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Question 1
Correct
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What is the primary factor that increases the risk of thiamine (vitamin B1) deficiency?
Your Answer: Chronic alcohol excess
Explanation:Thiamine: Its Roles, Sources, Deficiency States, and Manifestations
Thiamine is a vital nutrient that plays several roles in the body. It acts as a cofactor to enzymes involved in energy production, metabolism of branched chain amino acids, and regulation of nerve and muscle action potentials. It is found in many foods, including wheat, oats, and yeast-containing products. However, deficiency states can occur in chronic alcohol dependence, renal dialysis, and cultures that mainly consume white rice. The deficiency can manifest as ‘dry’ beriberi, which causes peripheral neuropathy, muscle weakness, fatigue, and reduced concentration, or ‘wet’ beriberi, which also involves heart failure and edema. In severe cases, Wernicke-Korsakoff syndrome can develop, which is an emergency requiring urgent IV replacement of thiamine. If left untreated, it can lead to irreversible amnesia, confabulation, and dementia. Therefore, all patients with alcohol-related admissions should be considered for Pabrinex, a B vitamin infusion.
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This question is part of the following fields:
- Basic Sciences
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Question 2
Incorrect
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What are the potential clinical consequences of a lack of vitamin E?
Your Answer: Premature dementia
Correct Answer: Ataxia
Explanation:Vitamin E Deficiency
Vitamin E deficiency is a rare condition that is more likely to occur in individuals with problems affecting the absorption of dietary fats. This includes those with a history of bowel surgery, pancreatic insufficiency, and cystic fibrosis. Premature infants are also at a higher risk of developing this deficiency as vitamin E does not easily cross the placenta. However, supplementation with vitamin E can reverse the damage in some cases.
The effects of vitamin E deficiency can be severe and can cause spinocerebellar degeneration, which includes limb ataxia, loss of joint position sense, loss of sensation of vibration, and loss of deep tendon reflexes. Additionally, it can cause degeneration of retinal pigments, leading to blindness. In premature infants, it can cause haemolytic anaemia, thrombocytosis, and oedema.
Overall, vitamin E deficiency is crucial in preventing and treating its effects. It is important to identify individuals who are at a higher risk of developing this deficiency and provide them with appropriate supplementation to prevent any long-term damage.
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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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The Krebs or TCA cycle is a series of metabolic processes beginning with the synthesis of citrate from acetyl-CoA which results in a number of important metabolic products. Where in the cell does this cycle occur?
Your Answer: Mitochondria
Explanation:Cellular Processes and Organelles
Metabolic processes in the cell occur in specific locations. Acetyl-CoA production and the Krebs cycle take place in the mitochondrium, while glycolysis occurs in the cytoplasm. The nucleus is the central structure of the cell that contains DNA and is double membrane-bound. The rough endoplasmic reticulum is responsible for packaging and transporting proteins, while the smooth endoplasmic reticulum performs a similar function but lacks ribosomes.
It is important to understand where these processes occur in the cell to better understand their functions and how they contribute to the overall functioning of the cell. The mitochondrium is responsible for producing energy in the form of ATP, while the cytoplasm is where glucose is broken down during glycolysis. The nucleus is where genetic information is stored and replicated, and the endoplasmic reticulum is involved in protein synthesis and transport.
In summary, the cell is a complex system with various organelles that perform specific functions. where these processes occur in the cell is crucial to how they contribute to the overall functioning of the cell.
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This question is part of the following fields:
- Basic Sciences
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Question 4
Correct
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Which process occurs mainly in the smooth endoplasmic reticulum?
Your Answer: Steroid synthesis
Explanation:The Functions of Endoplasmic Reticulum and Lysosomes
The endoplasmic reticulum (ER) is a complex network of membranes that is divided into two types: rough and smooth. The rough ER is characterized by the presence of ribosomes on its cytosolic side, which makes it an important site for protein production, modification, and transport. On the other hand, the smooth ER is involved in cholesterol and steroid handling, as well as calcium storage in some cells. This type of ER is particularly prominent in cells that produce large amounts of steroid hormones, such as those found in the adrenal cortex.
