Categoría: Noticias
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New tool uncovers overlooked disease-linked genes by accounting for ancestry and family ties
Every person’s DNA tells a unique story. To unlock the full potential of genetic research, scientists need tools that reflect the complexity of the people they study.
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New tool uncovers overlooked disease-linked genes by accounting for ancestry and family ties
Every person’s DNA tells a unique story. To unlock the full potential of genetic research, scientists need tools that reflect the complexity of the people they study.
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Three genetic modifiers may alter inherited Alzheimer’s onset and progression
Autosomal dominant Alzheimer’s disease (ADAD) is a genetically inherited form of Alzheimer’s disease that accounts for only about 1% of Alzheimer’s disease cases. However, because individuals with the gene mutations are extremely likely to develop Alzh…
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Three genetic modifiers may alter inherited Alzheimer’s onset and progression
Autosomal dominant Alzheimer’s disease (ADAD) is a genetically inherited form of Alzheimer’s disease that accounts for only about 1% of Alzheimer’s disease cases. However, because individuals with the gene mutations are extremely likely to develop Alzh…
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Same carcinogen, different tumors: Mouse study reveals the role of genetic background
Why do cancers develop differently in different people—even when they are exposed to the same risk factors? An international research group, including the German Cancer Research Center (DKFZ), has demonstrated in mice that an organism’s genetic makeup …
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Same carcinogen, different tumors: Mouse study reveals the role of genetic background
Why do cancers develop differently in different people—even when they are exposed to the same risk factors? An international research group, including the German Cancer Research Center (DKFZ), has demonstrated in mice that an organism’s genetic makeup …
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Personalized gene therapy helps teen with rare form of severe epilepsy walk independently
SCN2A-related developmental epileptic encephalopathy (DEE) is a rare, severe form of childhood epilepsy and one of the most common causes of monogenic autism. The condition is caused by single mutations in the sodium voltage-gated channel alpha subunit…
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Personalized gene therapy helps teen with rare form of severe epilepsy walk independently
SCN2A-related developmental epileptic encephalopathy (DEE) is a rare, severe form of childhood epilepsy and one of the most common causes of monogenic autism. The condition is caused by single mutations in the sodium voltage-gated channel alpha subunit…
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Sudden cardiac death condition shown to have linked genetic variations
Scientists have found that the «sudden» cardiac death condition related to high-profile deaths or major medical episodes of sports stars including Fabrice Muamba, Christian Erikson and Mark-Vivian Foe, has numerous linked gene variations that highlight…
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Sudden cardiac death condition shown to have linked genetic variations
Scientists have found that the «sudden» cardiac death condition related to high-profile deaths or major medical episodes of sports stars including Fabrice Muamba, Christian Erikson and Mark-Vivian Foe, has numerous linked gene variations that highlight…