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Question 1
Incorrect
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At what stage of meiosis does the process of homologous recombination occur?
Your Answer: Metaphase II
Correct Answer: Prophase I
Explanation:Homologous Recombination: A Mechanism for DNA Repair and Genetic Variation
Homologous recombination is a process that allows for the exchange of nucleotide sequences between two similar or identical DNA molecules. This occurs during meiosis, specifically during the second phase of prophase I, where sister chromatids swap sequences. The primary purpose of homologous recombination is to accurately repair harmful double-strand DNA breaks. This process results in new combinations of DNA sequences that provide genetic variation in daughter cells and, ultimately, the organism’s offspring.
In prokaryotic organisms such as bacteria and viruses, homologous recombination occurs during horizontal gene transfer. This process involves the exchange of genetic material between different strains and species. Homologous recombination plays a crucial role in the evolution of these organisms by allowing for the acquisition of new traits and adaptations.
Overall, homologous recombination is a vital mechanism for DNA repair and genetic variation. It ensures the accuracy of DNA replication and contributes to the diversity of life on Earth.
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This question is part of the following fields:
- Basic Sciences
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Question 2
Correct
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While taking a patient's medical history, you discover that their family has a strong history of a certain disease. Autosomal dominant diseases are often caused by defects in structural genes and typically present in early adulthood, affecting both males and females equally. Which of the following diseases does not follow an autosomal dominant pattern of inheritance?
Your Answer: Haemochromatosis
Explanation:Abnormal Binding Proteins and Iron Deposition: A Genetic Disorder
Abnormal binding proteins can lead to the deposition of iron in the body, resulting in various health complications. This genetic disorder is inherited in an autosomal recessive manner. The deposition of iron can cause cardiomyopathy, cirrhosis, pancreatic failure due to fibrosis, and skin pigmentation.
In general, disorders that affect metabolism or DNA replication on a cellular or genetic level tend to be autosomal recessive. On the other hand, genetic disorders that affect the structure of the body on a larger level are usually autosomal dominant. While there may be exceptions to these rules, they can serve as a helpful guide for exam preparation. Proper of this genetic disorder can aid in its diagnosis and management.
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This question is part of the following fields:
- Basic Sciences
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Question 3
Correct
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What is the fundamental meaning of carbohydrate?
Your Answer: A compound following the formula Cx(H2O)y
Explanation:Carbohydrates: Building Blocks of Energy and Storage
Carbohydrates are organic compounds made up of carbon, hydrogen, and oxygen, with a general formula of Cx(H2O)y. They can be classified as either aldehydes or ketones and contain multiple hydroxyl groups. Monosaccharides are the simplest form of carbohydrates, consisting of a single unit. They are categorized based on the number of carbon atoms they contain, with trioses having three, pentoses having five, and hexoses having six carbon atoms. These monosaccharides are essential for energy production and building larger carbohydrate structures.
Disaccharides are formed when two monosaccharides are joined together through a condensation reaction, releasing a water molecule. The most common disaccharides are lactose, maltose, and sucrose. Polysaccharides, on the other hand, are long, branched polymers made up of multiple single units. They serve as convenient storage molecules for energy reserves, such as glycogen in humans and starch in plants.
In summary, carbohydrates are vital building blocks for energy production and storage in living organisms. Monosaccharides, disaccharides, and polysaccharides all play important roles in maintaining the body’s energy balance and overall health.
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This question is part of the following fields:
- Basic Sciences
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Question 4
Incorrect
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A 50-year-old female patient with varicose veins presents to the vascular clinic for evaluation.
During the assessment, a test is conducted to determine the location of incompetence. The patient is instructed to lie down, and the veins are emptied by elevating her legs off the couch. The examiner then identifies the site of the sapheno-femoral junction and applies pressure with their fingers. The patient is then asked to stand up to evaluate vein filling.
What is the name of this test?Your Answer: Perthe's test
Correct Answer: Trendelenburg's test
Explanation:Assessing Varicose Vein Site of Incompetence
The Trendelenburg and tourniquet tests are both used to evaluate the site of incompetence in varicose veins at the sapheno-femoral junction. During the Trendelenburg test, the examiner applies pressure with their fingers over the junction site, while in the tourniquet test, a tourniquet is placed just below the junction level.