Lysosomes, on the other hand, are organelles that are responsible for breaking down and recycling cellular waste. They are formed by the Golgi apparatus, which is another complex network of membranes found in eukaryotic cells. Lysosomes contain a variety of enzymes that are capable of breaking down different types of molecules, including proteins, lipids, and carbohydrates.
In summary, the ER and lysosomes are two important organelles in eukaryotic cells that play different roles in cellular metabolism. While the ER is involved in protein production, modification, and transport, the lysosomes are responsible for breaking down and recycling cellular waste.
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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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Which food is a rich source of vitamin D in the diet?
Your Answer: Oily fish
Explanation:Sources of Vitamin D
Vitamin D is a type of fat-soluble vitamin that can be found in certain foods such as cheese, butter, eggs, and oily fish. However, vegetable sources of vitamin D are limited, although some foods are fortified with this vitamin. For instance, 100 grams of sundried shiitake mushrooms contain 1600 IU of vitamin D, while one egg contains 20 IU. Wild salmon is also a good source of vitamin D, with 100 grams containing 800 IU, while farmed salmon contains 200 IU.
Aside from food sources, sunlight is also a good source of vitamin D. Exposure of arms and legs to sunlight for 10-15 minutes can provide 3000 IU of vitamin D. However, it is difficult to obtain the daily requirement of 25-50 IU of vitamin D through sunlight alone, especially for people living in temperate climates. As a result, many people may have insufficient vitamin D levels. It is important to ensure that we get enough vitamin D through a combination of food sources and sunlight exposure.
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This question is part of the following fields:
- Basic Sciences
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Question 6
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 7
Incorrect
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What is the estimated percentage of oxygen in the blood that is attached to haemoglobin?
Your Answer: 60%
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 8
Incorrect
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What is the primary function of riboflavin in the B vitamin group?
Your Answer: Nervous transmission
Correct 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 9
Incorrect
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Which form of vitamin D is the most active in the human body?
Your Answer: 24,25 (OH) 2 vitamin D
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 10
Correct
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During which phase of aerobic respiration is FADH2 generated?
Your Answer: Krebs cycle
Explanation:The Krebs Cycle and the Role of FADH2
The Krebs cycle is a crucial part of aerobic respiration in cells. It involves a series of reactions that convert acetate, derived from carbohydrates, fats, and proteins, into carbon dioxide and energy in the form of ATP. Additionally, the Krebs cycle produces precursors for some amino acids and reducing agents like NADH and FADH2 that are involved in other metabolic pathways.
FAD is a redox cofactor that plays a vital role in the Krebs cycle. It receives two electrons from the sixth reaction of the cycle, where succinate dehydrogenase converts succinate into fumarate by removing two hydrogen atoms and attaching them onto FAD. This process results in FAD gaining two electrons and reducing into FADH2.
FADH2 then donates the electrons to the electron transport chain, which is another part of cellular respiration. This mechanism helps compensate for the relatively low amount of ATP produced by the Krebs cycle (2.5 molecules of ATP per turn) compared to the electron transport chain (26-28 molecules of ATP). Overall, the Krebs cycle and the role of FADH2 are essential for generating energy in cells.
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This question is part of the following fields:
- Basic Sciences
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Question 11
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: Buerger'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 12
Incorrect
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What are the typical clinical manifestations of a deficiency in vitamin B6 (pyridoxine)?
Your Answer: Renal impairment
Correct Answer: Sensory neuropathy
Explanation:The Importance of Pyridoxine in the Body
Pyridoxine is a group of B-vitamins that are crucial in various bodily functions. They act as essential cofactors in many reactions, particularly in the metabolism of amino acids and neurotransmitters. Pyridoxine also plays a role in regulating gene transcription and controlling steroid hormones.
