-
Question 1
Correct
-
Critical shortening of Telomeres result in:
Your Answer: Activation of p53 and prb and cell crisis
Explanation:Telomeres are repetitive nucleotide sequences at the ends of chromosomes that protect them from deterioration or from fusion with neighboring chromosomes. Each time a cell divides, its telomeres shorten. When they become critically short, they can no longer protect the chromosome ends, triggering a DNA damage response.
This response leads to the activation of tumor suppressor proteins p53 and pRb (retinoblastoma protein). Activated p53 can induce cell cycle arrest, allowing time for DNA repair or triggering apoptosis if the damage is irreparable. Similarly, pRb helps regulate cell cycle progression and can halt the cell cycle to prevent the proliferation of cells with damaged DNA.
As a result, the cell enters a state of crisis, characterized by widespread cell death and genomic instability, which ultimately prevents the propagation of cells with critically shortened telomeres.
Therefore, the correct answer is:
Activation of p53 and pRb and cell crisis
-
This question is part of the following fields:
- Genetics
- Medicine
-
-
Question 2
Correct
-
Which of the following is a granulocyte?
Your Answer: Eosinophil
Explanation:Granulocytes are a category of white blood cells characterized by the presence of granules in their cytoplasm. There are three principal types of granulocytes, distinguished by their appearance under Wright’s stain:
- Basophil granulocytes
- Eosinophil granulocytes
- Neutrophil granulocytes
-
This question is part of the following fields:
- Haematology
- Medicine
-
-
Question 3
Correct
-
Question 4
Correct
-
Which of the following is least recognised as a potential complication of acromegaly?
Your Answer: Mental retardation
Explanation:Acromegaly is a condition that results from excess growth hormone (GH) after the growth plates have closed. It is typically due to the pituitary gland producing too much growth hormone. In more than 95% of people the excess production is due to a benign tumour, known as a pituitary adenoma. The condition is not inherited.Complications:Severe headacheArthritis and carpal tunnel syndromeEnlarged heartLiver fibrosis and bile duct hyperplasiaHypertensionDiabetes mellitus (excess of GH leads to insulin resistance)Heart failureKidney failureColorectal cancerCompression of the optic chiasm leading to loss of vision in the outer visual fields (typically bitemporal hemianopia.)Increased palmar sweating and sebum production over the face (seborrhoea) are clinical indicators of active GH-producing pituitary tumours.hypertensiondiabetes (>10%)cardiomyopathycolorectal cancer
-
This question is part of the following fields:
- Endocrinology
- Medicine
-
-
Question 5
Correct
-
A 32 year old male who has recently returned from a trip to Thailand presents with congestion of eyes and swelling of the knee joint. He completed a course of antibiotics for dysentery 4 weeks back. He experiences no dysuria and urine examination is normal. Which further information would be most useful in establishing a diagnosis?
Your Answer: History and physical examination
Explanation:The patient most likely has reactive arthritis which is usually diagnosed on history and clinical examination. The classic triad of symptoms include conjunctivitis, urethritis and arthritis. Arthritis and conjunctivitis may occur 4-6 weeks after a gastrointestinal or genitourinary infection. Arthritis usually occurs acutely, mostly involving the lower limb and is asymmetrical. Blood culture, urine culture and arthrocentesis (joint aspiration) will not yield positive results.
-
This question is part of the following fields:
- Connective Tissue
- Medicine
-
-
Question 6
Correct
-
Which enzyme hydrolyses triglycerides in lipoproteins into free fatty acids for storage in fat cells?
Your Answer: Lipoprotein lipase
Explanation:Lipoprotein lipase is a water-soluble enzyme that hydrolyses triglycerides in lipoproteins, such as those found in chylomicrons and very low-density lipoproteins (VLDL), into two free fatty acids and one monoacylglycerol molecule.
-
This question is part of the following fields:
- Medicine
- Metabolism
-
-
Question 7
Correct
-
Which substance is produced by anterograde neurons?
Your Answer: Nitric oxide
Explanation:Nitric oxide is thought to act as an anterograde neurotransmitter. Classically in the peripheral nervous system, it diffuses from a presynaptic nerve ending to the post synaptic effecter cell which is mainly smooth muscle cells in the gastrointestinal, respiratory and urogenital tracts.
-
This question is part of the following fields:
- Gastrointestinal
- Medicine
-
-
Question 8
Correct
-
Which one of the following cells originates from a monocyte and resembles a macrophage?
Your Answer: Microglia
Explanation:Microglia act as the macrophages of the central nervous system, and they contribute to innate and adaptive immune responses. Studies have shown that microglial cells recognize monocyte antigens, and there are similarities between them that demonstrate that they originate from these monocytes.
-
This question is part of the following fields:
- Medicine
- Neurology
-
-
Question 9
Correct
-
Which of the following is not true regarding mitochondrial chromosome disorders?
Your Answer: Because mitochondrial chromosomes have no introns in their genes, any point mutation has a low likelihood of having an effect.
Explanation:Mitochondrial DNA (mtDNA) does indeed lack introns, meaning that its genes are closely packed with coding sequences. This actually means that any point mutation in the mtDNA is more likely to have an effect, not less. The lack of introns means there are fewer non-coding regions where mutations can occur without affecting gene function. Thus, mutations in mtDNA often have significant consequences because they are more likely to alter essential coding sequences.
The other statements are true:
- Most mitochondrial diseases are myopathies and neuropathies with a maternal pattern of inheritance: This is correct because mtDNA is inherited maternally, and many mitochondrial disorders affect muscle and nerve function.
- Retinal degeneration, diabetes mellitus, and some forms of hearing loss are some of the other diseases attributed to mitochondrial chromosome defects: These are indeed conditions associated with mitochondrial defects.
- Mitochondrial chromosome defects are inherited from one’s mother: This is correct, as mtDNA is passed from mother to offspring.
- Leber’s hereditary optic neuropathy (LHON), the commonest cause of blindness in young men, is an example of a mitochondrial chromosome defect: This is true; LHON is a well-known mitochondrial disorder.
-
This question is part of the following fields:
- Genetics
- Medicine
-
-
Question 10
Correct
-
Which enzyme is responsible for the formation of the active endopeptidases from their inactive precursors?
Your Answer: Enterokinase
Explanation:Enterokinase is a brush border enzyme of the duodenum that activates proteolytic enzymes for further digestion of proteins. Trypsinogen is converted to trypsin by the action of enterokinase. Trypsin and chymotrypsin are secreted by the pancreatic acinar cells and are enzymes that aid in protein digestion. Pepsin is secreted by chief cells of gastric mucosa. Procarboxydase is the inactive form of carboxypeptidase which is converted to its active form by trypsin and is secreted by pancreatic acinar cells.
-
This question is part of the following fields:
- Gastrointestinal
- Medicine
-
SESSION STATS - PERFORMANCE PER SPECIALTY
