Sox18 mutations in theragged mouse allelesragged-like andopossum (Q60411801)

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3 November 2019

title

Sox18 mutations in the ragged mouse alleles ragged-like and opossum (English)

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3 November 2019

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3

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3 November 2019

George Muscat

4

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3 November 2019

Peter Koopman

5

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3 November 2019

author name string

Kristy James

1

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3 November 2019

Brett Hosking

2

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3 November 2019

publication date

1 May 2003

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3 November 2019

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3 November 2019

volume

36

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3 November 2019

issue

1

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3 November 2019

page(s)

1-6

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Genetic evidence equating SRY and the testis-determining factor

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Sox9 is required for cartilage formation

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Direct interaction of SRY-related protein SOX9 and steroidogenic factor 1 regulates transcription of the human anti-Müllerian hormone gene

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Trans-activation and DNA-binding properties of the transcription factor, Sox-18

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Cloning and functional analysis of the Sry-related HMG box gene, Sox18

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

SOX18 directly interacts with MEF2C in endothelial cells

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

A human XY female with a frame shift mutation in the candidate testis-determining gene SRY.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Pairing SOX off: with partners in the regulation of embryonic development

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Sox1 directly regulates the gamma-crystallin genes and is essential for lens development in mice

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Sox18 expression in blood vessels and feather buds during chicken embryogenesis.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Mice null for sox18 are viable and display a mild coat defect

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Structure, mapping, and expression of human SOX18.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

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/10.1002%2FGENE.10190

7 January 2021

The transcription factors L-Sox5 and Sox6 are essential for cartilage formation

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

SOX7 transcription factor: sequence, chromosomal localisation, expression, transactivation and interference with Wnt signalling

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

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/10.1002%2FGENE.10190

7 January 2021

Analysis of genetic control of chylous ascites in ragged mice

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

From head to toes: the multiple facets of Sox proteins

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Matching SOX: partner proteins and co-factors of the SOX family of transcriptional regulators

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Developmental-specific activity of the FGF-4 enhancer requires the synergistic action of Sox2 and Oct-3

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10190

7 January 2021

Identifiers

DOI

10.1002/GENE.10190

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12748961%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference