Results 1 to 10 of about 10,690,340 (404)

Natural selection reduced diversity on human Y chromosomes [PDF]

open access: yesarXiv, 2013
The human Y chromosome exhibits surprisingly low levels of genetic diversity. This could result from neutral processes if the effective population size of males is reduced relative to females due to a higher variance in the number of offspring from males than from females.
Lohmueller, Kirk E.   +2 more
arxiv   +12 more sources

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

Forensic use of Y-chromosome DNA: a general overview [PDF]

open access: yesHuman Genetics, 2017
The male-specific part of the human Y chromosome is widely used in forensic DNA analysis, particularly in cases where standard autosomal DNA profiling is not informative.
M. Kayser
semanticscholar   +5 more sources

Complex genomic rearrangements of the Y chromosome in a premature infant [PDF]

open access: yesMolecular Cytogenetics
Background Chromoanagenesis is an umbrella term used to describe catastrophic “all at once” cellular events leading to the chaotic reconstruction of chromosomes. It is characterized by numerous rearrangements involving a small number of chromosomes/loci,
Stephanie A. Balow   +6 more
doaj   +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

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

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

48,XYYY: A Rare Case Report

open access: yesBalkan Journal of Medical Genetics, 2022
A case study of a 4 year old child with hypospadias and cryptorchidism on the right side is presented. Combined analysis by Karyotype and FISH showed a mosaic pattern of 48, XYYY (73%); 47,XYY (7%); 46,XY (7%) and 45,X (13%).
Sabnis AS, Bhusare D
doaj   +1 more source

Multiplex-Polymerase Chain Reaction for Detecting Microdeletions in The Azoospermia Factor Region of Y Chromosome in Iranian Couples with Non-Obstructive Infertility and Recurrent Pregnancy Loss [PDF]

open access: yesInternational Journal of Fertility and Sterility, 2018
Background Approximately 15% of couples are infertile with the male factor explaining approximately 50% of the cases. One of the main genetic factors playing a role in male infertility is Y chromosomal microdeletions within the proximal long arm of the Y
Afsaneh Mojtabanezhad Shariatpanahi   +4 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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