If the veins fill quickly upon standing, it indicates that the sapheno-femoral junction is not the source of the incompetence. These tests are essential in determining the location of the varicose vein site of incompetence, which is crucial in planning the appropriate treatment. By identifying the site of incompetence, physicians can perform targeted interventions to improve venous function and alleviate symptoms. Therefore, the Trendelenburg and tourniquet tests are valuable tools in the diagnosis and management of varicose veins.
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This question is part of the following fields:
- Basic Sciences
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Question 5
Correct
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Over the last five years, the total number of patients admitted and deaths in the East and North Hertfordshire NHS Trust have been recorded. In the year 2010/2011, there were 95,071 patients admitted and 1,912 deaths. What is the crude mortality ratio for this group in that year (per 100 admissions)?
Your Answer: 2
Explanation:In this scenario, the crude mortality ratio is established by comparing the number of deaths occurring within the hospital in a given year to the total number of admissions, disregarding age or gender-specific mortality rates. For instance, with 1,912 deaths out of 95,071 admissions, the ratio computes to 0.02, or 2.0% when calculated per 100 admissions (1,912/95,071 = 0.02/100= 2.0%. When recalculated per 1,000 admissions, the crude admission rate would be 20 per 1,000.
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This question is part of the following fields:
- Basic Sciences
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Question 6
Incorrect
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Which statement regarding microtubules is accurate in relation to Chédiak-Higashi syndrome?
Your Answer: They have a fixed length
Correct Answer: They are arranged in a 9+2 formation in cilia
Explanation:Microtubules and Chédiak-Higashi Syndrome
Microtubules are made up of alpha and beta tubulin dimers that are arranged in a helix and can be added or removed to change the length. They are found in structures such as flagella, mitotic spindles, and cilia, where they have a 9+2 arrangement. These structures are important for cell movement and division. Chemotherapy agents, such as taxanes, target microtubules and are used in breast cancer treatment.
Chédiak-Higashi syndrome is a rare inherited immunodeficiency disorder caused by mutations in the LYST gene. This condition is characterized by neutrophil inclusions, albinism, recurrent infections, and peripheral neuropathy. The neutrophil inclusions are thought to be caused by abnormal microtubule function, which affects the immune system’s ability to fight infections. While there is no cure for Chédiak-Higashi syndrome, treatment focuses on managing symptoms and preventing infections.
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This question is part of the following fields:
- Basic Sciences
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Question 7
Correct
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A premature baby is born and the anaesthetists are struggling to ventilate the lungs because of insufficient surfactant. How does Laplace's law explain the force pushing inwards on the walls of the alveolus caused by surface tension between two static fluids, such as air and water in the alveolus?
Your Answer: Inversely proportional to the radius of the alveolus
Explanation:The Relationship between Alveolar Size and Surface Tension in Respiratory Physiology
In respiratory physiology, the alveolus is often represented as a perfect sphere to apply Laplace’s law. According to this law, there is an inverse relationship between the size of the alveolus and the surface tension. This means that smaller alveoli experience greater force than larger alveoli for a given surface tension, and they will collapse first. This phenomenon explains why, when two balloons are attached together by their ends, the smaller balloon will empty into the bigger balloon.
In the lungs, this same principle applies to lung units, causing atelectasis and collapse when surfactant is not present. Surfactant is a substance that reduces surface tension, making it easier to expand the alveoli and preventing smaller alveoli from collapsing. Therefore, surfactant plays a crucial role in maintaining the proper functioning of the lungs and preventing respiratory distress. the relationship between alveolar size and surface tension is essential in respiratory physiology and can help in the development of treatments for lung diseases.
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This question is part of the following fields:
- Basic Sciences
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Question 8
Correct
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The arrangement of amphipathic phospholipids in the mammalian cell membrane, what is it like?
