Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
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A multi-platform draft de novo genome assembly and comparative analysis for the Scarlet Macaw (Ara macao)SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexesBiochemical and functional characterization of six SIX1 Branchio-oto-renal syndrome mutationsSix1 and Eya1 expression can reprogram adult muscle from the slow-twitch phenotype into the fast-twitch phenotypeMisexpression of Six2 is associated with heritable frontonasal dysplasia and renal hypoplasia in 3H1 Br miceCreating a framework for online cancer services research to facilitate timely and interdisciplinary applicationsTranscription factor SIX5 is mutated in patients with branchio-oto-renal syndromeMultiple Functions of the Eya Phosphotyrosine PhosphataseStructure-function analyses of the human SIX1–EYA2 complex reveal insights into metastasis and BOR syndromeTranscriptional regulation of cranial sensory placode developmentThe role of Six1 in mammalian auditory system developmentEYA1 and SIX1 drive the neuronal developmental program in cooperation with the SWI/SNF chromatin-remodeling complex and SOX2 in the mammalian inner earSIX1 acts synergistically with TBX18 in mediating ureteral smooth muscle formation.Eya1 and Six1 are essential for early steps of sensory neurogenesis in mammalian cranial placodesSix1 is required for the early organogenesis of mammalian kidneyEya1 regulates the growth of otic epithelium and interacts with Pax2 during the development of all sensory areas in the inner earPatterning of the third pharyngeal pouch into thymus/parathyroid by Six and Eya1Determination of the embryonic inner ear.EYA1 mutations associated with the branchio-oto-renal syndrome result in defective otic development in Xenopus laevisUsing 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 absentThe Eye Specification Network in DrosophilaMulticystic renal dysplasia: a diagnostic dilemmaBOR-syndrome-associated Eya1 mutations lead to enhanced proteasomal degradation of Eya1 proteinThe SIX1-EYA transcriptional complex as a therapeutic target in cancer.Congenital anomalies of kidney and hand: a review.SIX1 overexpression in diffuse-type and grade III gastric tumors: Features that are associated with poor prognosis.Induction and specification of the vertebrate ectodermal placodes: precursors of the cranial sensory organs.Differential regulation of mouse and human nephron progenitors by the Six family of transcriptional regulatorsThe Eyes Absent proteins in development and disease.The phosphatase-transcription activator EYA1 is targeted by anaphase-promoting complex/Cdh1 for degradation at M-to-G1 transition.Branchio-oto-renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BOR.Eya1 gene dosage critically affects the development of sensory epithelia in the mammalian inner ear.CDK6 binds and promotes the degradation of the EYA2 proteinTranscription factors in parathyroid development: lessons from hypoparathyroid disorders.The EYA-SO/SIX complex in development and disease.Six1: a critical transcription factor in tumorigenesis.Establishing the pre-placodal region and breaking it into placodes with distinct identities.Signaling during Kidney DevelopmentEya-six are necessary for survival of nephrogenic cord progenitors and inducing nephric duct development before ureteric bud formation.Eya1-Six1 interaction is sufficient to induce hair cell fate in the cochlea by activating Atoh1 expression in cooperation with Sox2.
P2860
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P2860
Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
description
2001 nî lūn-bûn
@nan
2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
@ast
Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
@en
Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
@nl
type
label
Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
@ast
Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
@en
Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
@nl
prefLabel
Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
@ast
Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
@en
Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
@nl
P2093
P921
P356
P1476
Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome
@en
P2093
P304
P356
10.1093/HMG/10.24.2775
P407
P577
2001-11-15T00:00:00Z