(Q33300786)

25 July 2017

title

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

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25 July 2017

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2

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25 July 2017

3

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25 July 2017

4

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25 July 2017

14

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25 July 2017

João Gonçalves

16

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Paulo Navarro-Costa

object named as

Paulo Navarro-Costa

1

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Carlos E Plancha

object named as

Carlos E Plancha

15

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author name string

Carmen Proença

5

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25 July 2017

Pedro Marques-Vidal

6

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25 July 2017

Tiago Rocha

7

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25 July 2017

Sónia C Correia

8

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25 July 2017

Sónia Jorge

9

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25 July 2017

António Neves

10

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25 July 2017

Ana P Soares

11

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25 July 2017

Joaquim Nunes

12

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25 July 2017

Carlos Calhaz-Jorge

13

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25 July 2017

language of work or name

English

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publication date

28 September 2007

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25 July 2017

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25 July 2017

volume

8

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25 July 2017

page(s)

342

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https://scigraph.springernature.com/pub.10.1186/1471-2164-8-342

25 July 2017

exact match

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cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

Micro-phylogeographic and demographic history of Portuguese male lineages

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

Y chromosome variants and male reproductive function

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

DNA Commission of the International Society of Forensic Genetics (ISFG): an update of the recommendations on the use of Y-STRs in forensic analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

Phylogeography of Y-chromosome haplogroup I reveals distinct domains of prehistoric gene flow in europe

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

Hierarchical analysis of 30 Y-chromosome SNPs in European populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

Phylogeographic analysis of haplogroup E3b (E-M215) y chromosomes reveals multiple migratory events within and out of Africa

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

Excavating Y-chromosome haplotype strata in Anatolia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

Divergence in the spatial pattern of gene expression between human duplicate genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

Functional coherence of the human Y chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2151955

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

31 October 2018

1 reference

12 December 2020

DAZ1/DAZ2 cluster deletion mediated by gr/gr recombination per se may not be sufficient for spermatogenesis impairment: a study of Chinese normozoospermic men

1 reference

12 December 2020

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

1 reference

12 December 2020

Y chromosome microdeletion in a father and his four infertile sons

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

Effects of transmission of Y chromosome AZFc deletions

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2164-8-342

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/fxjy4ucuezbnfjgofqvlxer72q

30 July 2022

Dimensions Publication ID

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2164-8-342

release_fxjy4ucuezbnfjgofqvlxer72q

9 September 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/fxjy4ucuezbnfjgofqvlxer72q

30 July 2022

https://api.fatcat.wiki/v0/release/fxjy4ucuezbnfjgofqvlxer72q

1 reference

30 July 2022

https://api.fatcat.wiki/v0/release/fxjy4ucuezbnfjgofqvlxer72q

1 reference

30 July 2022