Structures within the Cell Flashcards

1
Q

command center of the cell

A

nucleus

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2
Q

the outernuclear membrane is continous with what structure

A

endoplasmic reticulum

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3
Q

this form of chromatin is most abundant

A

Euchromatin

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4
Q

site of dna transcription

A

nucleus

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5
Q

responsible for ribosomal rna synthesis

A

nucleolus

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6
Q

this form of chromatin is transcriptionally inactive

A

heterochromatin

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7
Q

this is a complex of dna, histone proteins

A

chromatin

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8
Q

barr bodies

A

heterochromatin

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9
Q

basic repeating unit of chromatin fibers

A

nucleosome

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10
Q

condensed/dark inactive barr bodies

A

heterochromatin

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11
Q

dispersed/light actively transcribed

A

euchromatin

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12
Q

1 47 xxy bar body

A

klinefelter’s syndrome

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13
Q

2 47 xxx bar body

A

super female

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14
Q

contains their own set of DNA

A

mitochondria

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15
Q

site of post tranlational modification

A

Golgi apparatus

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16
Q

sequestration and release of calcium ions in striated muscle.

A

sarcoplasmic reticulum

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17
Q

consists of large and small subunits

A

ribosomes

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18
Q

synthesis of steroid hormones, phospholipids and TAG

A

smooth reticulum

19
Q

protein sorting and packaging

A

Golgi apparatus

20
Q

site of synthesis of secretory proteins, membrane bound protein and lysosomal enzymes

A

rough er

21
Q

involved in the production of Coa, TCA, beta oxidation and oxidative phosphorylation

A

mitochondria

22
Q

disease associated with mitochondrial genome defect

A

MELAS

23
Q

muscle weakness, pain, seizure, hemiparesis, dementia

A

MELAS

24
Q

drug detoxification

A

smooth er

25
Q

abundant in ovaries, testis, and adrenals

A

smooth er

26
Q

abundant in neurons

A

Rough Er

27
Q

abundant in pancreas and thyroid

A

Rough Er

28
Q

abundant in red muscle fibers

A

mitOchondria

29
Q

site of protein synthesis for the nucleus, peroxisomes and mitochondria

A

free ribosomes

30
Q

site of protein synthesis, synthesis if secretory protein, membrane protein and lysosomal enzymes.

A

rough Er

31
Q

involved in membrane cycling.

A

Golgi apparatus

32
Q

cell’s garbage disposal system

A

lysosomes

33
Q

contains oxidative enzymes and synthesis of hydrogen peroxide.

A

ribosomes

34
Q

contains hydrolytic enzymes

A

lysosomes

35
Q

involved in beta oxidation of long chain fatty acid

A

peroxisomes

36
Q

suicide bags

A

lysosomes

37
Q

catalase is the major enzymes

A

peroxisomes

38
Q

participate in bile acid synthesis

A

peroxisomes

39
Q

acid hydrolase is the major protein.

A

lysosomes

40
Q

enzymes are produced in free ribosomes

A

peroxisomes

41
Q

enzymes are produced in the RER

A

lysosomes

42
Q

glycogen storage disease that involves a defect in lysosomal metabolism

A

Pompe disease

43
Q

acid maltase deficiency, muscle weakness, cardiorespiratory failure

A

Pompe disease