(Q24656897)

1

0 references

R Critcher

2

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N Hastie

3

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P N Goodfellow

Proceedings of the National Academy of Sciences of the United States of America

4

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language of work or name

English

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publication date

1 September 1998

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published in

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volume

95

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issue

18

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page(s)

10649-54

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cites work

Sex reversal by loss of the C-terminal transactivation domain of human SOX9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

A comparison of the properties of Sox-3 with Sry and two related genes, Sox-1 and Sox-2

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

Sox-4, an Sry-like HMG box protein, is a transcriptional activator in lymphocytes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

A clinical and genetic study of campomelic dysplasia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

A conserved family of genes related to the testis determining gene, SRY

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

SOX9 directly regulates the type-II collagen gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

SOX9 binds DNA, activates transcription, and coexpresses with type II collagen during chondrogenesis in the mouse

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

A male-specific role for SOX9 in vertebrate sex determination

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

SOX9 is a potent activator of the chondrocyte-specific enhancer of the pro alpha1(II) collagen gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

Sox9 expression during gonadal development implies a conserved role for the gene in testis differentiation in mammals and birds

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

Dicistronic targeting constructs: reporters and modifiers of mammalian gene expression.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

Evidence for a locus activation region: the formation of developmentally stable hypersensitive sites in globin-expressing hybrids

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

Male development of chromosomally female mice transgenic for Sry.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

[49] Yeast artificial chromosome modification and manipulation

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.95.18.10649

YAC transfer by microinjection.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27949

Use of YAC fragmentation to delimit a duplicated region on human chromosome 21

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9724758

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9724758

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Sex-reversed XY females with campomelic dysplasia are H-Y negative

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9724758

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.95.18.10649

1 reference

ADS bibcode

1998PNAS...9510649W

0 references

1 reference

1 reference

PubMed publication ID

9724758

1 reference