Results 11 to 20 of about 10,446,015 (290)

Massive gene amplification on a recently formed Drosophila Y-chromosome [PDF]

open access: yesNature Ecology & Evolution, 2018
Widespread loss of genes on the Y is considered a hallmark of sex chromosome differentiation. Here we show that the initial stages of Y evolution are driven by massive amplification of distinct classes of genes. The neo-Y chromosome of Drosophila miranda
D. Bachtrog   +2 more
semanticscholar   +3 more sources

Y-Chromosome Microdeletions: A Review of Prevalence, Screening, and Clinical Considerations

open access: greenThe Application of Clinical Genetics, 2021
Matthew J Rabinowitz, Phillip J Huffman, Nora M Haney, Taylor P Kohn The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USACorrespondence: Taylor P KohnJames Buchanan Brady Urological Institute ...
Rabinowitz MJ   +3 more
openalex   +2 more sources

Chromosomal aneuploidies and associated rare genetic syndromes involved in male infertility [PDF]

open access: yesJournal of Men's Health, 2021
Background and objectives: Recent investigations have reported more than 70 genetic syndromes involved in male infertility; however, the majority of these syndromes are extremely rare.
Eisa Tahmasbpour Marzouni   +2 more
doaj   +1 more source

Mosaic Turner Variant Adult Female Presenting with XO/XY Karyotype

open access: yesJournal of Human Reproductive Sciences, 2023
Turner syndrome (TS) is the most frequently detected chromosomal abnormality in females caused by the partial or complete absence of second X chromosome.
Sigin George   +3 more
doaj   +1 more source

Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality

open access: yesScience, 2022
Hematopoietic mosaic loss of Y chromosome (mLOY) is associated with increased risk of mortality and age-related diseases in men, but the causal and mechanistic relationships have yet to be established. Here, we show that male mice reconstituted with bone
S. Sano   +24 more
semanticscholar   +1 more source

Development and Forensic Application of EX20+30Y Kit

open access: yesFayixue Zazhi, 2021
ObjectiveTo develop a multiplex PCR amplification system (EX20+30Y for short) of 19 autosomes, 30 Y-STR loci plus the gender indicator, and evaluate its forensic application value.MethodsWith the six-color fluorescence labeling technology, a multiplex ...
ZHOU Xu-ming, GAO Deng-xing, LI Fa-yuan
doaj   +1 more source

Telomere-to-telomere assembly of a fish Y chromosome reveals the origin of a young sex chromosome pair

open access: yesGenome Biology, 2021
The origin of sex chromosomes requires the establishment of recombination suppression between the proto-sex chromosomes. In many fish species, the sex chromosome pair is homomorphic with a recent origin, providing species for studying how and why ...
Lingzhan Xue   +8 more
semanticscholar   +1 more source

Frequency of Y chromosome Microdeletions in Turkish Infertile Men: Single Center Experience

open access: yesGenel Tıp Dergisi, 2022
Objective: Infertility is defined as the failure to achieve a clinical pregnancy after twelve months of regular unprotected sexual intercourse. Both genetic and environmental factors affect infertility.
Aysel Kalaycı Yiğin   +3 more
doaj   +1 more source

Comparison between Real Time PCR and Gel based PCR Technique in Diagnosis Y Chromosome microdeletions in infertile azoospermia males in the Iraqi Kurdish Population

open access: yesBioMed Target Journal, 2023
Infertility is a disorder of the reproductive system characterized by a couple's inability to conceive after at least one year of regular, unprotected sexual activity. Approximately 15% of couples worldwide struggle with infertility.
Muhsin Jamil Abdulwahid   +1 more
doaj   +1 more source

Recognition of the Y chromosome in Turner syndrome using peripheral blood or oral mucosa tissue [PDF]

open access: yesAnnals of Pediatric Endocrinology & Metabolism, 2021
Purpose Turner syndrome is defined as total or partial loss of the second sex chromosome in a phenotypically female patient. Due to the possibility of hidden mosaicism of fragments of the Y chromosome and development of gonadoblastoma, we evaluated the ...
Lene Garcia Barbosa   +3 more
doaj   +1 more source

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