Your Answer: A lipid bilayer with hydrophilic heads facing out and hydrophobic tails facing in
Explanation:The Function and Structure of the Mammalian Cell Membrane
The mammalian cell membrane serves as a protective barrier that separates the cytoplasm from the extracellular environment. It also acts as a filter for molecules that move across it. Unlike plant and prokaryotic cells, mammalian cells do not have a cell wall. The main component of the cell membrane is a bilayer of amphipathic lipids, which have a hydrophilic head and a hydrophobic tail. The phospholipids in the bilayer are oriented with their hydrophilic heads facing outward and their hydrophobic tails facing inward. This arrangement allows for the separation of the watery extracellular environment from the watery intracellular compartment.
It is important to note that the cell membrane is not a monolayer and the phospholipids are not linked head-to-tail. This is in contrast to DNA, which has a helical chain formation. Overall, the structure and function of the mammalian cell membrane are crucial for maintaining the integrity and proper functioning of the cell.
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This question is part of the following fields:
- Basic Sciences
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Question 9
Correct
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What is the conversion of pyruvate before it enters the Krebs cycle?
Your Answer: Acetyl-CoA
Explanation:The Krebs cycle occurs in the mitochondrion and involves the conversion of acetyl-CoA to oxaloacetate. This cycle produces six NADH, two FADH, and two ATP for each molecule of glucose. Pyruvate is converted to acetyl-CoA before entering the Krebs cycle, and water and carbon dioxide are end products. Acetic acid itself has no role in the cycle, but its acetyl group is used to form acetyl-CoA. Some anaerobic bacteria can convert sugars to acetic acid directly.
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This question is part of the following fields:
- Basic Sciences
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Question 10
Incorrect
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Which form of vitamin D is the most active in the human body?
Your Answer: Cholecalciferol
Correct Answer: 1, 25 (OH) 2 vitamin D
Explanation:The Process of Vitamin D Production and Activation
Vitamin D comes in two forms, D2 and D3. D3 can be produced in the skin through a reaction that requires UV light, while D2 cannot. Both forms can also be obtained through diet, with some foods now being supplemented with Vitamin D. However, the production of Vitamin D3 in the skin can be affected by various factors such as seasons, latitude, clothing, sun block, and skin tone, making it difficult for individuals to get adequate levels of Vitamin D through sunlight alone, especially in the UK during winter.
Once absorbed into the lymph, Vitamin D2 and D3 circulate in the bloodstream and reach the liver. Here, the liver enzyme 25-hydroxylase adds an OH group to the Vitamin D molecule, resulting in 25(OH) Vitamin D. The compound then travels to the kidney, where the enzyme 1-alpha hydroxylase adds another OH group, creating the active form of Vitamin D, 1,25 (OH)2Vitamin D. When there is enough of this active form, an inactive metabolite called 24,25 (OH)2Vitamin D is produced instead. this process is important in ensuring adequate Vitamin D levels for overall health and well-being.
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This question is part of the following fields:
- Basic Sciences
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Question 11
Correct
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A premature baby is born and the anaesthetists are struggling to ventilate the lungs because of insufficient surfactant. How does Laplace's law explain the force pushing inwards on the walls of the alveolus caused by surface tension between two static fluids, such as air and water in the alveolus?
Your Answer: Inversely proportional to the radius of the alveolus
Explanation:The Relationship between Alveolar Size and Surface Tension in Respiratory Physiology
In respiratory physiology, the alveolus is often represented as a perfect sphere to apply Laplace’s law. According to this law, there is an inverse relationship between the size of the alveolus and the surface tension. This means that smaller alveoli experience greater force than larger alveoli for a given surface tension, causing them to collapse first. This phenomenon is similar to what happens when two balloons of different sizes are attached together, with the smaller balloon emptying into the larger one.
In the lungs, this collapse of smaller alveoli can lead to atelectasis and collapse if surfactant is not present. Surfactant is a substance that reduces surface tension, making it easier to expand the alveoli and preventing smaller alveoli from collapsing. this relationship between alveolar size and surface tension is crucial in respiratory physiology, as it helps explain the importance of surfactant in maintaining proper lung function.
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This question is part of the following fields:
- Basic Sciences
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Question 12
Correct
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What occurs in eukaryotic prometaphase?
