Answer:
mitochondria
Explanation:
In aerobic glycolysis: NADH is transferred into mitochondria via the mitochondrial shuttle, where it is oxidized to NAD in the respiratory chain, ultimately producing ATP.
In chromatin, substitution mutations are most common in linker regions. Option d is the correct answer.
Mutation by substitution When one nucleotide base is replaced by another, this occurs. Mismatch mutation A type of substitution mutation in which a single nucleotide is replaced, resulting in the coding of an incorrect amino acid, which usually results in a malfunctioning protein. Silent mutations are the result of genetic code redundancy (degeneracy): This is false, as silent mutations are the result of a base substitution that has no discernible effect on a protein's amino acid sequence.
Learn motre more about subsitution here:
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Answer: D. Passed on from parent to offspring
Answer:
I'm pretty sure its either B or E. Depends on if you need a definition or example I think
Answer:
The short‑ear allele phenotypic ratio is 25%.
Explanation:
Genotype for homozygous short‑eared progenitor: ll
Genotype for homozygous long-eared progenitor: LL
Genotype for heterozygous: Ll
P) LL x ll
Gametes) L L l l
F1) LlLl
All of the individuals of the first progeny are long-eared heterozygote.
The cross of two heterozygous individuals:
Ll x Ll
Gametes) L l L l
F2) 25% Homozygote for the long ear: LL
25% Homozygote for the short ear: ll
50% Heterozygote: Ll
75% of progeny are Longed-ear animals
25% of progeny are Shorted-ear animals
