Washington [US], August 5 (ANI): During a recent study researchers have discovered how mitochondrial function, and dysfunction, play critical roles in numerous diseases, and even ageing.
San Diego (California) [US] August 2 (ANI): The body absorbs too much iron due to a condition known as hereditary hemochromatosis, which is brought on by a gene mutation. This causes tissue damage and diseases like liver disease, heart disease, and diabetes. However, scant and conflicting re
London [UK], July 19 (ANI): Non-coding 'junk' DNA, far from being innocuous and inactive, has been discovered by scientists to potentially contribute to the development of cancer.
Washington [US], July 16 (ANI): A preliminary study has shown that screening sperm may help identify potentially harmful new genetic mutations and help fertility specialists prevent them from being passed on to offspring.
Washington [US], July 12 (ANI): Screening sperm may help identify potentially harmful new genetic mutations and help fertility specialists prevent them from being passed on to offspring, shows a preliminary study. The results suggest a potential tool to help improve fertility treatment outco
Washington [US], July 10 (ANI): According to the long-standing canon in evolutionary biology, natural selection is cruelly selfish, favouring traits that help promote reproductive success. This usually means that the so-called "force" of selection is well equipped to remove harmful mutations
Washington [US], July 3 (ANI): According to a recent study, a group of scientists have stepped closer to understanding the unsolved Mendelian diseases. They have found that Mendelian diseases are inherited from either parent due to gene mutations in the developing egg or sperm by studying th
Washington [US], July 2 (ANI): Scientists have discovered a convergent mechanism that may be responsible for how two top-ranked genetic risk factors for autism spectrum disorder/intellectual disability (ASD/ID) lead to these neurodevelopmental disorders.
Washington [US], June 30 (ANI): Scientists have discovered a new way to interpret unsolved Mendelian diseases which are inherited from either parent due to gene mutations in the developing egg or sperm through studying the inheritance of a protein known as SMCHD1 which is coded by the SMCHD1
Washington [US], June 21 (ANI): Scientists have built a computer model that can rapidly scan the entire genome of cancer cells and identify mutations that occur more frequently than expected, suggesting that they are driving tumour growth.
New York [US], June 19 (ANI): A new algorithm can analyse thousands of mutations across the genome and determine a person's risk of getting chronic kidney disease, according to a recent study.
Washington [US], June 14 (ANI): A research study by the Dana-Farber Cancer Institute sheds light on that mystery, providing clues that may link mutations to epigenetic changes, and may point to potential drug targets to reduce the risk for people born with certain genetic mutations.