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SOX9 in organogenesis: shared and unique transcriptional functions

SOX9 in organogenesis: shared and unique transcriptional functions

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9482574

SOX9 in organogenesis: shared and unique transcriptional functions

About this item

Full title

SOX9 in organogenesis: shared and unique transcriptional functions

Publisher

Cham: Springer International Publishing

Journal title

Cellular and molecular life sciences : CMLS, 2022-10, Vol.79 (10), p.522-522, Article 522

Language

English

Formats

Publication information

Publisher

Cham: Springer International Publishing

More information

Scope and Contents

Contents

The transcription factor SOX9 is essential for the development of multiple organs including bone, testis, heart, lung, pancreas, intestine and nervous system. Mutations in the human
SOX9
gene led to campomelic dysplasia, a haploinsufficiency disorder with several skeletal malformations frequently accompanied by 46, XY sex reversal. The mechan...

Alternative Titles

Full title

SOX9 in organogenesis: shared and unique transcriptional functions

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9482574

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9482574

Other Identifiers

ISSN

1420-682X

E-ISSN

1420-9071

DOI

10.1007/s00018-022-04543-4

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