Associated Papers
Novel TEAD1 gene variant in a Serbian family with Sveinsson's chorioretinal atrophy.
Grubisa I et al.
Experimental Eye Research, 2021
The Hippo Tumor Suppressor Pathway (YAP/TAZ/TEAD/MST/LATS) and EGFR-RAS-RAF-MEK in cancer metastasis.
Zinatizadeh MR et al.
Genes & Diseases, 2021
The Hippo Signaling Pathway in Development and Disease.
Zheng Y et al.
Developmental Cell, 2019
Molecular and structural characterization of a TEAD mutation at the origin of Sveinsson's chorioretinal atrophy.
Bokhovchuk F et al.
The Febs Journal, 2019
Regulation of the Hippo Pathway Transcription Factor TEAD.
Lin KC et al.
Trends in Biochemical Sciences, 2017
Crystal structure of TAZ-TEAD complex reveals a distinct interaction mode from that of YAP-TEAD complex.
Kaan HYK et al.
Scientific Reports, 2017
Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage.
Komor AC et al.
Nature, 2016
27096365 (PubMed )
Supplement: NIHMS774092-supplement-1.pdf
A De Novo Mutation in TEAD1 Causes Non-X-Linked Aicardi Syndrome.
Schrauwen I et al.
Investigative Ophthalmology & Visual Science, 2015
Regulation of the Hippo pathway and implications for anticancer drug development.
Park HW et al.
Trends in Pharmacological Sciences, 2013
Structures of YAP protein domains reveal promising targets for development of new cancer drugs.
Sudol M et al.
Seminars in Cell & Developmental Biology, 2012
Alteration of TEAD1 expression levels confers apoptotic resistance through the transcriptional up-regulation of Livin.
Landin Malt A et al.
Plos One, 2012
PhenoHM: human-mouse comparative phenome-genome server.
Sardana D et al.
Nucleic Acids Research, 2010
20507906 (PubMed )
Supplement: gkq472_nar-00429-web-b-2010-File006.xls › MPO_to_OMIM_allelic_Variants
Structural basis of YAP recognition by TEAD4 in the hippo pathway.
Chen L et al.
Genes & Development, 2010
Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.
Tosi J et al.
Ophthalmology, 2009
A Sveinsson's chorioretinal atrophy-associated missense mutation in mouse Tead1 affects its interaction with the co-factors YAP and TAZ.
Kitagawa M
Biochemical and Biophysical Research Communications, 2007
A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration).
Fossdal R et al.
Human Molecular Genetics, 2004
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