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Reproduction
Focuses on human reproductive issues.
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Previously unknown genetic links provide insights into autism's prevalence among males

Previously unknown genetic links provide insights into autism's prevalence among males

byThe Hospital for Sick ChildrenCredit: Pixabay/CC0 Public DomainResearch published inThe American Journal of Human Geneticshas identified a previously unknown genetic link to autism

Previously unknown genetic links provide insights into autism's prevalence among males

byThe Hospital for Sick ChildrenCredit: Pixabay/CC0 Public DomainResearch published inThe American Journal of Human Geneticshas identified a previously unknown genetic link to autism
How a former navy mechanic defied the genetic odds of inherited Alzheimer's disease

How a former navy mechanic defied the genetic odds of inherited Alzheimer's disease

by Justin Jackson , Medical XpressSchematic representation of the pedigree for the DIAN family carriers of the pathogenic mutation PSEN2 p.Asn141Ile. Credit:Nature Medicine(2025). DOI: 10.

How a former navy mechanic defied the genetic odds of inherited Alzheimer's disease

by Justin Jackson , Medical XpressSchematic representation of the pedigree for the DIAN family carriers of the pathogenic mutation PSEN2 p.Asn141Ile. Credit:Nature Medicine(2025). DOI: 10.
Boosting autophagy in eggs may reduce DNA damage and reproductive complications

Boosting autophagy in eggs may reduce DNA damage and reproductive complications

by Brian Consiglio,University of MissouriSchematic model summarizing the impact of DNA double-strand breaks on oocyte meiosis I and the role of autophagy in DNA damage repair. Credit:Natur

Boosting autophagy in eggs may reduce DNA damage and reproductive complications

by Brian Consiglio,University of MissouriSchematic model summarizing the impact of DNA double-strand breaks on oocyte meiosis I and the role of autophagy in DNA damage repair. Credit:Natur
Research reveals possible link between protein G3BP1 and amyotrophic lateral sclerosis

Research reveals possible link between protein G3BP1 and amyotrophic lateral sclerosis

byFree University of BrusselsLiquid–liquid phase separation of G3BP1 is aggravated by R-rich C9orf72 DPRs. Credit:Proceedings of the National Academy of Sciences(2024). DOI: 10.1073/

Research reveals possible link between protein G3BP1 and amyotrophic lateral sclerosis

byFree University of BrusselsLiquid–liquid phase separation of G3BP1 is aggravated by R-rich C9orf72 DPRs. Credit:Proceedings of the National Academy of Sciences(2024). DOI: 10.1073/
Ancient viral DNA in the human genome linked to multiple sclerosis and amyotrophic lateral sclerosis

Ancient viral DNA in the human genome linked to multiple sclerosis and amyotrophic lateral sclerosis

byKing's College LondonRetrotranscriptome-wide association studies of neurodegenerative diseases. Credit:Brain, Behavior, and Immunity(2024). DOI: 10.1016/j.bbi.2024.10.020New re

Ancient viral DNA in the human genome linked to multiple sclerosis and amyotrophic lateral sclerosis

byKing's College LondonRetrotranscriptome-wide association studies of neurodegenerative diseases. Credit:Brain, Behavior, and Immunity(2024). DOI: 10.1016/j.bbi.2024.10.020New re
Genomics research focuses on health solutions in the tropics

Genomics research focuses on health solutions in the tropics

byJames Cook UniversityCredit: CC0 Public DomainScientists believe the lives of much of the world's population could be improved if DNA technology is applied in an integrated way in three ar

Genomics research focuses on health solutions in the tropics

byJames Cook UniversityCredit: CC0 Public DomainScientists believe the lives of much of the world's population could be improved if DNA technology is applied in an integrated way in three ar
Research team reveals how TREM2 genetic mutation affects late-onset Alzheimer's

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

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
Unexpected X chromosome findings challenge assumptions about sex differences in human disease

Unexpected X chromosome findings challenge assumptions about sex differences in human disease

by Karin Söderlund Leifler,Linköping UniversitySome of the group members in the Nestor lab at Linköping University. Credit: Johan Sjöholm/Linköping UniversityResearchers at Linköping University

Unexpected X chromosome findings challenge assumptions about sex differences in human disease

by Karin Söderlund Leifler,Linköping UniversitySome of the group members in the Nestor lab at Linköping University. Credit: Johan Sjöholm/Linköping UniversityResearchers at Linköping University
Consortium creates a robust, open-access platform to define the clinical relevance of genes and variants

Consortium creates a robust, open-access platform to define the clinical relevance of genes and variants

by Molly Chiu,Baylor College of MedicineCredit:Genetics in Medicine(2024). DOI: 10.1016/j.gim.2024.101228The Clinical Genome Resource (ClinGen), a resource that works to define the c

Consortium creates a robust, open-access platform to define the clinical relevance of genes and variants

by Molly Chiu,Baylor College of MedicineCredit:Genetics in Medicine(2024). DOI: 10.1016/j.gim.2024.101228The Clinical Genome Resource (ClinGen), a resource that works to define the c