(Q24634263)

Human Reproduction Update

18 March 2010

5 references

14 March 2019

30 June 2019

14 September 2019

12 October 2019

28 November 2023

5 references

14 March 2019

30 June 2019

14 September 2019

12 October 2019

28 November 2023

16

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page(s)

525-42

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issue

5

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copyright license

Creative Commons Attribution-NonCommercial 2.5 Generic

5 references

14 March 2019

30 June 2019

14 September 2019

12 October 2019

on focus list of Wikimedia project

28 November 2023

ScienceSource

0 references

cites work

Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

The DAZL family proteins are PABP-binding proteins that regulate translation in germ cells.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Identification and characterization of human VCY2-interacting protein: VCY2IP-1, a microtubule-associated protein-like protein

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Specific expression of VCY2 in human male germ cells and its involvement in the pathogenesis of male infertility

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

VCY2 protein interacts with the HECT domain of ubiquitin-protein ligase E3A

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Previously uncharacterized histone acetyltransferases implicated in mammalian spermatogenesis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

A nomenclature system for the tree of human Y-chromosomal binary haplogroups

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

The b2/b3 subdeletion shows higher risk of spermatogenic failure and higher frequency of complete AZFc deletion than the gr/gr subdeletion in a Chinese population

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

The mechanism of human nonhomologous DNA end joining

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

High mutation rates have driven extensive structural polymorphism among human Y chromosomes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

AZF deletions and Y chromosomal haplogroups: history and update based on sequence

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Large-scale copy number polymorphism in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

The human Y chromosome: an evolutionary marker comes of age

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Polymorphic DAZ gene family in polymorphic structure of AZFc locus: Artwork or functional for human spermatogenesis?

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

The origins, patterns and implications of human spontaneous mutation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

The double-strand-break repair model for recombination

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Dazl can bind to dynein motor complex and may play a role in transport of specific mRNAs

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Hierarchical analysis of 30 Y-chromosome SNPs in European populations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative endings

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Replication validity of genetic association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Human DAZL, DAZ and BOULE genes modulate primordial germ-cell and haploid gamete formation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Isodicentric Y chromosomes and sex disorders as byproducts of homologous recombination that maintains palindromes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Y chromosome gr/gr deletions are a risk factor for low semen quality

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Gene conversion causing human inherited disease: evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Copy number variation on the human Y chromosome.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Unique signatures of natural background radiation on human Y chromosomes from Kerala, India

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Polymorphic expression of DAZ proteins in the human testis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Ectopic gene conversions in the human genome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

The Y chromosome and male infertility

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Gene conversion and end-joining-repair double-strand breaks in the Caenorhabditis elegans germline

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Double-strand breaks associated with repetitive DNA can reshape the genome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

A mechanism for DNA-PK activation requiring unique contributions from each strand of a DNA terminus and implications for microhomology-mediated nonhomologous DNA end joining

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Dynamic nature of the proximal AZFc region of the human Y chromosome: multiple independent deletion and duplication events revealed by microsatellite analysis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

An evolutionary perspective on Y-chromosomal variation and male infertility

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Restricted expression of the human DAZ protein in premeiotic germ cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Genetics of azoospermia: current knowledge, clinical implications, and future directions. Part II: Y chromosome microdeletions.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Microarray detection of Y chromosome deletions associated with male infertility.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Gene polymorphisms and male infertility--a meta-analysis and literature review

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Characterizing partial AZFc deletions of the Y chromosome with amplicon-specific sequence markers

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Gene conversion: mechanisms, evolution and human disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Biased clustered substitutions in the human genome: the footprints of male-driven biased gene conversion

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Partial deletions are associated with an increased risk of complete deletion in AZFc: a new insight into the role of partial AZFc deletions in male infertility

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Partial duplication at AZFc on the Y chromosome is a risk factor for impaired spermatogenesis in Han Chinese in Taiwan

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Y-chromosome haplogroups and susceptibility to azoospermia factor c microdeletion in an Italian population

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Y chromosome and male infertility: update, 2006.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Genome-wide identification of pseudogenes capable of disease-causing gene conversion.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

The human Y chromosome: a masculine chromosome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

The Y deletion gr/gr and susceptibility to testicular germ cell tumor

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Role of the DAZ genes in male fertility

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Genomic heterogeneity and instability of the AZF locus on the human Y chromosome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Establishment of genetic associations for complex diseases is independent of early study findings

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Putative biological functions of the DAZ family

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Intense and highly localized gene conversion activity in human meiotic crossover hot spots

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Cdyl: a new transcriptional co-repressor

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Abundant gene conversion between arms of palindromes in human and ape Y chromosomes.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Problems of reporting genetic associations with complex outcomes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the Y chromosome, and of 18 children conceived via ICSI.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

