

1. The biological science that is as complex as immunology is: B. Biochemistry

Immunology is the study of the immune system and how it works to fight off pathogens. Biochemistry is the study of chemical processes and substances in living organisms. Both fields can be quite complex, but biochemistry can be just as complex as immunology.

2. Mucous membranes are a part of the: C. physical barrier

Mucous membranes are a type of physical barrier in the body's defense against infection. They line various organs and body cavities, such as the nose, mouth, throat, lungs, and reproductive organs. The mucus produced by these membranes helps trap pathogens and prevent them from entering the body.

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PLEASE HELP ME DUE IN 2 HOURS FROM NOW.
What is the goal of personalized medicine? How will the study of genomics aid in the development of personalized medicine approaches?

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Personalized medicine is an innovative field that focuses on tailoring medical care to each individual's unique genetic and biological makeup. Its main goal is to develop treatments that are specific to each patient's genetic and biological characteristics, making them more effective and personalized.

This approach will make medical care more accurate and targeted to each patient's individual needs and can lead to better clinical outcomes.The study of genomics will play a critical role in the development of personalized medicine. It is the study of the human genome, including its structure, function, and interactions with the environment. Genomic medicine will offer clinicians insights into the genetic makeup of each patient, enabling them to predict the likelihood of certain diseases, select the most effective medications, and determine the most appropriate dosages. As a result, this field will revolutionize the way we practice medicine, as it will lead to better outcomes for patients, reduce the burden of healthcare costs, and enhance the quality of life.

Personalized medicine is a promising field that has the potential to improve medical outcomes and reduce healthcare costs. With the study of genomics, researchers and clinicians will be able to develop personalized treatments that are tailored to each patient's unique needs, resulting in better clinical outcomes. In the future, this approach will become more widespread, and more people will benefit from it. It is an exciting time for personalized medicine and genomic research.

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1. Form and function are products of evolution. What are the conditions that must be satisfied in order for adaptive evolution to occur?

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In order for adaptive evolution to occur, certain conditions must be satisfied:

Variation: There must be genetic variation within a population, which arises through mutations, recombination, and genetic drift. This variation serves as the raw material for natural selection to act upon. Inheritance: The genetic variations must be heritable, meaning they can be passed from one generation to the next. Differential Fitness: The variations in traits must lead to differences in fitness, or reproductive success. Individuals with advantageous traits that enhance their survival and reproductive success are more likely to pass on their genes to the next generation. Selective Pressure: There must be selective pressure in the environment that favors certain traits over others.

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3. Assume a person receives the Johnson&Johnson vaccine. Briefly list the cellular processes or molecular mechanisms that will take place within the human cells that will result in the expression of the coronavirus antigen.

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Processes include viral vector entry into cells, vector replication, expression of the viral spike protein gene, translation of the spike protein mRNA, and presentation of the spike protein on the cell surface.

The Johnson & Johnson vaccine utilizes a viral vector-based approach to generate an immune response against the coronavirus antigen. The vaccine uses a modified adenovirus, specifically Ad26, as the viral vector. Once the vaccine is administered, several cellular processes and molecular mechanisms come into play.

Firstly, the viral vector (Ad26) enters human cells, typically muscle cells near the injection site. This is facilitated by the specific interactions between viral proteins and cell surface receptors.

After the entry, the viral vector undergoes replication within the host cells. This replication allows for the amplification of the viral genetic material and subsequent gene expression.

The coronavirus antigen expression is achieved through the insertion of the genetic material encoding the spike protein of the SARS-CoV-2 virus into the viral vector genome. The spike protein gene is under the control of specific regulatory elements to ensure its expression.

Once the spike protein mRNA is transcribed, it undergoes translation, resulting in the synthesis of spike protein molecules within the host cells. These spike proteins are similar to those found on the surface of the SARS-CoV-2 virus and act as antigens.

Finally, the host cells present the spike protein antigens on their surface using major histocompatibility complex (MHC) molecules. This antigen presentation allows immune cells, such as T cells and B cells, to recognize and mount an immune response against the spike protein.

In summary, upon receiving the Johnson & Johnson vaccine, the viral vector enters human cells, undergoes replication, and expresses the coronavirus spike protein gene.

