<span>Roan is a combination of white hairs with red hairs. When we see cattle like this, they look pink because it resulted from a mix of white and red.
Red allele: A
White allele: a
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<span>A heterozygotic animal has this genotype: Aa
Like i said previously this is the mixture of colors so the animal would be pink.
A red coat color has this genotype: AA
A white coat color has this genotype: aa
To get all the herd to be</span><span> roan-colored cattle the combination of parents should be: AA x aa. -> 100% roan
Another possible way to obtain would be</span><span>roan-colored cattle: Aa x Aa or aa x Aa (in this case there would be less probabable to obtain road).</span>
Answer: Option A
Explanation:
A tunicate is marine invertebrate animal which is a part of chordates. They have notochords and dorsal nerve chord. The subphylum of the organism is called as Urochordata.
The adult urochordates lack notochord but the larval stage of the urochordates have notochord. This is because it helps in swimming of the organism which is required only at the larval stage.
The adult stage of the tunicates is sessile and they do not swim so they do not require notochord.
Answer:
wheat is like a crop because first you have that to plant to get corn
Explanation:
<span>Lafora disease is the most severe teenage-onset progressive epilepsy, a unique form of glycogenosis with perikaryal accumulation of an abnormal form of glycogen, and a neurodegenerative disorder exhibiting an unusual generalized organellar disintegration. The disease is caused by mutations of the EPM2A gene, which encodes two isoforms of the laforin protein tyrosine phosphatase, having alternate carboxyl termini, one localized in the cytoplasm (endoplasmic reticulum) and the other in the nucleus. To date, all documented disease mutations, including the knockout mouse model deletion, have been in the segment of the protein common to both isoforms. It is therefore not known whether dysfunction of the cytoplasmic, nuclear, or both isoforms leads to the disease. In the present work, we identify six novel mutations, one of which, c.950insT (Q319fs), is the first mutation specific to the cytoplasmic laforin isoform, implicating this isoform in disease pathogenesis. To confirm this mutation's deleterious effect on laforin, we studied the resultant protein's subcellular localization and function and show a drastic reduction in its phosphatase activity, despite maintenance of its location at the endoplasmic reticulum.
I got my information from </span>https://www.ncbi.nlm.nih.gov/pubmed/14722920
