(Q22009352)

anatomical structure morphogenesis

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Jeroen P Roose

1 reference

ORCID Public Data File 2021

author name string

J Roose

1

0 references

W Korver

2

W

Korver

1 reference

7 February 2023

R de Boer

3

R

de Boer

1 reference

7 February 2023

J Kuipers

4

J

Kuipers

1 reference

7 February 2023

J Hurenkamp

5

J

Hurenkamp

1 reference

7 February 2023

H Clevers

6

H

The human SOX11 gene: cloning, chromosomal assignment and tissue expression

Clevers

1 reference

7 February 2023

language of work or name

English

0 references

publication date

15 April 1999

0 references

published in

Genomics

0 references

volume

57

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issue

2

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page(s)

301-5

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cites work

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

Cloning and characterization of SOX5, a new member of the human SOX gene family

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

cDNA cloning of a novel rainbow trout SRY-type HMG box protein, rtSox23, and its functional analysis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

Sox genes find their feet

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

The Xenopus Wnt effector XTcf-3 interacts with Groucho-related transcriptional repressors

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

Defects in cardiac outflow tract formation and pro-B-lymphocyte expansion in mice lacking Sox-4

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

Identification of two Sox17 messenger RNA isoforms, with and without the high mobility group box region, and their differential expression in mouse spermatogenesis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

The human SRY transcript

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

SOX22 is a new member of the SOX gene family, mainly expressed in human nervous tissue

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

The murine Sox-4 protein is encoded on a single exon

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

High expression of the HMG box factor sox-13 in arterial walls during embryonic development

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

A gene that is related to SRY and is expressed in the testes encodes a leucine zipper-containing protein

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

SRY and sex determination in mammals

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021

Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5779

7 January 2021