Your Answer: The nuclear membrane and the nucleoli disintegrate and kinetochores appear
Explanation:The Significance of Prometaphase in Cell Division
Prometaphase is a crucial phase in cell division that marks the transition from prophase to metaphase. Although it is often considered as a part of these two phases, it has distinct events that make it an individual phase. During prometaphase, the nuclear membrane disintegrates, and the nucleoli are no longer visible. Additionally, each chromosome forms two kinetochores near the centromere, which serve as attachment points for spindle fibers. These fibers connect to the opposite poles of the cell, forming travelling lines that will separate the sister chromatids during anaphase.
Prophase is characterized by chromatin condensation, while DNA and centrosome duplication occur during interphase. Chromosome alignment takes place during metaphase, and the sister chromatids separate during anaphase. Prometaphase, therefore, plays a crucial role in preparing the chromosomes for separation during anaphase. Its distinct events make it an essential phase in cell division, and its proper execution is necessary for successful cell division.
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This question is part of the following fields:
- Basic Sciences
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Question 13
Correct
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What is the primary function of riboflavin in the B vitamin group?
Your Answer: Mopping up free radicals
Explanation:The Role of Riboflavin in the Body
Riboflavin, also known as vitamin B2, is a B-vitamin that plays a crucial role in the body. One of its functions is to act as an antioxidant, mopping up free radicals that can cause damage to cells. However, if the metabolites formed during this process are not excreted promptly, the free radicals can be generated again. Riboflavin is also involved in the production of blue-light sensitive pigments in the eye, which help establish the circadian rhythm. This function is not related to visual acuity.
Riboflavin is found in a variety of foods, including milk and offal. Deficiency of this vitamin is rare, but when it does occur, it can cause non-specific effects on the skin and mucous membranes. There is no evidence of clear long-lasting damage from riboflavin deficiency. Overall, riboflavin is an important nutrient that plays a vital role in maintaining good health.
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This question is part of the following fields:
- Basic Sciences
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Question 14
Correct
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At what stage of eukaryotic mitosis do the centromeres of chromosomes separate?
Your Answer: Anaphase
Explanation:Chromosome Division during Anaphase
Chromosomes are joined together in an X shape at the centromere. During anaphase, the centromeres break down and the chromosomes divide into two identical pairs called sister chromatids. These sister chromatids then move to opposite sides of the cell along a network of spindle fibres. When the cell divides during telophase, each daughter cell receives one sister chromatid from the parent cell. This ensures the accurate copying and propagation of genes. The process of chromosome division during anaphase is crucial for the proper distribution of genetic material in cells.
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This question is part of the following fields:
- Basic Sciences
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Question 15
Correct
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A couple in their late 30s come to the clinic seeking information about the risk of their three children inheriting Huntington's disease. The husband has recently been diagnosed with the disease, while the wife is not affected. What is the likelihood, expressed as a percentage, that their children will inherit the disease?
Your Answer: 50%
Explanation:Huntington’s Disease
Huntington’s disease is a genetic disorder that typically appears later in life and is characterized by symptoms such as chorea, cognitive decline, and personality changes. It is an autosomal dominant disease, meaning that there is a 50% chance of passing it on to offspring. If the gene is inherited from an unaffected parent, the child will not be affected. This is different from autosomal recessive inheritance, where both parents must pass on the gene for it to affect their children.
The disease is caused by an increase in the length of a repeating trinucleotide sequence (CAG) in the Huntington protein. This sequence can change in length through generations, and longer sequences are associated with earlier onset of symptoms (genetic anticipation). Since Huntington’s disease usually presents itself after people have already started their families, there are many issues associated with genetic testing.
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This question is part of the following fields:
- Basic Sciences
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Question 16
Correct
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What RNA base pairs with adenine when synthesizing a complementary RNA strand from DNA, using RNA polymerase to split the helix at specific points?
Your Answer: Uracil
Explanation:Differences between DNA and RNA
DNA and RNA differ in several ways. The primary sugar in DNA is deoxyribose, while in RNA it is ribose. Additionally, DNA is double stranded, while RNA is single stranded. This single stranded structure with un-paired bases allows for transcription to occur when the DNA bases are freed. Each base has a specific pairing, with guanine always binding to cytosine and adenine always binding to thymine in the DNA strand. During transcription, the same complementary RNA bases assemble with the DNA bases, except for thymine, which is not an RNA base. Instead, uracil serves as the RNA pyrimidine base equivalent of thymine. Finally, lysine is an amino acid coded for by the RNA base triplet AAA, where A represents adenine.