The spike protein mRNA is translated into spike protein molecules, which are presented on the cell surface, leading to the subsequent immune response against the coronavirus antigen.

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What are the two types of Speciation? 4.3
There are two pathways to speciation: PG: 137
1) Transformation: One species evolves into another species
2) Divergence: One or more species arise from a parent species

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The two types of speciation are allopatric speciation and sympatric speciation.

Allopatric speciation: Allopatric speciation occurs when a population is geographically isolated, leading to reproductive isolation and the formation of new species. The physical barrier prevents gene flow between the separated populations, allowing for independent evolutionary changes to accumulate over time. The accumulation of genetic and phenotypic differences can eventually result in reproductive isolation, where individuals from the separated populations can no longer produce viable offspring if brought back into contact.

Sympatric speciation: Sympatric speciation occurs without geographic isolation, where a new species arises within the same geographic area as the parent population. Reproductive isolation is achieved through other mechanisms such as ecological, behavioral, or genetic factors. These mechanisms can lead to the development of reproductive barriers that prevent gene flow between different subgroups within the population. Over time, these subgroups accumulate genetic and phenotypic differences, eventually leading to the formation of new species.

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A SOAP must always be written in this order: "Subjective,
Objective, Assessment, and Plan".
A. True
B. False

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The statement "A SOAP must always be written in this order: "Subjective, Objective, Assessment, and Plan" is A. True

A SOAP (Subjective, Objective, Assessment, Plan) note is a standard format used in medical documentation and patient charting. It is typically organized in that order to provide a logical and structured approach to documenting patient encounters and facilitating communication between healthcare providers.

The subjective section includes the patient's reported symptoms and history, the objective section includes the healthcare provider's observations and objective findings, the assessment section includes the provider's assessment and diagnosis, and the plan section outlines the proposed treatment plan.

Following this order helps ensure consistency and clarity in medical documentation. Therefore, the correct answer is option (A).

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Prepare a 500-800 word essay using correct grammar and spelling. Why is there no reason for a cheat meal or day? What is meant by the statement, there are no good foods or bad foods? When people disclose they are craving a food or they emotionally eat, what would be a practical tip or suggestion that might help them address the challenge? What benefits could our society gain by adopting a Health at Every Size approach?

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A cheat meal or day is defined as a planned indulgence or reward that enables an individual to indulge in their favorite foods or meals without feeling guilty.

The problem with a cheat meal is that it tends to create negative feelings of guilt, shame, and anxiety for people, especially those struggling with weight loss. There is no reason for a cheat meal or day because it promotes the diet mentality and suggests that there are good and bad foods. However, this is not true because food is neutral, and it is the relationship with food that is either positive or negative. What is meant by the statement, there are no good foods or bad foods? There are no good or bad foods. Foods are not inherently good or bad; they are simply foods.

When we label foods as good or bad, we tend to create an unhealthy relationship with food. For instance, we may restrict ourselves from eating certain foods, which may lead to overeating or binge eating. This is because labeling food creates a sense of morality, which affects the way we think and feel about ourselves. Therefore, it is essential to view food as neutral. When people disclose they are craving a food or they emotionally eat, what would be a practical tip or suggestion that might help them address the challenge? When people disclose they are craving a food or they emotionally eat, it is essential to acknowledge their feelings. One practical suggestion that may help is to identify the emotion that is driving the craving.

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1. A 48-year-old woman comes to the emergency department because of a 3-hour history of periumbilical pain radiating to the right lower and upper of the abdomen. She has had nausea and loss of appetite during this period. She had not had diarrhea or vomiting. Her temperature is 38°C (100.4 °F). Abdominal examination show diffuse guarding and rebound tenderness localized to the right lower quadrant. Pelvic examination shows no abnormalities. Laboratory studies show marked leukocytosis with absolute neutrophils and a shift to the left. Her serum amylase active is 123 U/L, and serum lactate dehydrogenase activity is an 88 U/L. Urinalysis within limits. An x-ray and ultrasonography of the abdomen show no free air masses. Which of the following best describes the pathogenesis of the patient's disease?
A. Contraction of the sphincter of Oddi with autodigestion by trypsin, amylase, and lipase
B. Fecalith formation of luminal obstruction and ischemia
C. Increased serum cholesterol and bilirubin concentration with crystallization and calculi formation
D. Intussusception due to polyps within the lumen of the ileum E. Multiple gonococcal infections with tubal plical scaring

Answers

The patient's symptoms, physical examination findings, and laboratory studies are consistent with acute appendicitis, which is characterized by inflammation and obstruction of the appendix.

