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  • Dina

  • 問題数 35 • 11/14/2023

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    問題一覧

  • 1

    what’s niche?

    Adult stem cells that are found in few places in the body like bone marrow and gonads

  • 2

    at. homologous chromosomes recombination occurs

    prophase

  • 3

    ____is a multi step process by which signal is transmitted through cell leading to an event

    signal transduction

  • 4

    ________ Involves reprogramming of undifferentiated stem cells

    metaplasia

  • 5

    ________may be the fastest growing form and have increased rate of mitosis

    anaplastic tumors

  • 6

    what’s the meaning of staging

    extent of spread of the tumor within the patient

  • 7

    The checkpoint factor that controls the process of cell differentiation is ———————— which functions is in late G1.

    Restriction check points

  • 8

    what type of molecule is cadherin-catenin complex and what’s its function ?

    it’s CAM (Cell adhesion molecule) and its function is to join cells together

  • 9

    _________Fibrous proteins that provide the nucleus with mechanical support

    nuclear lamina

  • 10

    solenoid structures are tightly packed————-?

    Nucleosomes

  • 11

    what’s a gene?

    a nucleotide sequence in a dna molecule

  • 12

    what are the regulatory expressed genes?

    expression of inducible genes increase in response to inducer or activator such as enzymes in catabolic pathways

  • 13

    difference between cell types result from———?

    differential Jene expression

  • 14

    ——————- is a sequence in eukaryotic mRNA, which plays a major role in the initiation of the translation process.

    Kozak sequence

  • 15

    •——————- assist the ribosome in recognising the stop codon and terminating translation. and an example of it in eukaryotics could be—————

    release factor,eRF

  • 16

    serum albumin secretion could be an example of which protein secretion?

    constitute secretion

  • 17

    non folded aggregated proteins are associated with ——— and misfolded proteins form———

    prion diseases,amyloid fibrils

  • 18

    which post transitional modification process is important in cell cell communication?

    glycosylation

  • 19

    methylation is an important process of PTMs because it influences the availability of————for transcription

    DNA

  • 20

    what causes zellweger syndrome ?

    cells have small or absent peroxisome resulting from faults in transporting their specific enzymes to them from the endoplasmic reticulum

  • 21

    when signal peptide on the N terminal is removed in collagen biosynthesis we get______

    pro peptide

  • 22

    when collagen peptidase remove the loose ends of pro collagen molecule————- is formed

    Tripp collagen

  • 23

    what’s a probe

    a single stranded polynucleotide of dna and rna

  • 24

    Extracellular water includes…..

    plasma , interstitial water

  • 25

    The difference in percentage of water between cells depends on

    metabolic activity and age of the cell

  • 26

    primary microcephaly is a brain disorder that is caused by mutation in ………

    spindles

  • 27

    What do enzymes do to bond tropocollagen molecules in collagen biosynthesis?

    Enzymes bond tropocollagen molecules to form the collagen fibril in collagen biosynthesis

  • 28

    What enzymes remove the “loose ends” of the pro-collagen molecule in collagen biosynthesis?

    Collagen peptidases, membrane enzymes, remove the “loose ends” of the pro-collagen molecule in collagen biosynthesis.

  • 29

    What is removed during pro-peptide formation in collagen biosynthesis?

    The signal peptide on the N-terminal is removed during pro-peptide formation in collagen biosynthesis.

  • 30

    People with this disease lack an enzyme that breaks down lipids, causing lipids accumulation in the brain and other parts of the nervous system.

    tay sacks disease which is also an example of incomplete dominance

  • 31

    what’s pleiotropy and what could be a disease caused by its defect?

    when one gene has a wide affect,marfan’s syndrome

  • 32

    in some cases this disease inherited as an autosomal recessive trait. Some cases are inherited in X-linked recessive pattern, and some have some have mitochondrial inheritance pattern (maternal inheritance)

    leigh syndrome

  • 33

    What is the cause of Xeroderma Pigmentosum?

    Defect/deficiency in endonuclease enzyme (mutation in at least 9 genes) in nucleotide excision repair mechanism.Defect/deficiency in endonuclease enzyme (mutation in at least 9 genes) in nucleotide excision repair mechanism.

  • 34

    What effect does XP have on DNA when exposed to UV sunlight?

    It allows thymine dimers formed upon exposure to UV sunlight to persist and block replication.

  • 35

    Why is cancer extremely common in individuals with XP?

    XP leads to an inability to repair DNA, increasing the frequency of mutations. Cancer develops once proto-oncogenes or tumor suppressor genes mutate.