Susceptibility of gr/gr rearrangements to azoospermia or oligozoospermia is dependent on DAZ and CDY1 gene copy deletions
Explore this paper's citation graph
Summary
AZFc subdeletions are a major risk factor for male infertility in the Indian population and the deletion of DAZ and CDY1 gene copies increases its susceptibility to azoospermia or severe oligozoospermia.
- Type
- article
- Published
- 2015-07-07
- Cited by
- 32
- References
- 47
- Access
- Open access
- OpenAlex
- https://openalex.org/W1855227091
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:1451083
Keywords
Azoospermia, Male infertility, Genetics, Biology, Infertility
References
- Gene copy number reduction in the azoospermia factor c (AZFc) region and its effect on total motile sperm count.
- Genetic causes of spermatogenic failure.
- Spermatogenic Patterns and Early Embryo Development After Intracytoplasmic Sperm Injection in Severe Oligoasthenozoospermia
- Screening for AZFc Partial Deletions in Dravidian Men with Nonobstructive Azoospermia and Oligozoospermia
- Previously uncharacterized histone acetyltransferases implicated in mammalian spermatogenesis
- Clinical and laboratory evaluation of idiopathic male infertility in a secondary referral center in India
- Levels of Tektin 2 and CatSper 2 in normozoospermic and oligoasthenozoospermic men and its association with motility, fertilization rate, embryo quality and pregnancy rate
- Y chromosome analysis of infertile men and their sons conceived through intracytoplasmic sperm injection: vertical transmission of deletions and rarity of de novo deletions.
- A unique view on male infertility around the globe
- Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection
- Clinical relevance of Y-linked CNV screening in male infertility: new insights based on the 8-year experience of a diagnostic genetic laboratory
- Association of progesterone receptor gene polymorphism with male infertility and clinical outcome of ICSI
- Human DAZL, DAZ and BOULE genes modulate primordial germ cell and haploid gamete formation
- Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment.
- Y chromosome and male infertility: update, 2006.
- Partial Microdeletions in the Y-Chromosome AZFc Region Are Not a Significant Risk Factor for Spermatogenic Impairment in Tunisian Infertile Men
- Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background
- Impaired Spermatogenesis and gr/gr Deletions Related to Y Chromosome Haplogroups in Korean Men
- DAZ (Deleted in AZoospermia) genes encode proteins located in human late spermatids and in sperm tails.
- Associations of Y-chromosome subdeletion gr/gr with the prevalence of Y-chromosome haplogroups in infertile patients
Cited by
- Deletion of GOLGA2P3Y but not GOLGA2P2Y is a risk factor for oligozoospermia.
- Analysis of partial azoospermia factor c deletion and DAZ copy number in azoospermia and severe oligozoospermia
- Gr/gr deletions on Y-chromosome correlate with male infertility: an original study, meta-analyses, and trial sequential analyses
- Y chromosome b2/b3 deletions and male infertility: A comprehensive meta-analysis, trial sequential analysis and systematic review.
- eNOS gene T786C, G894T and 4a4b polymorphisms and male infertility susceptibility: a meta‐analysis
- gr/gr-DAZ2-DAZ4-CDY1b deletion is a high-risk factor for male infertility in Tunisian population.
- Male infertility: screening of azoospermia factor (azf) microdeletion in idiopathic infertile men
- Role of nuclear and mitochondrial genes in human male infertility: a review
- Role of Y Chromosome Microdeletions in the Clinical Evaluation of Infertile Males
- Analyse des variations du nombre de copies d'ADN dans une cohorte d'hommes infertiles et génération de modèles génétiques d’étude de la méiose à partir de cellules iPS de patients infertiles
- Genetics of the human Y chromosome and its association with male infertility
- Paternal factors contributing to embryo quality
- Germline deletion of Cdyl causes teratozoospermia and progressive infertility in male mice
- Consequences of Y chromosome microdeletions beyond male infertility
- AZF deletions in Indian populations: original study and meta-analyses
- Chromosomal microarray analysis of infertile men with azoospermia factor microdeletions.
- The effects of Y chromosome microdeletions on in vitro fertilization outcomes, health abnormalities in offspring and recurrent pregnancy loss
- Hypomethylation of the DAZ3 promoter in idiopathic asthenospermia: a screening tool for liquid biopsy
- Poor intracytoplasmic sperm injection outcome in infertile males with azoospermia factor c microdeletions.
- Evaluation of association between methylenetetrahydrofolate reductase and azoospermia
Related papers
- [Screening and clinical phenotype analysis of microdeletions of azoospermia factor region on Y chromosome in 1011 infertile men].
- Analysis of microdeletions of azoospermia factor on Y chromosome in male infertile patients from a city
- Examination on microdeletions of azoospermia factor in male infertility
- Screening for the microdeletions of azoospermia factoron the Y chromosome with multiplex PCR
- Spontaneous transmission from a father to his son of a Y chromosome microdeletion involving the deleted in azoospermia (DAZ) gene
- Analysis of microdeletions of azoospermia factor on the Y chromosome in male infertile patients
- [Chromosome Y microdeletions in the pathogenesis of male infertility].
- Y chromosome microdeletion and gene deletion screening in infertile men with idiopathic azoospermia and oligospermia
- The clinical significance of Y chromosomal microdeletions detection in male infertility