Based on the given information, the patient presents with classic signs and symptoms of acute appendicitis. The periumbilical pain that radiates to the right lower and upper abdomen, accompanied by nausea, loss of appetite, and fever, are indicative of appendiceal inflammation. The presence of diffuse guarding and rebound tenderness localized to the right lower quadrant on abdominal examination further supports this diagnosis.

Laboratory studies reveal marked leukocytosis with absolute neutrophils, indicating an inflammatory response, and a shift to the left, suggesting an increase in immature forms of white blood cells. These findings are consistent with an infectious process, such as acute appendicitis.

Imaging studies, including an x-ray and ultrasonography of the abdomen, show no free air masses, ruling out perforation of the appendix. This supports the diagnosis of early or uncomplicated appendicitis, where the appendix is inflamed but not yet perforated.

In summary, the patient's clinical presentation, examination findings, and laboratory and imaging results are most consistent with acute appendicitis, which is caused by inflammation and obstruction of the appendix. Early recognition and prompt surgical intervention are crucial to prevent complications and ensure the patient's recovery.

the clinical presentation, diagnosis, and management of acute appendicitis to understand the importance of timely intervention in this condition.

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When pyrimidines undergo catabolism the result is: Pyrimidines are eventually broken down into ammonia and eliminated as nitrogenous waste or reused in purine synthesis Production and elimination of uric acid Production of malonyl-CoA which is then reused in fatty acid and polyketide Synthesis. Production of chorismic acid and integration into polyketide synthesis

Answers

The correct answer is 1. Pyrimidines are eventually broken down into ammonia and eliminated as nitrogenous waste or reused in purine synthesis.

Pyrimidines are broken down by a series of enzymes into ammonia, carbon dioxide, and β-alanine. The ammonia can be used to synthesize new pyrimidines, or it can be excreted as a waste product.

The other options are incorrect.

Uric acid is a product of purine catabolism, not pyrimidine catabolism.

Malonyl-CoA is not produced from pyrimidine catabolism. It is produced from acetyl-CoA in the fatty acid synthesis pathway.

Chorismic acid is not produced from pyrimidine catabolism. It is produced from the amino acid tryptophan in the biosynthesis of aromatic amino acids, including phenylalanine, tyrosine, and tryptophan.

Therefore, (1) Pyrimidines are eventually broken down into ammonia and eliminated as nitrogenous waste or reused in purine synthesis is the correct option.

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Why are peptidase inhibitors a promising class of drugs that may be used to treat a broad spectrum of coronavirus strains and variants?
A. Because coronaviruses contain genes for two highly conserved peptidase enzymes.
B. Because coronaviruses express polyproteins that are activated by proteolysis into individual viral proteins.
C. Because the coronavirus-encoded peptidases are essential for polyprotein activation, and therefore for viral replication.
D. All of the above

Answers

The correct answer is: C. Because the coronavirus-encoded peptidases are essential for polyprotein activation, and therefore for viral replication.

Peptidase inhibitors are a promising class of drugs to treat coronavirus strains and variants because coronavirus-encoded peptidases play a crucial role in polyprotein activation, which is necessary for viral replication. Coronaviruses express polyproteins that need to be processed by proteolysis into individual viral proteins for the virus to replicate effectively. These polyproteins contain genes for highly conserved peptidase enzymes that are responsible for cleaving the polyproteins into functional units. By inhibiting the activity of these peptidases, the processing of viral polyproteins can be disrupted, leading to a reduction in viral replication.

Option A is incorrect because not all coronaviruses necessarily contain genes for two highly conserved peptidase enzymes. Option B is also incorrect because it describes the process of polyprotein activation but does not specifically address the role of peptidase inhibitors. Option C is the correct answer as it highlights the essential nature of coronavirus-encoded peptidases for polyprotein activation and viral replication. Therefore, option D is incorrect because it includes incorrect information (option A) alongside the correct explanation (option C).

