Describing a previously unknown genetic condition that affects children, researchers at University of California San Diego School of Medicine and Rady Children's Institute for Genomic Medicine say they also found a potential ...
Sep 29, 2021
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Acquired aplastic anemia (AA) is a rare blood disorder that causes the individual to have suppressed levels of hematopoietic stem progenitor cells, which ultimately mature into various types of blood cells. In many individuals ...
Sep 27, 2021
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Glioblastoma is the most lethal and malignant adult brain cancer that may arise from neuroglial stem or progenitor cells. Certain gene mutations or those with a known history of other cancers and radiation therapy may predispose ...
Sep 15, 2021
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Mutations in a protein known to cause Parkinson's Disease derange transportation in and out of brain cells, reports a team of UConn Health researchers in the 27 July issue of Science Signaling. The toxic traffic jams that ...
Sep 15, 2021
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Some types of chemotherapy eliminate cancer cells by damaging their DNA. These drugs can also affect healthy cells, where the damage can generate mutations that persist after the end of the treatment.
Sep 14, 2021
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Right now, in your body, lurk thousands of cells with DNA mistakes that could cause cancer. Yet only in rare instances do these DNA mistakes, called genetic mutations, lead to a full-blown cancer. Why?
Sep 2, 2021
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Talazoparib, a new precision drug, can keep cancer in check in some men with advanced prostate cancer who have run out of options, a phase II clinical trial shows.
Aug 23, 2021
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A new study led by University of California, Irvine (UCI) researchers identifies two ways in which APOBEC3A— a vital enzyme that is responsible for genetic changes resulting in a variety of cancers while protecting our ...
Aug 13, 2021
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Throughout development, life and the processes of aging, all human cells accumulate mutations, resulting in what is called mosaicism, a condition in which different cells in the same person have different DNA sequences or ...
Aug 13, 2021
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Hypertrophic cardiomyopathy (HCM) is the most common of all genetic heart diseases and is the leading cause of sudden cardiac death. It is characterized by an abnormal thickening of the heart muscle, which over time can lead ...
Aug 12, 2021
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