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Fossil Evidence
Fossil Evidence
XUJIAYAO HOMINID POSSESSED THE LARGEST KNOWN BRAIN IN THE MIDDLE PLEISTOCENE
August 18, 2025
Xujiayao hominid’s brain is biggest known brain Hong Ao et. al., Journal of Human Evolution, [...]
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Neanderthals Cared for a Child with Down Syndrome
August 20, 2025
NEANDERTHALS CARED FOR 6-YEAR-OLD WITH DOWN SYNDROME Research conducted by: MERCEDES CONDE-VALVERDE[...]
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Featured Posts
Improved Prime Editing System Enables Gene-Sized Edits in Human Cells at Therapeutic Levels
The largest and most diverse study on recessive genetic changes in developmental disorders reveals that over 80% of cases caused by recessive variants are linked to known genes. Researchers analyzed data from nearly 30,000 families and found that a shift in focus from gene discovery to interpreting changes in known genes could double diagnosis rates. • The study highlights the importance of genetic background in diagnosis and suggests that some patients may have multiple contributing genetic factors. These findings could lead to more personalized and accurate diagnoses for families affected by developmental disorders. • They include Joubert syndrome, Bardet-Biedl syndrome and TaySachs disease. Until now, overall quantification of these recessive genetic causes across diverse populations has not been done. • The team found the number of patients affected by recessive genetic variants varied greatly between different ancestry groups, ranging from two to 19 per cent of cases. This variation is strongly linked to the prevalence of unions between close relatives – consanguinity – in these groups.
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