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Producers uptake molecules. molecules and use energy from sunlight; animals; energy-rich energy-poor; sunlight; energy-rich energy-rich; sunlight: energy-poor O energy-rich; animals; energy-poor O energy-poor; animals; energy-rich to convert them into 2 pts

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Producers uptake energy-rich molecules and use energy from sunlight to convert them into energy-rich molecules.

Producers uptake energy-rich molecules and use energy from sunlight to convert them into energy-rich molecules. Producers are autotrophic organisms that can produce their food. They convert light energy from the sun into food energy through a process called photosynthesis. During this process, producers uptake carbon dioxide and water molecules from the environment and convert them into glucose and oxygen molecules using energy from sunlight.

They use this energy to produce energy-rich molecules that can be used as food or stored in the cells. This process is crucial for the survival of producers and also provides food for consumers. Consumers, on the other hand, obtain their food energy by consuming other organisms. Therefore, producers play a crucial role in the food chain and provide energy for the entire ecosystem.

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A couple, both of whom have autosomal recessive deafness, have a child who can hear. provide scientific and genetically relevant explanation for this (other than a de novo mutation in the child, which is extremely unlikely

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The child's ability to hear despite having parents with autosomal recessive deafness suggests that the child inherited at least one dominant allele for hearing from one of the parents. This could be due to a phenomenon called "gene conversion" or "gene crossover."

In autosomal recessive conditions, both parents must carry two copies of the recessive allele to pass it on to their child. However, if one of the parents carries a dominant allele for hearing alongside the recessive allele for deafness, the child has a chance of inheriting the dominant allele and thus having normal hearing.

One possible explanation is gene conversion or gene crossover. During the formation of reproductive cells (sperm or eggs), genetic material from homologous chromosomes can exchange segments. In this case, it is possible that the parent with autosomal recessive deafness underwent gene conversion or crossover, resulting in the transfer of the dominant allele for hearing to the reproductive cells.

As a result, the child inherits the dominant allele for hearing from the parent and can hear despite both parents having autosomal recessive deafness. This scenario allows for the child's normal hearing ability without the need to invoke a de novo mutation, which is highly unlikely in this context.

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The lab instruction states that SDS is used in the process of isolating DNA from cells because it dissolves lipids. What structural part of cells is composed of lipids (and what type of lipid is this structural component)?

Answers

The structural component of cells composed of lipids is the cell membrane, which is primarily made up of phospholipids.

The cell membrane, also known as the plasma membrane, is a vital component of cells that separates the intracellular environment from the extracellular environment. It acts as a selectively permeable barrier, controlling the movement of substances in and out of the cell. The cell membrane is composed of lipids, primarily phospholipids.

Phospholipids are a type of lipid consisting of a hydrophilic (water-loving) head and hydrophobic (water-fearing) tails. The hydrophilic head of a phospholipid molecule contains a phosphate group, while the hydrophobic tails consist of fatty acid chains. These phospholipids arrange themselves in a bilayer structure, with their hydrophilic heads facing the aqueous environment both inside and outside the cell, and their hydrophobic tails pointing inward, shielded from the water.

SDS (sodium dodecyl sulfate) is an anionic detergent commonly used in molecular biology and biochemistry. It has the ability to disrupt lipid-lipid and lipid-protein interactions by binding to the hydrophobic regions of lipids and proteins. In the process of isolating DNA from cells, SDS is added to lyse the cell membrane, as it dissolves the lipids of the cell membrane, thereby releasing the cellular contents, including DNA.

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What muscle causes the downward pull on the first
metatarsal?
What ligament partially inserts on the medial talar
tubercle?
What bone does the medial malleoulus part of?
What ligament connects the sus

Answers

The tibialis anterior muscle pulls downward on the first metatarsal. The deltoid ligament inserts on the medial talar tubercle. The medial malleolus is part of the tibia bone. The spring ligament connects the sustentaculum tali to the navicular bone.

