Aug 17, 2021 ... Such mutations are typical of Noonan syndrome and suggests the syndrome may be a cause of unrecognized sudden death in infancy. The case is ...

Jul 26, 2021 ... A genetic mutation associated with a hereditary disorder in the cardiac electrical system has been identified, researchers at Yale School of ...

Dec 12, 2022 ... Returning to India in 2005, Bhat has been providing clinical-genetic services at the Centre for Human Genetics (CHG), Bangalore, which she ...

May 19, 2020 ... A collaboration between scientists at the Medical University of South Carolina and clinicians at the Greenwood Genetic Center has yielded ...

Feb 8, 2024 ... The team found two key human genetic factors that could help explain why some people develop severe Lassa fever, and a set of LARGE1 variants ...

Feb 10, 2022 ... Researchers from the Université Laval Faculty of Medicine and CHU de Québec–Université Laval Research Centre have successfully edited the ...

Jan 10, 2019 ... Researchers have created a method for modifying blood stem cells to reverse the genetic mutation that causes a life-threatening autoimmune ...

Nov 27, 2013 ... Study uses patient-derived stem cells to show that a mutation in the α-synuclein gene causes increased vulnerability to pesticides, ...

Mar 23, 2021 ... Moreover, the brother with the mutation had severe COVID-19, while his brother with normal interferon genes was asymptomatic. "Our results show ...

Jan 10, 2022 ... Related Stories ... Experts identified mutations in the gene RBM5 in multiple infertile men. Previous research carried out in mice has shown that ...

Genetic mutation implicated in 'broken' heart. Date: February 15, 2012; Source: Harvard Medical School; Summary: Researchers have found that mutations in a ...

Jan 15, 2013 ... Researchers have identified a new genetic mutation for amyotrophic lateral sclerosis (ALS), opening the door to future targeted therapies.

Jun 23, 2022 ... Researchers at the John T. Macdonald Department of Human Genetics and John P. Hussman Institute for Human Genomics at the University of ...

Aug 1, 2022 ... A disorder called hereditary hemochromatosis, caused by a gene mutation, results in the body absorbing too much iron, leading to tissue ...

Jan 17, 2012 ... After a 20-year quest to find a genetic driver for prostate cancer that strikes men at younger ages and runs in families, researchers have ...

Mar 24, 2021 ... ... DNA, Endocrinology, Gene, Genes, Genetic, Genetics, Genomics, Marriage, Medical Research, Medicine, Mental Health, Mutation, Neuron, Neurons ...

Dec 8, 2021 ... "What that means is that the gene is causing heart damage slowly over time," said Amanda C. Coniglio, M.D., the lead author of the study and a ...

Mar 30, 2014 ... Using a new gene-editing system based on bacterial proteins, researchers have cured mice of a rare liver disorder caused by a single genetic ...

Sep 8, 2013 ... ... gene, which may increase the risk of developing ALL. The inherited genetic mutation is located in a gene called PAX5, which is known to play ...

Jul 9, 2021 ... A team of Australian researchers say they have discovered the underlying mechanism of a rare genetic mutation that can cause epilepsy.