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This question is part of the following fields:
- Basic Sciences
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Question 17
Correct
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In scientific experimentation, what is the term used to describe the movement of charged particles or solutes in a liquid medium due to an electric field?
Your Answer: Electrophoresis
Explanation:Electrophoresis: Separating Molecules Based on Charge and Mass
Electrophoresis is a technique that separates solutes, molecules, or nucleic acids based on their mass and charge. It involves the migration of charged particles in a liquid medium under the influence of an electric field. The apparatus consists of two electrodes placed at either end of a support medium, or gel, which is suspended in a buffer solution. The sample is inserted into a well and a current is applied. Over time, positively charged solutes move towards the negative electrode, while negatively charged substances move towards the positive electrode. Once the migration is complete, the gel is removed and stained to color the substance being tested for, such as protein.
This technique is widely used in medical testing, but it requires a higher degree of operational and interpretive skill than many other tests, which is why it often takes longer to get a result. Electrophoresis has various uses and adaptations, such as standard electrophoresis for protein detection in the diagnosis of myeloma, identification of unusual lipid fractions in patients with inherited diseases, and detection of viral DNA through Southern Blotting. There is also Northern blotting, primarily a research technique at present, which uses electrophoresis to separate RNA. Additionally, Western blotting is used to test for the presence of antibodies to DNA through protein separation.
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This question is part of the following fields:
- Basic Sciences
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Question 18
Incorrect
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What is the primary reason for malnutrition?
Your Answer: Inadequate intake of multiple vitamins
Correct Answer: Inadequate intake of calories in any form
Explanation:Malnutrition
Malnutrition refers to a state where the dietary intake is insufficient to maintain a healthy state and stable weight. It can be caused by over- or under-nutrition, but it is commonly used to describe under-nutrition. Malnutrition can be defined as a state of nutrition where a deficiency, excess, or imbalance of energy, protein, and other nutrients causes measurable adverse effects on tissue, function, and clinical outcome. Protein malnutrition is the most severe form of malnutrition, causing significant mortality and clinical effects such as kwashiorkor. Carbohydrate malnutrition is less common as carbohydrate sources are widely grown and cheap. Fat malnutrition rarely results in problems if there is adequate dietary protein and carbohydrate. Deficiencies of fat-soluble vitamins can result in various clinical effects. Body size can give some indication of nutritional status, but many obese patients may have nutritional deficiencies due to their faddy diets.
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This question is part of the following fields:
- Basic Sciences
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Question 19
Incorrect
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What is the estimated percentage of oxygen in the blood that is attached to haemoglobin?
Your Answer: 80%
Correct Answer: 100%
Explanation:Calculation of Oxygen in Blood
The majority of oxygen in the blood is bound to haemoglobin, with the exact amount varying based on the oxygen saturation and haemoglobin level. To calculate the amount of oxygen per litre of blood, the formula (13.9 × Hb × sats/100) + (PaO2 × 0.03) can be used. For example, an average man with an Hb of 14, saturations of 98% on room air, and a PaO2 of 12 would have 191 ml of oxygen per litre of blood. It is important to note that only 0.36 ml of this oxygen is dissolved in the blood.
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This question is part of the following fields:
- Basic Sciences
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Question 20
Correct
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What role does the nucleolus play in eukaryotic cells?
Your Answer: To transcribe ribosomal RNA and assemble ribosomes
Explanation:The Nucleolus: Structure and Function
The nucleolus is a non-membrane-bound structure that takes up about a quarter of the nuclear volume. It is composed mainly of proteins and nucleic acids and is responsible for transcribing ribosomal RNA (rRNA) and assembling ribosomes in the cell. Nucleoli are formed in nucleolar organizing regions (NORs), which are also the regions of the genes for three of the four eukaryotic rRNAs.
During ribosome assembly, ribosomal proteins enter the nucleolus from the cytoplasm and begin to assemble on an rRNA precursor. As the pre-rRNA is cleaved to produce 5.8S, 18S, and 28S rRNAs, additional ribosomal proteins and the 5S rRNA (which is synthesized elsewhere in the nucleus) assemble to form preribosomal subunits. These subunits then exit the nucleolus into the cytoplasm and combine to produce the final 40S and 60S ribosomal subunits.
