TFAP2 paralogs regulate melanocyte differentiation in parallel with MITF

Author:

Seberg Hannah E.ORCID,Van Otterloo EricORCID,Loftus Stacie K.,Liu Huan,Bonde GregORCID,Sompallae Ramakrishna,Gildea Derek E.,Santana Juan F.,Manak J. Robert,Pavan William J.,Williams Trevor,Cornell Robert A.

Funder

National Institute of Arthritis and Musculoskeletal and Skin Diseases

National Institute of Dental and Craniofacial Research

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference117 articles.

1. Deletion of the SLUG (SNAI2) gene results in human piebaldism;M Sanchez-Martin;Am J Med Genet A,2003

2. Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I);CF Hoth;Am J Hum Genet,1993

3. SLUG (SNAI2) deletions in patients with Waardenburg disease;M Sanchez-Martin;Hum Mol Genet,2002

4. Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene;M Tassabehji;Nat Genet,1994

5. Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4;N Bondurand;Am J Hum Genet,2007

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