Research team reveals how TREM2 genetic mutation affects late-onset Alzheimer's

byUniversity of California, IrvineMERFISH spatial transcriptomics enables spatial variation analysis of the transcriptome at the cell type level. A Dataset overview consisting of 15 samples, fro

Updated on: August 08,2024 0

Research team reveals how TREM2 genetic mutation affects late-onset Alzheimer's

byUniversity of California, IrvineMERFISH spatial transcriptomics enables spatial variation analysis of the transcriptome at the cell type level. A Dataset overview consisting of 15 samples, fro

Updated on:August 08,2024 0

Exploring how our first language is echoed in our genes

by Mary-Lou Watkinson,Vanderbilt UniversityWorldwide variation in the relationship between genetics and language. Credit:Proceedings of the National Academy of Sciences(2024). DOI: 1

Updated on: December 11,2024 0

Exploring how our first language is echoed in our genes

by Mary-Lou Watkinson,Vanderbilt UniversityWorldwide variation in the relationship between genetics and language. Credit:Proceedings of the National Academy of Sciences(2024). DOI: 1

Updated on:December 11,2024 0

Discovery identifies key factor for balancing saturated and unsaturated fatty acids in the body

byOsaka UniversityThe possible roles of adipocyte Armc5 invivo. Credit:Journal of Biological Chemistry(2024). DOI: 10.1016/j.jbc.2024.107953Researchers at Osaka University iden

Updated on: December 12,2024 0

Discovery identifies key factor for balancing saturated and unsaturated fatty acids in the body

byOsaka UniversityThe possible roles of adipocyte Armc5 invivo. Credit:Journal of Biological Chemistry(2024). DOI: 10.1016/j.jbc.2024.107953Researchers at Osaka University iden

Updated on:December 12,2024 0

Newborn screening by genome sequencing shown to be safe and effective in two clinical studies

by Rady Children's Institute for Genomic MedicineCredit: Unsplash/CC0 Public DomainTwo studies published in theAmerican Journal of Human Geneticsshow the potential for genomic screenin

Updated on: December 11,2024 0

Newborn screening by genome sequencing shown to be safe and effective in two clinical studies

by Rady Children's Institute for Genomic MedicineCredit: Unsplash/CC0 Public DomainTwo studies published in theAmerican Journal of Human Geneticsshow the potential for genomic screenin

Updated on:December 11,2024 0

Study finds omega-3 supplements reduce genetic risk of high total cholesterol, LDL and triglyceride levels

byUniversity of GeorgiaCredit: Pixabay/CC0 Public DomainFish oil supplements are a multi-billion dollar industry in the U.S. and abroad, with about 2 out of every 25 people popping the popular o

Updated on: August 08,2024 0

Study finds omega-3 supplements reduce genetic risk of high total cholesterol, LDL and triglyceride levels

byUniversity of GeorgiaCredit: Pixabay/CC0 Public DomainFish oil supplements are a multi-billion dollar industry in the U.S. and abroad, with about 2 out of every 25 people popping the popular o

Updated on:August 08,2024 0

Plastic chemical phthalate causes DNA breakage and chromosome defects in sex cells, new study finds

byPublic Library of ScienceBBP exposure causes chromosome organization defects in the female germline. Carnoy's fixed and DAPI-stained images of gonads at the pachytene stage following expos

Updated on: October 31,2024 0

Plastic chemical phthalate causes DNA breakage and chromosome defects in sex cells, new study finds

byPublic Library of ScienceBBP exposure causes chromosome organization defects in the female germline. Carnoy's fixed and DAPI-stained images of gonads at the pachytene stage following expos

Updated on:October 31,2024 0

Study identifies the main culprit behind flare-ups in a rare genetic disorder

byKyoto UniversityCredit:EMBO Molecular Medicine(2024). DOI: 10.1038/s44321-024-00174-3Through a series of cell and animal studies, a research team has identified the principal culpr

Updated on: December 12,2024 0

Study identifies the main culprit behind flare-ups in a rare genetic disorder

byKyoto UniversityCredit:EMBO Molecular Medicine(2024). DOI: 10.1038/s44321-024-00174-3Through a series of cell and animal studies, a research team has identified the principal culpr

Updated on:December 12,2024 0

BRCA1 gene mutation may increase the risk of impaired fertility, study shows

byMonash University(a) Human cortical ovarian tissues from BRCA1 (n=8) and BRCA2 (n=10) mutation carriers (mc) were immunohistochemically stained for DDX4 as a marker of

Updated on: August 08,2024 0

BRCA1 gene mutation may increase the risk of impaired fertility, study shows

byMonash University(a) Human cortical ovarian tissues from BRCA1 (n=8) and BRCA2 (n=10) mutation carriers (mc) were immunohistochemically stained for DDX4 as a marker of

Updated on:August 08,2024 0

New method for evaluating male subfertility based on trace element analysis

byUniversity of TsukubaCredit: Unsplash/CC0 Public DomainWith declining birthrate becoming a social problem, the number of couples in Japan suffering from subfertility due to male factors is rep

Updated on: November 23,2024 0

New method for evaluating male subfertility based on trace element analysis

byUniversity of TsukubaCredit: Unsplash/CC0 Public DomainWith declining birthrate becoming a social problem, the number of couples in Japan suffering from subfertility due to male factors is rep

Updated on:November 23,2024 0

Bioinformatics techniques uncover hidden prevalence of repeat expansion disorders

byQueen Mary, University of LondonCredit: Pixabay/CC0 Public DomainResearch led by scientists at Queen Mary University of London is signaling a new era for genetic sequencing and testing. In the

Updated on: October 09,2024 0

Bioinformatics techniques uncover hidden prevalence of repeat expansion disorders

byQueen Mary, University of LondonCredit: Pixabay/CC0 Public DomainResearch led by scientists at Queen Mary University of London is signaling a new era for genetic sequencing and testing. In the

Updated on:October 09,2024 0

Study deciphers pathological mechanisms of spermatogenic impairment in cryptorchidism

byChinese Academy of SciencesSpermatogenic failure in cryptorchidism is due to abnormal spermatogonia, activated mast cells, and impaired testicular niche. Credit: Wang Xiaoyan and Zhuang ZiyanC

Updated on: September 14,2024 0

Study deciphers pathological mechanisms of spermatogenic impairment in cryptorchidism

byChinese Academy of SciencesSpermatogenic failure in cryptorchidism is due to abnormal spermatogonia, activated mast cells, and impaired testicular niche. Credit: Wang Xiaoyan and Zhuang ZiyanC

Updated on:September 14,2024 0

Cutting corners results in rare genetic diseases being undiagnosed, say scientists

byUniversity of ManchesterCommunity of practice-driven development. Credit:Nature Genetics(2024). DOI: 10.1038/s41588-024-01938-wInaccurate naming of genetic diseases is resulting in

Updated on: October 09,2024 0

Cutting corners results in rare genetic diseases being undiagnosed, say scientists

byUniversity of ManchesterCommunity of practice-driven development. Credit:Nature Genetics(2024). DOI: 10.1038/s41588-024-01938-wInaccurate naming of genetic diseases is resulting in

Updated on:October 09,2024 0