Gurugram (Haryana) [India], August 8: Gurugram-based Dr. Gitanjali Ramchandani and Siddhant Minocha have developed a new AI technology designed to detect chronic diseases years in advance. Their platform, Purna AI, identifies over 75 clinical and sub-clinical patterns using blood biomarkers,
To get to the bottom of this, the National Institute of Mental Health (NIMH) initiated a consortium called SSPsyGene (sspsygene.ucsc.edu) in 2023, uniting research teams from renowned US universities with the joint goal of characterising the genetic origins of NPD, focusing on 250 selected h
A team of researchers discovered a genetic mutation in a non-coding region of DNA that changes thyroid regulation, resulting in a rare type of congenital thyroid abnormality.
Ahmedabad (Gujarat) [India], March 14: In a significant stride towards making advanced cancer treatment accessible to all, Zydus has launched Olaparib, a PARP inhibitor, under the brand name IBYRA in India. The drug will target specific genetic mutations prevalent in certain types of cancers
The Similipal Tiger Reserve in Odisha's Mayurbhanj district is the only tiger reserve in India that houses the rare black tiger (pseudo-melanistic), which has distinctive dark stripe patterns due to a genetic mutation. The reserve is located in the Mayurbhanj district, at the eastern end of
African Americans have long been known to be at a higher risk of kidney disease due to a dangerous genetic mutation that creates a hole in the kidney cells, but Vanderbilt University Medical Centre (VUMC) researchers have now discovered a protective genetic mutation that covers the hole, the
Researchers have identified a further possible origin for the genetic abnormalities that give rise to uncommon diseases like Huntington's disease (HD).
In the ageing population, the Apolipoprotein-4 allele has been associated with an increased risk for a variety of illnesses, particularly Alzheimer's and cardiovascular disease. Despite its negative effects, this genetic mutation is nevertheless prevalent in roughly 20 per cent of the popula
The Apolipoprotein-4 allele has been linked to an increased risk for a number of diseases in ageing populations, particularly Alzheimer's and cardiovascular disease. Nevertheless, this genetic mutation continues to be common in about 20% of the human population despite its harmful effects. A
A study performed by Sanford Burnham Prebys researchers discovered that specific genetic abnormalities are linked to treatment-resistant breast cancer in young women. These mutations do not appear to be associated with treatment-resistant breast cancer in older women.
An estimated 15-20 per cent of children diagnosed with Dravets Syndrome die before reaching adulthood. There is no cure, and current treatment focuses on simply reducing seizures.
A discovery that may result in novel medicines to halt or reverse the disease could be beneficial to patients with a rare genetic bone marrow problem who are at an elevated risk of blood malignancies.