Overall, the nucleolus plays a crucial role in protein synthesis by producing the components necessary for ribosome assembly. Its unique structure and function make it an essential component of the cell’s machinery.
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This question is part of the following fields:
- Basic Sciences
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Question 21
Incorrect
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What is the apoptotic event that occurs just before the formation of an apoptosome?
Your Answer: Binding of small mitochondria-derived activators of caspases (SMACs) to inhibitor of apoptosis proteins (IAPs)
Correct Answer: Release of cytochrome c from mitochondria
Explanation:Apoptosis and the Role of the Apoptosome
Apoptosis, also known as programmed cell death, is a natural process that occurs in all multicellular organisms. It involves a series of changes in cell morphology, including membrane blebbing, cell shrinkage, nuclear fragmentation, chromatin condensation, and chromosomal DNA fragmentation. The formation of the apoptosome is a crucial part of the apoptosis cascade. It is a large protein structure that is triggered by the release of cytochrome c from the mitochondria in response to various stimuli, such as DNA damage, infections, or developmental signals.
The apoptosome is formed when cytochrome c binds to Apaf-1, a cytosolic protein, in a 1:1 ratio. This triggers the recruitment and activation of the initiator pro-caspase-9, which then activates effector caspases, a family of apoptotic proteases, to initiate the apoptotic cascade. It is important to note that the activation of caspase-9 occurs only after the formation of the apoptosome.
In summary, apoptosis is a natural process that occurs in multicellular organisms, and the apoptosome plays a crucial role in triggering the apoptotic cascade. the mechanisms behind apoptosis and the formation of the apoptosome can provide insights into various diseases and developmental processes.
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This question is part of the following fields:
- Basic Sciences
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Question 22
Correct
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A 40-year-old male complains of a painful and swollen right calf. The possibility of deep vein thrombosis (DVT) is being considered. What tests should be conducted to confirm the diagnosis?
Your Answer: Dopplers of the leg veins
Explanation:Diagnostic Methods for Deep Vein Thrombosis
When it comes to diagnosing deep vein thrombosis (DVT), there are several methods available. The most common ones are Doppler studies and venography. Doppler studies use B mode ultrasonography to examine the venous system, while venography involves injecting a contrast dye into the veins and taking X-rays. CT scans are not typically used for DVT diagnosis because they require contrast and expose the patient to radiation. D-Dimer concentrations can help rule out DVT if they are negative, but they cannot diagnose it. MRI scans are useful for examining soft tissues and bones, but they are not the best option for visualizing the vasculature. Finally, oxygen saturation of the limbs is not a reliable diagnostic method because tissue perfusion can be the same even if there is arterial disease. Overall, Doppler studies and venography are the most effective methods for diagnosing DVT.
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This question is part of the following fields:
- Basic Sciences
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Question 23
Correct
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What function does vitamin E serve in the body?
Your Answer: Antioxidant
Explanation:Vitamin E and its Functions
Several substances are classified as vitamin E, with alpha-tocopherol being the most common, accounting for 90% of human vitamin E. Alpha-tocopherol is composed of two carbon rings and a long saturated hydrocarbon chain, making it hydrophobic. It has an aromatic ring with an OH- group attached to it. Other substances with vitamin E activity include other tocopherols and tocotrienols, all of which act as antioxidants. Alpha-tocopherol is particularly important in cell membranes, preventing the peroxidation of unsaturated fatty acids by free radicals. It also has other functions, such as regulating gene transcription, inhibiting clotting formation, reducing proliferation of vascular smooth muscle, and playing a role in immunity.
Despite claims that taking vitamin E can reduce the risk of heart disease, cancer, and enhance sexual performance, there is currently no strong evidence to support these claims.
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This question is part of the following fields:
- Basic Sciences
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Question 24
Incorrect
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What significance do linoleic and alpha-linolenic acids hold?
