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Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoske...

Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoske...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2e4d09eb836c4822bbc833719b711875

Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoskeletal defects

About this item

Full title

Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoskeletal defects

Publisher

England: The Company of Biologists Ltd

Journal title

Disease models & mechanisms, 2019-06, Vol.12 (6)

Language

English

Formats

Publication information

Publisher

England: The Company of Biologists Ltd

More information

Scope and Contents

Contents

In a screen for organogenesis defects in N-ethyl-N-nitrosourea (ENU)-induced mutant mice, we discovered a line carrying a mutation in Colgalt1 [collagen beta(1-O)galactosyltransferase type 1], which is required for proper galactosylation of hydroxylysine residues in a number of collagens. Colgalt1 mutant embryos have not been previously characteriz...

Alternative Titles

Full title

Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoskeletal defects

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_2e4d09eb836c4822bbc833719b711875

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2e4d09eb836c4822bbc833719b711875

Other Identifiers

ISSN

1754-8403

E-ISSN

1754-8411

DOI

10.1242/dmm.037176

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