Associated Papers
An ENU-induced mutation in Twist1 transactivation domain causes hindlimb polydactyly with complete penetrance and dominant-negatively impairs E2A-dependent transcription.
Chen RZ et al.
Scientific Reports, 2020
32051525 (PubMed )
Supplement: 41598_2020_59455_MOESM2_ESM.pdf
Twist1 controls a cell-specification switch governing cell fate decisions within the cardiac neural crest.
Vincentz JW et al.
Plos Genetics, 2013
Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlations.
Passos-Bueno MR et al.
Frontiers of Oral Biology, 2008
Mutations in the basic domain and the loop-helix II junction of TWIST abolish DNA binding in Saethre-Chotzen syndrome.
El Ghouzzi V et al.
Febs Letters, 2001
Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations.
Paznekas WA et al.
American Journal of Human Genetics, 1998
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