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chromosome
8 studies tagged chromosome, dated 1992-12-01 to 2021-04-10. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Immune cells lacking Y chromosome show dysregulation of autosomal gene expression 2021-04-10
- Mosaic loss of human Y chromosome: what, how and why 2020-02-04
- Longitudinal changes in the frequency of mosaic chromosome Y loss in peripheral blood cells of aging men varies profoundly between individuals 2019-10-25
Studies
8 studies carry this tag.
Date range
1992 to 2021
Top journals
- European journal of human genetics : EJHG 2
- Science (New York, N.Y.) 2
- Brain : a journal of neurology 1
- Cellular and molecular life sciences : CMLS 1
- Human genetics 1
6 journals in all.
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
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Epidemiological investigations show that mosaic loss of chromosome Y (LOY) in leukocytes is associated with earlier mortality and morbidity from many diseases in men.
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Y chromosome (ChrY), the male-specific sex chromosome, has been considered as a genetic wasteland.
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Mosaic loss of chromosome Y (LOY) is the most common somatic genetic aberration and is associated with increased risk for all-cause mortality, various forms of cancer and Alzheimer's disease, as well as other common human diseases.
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Age-related macular degeneration (AMD) is the leading cause of blindness in industrialised countries, and thereby a major individual but also a socio-economic burden.
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Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are both relentlessly progressive and ultimately fatal neurological disorders.
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The apolipoprotein E (APOE) gene is the only genetic risk factor that has so far been linked to risk for late-onset Alzheimer's disease (LOAD).
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Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease, affecting approximately 1 percent of the population over age 50.
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Familial Alzheimer's disease (FAD) has been shown to be genetically heterogeneous, with a very small proportion of early onset pedigrees being associated with mutations in the amyloid precursor protein (APP) gene on chromosome 21, and some late onset pedigrees showing associations with markers on chromosome 19.