The muscle that causes the downward pull on the first metatarsal is the tibialis anterior. The ligament that partially inserts on the medial talar tubercle is the deltoid ligament.The medial malleoulus is part of the tibia bone.The ligament that connects the sustentaculum tali of the calcaneus bone to the navicular bone is the spring ligament.In summary:Muscle causing downward pull on first metatarsal is Tibialis Anterior.The deltoid ligament partially inserts on the medial talar tubercle.The medial malleolus is part of the tibia bone.The spring ligament connects the sustentaculum tali of the calcaneus bone to the navicular bone.The tibialis anterior muscle pulls downward on the first metatarsal. The deltoid ligament inserts on the medial talar tubercle. The medial malleolus is part of the tibia bone. The spring ligament connects the sustentaculum tali to the navicular bone.content loadedWhat muscle causes the downward pull on the firstmetatarsal?What ligament partially inserts on the medial talartubercle?What bone does the medial malleoulus part of?What ligament connects the sus

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1. What are the factors and conditions that can increase
bleeding time?

Answers

Several factors and conditions can contribute to an increase in bleeding time. These include certain medications, underlying medical conditions, platelet disorders, and deficiencies in clotting factors.

Bleeding time refers to the duration it takes for blood to clot after an injury. Several factors and conditions can affect bleeding time. Certain medications, such as anticoagulants (e.g., aspirin, warfarin) and nonsteroidal anti-inflammatory drugs (NSAIDs), can interfere with platelet function and prolong bleeding time.

Additionally, underlying medical conditions like liver disease, kidney disease, and vitamin K deficiency can impair the synthesis of clotting factors, leading to prolonged bleeding.

Platelet disorders can also contribute to increased bleeding time. Conditions like thrombocytopenia (low platelet count), von Willebrand disease (deficiency or dysfunction of von Willebrand factor, a protein involved in clotting), and platelet function disorders (e.g., Glanzmann's thrombasthenia) can result in impaired platelet aggregation and clot formation, leading to prolonged bleeding time.

Furthermore, deficiencies in clotting factors, such as hemophilia (inherited clotting factor deficiencies), can cause prolonged bleeding time. Hemophilia A (deficiency of factor VIII) and hemophilia B (deficiency of factor IX) are the most common types of hemophilia.

It is important to note that if you experience prolonged or excessive bleeding, it is essential to consult a healthcare professional for proper evaluation and diagnosis, as the underlying cause needs to be addressed appropriately.

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Transaminases need cofactor. Vitamin B6 Vitamin B3 Vitamin B9 Vitamin B12

Answers

The transaminases primarily rely on vitamin B6 as a cofactor, they do not require other B vitamins such as niacin (vitamin B3), folic acid (vitamin B9), or cobalamin (vitamin B12) for their enzymatic activity.

Transaminases are a group of enzymes that play a vital role in various biochemical reactions in the body, particularly in amino acid metabolism. These enzymes facilitate the transfer of amino groups between different amino acids, thereby allowing the synthesis of new amino acids and the breakdown of others.

To carry out their function, transaminases require a coenzyme known as pyridoxal phosphate (PLP), which is derived from vitamin B6.

Vitamin B6, also known as pyridoxine, is a water-soluble vitamin that serves as a cofactor for many enzymes, including transaminases.

It is involved in numerous metabolic reactions, including the conversion of amino acids and the synthesis of neurotransmitters and hemoglobin. Vitamin B6 is converted into its active form, PLP, which binds to transaminases and acts as a coenzyme, facilitating the transfer of amino groups.

These vitamins play essential roles in other aspects of metabolism but are not directly involved in transamination reactions.

Niacin (vitamin B3) is involved in energy metabolism and DNA repair, while folic acid (vitamin B9) is necessary for DNA synthesis and cell division.

Cobalamin (vitamin B12) participates in DNA synthesis, red blood cell formation, and nerve function.

Although these B vitamins are crucial for overall health and well-being, they do not serve as cofactors for transaminases.

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Enzymes are: (select all correct responses)
a. highly specific
b. carbohydrates
c. consumed/destroyed in reactions
d. used to increase the activation energy of a reaction
e. catalysts

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The correct responses are: a. Highly specific, e. Catalysts, enzymes are highly specific catalysts that accelerate chemical reactions by lowering the activation energy barrier.

Enzymes are highly specific (option a) in their ability to catalyze specific reactions. Each enzyme is designed to interact with a specific substrate or group of substrates, enabling them to perform their function with precision. Enzymes are not carbohydrates (option b). Carbohydrates are a type of biomolecule that includes sugars, starches, and cellulose, whereas enzymes are proteins or sometimes RNA molecules known as ribozymes.

