Tag: Mutation
Redcliffe Labs reports India’s first USP18 gene mutation tied to rare...
The study identifies a rare USP18 gene mutation, offering crucial insights into a neurological disorder previously documented in only 11 cases worldwide and now reported for the first time in India
Servier India partners MedGenome and Strand Life Sciences to advance biomarker...
The panel will be available to healthcare professionals across private and government sectors
Genetic recombination made Omicron more infectious
The Indian researchers have found that recombination events had escalated during the Omicron wave, which made the virus more immune-evasive and infectious.
CCMB scientists unearth potential diagnostic markers for male infertility
The new study which was conducted in collaboration with several other institutions and focused on the cause of infertility in the rest of the cases, has now identified eight defective genes in these men
Gene defect for allergic & autoimmune diseases discovered
A mutation of the IL-33 gene in the human genome that results in multiple allergic disease manifestations, and autoimmune disease has been discovered for the first time
First ever human patient dosed with Gene Therapy in Ocugen’s Phase...
This first patient dosing marks the beginning of the dose-escalating, observer-blind, Phase 1/2 safety and efficacy study
Treatment of progressive neurological, neuromuscular disorder gets a shot in the...
The researchers identified the compounds from a library of about 25 lakh small molecules maintained by the National Cancer Institute (NCI), United States of America
Study identifies genetic risk factors for heart failure
A gene called β-MYH7 is one of the major genes implicated in cardiac diseases globally
Zydus Cadila to supply 1 crore doses of its Covid-19 vaccine,...
ZyCoV-D is the first DNA plasmid vaccine in the world for human use, developed indigenously by the company against the Covid-19 virus
Latest research by NII scientists raises new hope for mitochondrial disorders
In the new study, the researchers at National Institute of Immunology focused on autosomal dominant progressive external ophthalmoplegia (adPEO) as it is one of the most common Mitochondrial disorders......................