The body can produce pyridoxine through bacterial flora in the gut, and it is also present in many dietary sources. However, overheating certain foods can destroy pyridoxine, and some medications can alter its metabolism. Pyridoxine is also used therapeutically to prevent neuropathy in the treatment of tuberculosis.
Deficiency in pyridoxine can lead to sensory neuropathy, skin changes, and damage to mucous membranes. On the other hand, deficiency in vitamin C can cause gingivitis and increased bleeding, while vitamin K deficiency can also lead to bleeding. Sleep disturbance is rarely attributed to vitamin B3 (niacin) deficiency.
In summary, pyridoxine is a vital nutrient that plays a crucial role in various bodily functions. Its deficiency can lead to various health problems, highlighting the importance of maintaining adequate levels of this vitamin in the body.
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This question is part of the following fields:
- Basic Sciences
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Question 13
Incorrect
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As part of your general practice placement, you have been tasked with conducting an audit on the duration of solid food introduction in the practice population. You review the data for the last six infants born within the practice:
6 months, 7 months, 8 months, 9 months, 10 months, 11 months.
What is the variance value for the duration of solid food introduction in the practice population?Your Answer: 8.6
Correct Answer: 74.9
Explanation:Variance and Standard Deviation in Breast Feeding Duration
Variance is a statistical measure that indicates how spread out a set of data is. In the case of breast feeding duration, variance can help us understand how much the duration varies from the mean. The formula for variance involves squaring the difference between each data point and the mean, then dividing the sum by n-1, where n is the total number of data points. In a sample population, n-1 is a better estimate of variance than n because it accounts for the variability within the sample.
For example, if the variance of breast feeding duration is 74.9 months, this indicates that the duration is widely distributed from the mean of 17.6 months. A smaller variance, such as 4.5 months, would indicate that the duration varies less and is closer to the mean. The standard deviation, which is the square root of the variance, is also important in the spread of data. In a normal distribution, 95% of observations will fall within two standard deviations of the mean.
In the case of breast feeding duration, the mean is 17.6 months, indicating that babies are breast fed for an average of 15 and a half months. The median, which is the middle number in the data set, is 15 months, meaning that half of the babies were breast fed for 15 months. variance and standard deviation can help us better understand the distribution of breast feeding duration and other medical measurements.
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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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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 15
Correct
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What are the clinical effects that can occur due to acute or chronic over-administration of multivitamins leading to Vitamin A toxicity?
Your Answer: Nausea, vomiting and headaches
Explanation:The Importance and Risks of Vitamin A
Vitamin A is an essential nutrient that plays a crucial role in various bodily functions such as growth and development, vision, enzyme signalling pathways, and the maintenance of epithelial membranes. However, excessive intake of vitamin A can lead to toxicity, which can cause several adverse effects. These include raised intracranial pressure resulting in headaches, nausea, vomiting, and visual loss, increased bone resorption leading to osteoporosis and hypercalcaemia, liver damage, hair loss, and skin changes. Moreover, there is a possible increased risk of malignancy, particularly among smokers. Pregnant women are also advised to avoid foods rich in vitamin A, such as liver and fish oils, due to the teratogenicity of vitamin A-derived drugs. Therefore, it is crucial to maintain a balanced intake of vitamin A to avoid the risks associated with its toxicity.
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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 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 17
Correct
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What are the defining features of an amino acid?
Your Answer: It has the formula H2N - CHR - COOH where R is the variable group
Explanation:The Versatility of Amino Acids and its Applications in Electrophoresis
Amino acids are the building blocks of proteins and are composed of a basic structure of H2N – CHR – COOH, where R represents the variable group that distinguishes one amino acid from another. The simplest amino acid is glycine, where the R group is just H. Amino acids are capable of forming complex and useful molecules due to their dipolar or amphoteric nature, which makes them simultaneously acidic and basic. In solution, they form zwitterions, which can act as either an acid or a base depending on the pH of the solution. This versatility of amino acids is what allows for the process of electrophoresis, which separates proteins based on their charge in a solution. By using solutions of different pH, different proteins can be assessed, making it a useful tool in the diagnosis of bone marrow malignancies like myeloma.