The human Y chromosome genes BPY2, CDY1 and DAZ are not essential for sustained fertility

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Small deletions of the short arm of the Y chromosome in 46,XY females

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

p49f, A highly polymorphic probe, that detects Taq1 RFLPs on the human Y chromosome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Dynamics of a human interparalog gene conversion hotspot

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Genetic evidence for a higher female migration rate in humans.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Y-chromosomal microdeletions and partial deletions of the Azoospermia Factor c (AZFc) region in normozoospermic, severe oligozoospermic and azoospermic men in Sri Lanka.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Duplications of the AZFa region of the human Y chromosome are mediated by homologous recombination between HERVs and are compatible with male fertility

30 May 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Identification of new breakpoints in AZFb and AZFc

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

High frequency of gr/gr chromosome Y deletions in consecutive oligospermic ICSI candidates

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Association of partial AZFc region deletions with spermatogenic impairment and male infertility

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Meiotic abnormalities in patients bearing complete AZFc deletion of Y chromosome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

The gr/gr deletion(s): a new genetic test in male infertility?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Case report: natural transmission of an AZFc Y-chromosomal microdeletion from father to his sons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Sons conceived by assisted reproduction techniques inherit deletions in the azoospermia factor (AZF) region of the Y chromosome and the DAZ gene copy number

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

AZFc somatic microdeletions and copy number polymorphism of the DAZ genes in human males exposed to natural background radiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

GR/GR deletions within the azoospermia factor c region on the Y chromosome might not be associated with spermatogenic failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Y-chromosome AZFc structural architecture and relationship to male fertility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Characterization of the genomic organization, localization and expression of four PRY genes (PRY1, PRY2, PRY3 and PRY4).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Expression pattern of the Y-linked PRY gene suggests a function in apoptosis but not in spermatogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Male-driven biased gene conversion governs the evolution of base composition in human alu repeats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Copy number of DAZ genes in infertile men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

A frequent Y chromosome b2/b3 subdeletion shows strong association with male infertility in Han-Chinese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

A frequent partial AZFc deletion does not render an increased risk of spermatogenic impairment in East Asians.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Y chromosome haplogroups and susceptibility to testicular cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Molecular and Clinical Characterization of Y Chromosome Microdeletions in Infertile Men: A 10-Year Experience in Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Partial AZFc deletions and duplications: clinical correlates in the Italian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

The Y chromosome gr/gr subdeletion is associated with male infertility

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Do we need to search for gr/gr deletions in infertile men in a clinical setting?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

A physical map of the human Y chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Partial deletions in the AZFc region of the Y chromosome occur in men with impaired as well as normal spermatogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Phenotypic expression of partial AZFc deletions is independent of the variations in DAZL and BOULE in a Han population.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

Clinical consequences of microdeletions of the Y chromosome: the extended Münster experience.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

A new case of Yq microdeletion transmitted from a normal father to two infertile sons

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2918367

No association found between gr/gr deletions and infertility in Brazilian males

28 November 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Study of AZFc partial deletion gr/gr in fertile and infertile Japanese males

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMUPD%2FDMQ005

Sex chromosome alignment at meiosis of azoospermic men with azoospermia factor microdeletion

21 January 2018

1 reference

12 December 2020

Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

1 reference

12 December 2020

Massive deletion in AZFb/b+c and azoospermia with Sertoli cell only and/or maturation arrest

1 reference

12 December 2020

Y chromosome microdeletion in a father and his four infertile sons

1 reference

12 December 2020

Y chromosome analysis of infertile men and their sons conceived through intracytoplasmic sperm injection: vertical transmission of deletions and rarity of de novo deletions

1 reference

12 December 2020

AZFc partial deletions in Chilean men with severe spermatogenic failure

1 reference

12 December 2020

[Analysis of an AZFc deletion family with natural transmission]

1 reference

12 December 2020

Distinct faces of the Ku heterodimer mediate DNA repair and telomeric functions

1 reference

12 December 2020

Spontaneous transmission from a father to his son of a Y chromosome microdeletion involving the deleted in azoospermia (DAZ) gene

1 reference

12 December 2020

Evidence for the association of Y-chromosome haplogroups with susceptibility to spermatogenic failure in a Chinese Han population

1 reference

12 December 2020

Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment

1 reference

12 December 2020

The fragility of fertility

1 reference

12 December 2020

The replication requirement

1 reference

12 December 2020

Reduced copy number of DAZ genes in subfertile and infertile men

1 reference

12 December 2020

The use of spermHALO-FISH to determine DAZ gene copy number

1 reference

12 December 2020

Identifiers

DOI

10.1093/HUMUPD/DMQ005

1 reference

3068296

3068296

1 reference

1 reference

1 reference