They help form D organ system which is the
digestive system
Answer:
<h2> Changes in population size may have important effects on genetic variation and on the survival potential of viral species. Genetic bottlenecks are evolutionary events that reduce genetic variation of a population in a stochastic manner and result in founding populations that can lead to genetic drift.</h2>
Explanation:
<h2>Hopes this helps. Mark as brainlest plz!</h2>
Answer:
All mammals, like dogs, cats, and humans; reptiles, amphibians, fish, birds, and even insects.
Explanation:
All mammals, like dogs, cats, and humans; reptiles, amphibians, fish, birds, and even insects are the animals that have a complete tube-like gut with two openings. A system having a tube with two openings i.e. mouth and an anus is called tubular system. In this tubular system, the animals eat with one opening and the other opening is used for excretion of waste and nitrogenous materials from the body so that's why most of the animals have two openings.
<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
Answer:
1/2.
Explanation:
The autosomal dominant trait may en defined as the trait that can express itself even in the heterozygous condition and in the homozygous dominant condition as well.
Let the B allele is responisble for the roll tongue and b is recessive allele. The woman can roll the tongue and she must have the genotype Bb because her one parents is normal. The woman married with a man with non roller ( bb). The Bb × bb cross results in the following progeny Dd, Dd ( roller), dd and dd ( non roller). The probability of the child being a roller is 1/2,
Thus, the answer is 1/2.
