Molecular Dissection Using Array Comparative Genomic Hybridization and Clinical Evaluation of An Infertile Male Carrier of An Unbalanced Y;21 Translocation: A Case Report and Review of The Literature [PDF]
International Journal of Fertility and Sterility, 2016 Chromosomal defects are relatively frequent in infertile men however, translocations between the Y chromosome and autosomes are rare and less than 40 cases of Y-autosome translocation have been reported.
Alfredo Orrico +7 more
doaj +1 more source
The outcomes of fetal cell microchimerism in the mother
Biomedical Research Journal, 2021 The presence of small quantities of genetically heterogeneous cells in an organism is known as microchimerism. Fetal microchimerism is the presence of small quantities of fetal cells in the maternal system during and after pregnancy.
Anushka Nikhil Alekar
doaj +1 more source
Assessment of Correlation between Androgen Receptor CAG Repeat Length and Infertility in Infertile Men Living in Khuzestan, Iran [PDF]
International Journal of Fertility and Sterility, 2015 Background The androgen receptor (AR) gene contains a polymorphic trinucleotide repeat that encodes a polyglutamine tract in its N-terminal transactivation domain (N- TAD).
Saeid Reza Khatami +4 more
doaj +1 more source
Association of X Chromosome Aberrations with Male Infertility
Acta Medica Bulgarica, 2021 Male infertility is caused by spermatogenetic failure, clinically noted as oligoor azoospermia. Approximately 20% of infertile patients carry a genetic defect.
Xharra S. +5 more
doaj +1 more source
Genome Biology, 2020 Heteromorphic sex chromosomes have evolved repeatedly across diverse species. Suppression of recombination between X and Y chromosomes leads to degeneration of the Y chromosome. The progression of degeneration is not well understood, as complete sequence
C. Peichel +10 more
semanticscholar +1 more source
Quantitative analysis of Y-Chromosome gene expression across 36 human tissues
Genome Research, 2020 Little is known about how human Y-Chromosome gene expression directly contributes to differences between XX (female) and XY (male) individuals in nonreproductive tissues.
Alexander K. Godfrey +7 more
semanticscholar +1 more source
The Y chromosome may contribute to sex-specific aging in Drosophila
Nature Ecology & Evolution, 2020 Heterochromatin suppresses repetitive DNA, and a loss of heterochromatin has been observed in aged cells of several species, including humans and Drosophila.
E. J. Brown +2 more
semanticscholar +1 more source
Balkan 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
Lack of Association Between Partial Y chromosome AZFc-gr/gr Deletions and Male Infertility
BioMed Target Journal, 2023 A microdeletion in the azoospermia factor (AZF) region of the human Y chromosome long arm is the second most common genetic factor causing male infertility and spermatogenetic failure. The current study aimed to evaluate the occurrence of AZFc-partial gr/
Muhsin Jamil Abdulwahid +1 more
doaj +1 more source
A family case of fertile human 45,X,psu dic(15;Y) males [PDF]
, 2006 We report on a familial case including four male probands from three generations with a 45,X,psu dic(15;Y)(p11.2;q12) karyotype. 45,X is usually associated with a female phenotype and only rarely with maleness, due to translocation of small Y chromosomal
Andersson M +29 more
core +1 more source