Difference between revisions of "Developmental Signals - TGF-beta"
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[[File:TGF-beta signaling pathway.jpg|thumb|TGF-beta signaling pathway]]
[[File:TGF-beta signaling pathway.jpg|thumb|TGF-beta signaling pathway
Revision as of 16:03, 10 September 2011
[[File:TGF-beta signaling pathway.jpg|thumb|TGF-beta signaling pathwayCite error: Closing
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(data from Expasy)
- WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 3A; WNT3A
- WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 7A; WNT7A
- CATENIN, BETA-1; CTNNB1
About OMIM "Online Mendelian Inheritance in Man OMIM is a comprehensive, authoritative, and timely compendium of human genes and genetic phenotypes. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 12,000 genes. OMIM focuses on the relationship between phenotype and genotype. It is updated daily, and the entries contain copious links to other genetics resources." OMIM
Search PubMed: TGF-beta
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Cite this page: Hill, M.A. (2019, November 18) Embryology Developmental Signals - TGF-beta. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Developmental_Signals_-_TGF-beta
- © Dr Mark Hill 2019, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G