An international study led by the University of Colorado Cancer Center has uncovered why a widely used treatment for acute ...

Mumbai: Nearly 28 out of every 100 children clinically suspected of having inherited blood disorders were found to be ...

Rapidly mutating DNA regions were mapped using a multi-generational family and advanced sequencing tools. Understanding how ...

Identifying and classifying gene mutations—which are the permanent changes in a person's DNA genetic code—are critical in ...

Blood samples from four individuals of the same family, a 3 m/o male, 35 y/o father, 31 y/o mother, and 27 y/o paternal aunt, were collected by vacuum venipuncture and used for biochemical laboratory ...

A mutation in salt-induced kinase 3 (hSIK3-N783Y) is identified in a human subject exhibiting the natural short sleep duration trait. A mouse model carrying this homologous mutation demonstrates ...

Professor Chris Whitty, England's chief medical officer, said he had alerted the World Health Organisation to its existence - and would be concentrating on analysing data related to the mutation's ...

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But her case is caused by a rare genetic mutation, so medications that work for 90% of people with cystic fibrosis won’t help her. The same dynamic plays out in other genetic conditions.

But her case is caused by a rare genetic mutation, so medications that work for 90% of people with cystic fibrosis won’t help her.