Research reveals childhood kidney cancer's complex genetic landscape, paving the way for innovative treatments. ...

Researchers have uncovered that some childhood cancers have a substantially higher number of DNA changes than previously ...

Researchers have uncovered that some childhood cancers have a substantially higher number of DNA changes than previously ...

Researchers have uncovered that some childhood cancers have a substantially higher number of DNA changes than previously ...

With gene therapy offering new hope for thalassemia, experts urge Indian govt to invest in early diagnosis, genetic testing, ...

Autosomal recessive bestrophinopathy (ARB) is a rare retinal dystrophy caused by homozygous or compound heterozygous null variants in the BEST1 gene. Clinically, ARB presents with variable features ...

A new study reveals that over one in four Indian children under 12 carry inherited blood disorders. The findings highlight ...

Somatic hypermutation (SHM) of immunoglobulin variable (V) regions modulates antibody-antigen affinity is initiated by activation-induced cytidine deaminase (AID) on single-stranded DNA (ssDNA).

A three-year study by Metropolis Healthcare reveals that 28.4 per cent of nearly 20,000 children screened for ...

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

Now he faces the challenge of dismantling the Iranian program. By David E. Sanger and Farnaz Fassihi David E. Sanger has covered the Iranian nuclear program for more than two decades. He reported ...

“Despite the existence of more advanced methods, Sanger Sequencing developed by Frederick Sanger remains the gold standard in various applications due to its reliability,” says NLM. Sanger ...