Answer:
The correct answer is d) genomic imprinting.
Explanation:
Genomic imprinting is a biological process by which specific modifications in the germ line that produce differences in the expression of the genetic material that is biochemically marked indicating its parental origin. The Prader-Willi syndrome is one of the best known and most studied examples in relation to pathologies produced by genomic imprinting. Prader-Willi syndrome is a complex genetic disease that is fundamentally neurological. Its appearance is due to a deletion of a fragment of chromosome 15 derived from the father.
Answer:
Make up the skull and composed of the brain
Explanation:
Activation energy - is the minimum quantity of energy that the reacting species must possess in order to undergo a specified reaction.
Hepatocyte growth factor (HGF) is the only known growth factor that activates quiescent satellite cells in skeletal muscle.
Hepatocyte growth factor regulates cell growth, cell motility, and morphogenesis by activating a tyrosine kinase signaling cascade after binding to the proto-oncogenic c-Met receptor. Hepatocyte growth factor is secreted by mesenchymal cells and acts as a multi-functional cytokine on cells of mainly epithelial origin.
HGF, produced by some cancer cells, stimulates c-Met, through activation of the autocrine signaling system. Hepatocyte growth factor (HGF) is a paracrine hormone that plays an important role in epithelial-mesenchymal transition. HGF secreted by mesenchymal cells affects many properties of epithelial cells, such as proliferation, motility, and morphology.
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