Enzymes are not consumed or destroyed in reactions (option c). They are not altered or used up during the catalytic process. Instead, enzymes facilitate reactions by lowering the activation energy required for the reaction to occur. Enzymes are catalysts (option e). They increase the rate of chemical reactions by lowering the activation energy barrier, thereby accelerating the conversion of substrates into products. Enzymes achieve this by providing an alternative reaction pathway with a lower energy barrier, making the reaction more favorable.

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Which of the following would not be expected to lead to fixation? A ongoing bottlenecks impacting a small population B. negative frequency-dependent selection on a large population (such as with a large population of purple and yellow elderflower orchids) Cunderdominance D. ongoing strong directional selection on a highly heritable trait across an entire population

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The option which would not be expected to lead to fixation is B: negative frequency-dependent selection on a large population (such as with a large population of purple and yellow elderflower orchids).

Fixation refers to the situation when all members of a population carry only one allele. Fixation can occur when a population's gene pool lacks diversity.

Fixation can be a gradual process or an abrupt one. However, fixation's genetic consequence is the same: a homozygous gene pool.Below are explanations on why the other options would lead to fixation:A.

Ongoing bottlenecks impacting a small Population bottlenecks can happen due to natural events such as droughts, fires, or floods.

It can also happen because of human activity. In either case, when a population bottleneck occurs, there is a reduction in population size, and there is a loss of genetic variation.

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In which cases are prezygotic isolating mechanisms expected to strengthen primarily due to the indirect effects of linkage or pleiotropy, or by genetic drift, rather than by the direct effect of natural selection for prezygotic barriers? [Choose all answers that apply.] a. the populations are allopatric. b. mating between the members of populations occurs readily in nature, but the hybrids are sterile. c. members of each population do not mate with members of the other population because mating occurs at different times of year. d. introgression occurs between members of populations at a secondary hybrid zone, but the hybrids are less fit than either parent.

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Prezygotic isolating mechanisms expected to strengthen primarily due to the indirect effects of linkage or pleiotropy, or by genetic drift, rather than by the direct effect of natural selection for prezygotic barriers in the following cases the populations are allopatric. introgression occurs between members of populations

at a secondary hybrid zone, but the hybrids are less fit than either parent. What are Prezygotic isolating mechanisms Prezygotic isolating mechanisms are biological mechanisms that prevent hybridization between two species by preventing the formation of a zygote. These mechanisms are in effect before fertilization and include many forms of mate selection. Prezygotic isolating mechanisms are often influenced by genetic drift, pleiotropy, and linkage. Some species exhibit prezygotic isolating mechanisms that have evolved to prevent cross-species mating. Allopatric populations are those that have been separated geographically. In the case of allopatric populations, prezygotic isolation mechanisms are often the only barriers to interbreeding between populations. Therefore, they are likely to evolve quickly.

In populations that are parapatric or sympatric, direct natural selection is more likely to act on prezygotic barriers because individuals are more likely to come into contact with other species. Prezygotic isolating mechanisms are expected to strengthen primarily due to genetic drift, linkage, and pleiotropy when populations are allopatric. It is also expected to strengthen when introgression occurs between members of populations at a secondary hybrid zone, but the hybrids are less fit than either parent.

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1) 1) The centromere is a region in which A) new spindle microtubules form at either end. B) chromosomes are grouped during telophase. the nucleus is located prior to mitosis. D) chromatids remain attached to one another until anaphase. E) metaphase chromosomes become aligned at the metaphase plate. 2) 2) If there are 20 chromatids in a cell, how many centromeres are there? A) 80 B) 10 C) 30 D) 40 E) 20 3) 3) Which is the longest of the mitotic stages? A) anaphase B) telophase prometaphase D) metaphase E) prophase 4) 4) A cell containing 92 chromatids at metaphase of mitosis would, at its completion, produce two nuclei each containing how many chromosomes? A) 92 B) 16 C) 23 D) 46 E) 12 5) Cytokinesis usually, but not always, follows mitosis. If a cell completed mitosis but not cytokinesis, 5) the result would be a cell with A) two nuclei but with half the amount of DNA. B) a single large nucleus. two nuclei. D) two abnormally small nuclei. E) high concentrations of actin and myosin. 6) The formation of a cell plate is beginning across the middle of a cell and nuclei are re-forming at opposite ends of the cell. What kind of cell is this? A) an animal cell undergoing cytokinesis B) an animal cell in telophase C) an animal cell in metaphase D) a plant cell undergoing cytokinesis E) a plant cell in metaphase 7) 7) Chromosomes first become visible during which phase of mitosis? A) metaphase B) prometaphase 9) telophase D) prophase E) anaphase

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1) The centromere is a region in which chromatids remain attached to one another until anaphase.

