Impaired interactions between mouse Eyal harboring mutations found in patients with branchio-oto-renal syndrome and Six, Dach, and G proteins
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Ski regulates muscle terminal differentiation by transcriptional activation of Myog in a complex with Six1 and Eya3Molecular interaction and synergistic activation of a promoter by Six, Eya, and Dach proteins mediated through CREB binding proteinSix1 and Eya1 expression can reprogram adult muscle from the slow-twitch phenotype into the fast-twitch phenotypeCrystal structure of ED-Eya2: insight into dual roles as a protein tyrosine phosphatase and a transcription factorTranscriptional regulation of cranial sensory placode developmentFibroblast growth factor signaling regulates Dach1 expression during skeletal developmentUsing Xenopus to discover new genes involved in branchiootorenal spectrum disordersThe sine oculis homeobox (SIX) family of transcription factors as regulators of development and diseaseDetermination of the embryonic inner ear.Using Drosophila to decipher how mutations associated with human branchio-oto-renal syndrome and optical defects compromise the protein tyrosine phosphatase and transcriptional functions of eyes absentMutational analysis of EYA1, SIX1 and SIX5 genes and strategies for management of hearing loss in patients with BOR/BO syndrome.BOR-syndrome-associated Eya1 mutations lead to enhanced proteasomal degradation of Eya1 proteinFunctional dissection of eyes absent reveals new modes of regulation within the retinal determination gene network.Induction and specification of the vertebrate ectodermal placodes: precursors of the cranial sensory organs.Decreased DACH1 expression in glomerulopathy is associated with disease progression and severity.The EYA-SO/SIX complex in development and disease.Establishing the pre-placodal region and breaking it into placodes with distinct identities.Early steps in inner ear development: induction and morphogenesis of the otic placode.Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney developmentA comparative study of Eya1 and Eya4 protein function and its implication in branchio-oto-renal syndrome and DFNA10Identification of a novel nonsynonymous mutation of EYA1 disrupting splice site in a Korean patient with BOR syndrome.Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development.Branchio-oto-renal syndrome associated mutations in Eyes Absent 1 result in loss of phosphatase activity.A novel mutation in EYA1 in a Chinese family with Branchio-oto-renal syndrome
P2860
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P2860
Impaired interactions between mouse Eyal harboring mutations found in patients with branchio-oto-renal syndrome and Six, Dach, and G proteins
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2002 թուականին հրատարակուած գիտական յօդուած
@hyw
2002 թվականին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2002
@ast
im Januar 2002 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: 2002)
@en
vedecký článok (publikovaný 2002)
@sk
vědecký článek publikovaný v roce 2002
@cs
wetenschappelijk artikel (gepubliceerd in 2002)
@nl
наукова стаття, опублікована у 2002
@uk
مقالة علمية (نشرت عام 2002)
@ar
name
Impaired interactions between ...... and Six, Dach, and G proteins
@ast
Impaired interactions between ...... and Six, Dach, and G proteins
@en
Impaired interactions between ...... and Six, Dach, and G proteins
@nl
type
label
Impaired interactions between ...... and Six, Dach, and G proteins
@ast
Impaired interactions between ...... and Six, Dach, and G proteins
@en
Impaired interactions between ...... and Six, Dach, and G proteins
@nl
prefLabel
Impaired interactions between ...... and Six, Dach, and G proteins
@ast
Impaired interactions between ...... and Six, Dach, and G proteins
@en
Impaired interactions between ...... and Six, Dach, and G proteins
@nl
P2093
P356
P1476
Impaired interactions between ...... and Six, Dach, and G proteins
@en
P2093
Hidenori Ozaki
Keiko Ikeda
Kiyoshi Kawakami
Yoko Watanabe
P2888
P304
P356
10.1007/S100380200011
P407
P577
2002-01-01T00:00:00Z