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serious [3.7K]
3 years ago
8

What best describes the flow of genetic formation

Biology
1 answer:
marshall27 [118]3 years ago
5 0

The answer is C.Your welcome !!

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A scientist isolated a molecule with nucleotide bases A, C, G, and U and ribose sugars. What is it?
gogolik [260]

Answer:

The Answer is RNA.

Explanation:

Because RNA consists of four nitrogenous bases: adenine, cytosine, uracil, and guanine.  I am 100% sure that is the answer if it's wrong, very sorry.

7 0
3 years ago
Buffers resist change in ph of solutions by_____?
masha68 [24]
<span>A buffer is able to resist pH change because the two components (conjugate acid and conjugate base) are both present in appreciable amounts at equilibrium and are able to neutralize small amounts of other acids and bases (in the form of H 3O + and OH -) when the are added to the solution.</span>Feb 7, 2016
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Valentina is at the beach and decides to head out into the water for a swim. As she swims away from shore, she gets caught in a
lozanna [386]
Remain calm
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6 0
2 years ago
Read 2 more answers
Which part of bone marrow is
Thepotemich [5.8K]

Answer: the answer is B

Explanation: Yellow bone marrow is involved in the storage of fats. The fats in yellow bone marrow are stored in cells called adipocytes.

3 0
2 years ago
DELETION OF SNORD116, A PRADER-WILLI SYNDROME CANDIDATE GENE, DOES NOT AFFECT CIRCADIAN RHYTHMS IN MICE MODELS
Vlada [557]

Prader-Willi syndrome (PWS) is a gentic disorder which has an impact on numerous physiological systems. PWS affected individuals (specifically babies) experience delayed growth, significant hypotonia (low muscle tone), and feeding issues. It does effect circadian rhythms in mice models.

SNORD116, often referred to as HBII-85, is a non-coding RNA (ncRNA) molecule that contributes to the alteration of other small nuclear RNAs (snRNAs). Unlike the majority of other snoRNAs, SNORD116 is not significantly complementary to ribosomal RNA and is expressed widely in the brain (but not in PWS patients).

According to the studies, SNORD116 cause sleep defect in patients with Prader-Willi syndrome. Same observation was seen in mouse models too. Paternal expression of SNORD116 is thought to be a potential gene for the sleep disruptions/circadian rhythm’s that the majority of PWS sufferers.

To learn more about circadian rhythm click here

brainly.com/question/6434404

#SPJ4

3 0
1 year ago
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