Answer:
Its is a lysosomal storage disease!
Explanation:
<u>Hurler syndrome:-</u> is also known as mucopolysaccharidosis-I .
It Is due to the mutation on chromosome 4 .
There is a lack of of enzyme called alpha-L-iduronidase.This enzyme is present in lysosomes
It causes accumulation of mucopolysaccharides because of the absent of the enzyme in the lysosome
<u>Hunter syndrome:- </u>is also known as mucopolysaccharidosis-II
It occurs due to mutation in iduronate-2-sulfatase (IDS) gene.It is an X-linked disease
Answer:
Cross-bridges would form in the absence of an action potential from a motor neuron.
Explanation:
The injected calcium ions would bind to troponin. Troponin would make tropomyosin move away from the myosin-binding sites on actin. The presence of free binding sites on the actin would be followed by the contraction cycle. This would include hydrolysis of ATP to energize myosin heads and binding of these heads to actin to form cross-bridges. Therefore, cross-bridge formation would occur without any action potential if calcium ions are injected directly into the muscle.
Protist and fungi are placed in the same domain because both have a true nucleus, have complex cellular organelles, are large, and Eukaryotic.
- In the healthy individual, the walls of the intestine are covered by intestinal villi and their microvilli, which contribute to increase the absorption surface of the nutrients we ingest and lead them to the bloodstream so that they reach the organs according to their needs.
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<h2>BRAINLYMENTALMENTE</h2>
Answer:
Explanation
Given that 36% are recessive in traits
100-36 = 64% for dominant traits considering a whole population to be 100%
P=dominant allele
q= recessive allele
P2= dominant genotype
q2= recessive genotype
according to hardyweinberg principle, p+q=1
64/100= 0.64 frequency for dominant traits or genotype, therefore
p2=0.64
then
P=√0.64
p= 0.8
Therefore, dominant allele frequency (p) for the population is 0.8
