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Last updated 10:11 PM on 2/23/25
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59 Terms

1
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Theca cells are the source of __________ and testosterone.
androstenedione
2
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Phosphodiester bonds join the 5'-hydroxyl group of the deoxy-pentose of one nucleotide to the 3'-hydroxyl group of the deoxy-pentose of an adjacent nucleotide through a phosphate group. (T/F) __________.
True
3
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Gout is a disorder characterized by low levels of uric acid—the end product of purine catabolism—in blood (hypouricemia). (T/F) __________.
False
4
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DNA is negatively charged, histones and Mg2+ ions help to __________ the charge.
neutralize
5
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Dopamine and norepinephrine are __________ in the brain and function as neurotransmitters.
synthesized
6
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The main metalloporphyrin in the body is heme, which has a __________ Fe2+ iron atom coordinated by protoporphyrin IX.
ferrous
7
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Polymerases use only __________ as a template.
ssDNA
8
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Reduction of androstenedione at the C17 position results in the formation of __________, the most potent adrenal androgen.
Glucagon
9
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Cholera and pertussis toxins catalyze the __________ of G proteins, affecting signal transduction.
ADP ribosylation
10
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Estrogens are formed by the aromatization of androgens, which requires __________ and NADPH.
O2
11
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Unconjugated bilirubin is normally __________.
secreted
12
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The bile acids are __________ molecules that aid in lipid digestion.
amphipathic
13
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The liver synthesizes more heme than most other organs in order to maintain its high content of __________.
cytochromes
14
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Most of the urobilinogen is oxidized to __________, which turns the feces brown.
stercobilin
15
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Bilirubin is not very __________, so most of it is carried to the liver bound to albumin.
water-soluble
16
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Tyrosine is formed from __________ by phenylalanine hydroxylase.
phenylalanine
17
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Inside a polysome, ribosomes are translating __________ types of proteins.
different
18
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Niemann-Pick disease is caused by the inability to degrade __________.
sphingomyelin
19
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Catecholamine degradation results in the synthesis of __________ (VMA).
vanillylmandelic acid
20
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Heme is synthesized from glycine and succinyl-CoA in humans via a __________ pathway.
complex
21
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In obstructive jaundice, it is mainly __________ bilirubin that increases, because the liver is intact.
conjugated
22
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Creatinine is synthesized in the __________ and excreted by the kidney.
liver
23
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Bilirubin and biliverdin are both products of __________ catabolism.
heme
24
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The porphyrins are altered by decarboxylation and oxidation, and __________ IX is formed.
protoporphyrin
25
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Infant RDS (Respiratory distress syndrome) is caused by a deficiency of __________ surfactant.
lung
26
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Hormones are only synthesized in specialized organs called __________.
glands
27
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The first step in pyrimidine synthesis is the formation of __________ phosphate, catalyzed by carbamoyl phosphate synthetase II.
carbamoyl
28
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Citrulline is a non-protein amino acid that works as an intermediate in __________ biosynthesis.
urea
29
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5-hydroxytryptophan is decarboxylated to serotonin in a reaction requiring __________ phosphate (PLP).
pyridoxal
30
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Hyperuricemia is typically __________ and does not always lead to gout.
asymptomatic
31
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The B chains of insulin are identical in all species, while the distinct __________-chain imparts hormone uniqueness.
alpha
32
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Glycogen synthase and DNA synthase require a __________.
primer
33
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Bilirubin is conjugated in the __________ by glucuronyl transferase.
gallbladder
34
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Aminotransferases are intracellular enzymes, and their plasma concentration increases usually indicate __________.
pathology
35
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Degradation of glycolipids happens in the __________.
lysosome
36
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Cyclic AMP was the first intracellular second messenger signal identified in __________ cells.
mammalian
37
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DNA polymerases cannot initiate the synthesis of a complementary DNA strand without an __________ primer.
RNA
38
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Glutamate is converted to __________ by transamination reactions.
alanine
39
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The purine ring is constructed primarily in the __________.
liver
40
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Telomeres are complexes of noncoding DNA plus proteins located at the ends of __________ chromosomes.
linear
41
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Hemin inhibits ALA synthase via __________ regulation.
allosteric
42
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The urea cycle occurs only in the __________.
mitochondria
43
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Enzymes increase reaction rates by lowering __________ energy.
activation
44
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Fatty acid synthesis occurs in the __________.
cytoplasm
45
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The electron transport chain is located in the __________ mitochondrial membrane.
inner
46
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Peptide bonds are formed via __________ synthesis.
dehydration
47
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Ribosomes are composed of __________ and proteins.
RNA
48
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The pancreas secretes __________ to aid in fat digestion.
bile
49
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Histidine is an __________ amino acid.
essential
50
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DNA replication is __________.
semiconservative
51
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ATP is the primary __________ currency of the cell.
energy
52
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The lac operon is an example of __________ and negative gene regulation.
positive
53
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Glycogen is stored in the __________ and muscle tissues.
liver
54
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The main function of mitochondria is __________ synthesis.
ATP
55
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Allosteric enzymes have __________ active sites.
multiple
56
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The citric acid cycle produces __________, NADH, and FADH2.
ATP
57
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Hemoglobin and myoglobin have the same __________-binding affinity.
oxygen
58
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The Golgi apparatus modifies and __________ proteins.
packages
59
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The smooth ER is involved in __________ synthesis.
lipid