Analysis - Chimpanzees are humans' closest living relatives, sharing over 98% of our DNA. They are endangered, with fewer ...

Sickle cell disease (SCD) is a genetic disorder of the red blood cells caused by a mutation in the HBB gene. This gene encodes a protein that is a key component of hemoglobin, a protein complex whose ...

It is caused by a mutation in the HBB gene, which leads to the production of abnormal haemoglobin known as haemoglobin S. This results in the distortion of red blood cells into Read More ...

The 11-gene panel includes the most prevalent recommended ... The kit targets genes like CFTR, CYP21A2, F8 inversions, FMR1, GBA, HBA1, HBA2, HBB, SMN1, SMN2 and TNXB. Per a report by TechSci ...

Sickle cell disease (SCD) is a genetic disorder of the red blood cells caused by a mutation in the HBB gene. This gene encodes a protein that is a key component of hemoglobin, a protein complex ...

Zynext Ventures is investing in Illexcor Therapeutics to advance the clinical development of ILX002, its lead candidate for ...