Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndrome
about
Cooperation of six and eya in activation of their target genes through nuclear translocation of EyaGene expression in Wilms' tumor mimics the earliest committed stage in the metanephric mesenchymal-epithelial transitionEya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroidEYA1 and SIX1 drive the neuronal developmental program in cooperation with the SWI/SNF chromatin-remodeling complex and SOX2 in the mammalian inner earEya1 regulates the growth of otic epithelium and interacts with Pax2 during the development of all sensory areas in the inner earSix2 is required for suppression of nephrogenesis and progenitor renewal in the developing kidneyConnecting the ear to the brain: Molecular mechanisms of auditory circuit assembly.Expression of the Pax2 transcription factor is associated with vestibular phenotype in the avian inner earHair cell fate decisions in cochlear development and regenerationSix4, a putative myogenin gene regulator, is not essential for mouse embryonal development.A subtracted cDNA library from the zebrafish (Danio rerio) embryonic inner ear.Branching ducts similar to mesonephric ducts or ureteric buds in teratomas originating from mouse embryonic stem cells.The malformed kidney: disruption of glomerular and tubular development.Renal stromal miRNAs are required for normal nephrogenesis and glomerular mesangial survival.Differential selection within the Drosophila retinal determination network and evidence for functional divergence between paralog pairs.Mutational analysis of EYA1, SIX1 and SIX5 genes and strategies for management of hearing loss in patients with BOR/BO syndrome.Patterning of the mammalian cochlea.The Eyes Absent proteins in development and disease.Clinical aspects of hereditary hearing loss.Non-homeodomain regions of Hox proteins mediate activation versus repression of Six2 via a single enhancer site in vivo.Position dependent responses to discontinuities in the retinal determination network.Transcription factors in parathyroid development: lessons from hypoparathyroid disorders.Inherited hearing loss: molecular genetics and diagnostic testing.Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness.Therapeutic use of human renal progenitor cells for kidney regeneration.Evidence of progression and fluctuation of hearing impairment in branchio-oto-renal syndrome.Hearing loss and renal syndromes.
P2860
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P2860
Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndrome
description
1998 nî lūn-bûn
@nan
1998 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Eya1 expression in the develop ...... nchio-Oto-Renal (BOR) syndrome
@ast
Eya1 expression in the develop ...... nchio-Oto-Renal (BOR) syndrome
@en
Eya1 expression in the develop ...... nchio-Oto-Renal (BOR) syndrome
@nl
type
label
Eya1 expression in the develop ...... nchio-Oto-Renal (BOR) syndrome
@ast
Eya1 expression in the develop ...... nchio-Oto-Renal (BOR) syndrome
@en
Eya1 expression in the develop ...... nchio-Oto-Renal (BOR) syndrome
@nl
prefLabel
Eya1 expression in the develop ...... nchio-Oto-Renal (BOR) syndrome
@ast
Eya1 expression in the develop ...... nchio-Oto-Renal (BOR) syndrome
@en
Eya1 expression in the develop ...... nchio-Oto-Renal (BOR) syndrome
@nl
P2860
P50
P1476
Eya1 expression in the develop ...... nchio-Oto-Renal (BOR) syndrome
@en
P2093
P2860
P304
P356
10.1002/(SICI)1097-0177(199812)213:4<486::AID-AJA13>3.0.CO;2-L
P407
P577
1998-12-01T00:00:00Z