Polymorphisms associated with the DAZ genes on the human Y chromosome. (Q53662835)

17 May 2018

title

Polymorphisms associated with the DAZ genes on the human Y chromosome. (English)

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17 May 2018

author

Alberto Ferlin

9

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author name string

Yi-Wen Lin

1

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17 May 2018

Duyen Anh Doan Thi

2

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Pao-Lin Kuo

3

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Chao-Chin Hsu

4

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17 May 2018

Bor-Ding Huang

5

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Yueh-Hsiang Yu

6

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Peter H Vogt

7

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Walter Krause

8

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Carlo Foresta

10

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Thierry Bienvenu

11

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17 May 2018

Werner Schempp

12

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Pauline H Yen

13

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publication date

1 October 2005

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17 May 2018

published in

Genomics

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volume

86

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page(s)

431-438

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issue

4

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17 May 2018

Functional coherence of the human Y chromosome

cites work

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

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

7 January 2021

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

7 January 2021

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Divergent outcomes of intrachromosomal recombination on the human Y chromosome: male infertility and recurrent polymorphism

7 January 2021

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Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

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2003 Curt Stern Award address. On low expectation exceeded; or, the genomic salvation of the Y chromosome

7 January 2021

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The comings and goings of a Y polymorphism

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Putative biological functions of the DAZ family

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Four DAZ genes in two clusters found in the AZFc region of the human Y chromosome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

The human DAZ genes, a putative male infertility factor on the Y chromosome, are highly polymorphic in the DAZ repeat regions

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Reduced copy number of DAZ genes in subfertile and infertile men

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligozoospermia detected using a sequence-tagged site-based mapping strategy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Familial mosaicism of del(Y) and inv del(Y).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Analysis of the DAZ gene family in cryptorchidism and idiopathic male infertility.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Reduction in the DAZ gene copy number in two infertile men with impaired spermatogenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

The fragility of fertility

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Isolation of genomic clones homologous to transcribed sequences from human X chromosome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: implications for X-Y interchange

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Analysis of DNA replication by fluorescence in situ hybridization

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

Fibre-fluorescence in situ hybridization unravels apparently seven DAZ genes or pseudogenes clustered within a Y-chromosome region frequently deleted in azoospermic males.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2005.07.003

10.1016/J.YGENO.2005.07.003

7 January 2021

Identifiers

DOI

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17 May 2018

PubMed ID

16085382

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17 May 2018