Give an explanation why a mutation in the fibroblast growth factor receptor (FGFR) can disrupt embryonic...
Give an explanation why a mutation in the fibroblast growth factor receptor (FGFR) can disrupt embryonic development, even if the individual is heterozygous for this mutation.
Homework Answers
ANS)
--> FGFR3 quality encodes Fibroblast development consider receptor 3 protein people and is spoken to as CD333 (a bunch of separation 333). This quality is situated on chromosome 4, area p16.3 and the outflow of this receptor protein happens in ligament, cerebrum, digestive system, and kidneys. At the point when there is a transformation in this quality distinctive ailments are made and one among them is a birth infection called Achondroplasia. FGFR3 is a transmembrane receptor protein along these lines it partakes in flag course amid embryonic and fetal improvement. It has a significant job in vein arrangement and neural separation. Achondroplasia is brought about by a solitary nucleotide substitution in this quality, where a change of amino corrosive happens (Gly380Arg). Achondroplasia is an autosomal overwhelming legacy that is the reason it happens even in the heterozygous conditions.
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Give an explanation why a mutation in the fibroblast growth
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Can someone give a thorough explanation of why? Thank you so
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4. If V is known at only a single point in space, can E be found at that point? Explain your answer.
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