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This question is part of the following fields:
- Basic Sciences
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Question 18
Correct
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What is the final product of glycolysis besides ATP?
Your Answer: Pyruvate
Explanation:Glycolysis: The Energy-Producing Reaction
Glycolysis is a crucial energy-producing reaction that converts glucose into pyruvate while releasing energy to create ATP and NADH+. It is one of the three major carbohydrate reactions, along with the citric acid cycle and the electron transport chain. The reaction involves ten enzymatic steps that provide entry points to glycolysis, allowing for a variety of starting points. The most common starting point is glucose or glycogen, which produces glucose-6-phosphate.
Glycolysis occurs in two phases: the preparatory (or investment) phase and the pay-off phase. In the preparatory phase, ATP is consumed to start the reaction, while in the pay-off phase, ATP is produced. Glycolysis can be either aerobic or anaerobic, but it does not require nor consume oxygen.
Although other molecules are involved in glycolysis at some stage, none of them form its end product. Lactic acid is associated with anaerobic glycolysis. glycolysis is essential for how the body produces energy from carbohydrates.
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This question is part of the following fields:
- Basic Sciences
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Question 19
Correct
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At what stage of meiosis does the process of homologous recombination occur?
Your 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 20
Correct
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What is the main role of the Golgi apparatus in eukaryotic cells?
Your Answer: Process of proteins
Explanation:The Golgi Apparatus, Cell Division, and Homeostasis
The Golgi apparatus is a structure found in eukaryotic cells that consists of flattened membrane stacks. Its primary function is to modify proteins that have been synthesized in the rough endoplasmic reticulum, preparing them for secretion or transport within the cell. However, the Golgi apparatus is not directly involved in cell division, which is controlled by the nucleus.
Cell homeostasis, on the other hand, is primarily maintained by membrane-embedded channels or proteins such as the sodium-potassium pump. This mechanism ensures that the cell’s internal environment remains stable. The sodium-potassium pump is an active transport mechanism that involves the binding of three intracellular sodium ions to the protein. Adenosine triphosphate (ATP) donates a phosphate group to the protein, which causes it to change shape and release the sodium ions out of the cell.
The protein then accepts two extracellular potassium ions, and the donated phosphate group detaches, causing the protein to revert to its original shape. This allows the potassium ions to enter the cell, increasing the intracellular potassium concentration and decreasing the intracellular sodium concentration. This process is in contrast to the extracellular conditions.
In summary, the Golgi apparatus modifies proteins for secretion or transport, while cell division is controlled by the nucleus. Cell homeostasis is maintained by membrane-embedded channels or proteins such as the sodium-potassium pump, which actively transports ions to stabilize the cell’s internal environment.
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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: Activation of caspase-9
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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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: 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 23
Incorrect
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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: 100%
Correct 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 24
Correct
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What significance do leucine, lysine, and phenylalanine hold?
Your Answer: They are essential amino acids
Explanation:Essential Amino Acids and their Importance in the Diet
There are approximately 20 essential amino acids that are crucial for human health. These amino acids are considered essential because the body cannot produce them on its own and they must be obtained through the diet. While some of these essential amino acids can be used to create other non-essential amino acids, they are still necessary for overall health and wellbeing.
Some examples of essential amino acids include histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, and valine. However, the amount of these essential amino acids can vary depending on the type of dietary protein consumed. Additionally, cooking or preserving proteins can alter the amino acid composition, making them less effective for the body.
In summary, essential amino acids play a vital role in maintaining human health and must be obtained through the diet. the importance of these amino acids and their sources can help individuals make informed decisions about their dietary choices.
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This question is part of the following fields:
- Basic Sciences
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Question 25
Correct
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In which part of the cell are the electron transport chain carriers situated?