Your Answer: They are omega-3 fatty acids
Correct Answer: They are essential fatty acids
Explanation:The Importance of Essential Fatty Acids in the Diet
Essential fatty acids, such as linoleic and alpha-linolenic acids, are crucial components of a healthy diet. Although they are only required in small amounts, they play several important roles in the body. These fatty acids are necessary for the synthesis of phospholipids, which are essential components of cell membranes. They also help regulate cholesterol transport and synthesis, and serve as precursors for omega-3 fatty acids and arachidonic acid. Additionally, essential fatty acids are important for the synthesis of prostaglandins, leukotrienes, and thromboxanes.
A lack of adequate essential fatty acids in the diet can have negative consequences, particularly for brain growth in infancy. It can also lead to alopecia, dermatitis, and fatty liver. Therefore, it is important to ensure that the diet includes sources of these essential fatty acids, such as certain types of fish, nuts, and seeds. By doing so, individuals can support their overall health and well-being.
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This question is part of the following fields:
- Basic Sciences
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Question 25
Incorrect
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What is the term for the process described below in laboratory testing?
Enzymes are immobilised on a solid surface, such as a bead or well, and allowed to come into contact with the sample. After washing, another enzyme is added with a label allowing quantitation of the analyte.Your Answer: Sandwich assay
Correct Answer: Enzyme-linked immunosorbent assay
Explanation:ELISA: A Common Immunoassay in Medical Diagnostic Testing
An enzyme-linked immunosorbent assay (ELISA) is a type of immunoassay that is widely used in medical diagnostic testing. This method uses antibodies to identify and/or quantify the analyte being tested. The ELISA process involves several steps, including coating a plate with the antigen, adding the patient’s sample, washing the plate to remove any unbound material, adding an enzyme-linked antibody, washing the plate again, and adding a substrate to produce a measurable signal.
Over time, many modifications have been made to the ELISA, making it a versatile tool in the laboratory for measuring various analytes. Some of the substances that can be measured using immunoassays include thyroid hormone, testosterone, oestrogen, troponin, and vitamin D. The ELISA has been around for a long time and is still widely used today due to its accuracy, sensitivity, and specificity.
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This question is part of the following fields:
- Basic Sciences
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Question 26
Correct
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What is the statement of Henry's law?
Your Answer: The concentration of a gas when dissolved in liquid is proportional to its partial pressure
Explanation:Gas Laws
Gas laws are a set of scientific principles that describe the behavior of gases under different conditions. One of these laws is Avogadro’s law, which states that equal volumes of gases at a standardized temperature and pressure contain the same number of molecules. Another law is Boyle’s law, which explains that gases expand when the temperature is increased. Charles’ law, on the other hand, states that the pressure of a gas is inversely proportional to its volume at a standardized temperature. Lastly, Graham’s law explains that the rate of diffusion of a gas is in inverse proportion to its weight. The specific gas laws that you need to know may vary depending on your syllabus, but you should be able to recognize and apply them if given the formulae. It is unlikely that you will be expected to know the correct formula.
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This question is part of the following fields:
- Basic Sciences
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Question 27
Correct
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What occurs in eukaryotic prophase?
Your Answer: Chromatin condenses into chromosomes
Explanation:The Stages of Prophase in Eukaryotic Mitosis
Prophase is the first stage of eukaryotic mitosis, except for plant cells which have a preprophase stage. During prophase, the cell’s chromatin, which is made up of DNA and associated proteins, condenses into double rod-shaped structures called chromosomes. This process is facilitated by the condensin protein I and/or II complexes. As the chromosomes form, the nuclear membrane and nucleoli disintegrate and disappear, making the chromatin visible.
Before prophase, the cell’s DNA is replicated during interphase, resulting in identical pairs of chromosomes called chromatids. These chromatids attach to each other at a DNA element called the centromere. DNA and centrosome duplication occur during interphase, while chromosome alignment takes place during metaphase. The nuclear membrane and nucleoli re-form during telophase, and the sister chromatids separate during anaphase.
In summary, prophase is the initial stage of eukaryotic mitosis where chromatin condenses into chromosomes, and the nuclear membrane and nucleoli disappear. Chromosome alignment, DNA and centrosome duplication, and re-formation of the nuclear membrane and nucleoli occur in subsequent stages.