2) If there are 20 chromatids in a cell, there would be 20 centromeres.

3) The longest stage of mitosis is metaphase.

4) A cell containing 92 chromatids at metaphase of mitosis would, at its completion, produce two nuclei each containing 46 chromosomes.

5) If a cell completed mitosis but not cytokinesis, the result would be a cell with two nuclei but with half the amount of DNA.

6) The formation of a cell plate is beginning across the middle of a cell and nuclei are re-forming at opposite ends of the cell. This kind of cell is a plant cell undergoing cytokinesis.

7) Chromosomes first become visible during prophase of mitosis.

1) The centromere is a region in which D) chromatids remain attached to one another until anaphase.

The centromere is the specialized region of a chromosome where the two sister chromatids are joined together. During mitosis, the chromatids are held together at the centromere until anaphase, when they separate and move towards opposite poles of the cell. This ensures that each daughter cell receives the correct number of chromosomes.

2) If there are 20 chromatids in a cell, the number of centromeres would be E) 20.

Each chromatid contains one centromere. Since there are 20 chromatids, there would be 20 centromeres. Each chromatid is a replicated chromosome consisting of two sister chromatids held together at the centromere.

3) The longest stage of mitosis is D) metaphase.

Metaphase is the stage of mitosis where the replicated chromosomes align along the equatorial plane of the cell, known as the metaphase plate. This alignment ensures that each chromosome is correctly positioned before the separation of sister chromatids during anaphase. Metaphase can take a relatively longer time compared to other stages of mitosis.

4) A cell containing 92 chromatids at metaphase of mitosis would, at its completion, produce two nuclei each containing D) 46 chromosomes.

In metaphase of mitosis, each chromatid is still attached to its sister chromatid at the centromere. When the chromatids separate during anaphase and complete mitosis, each resulting daughter cell will receive the same number of chromosomes as the parent cell. Since there are 92 chromatids, there would be 46 chromosomes in each of the two nuclei produced at the completion of mitosis.

5) If a cell completed mitosis but not cytokinesis, the result would be a cell with A) two nuclei but with half the amount of DNA.

Cytokinesis is the process of dividing the cytoplasm and organelles to form two daughter cells. If mitosis is completed without cytokinesis, the result would be a single cell with two nuclei. However, the DNA content would not be halved because the chromosomes have already replicated during the S phase of the cell cycle. Therefore, each nucleus would still contain the same amount of DNA as the original cell.

6) The formation of a cell plate is beginning across the middle of a cell and nuclei are re-forming at opposite ends of the cell. This kind of cell is D) a plant cell undergoing cytokinesis.

The formation of a cell plate is a characteristic feature of cytokinesis in plant cells. During cytokinesis, a cell plate made of vesicles derived from the Golgi apparatus starts to form across the equatorial plane of the cell. This cell plate eventually develops into a new cell wall, dividing the cytoplasm into two daughter cells. The reformation of nuclei at opposite ends of the cell indicates that mitosis has already occurred.

7) Chromosomes first become visible during D) prophase of mitosis.

Prophase is the initial stage of mitosis where the chromatin fibers condense

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Can you explain solution of the question in detail
Sequence Alignment Compute the best possible global alignment for the following two sequences (filling the table below using dynamic programming), assuming a gap penalty of -5, a mismatch penalty of -

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The question involves computing the best global alignment for two sequences using dynamic programming. A gap penalty of -5 and a mismatch penalty of -2 are assumed. The table needs to be filled to determine the optimal alignment.

Sequence alignment is a method used to compare and find similarities between two sequences of characters, such as DNA or protein sequences. In this question, the goal is to compute the best global alignment for two given sequences.

Dynamic programming is a commonly used algorithmic technique for solving sequence alignment problems. It involves filling a table, known as a scoring matrix, to calculate the optimal alignment. Each cell in the matrix represents a specific alignment between two characters from the sequences.

