Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome
about
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) miceA natural allele of Nxf1 suppresses retrovirus insertional mutationsGene expression in Wilms' tumor mimics the earliest committed stage in the metanephric mesenchymal-epithelial transitionGenetics of hearing and deafnessTranscriptional regulation of cranial sensory placode developmentNotch signalling in the paraxial mesoderm is most sensitive to reduced Pofut1 levels during early mouse developmentEya 1 acts as a critical regulator for specifying the metanephric mesenchymeCatweasel mice: a novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome.Identification of strain-specific variants of mouse Adamts13 gene encoding von Willebrand factor-cleaving proteaseConnecting the ear to the brain: Molecular mechanisms of auditory circuit assembly.Tympanometry assessment of 61 inbred strains of mice.Branching ducts similar to mesonephric ducts or ureteric buds in teratomas originating from mouse embryonic stem cells.Zebrafish as a model for hearing and deafness.Renal anomalies associated with ectopic neurohypophysisMolecular conservation and novelties in vertebrate ear development.Genetic approaches to human renal agenesis/hypoplasia and dysplasia.Induction and specification of the vertebrate ectodermal placodes: precursors of the cranial sensory organs.Development and evolution of the vestibular sensory apparatus of the mammalian ear.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.A transgenic insertional inner ear mutation on mouse chromosome 1.Setting appropriate boundaries: fate, patterning and competence at the neural plate border.Establishing the pre-placodal region and breaking it into placodes with distinct identities.Developmental expression patterns of candidate cofactors for vertebrate six family transcription factors.Mutations of the Pendred syndrome gene (PDS) in patients with large vestibular aqueduct.High-fidelity CRISPR/Cas9- based gene-specific hydroxymethylation rescues gene expression and attenuates renal fibrosis
P2860
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P2860
Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome
description
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1999
@ast
im April 1999 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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vedecký článok (publikovaný 1999/04/01)
@sk
vědecký článek publikovaný v roce 1999
@cs
wetenschappelijk artikel (gepubliceerd op 1999/04/01)
@nl
наукова стаття, опублікована у квітні 1999
@uk
مقالة علمية (نشرت في أبريل 1999)
@ar
name
Inner ear and kidney anomalies ...... a mouse model of BOR syndrome
@ast
Inner ear and kidney anomalies ...... a mouse model of BOR syndrome
@en
Inner ear and kidney anomalies ...... a mouse model of BOR syndrome
@nl
type
label
Inner ear and kidney anomalies ...... a mouse model of BOR syndrome
@ast
Inner ear and kidney anomalies ...... a mouse model of BOR syndrome
@en
Inner ear and kidney anomalies ...... a mouse model of BOR syndrome
@nl
prefLabel
Inner ear and kidney anomalies ...... a mouse model of BOR syndrome
@ast
Inner ear and kidney anomalies ...... a mouse model of BOR syndrome
@en
Inner ear and kidney anomalies ...... a mouse model of BOR syndrome
@nl
P2093
P2860
P356
P1476
Inner ear and kidney anomalies ...... a mouse model of BOR syndrome
@en
P2093
A. N. Matthews
K. R. Johnson
L. C. Erway
L. P. Sanford
N. E. Paradies
R. A. Friedman
S. A. Cook
P2860
P304
P356
10.1093/HMG/8.4.645
P577
1999-04-01T00:00:00Z