(Q21563340)

inferred from abstract

Ethylin Wang Jabs

4

Ethylin Wang

Jabs

1 reference

19 August 2022

Song-Ro Yoon

1

Song-Ro

Yoon

1 reference

19 August 2022

Jian Qin

2

Jian

Qin

1 reference

19 August 2022

Rivka L Glaser

3

Rivka L

Glaser

1 reference

19 August 2022

Nancy S Wexler

5

Nancy S

Wexler

1 reference

19 August 2022

Rebecca Sokol

6

Rebecca

Sokol

1 reference

19 August 2022

Norman Arnheim

7

Norman

Arnheim

1 reference

19 August 2022

Peter Calabrese

8

Peter

Calabrese

1 reference

Creative Commons Attribution 4.0 International

19 August 2022

language of work or name

English

0 references

publication date

July 2009

0 references

published in

PLOS Genetics

0 references

volume

5

0 references

issue

7

0 references

page(s)

e1000558

0 references

copyright license

start time

10 July 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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The question of declining sperm density revisited: an analysis of 101 studies published 1934-1996

19 March 2017

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Have sperm densities declined? A reanalysis of global trend data

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Age and sex effects on human mutation rates: an old problem with new complexities

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Bad bones, absent smell, selfish testes: the pleiotropic consequences of human FGF receptor mutations

19 March 2017

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19 March 2017

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Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis

19 March 2017

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19 March 2017

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Evidence for decreasing quality of semen during past 50 years

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Understanding what determines the frequency and pattern of human germline mutations

7 April 2017

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A germ-line-selective advantage rather than an increased mutation rate can explain some unexpectedly common human disease mutations

12 September 2017

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Role of environmental factors in the timing of puberty

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12 September 2017

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Increased achondroplasia mutation frequency with advanced age and evidence for G1138A mosaicism in human testis biopsies

12 September 2017

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12 September 2017

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Gain-of-function amino acid substitutions drive positive selection of FGFR2 mutations in human spermatogonia

12 September 2017

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12 September 2017

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The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm

12 September 2017

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Evidence for selective advantage of pathogenic FGFR2 mutations in the male germ line

12 September 2017

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The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect

12 September 2017

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All you wanted to know about spermatogonia but were afraid to ask.

12 September 2017

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Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome

12 September 2017

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12 September 2017

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12 September 2017

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12 September 2017

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Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

12 September 2017

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12 September 2017

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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

12 September 2017

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12 September 2017

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Decrease in the number of human Ap and Ad spermatogonia and in the Ap/ Ad ratio with advancing age. New data on the spermatogonial stem cell

12 September 2017

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12 September 2017

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12 September 2017

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27 September 2017

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Extracellular point mutations in FGFR2 elicit unexpected changes in intracellular signalling

27 September 2017

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Birth prevalence study of the Apert syndrome

30 May 2018

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Genotype-phenotype correlation for nucleotide substitutions in the IgII- IgIII linker of FGFR2

30 May 2018

2 references

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000558

21 January 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700275

Spermatogenesis in man: an estimate of its duration.

29 November 2018

1 reference

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Extracellular point mutations in FGFR2 result in elevated ERK1/2 activation and perturbation of neuronal differentiation

21 January 2018

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Stature and pubertal stage assessment in American boys: the 1988–1994 Third National Health and Nutrition Examination Survey1 1The full text of this article is available via JAH Online at http://www.elsevier.com/locate/jahonline

21 January 2018

1 reference

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Detection of extremely rare alleles by bidirectional pyrophosphorolysis-activated polymerization allele-specific amplification (Bi-PAP-A): measurement of mutation load in mammalian tissues

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700275

Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700275

Stature and pubertal stage assessment in American boys: the 1988-1994 Third National Health and Nutrition Examination Survey

29 November 2018

1 reference

12 December 2020

Depletion of the spermatogonia from the seminiferous epithelium of the rhesus monkey after X irradiation

1 reference

12 December 2020

Direct estimates of human per nucleotide mutation rates at 20 loci causing Mendelian diseases

1 reference

12 December 2020

Secondary sexual characteristics in boys: estimates from the national health and nutrition examination survey III, 1988-1994

1 reference

12 December 2020

10.1371/JOURNAL.PGEN.1000558

Identifiers

DOI

1 reference

release_k5vfvugtrbfx3e6gqyxuvp5piq

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/k5vfvugtrbfx3e6gqyxuvp5piq

24 November 2022

mapped directly with Wikidata item

1 reference

1 reference

1 reference