To determine the best alignment, a scoring system is used, which includes penalties for gaps and mismatches. In this case, a gap penalty of -5 and a mismatch penalty of -2 are assumed. The alignment with the highest score is considered the best alignment.

The table needs to be filled using dynamic programming techniques, such as the Needleman-Wunsch algorithm or the Smith-Waterman algorithm. These algorithms consider the scores of neighboring cells to determine the optimal alignment. The alignment path with the highest score is traced back through the matrix to obtain the final alignment.

By following the dynamic programming approach and applying the given gap and mismatch penalties, the table can be filled to compute the best global alignment for the two sequences. The resulting alignment will show how the characters from the sequences are matched, taking into account the penalties and aiming to maximize the overall alignment score.

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Can you explain solution of the question in detail Sequence Alignment Compute the best possible global alignment for the following two sequences (filling the table below using dynamic programming), assuming a gap penalty of -5, a mismatch penalty of -1, and a match score of +3. Would your answer be any different if the gap penalty was -1. S1: AGCGTAT S1: ACGGTAT T A T G C G G G T A T A 0 A с

Metabolic fates of newly synthesized cholesterol are all but one. Choose the one. Olipoproteins bile salts O NAD+ membrane Question 12 (1 point) of the following types of lipoprotein particles, choose

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The metabolic fates of newly synthesized cholesterol include lipoproteins, bile salts, and membrane incorporation. NAD+ is not a metabolic fate of newly synthesized cholesterol. Option a is correct.

After synthesis, cholesterol undergoes various metabolic pathways in the body. One major fate of cholesterol is its association with lipoproteins. Lipoproteins are complexes of lipids and proteins that transport cholesterol and other lipids through the bloodstream. These lipoproteins include low-density lipoprotein (LDL) and high-density lipoprotein (HDL). LDL carries cholesterol from the liver to the peripheral tissues, while HDL helps transport excess cholesterol from peripheral tissues back to the liver for excretion.

Another fate of cholesterol is its conversion into bile salts. Bile salts are synthesized in the liver from cholesterol and are essential for the digestion and absorption of dietary fats. Bile salts are stored in the gallbladder and released into the small intestine during the digestion process.

Cholesterol can also be incorporated into cell membranes. It is an important component of cell membranes and plays a crucial role in maintaining their integrity and fluidity.

However, NAD+ is not a metabolic fate of newly synthesized cholesterol. NAD+ (nicotinamide adenine dinucleotide) is a coenzyme involved in various metabolic reactions, particularly in redox reactions. It is not directly involved in the metabolism or fate of cholesterol.

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The Complete question is

Metabolic fates of newly synthesized cholesterol are all but one. Choose the one.

a. lipoproteins bile salts

b. NAD+ membrane Question 12 (1 point) of the following types of lipoprotein particles, choose the one

a. lipids through the bloodstream

b. maintaining their integrity and fluidity

Describe the structure of the male and female reproductive systems, relating structure to function (AC 1.1). Use clear diagrams, either ones you have drawn or ones you have annotated Remember to relate structures to functions: how does the structure enable that function to effectively take place

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The male and female reproductive systems have distinct structures that enable their respective functions in the process of reproduction.

What are the structures and functions of the male and female reproductive systems?

Male Reproductive System:

The testes produce sperm through the process of spermatogenesis. Sperm mature and are stored in the epididymis before being transported through the vas deferens. The prostate gland and seminal vesicles contribute fluids to semen, which nourish and protect the sperm.

Female Reproductive System:

The ovaries produce eggs through oogenesis and also release hormones such as estrogen and progesterone. The fallopian tubes capture eggs released from the ovaries and provide a site for fertilization by sperm.

The fertilized egg then travels to the uterus, where it implants and develops into a fetus. The cervix acts as the entrance to the uterus and undergoes changes during the menstrual cycle. The vagina serves as the birth canal during childbirth and also facilitates sexual intercourse.

The structures of the male and female reproductive systems are specialized to perform their respective functions in reproduction. The male system is designed for the production, storage, and delivery of sperm, while the female system is responsible for producing and releasing eggs, facilitating fertilization, and supporting embryo development. These structures ensure the effective transfer of genetic material and the continuation of the species.

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