Your Answer: Mitochondrial cristae
Explanation:The Electron Transport Chain in Mitochondria
The electron transport chain (ETC) is a crucial process in cellular aerobic respiration that occurs in the mitochondrial cristae. These are folded membranes inside the organelle. During respiration, NADH and FADH produced from other parts of the process, such as glycolysis, transfer electrons from electron donors to electron acceptors through redox reactions. This electron transfer is coupled with proton transfer across the mitochondrial membrane, creating an electrochemical proton gradient. This gradient induces the production of ATP, which is used as an energy currency by the cell.
ATP is produced through a mechanism called chemiosmotic phosphorylation. The structure of the mitochondrion is essential for this process to occur. The cristae provide a large surface area for the ETC to take place, and the mitochondrial membrane is impermeable to protons, allowing for the creation of the proton gradient. The inner membrane also contains ATP synthase, the enzyme responsible for producing ATP through chemiosmotic phosphorylation.
In summary, the electron transport chain in mitochondria is a complex process that involves the transfer of electrons and protons across the mitochondrial membrane to create a proton gradient. This gradient is then used to produce ATP through chemiosmotic phosphorylation. The structure of the mitochondrion is crucial for this process to occur efficiently.
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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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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 27
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 28
Correct
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A 32-year-old snowboarder presents to the Emergency department complaining of pain and swelling around the first metacarpophalangeal joint (MCP joint) following a fall during practice.
Upon examination, there is significant swelling and bruising on the ulnar side of the joint.
What is the most probable injury that the patient has sustained?Your Answer: Ulnar collateral ligament
Explanation:Skier’s Thumb: A Common Injury in Winter Sports
Skier’s thumb, also known as gamekeeper’s thumb, is a common injury that occurs in winter sports. It is caused by damage or rupture of the ulnar collateral ligament, which is located at the base of the thumb. This injury can result in acute swelling and gross instability of the thumb. In severe cases where a complete tear of the ligament is suspected, an MRI may be necessary to confirm the diagnosis, and surgical repair may be required.
Once the acute swelling has subsided, treatment for skier’s thumb typically involves immobilization in a thumb spica. This is the standard therapy for cases of partial rupture.
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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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Which statement regarding microtubules is accurate in relation to Chédiak-Higashi syndrome?
Your Answer: They consist of beta tubulin subunits only
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 30
Correct
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What is the cause of the symptoms of weakness, dermatitis, diarrhoea and dementia in pellagra?
Your Answer: Deficiency of the vitamin niacin
Explanation:Niacin Deficiency and Other Genetic Diseases
Niacin, a vitamin present in two forms – nicotinamide and nicotinic acid, is found in a variety of plant and animal foodstuffs. However, in some cases, the form of the vitamin is not easily absorbed by the human body, leading to deficiency. This deficiency is common in areas where maize is the primary dietary carbohydrate. Additionally, niacin can be produced by the body from the amino acid tryptophan. Diseases that affect the availability of tryptophan, such as Hartnup disease and carcinoid syndrome, can also result in niacin deficiency.
Pellagra is a condition that arises from niacin deficiency. It initially presents with non-specific symptoms such as nausea, fatigue, and reduced appetite, followed by pigmented dermatitis in sun-exposed areas, gastrointestinal disturbance, mood disturbance, and dementia in severe cases.
Apart from niacin deficiency, genetic diseases affecting collagen synthesis, such as Ehlers Danlos, present with symptoms of fragile stretchy skin and joint hypermobility. Genetic diseases affecting haemoglobin, such as sickle cell anaemia, present with symptoms of pain, hepatosplenomegaly, shortness of breath, and anaemia. Deficiencies in B12 and folate can also lead to macrocytic anaemia, paresthesia, and lethargy.
In conclusion, the causes and symptoms of niacin deficiency and other genetic diseases is crucial for early diagnosis and effective treatment. A balanced diet and regular medical check-ups can help prevent and manage these conditions.
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This question is part of the following fields:
- Basic Sciences
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