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This question is part of the following fields:
- Basic Sciences
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Question 28
Incorrect
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A 50-year-old female patient presents to the vascular clinic for evaluation of varicose veins. During the assessment, a test is conducted to determine the site of incompetence. The patient is instructed to lie down, and her legs are raised to empty the veins. A constricting band is then placed below the sapheno-femoral junction, and the patient is asked to stand up to observe for varicose vein filling. What is the name of this test?
Your Answer: Trendelenburg's test
Correct Answer: Tourniquet test
Explanation:Tests for Varicose Veins and Arterial Insufficiency
The Trendelenburg and tourniquet tests are both used to evaluate the site of incompetence in varicose veins at the sapheno-femoral junction. During the Trendelenburg test, the examiner applies pressure with their fingers over the junction, while in the tourniquet test, a tourniquet is placed just below the junction. If the veins fill rapidly upon standing, it suggests that the sapheno-femoral junction is not the source of the incompetence.
Buerger’s test is used to assess the arterial circulation of the lower limb. The lower the angle at which blanching occurs, the more likely there is arterial insufficiency. This test is important in diagnosing peripheral artery disease.
The ankle-brachial pressure index (ABPI) is another test used to assess arterial insufficiency. Blood pressure cuffs are used to measure the systolic blood pressure in the ankle and arm. The ratio of the two pressures is calculated, and a lower ratio indicates a higher degree of claudication.
Finally, Perthe’s test is used to assess the patency of the deep femoral vein before varicose vein surgery. This test involves compressing the vein and observing the filling of the superficial veins. If the superficial veins fill quickly, it suggests that the deep femoral vein is patent and can be used for surgery.
In summary, these tests are important in diagnosing and evaluating varicose veins and arterial insufficiency. They help healthcare professionals determine the best course of treatment for their patients.
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This question is part of the following fields:
- Basic Sciences
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Question 29
Incorrect
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What is the most common method of assessing nutritional status in adults?
Your Answer: Albumin on blood testing
Correct Answer: Body mass index
Explanation:The Body Mass Index as a Measure of Nutritional Status
The measurement and assessment of nutritional status can be challenging, and there is no single test that can provide a complete picture. However, the body mass index (BMI) is a commonly used measurement in clinical practice. The BMI is calculated by dividing a person’s weight in kilograms by their height in meters squared. This measure is used to assess adiposity and nutritional status, and it is simple and quick to calculate and interpret.
Although the BMI is a convenient measure, it has limitations for assessing obesity in individual patients. It is best used to track trends in an individual patient’s BMI over time. In some cases, the BMI may overestimate fat mass in patients who are very tall or have a high proportion of lean tissue due to an active lifestyle. Additionally, the BMI may not be accurate for athletes and children.
Other measurements, such as skin fold thickness and weight, can also be useful, but the BMI is generally considered the better option. The ponderal index is used specifically for children. It is important to note that albumin is not a reliable marker of nutritional status, as it can also be affected by inflammation.
Overall, the BMI is a widely used measure of nutritional status and is recommended by the World Health Organization. However, it is important to consider its limitations and use it in conjunction with other measurements to obtain a more complete picture of a patient’s nutritional status.
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This question is part of the following fields:
- Basic Sciences
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Question 30
Correct
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What is the end result of meiosis in a cell?
Your Answer: 4 haploid cells
Explanation:Meiosis
Meiosis is a crucial process that occurs in the genetic cells of eukaryotic organisms. Its primary purpose is to recombine genes, which results in genetic variation while also ensuring genetic preservation. Although meiosis shares some similarities with mitosis, it is restricted to genetic cells, also known as gametes, of eukaryotic organisms.
During meiosis, a gamete duplicates each of its chromosomes and divides into two diploid cells. These cells then divide into four haploid cells by the end of the second stage of meiosis (telophase II and cytokinesis). These haploid cells are either sperm cells (male) or eggs (female) in mammals. When these haploid cells fuse together, they produce a diploid zygote that contains two copies of parental genes.
In summary, meiosis is a crucial process that ensures genetic variation and preservation in eukaryotic organisms. It involves the duplication and division of genetic cells into haploid cells, which can then fuse together to produce a diploid zygote.
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This question is part of the following fields:
- Basic Sciences
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