Prader-Willi syndrome (PWS) is a gentic disorder which has an impact on numerous physiological systems. PWS affected individuals (specifically babies) experience delayed growth, significant hypotonia (low muscle tone), and feeding issues. It does effect circadian rhythms in mice models.
SNORD116, often referred to as HBII-85, is a non-coding RNA (ncRNA) molecule that contributes to the alteration of other small nuclear RNAs (snRNAs). Unlike the majority of other snoRNAs, SNORD116 is not significantly complementary to ribosomal RNA and is expressed widely in the brain (but not in PWS patients).
According to the studies, SNORD116 cause sleep defect in patients with Prader-Willi syndrome. Same observation was seen in mouse models too. Paternal expression of SNORD116 is thought to be a potential gene for the sleep disruptions/circadian rhythm’s that the majority of PWS sufferers.
To learn more about circadian rhythm click here
brainly.com/question/6434404
#SPJ4
ATP, the molecule of energy, has three phosphates (hence the “T” and “P”). When one phosphate group is BROKEN OFF, it releases lots of ENERGY.
Answer:B)food
everything else is transported from those options except food. Hopefully this is right.
Answer:
They once thought that humans came from monkeys and apes but now they think they come from a ancient ancestor not from the monkey or ape family.
Explanation: