about
Mowat-Wilson syndromeThe "domestication syndrome" in mammals: a unified explanation based on neural crest cell behavior and geneticsEpilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotypeSmad-interacting protein-1 (Zfhx1b) acts upstream of Wnt signaling in the mouse hippocampus and controls its formationAutosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation.Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes.Clinical review of genetic epileptic encephalopathiesNeuroimaging findings in Mowat-Wilson syndrome: a study of 54 patientsGenetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia.Differences in human and chimpanzee gene expression patterns define an evolving network of transcription factors in brainCritical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndromeClinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.Retroviral insertional mutagenesis identifies Zeb2 activation as a novel leukemogenic collaborating event in CALM-AF10 transgenic mice.Integrated analysis of clinical signs and literature data for the diagnosis and therapy of a previously undescribed 6p21.3 deletion syndromeDifferential proteomic analysis of mammalian tissues using SILAM.Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.Loss of Sip1 leads to migration defects and retention of ectodermal markers during lens development.Complex pathogenesis of Hirschsprung's disease in a patient with hydrocephalus, vesico-ureteral reflux and a balanced translocation t(3;17)(p12;q11).Combined transcriptome analysis of fetal human and mouse cerebral cortex exposed to alcohol.Mowat-Wilson syndrome in a Moroccan consanguineous familyOcular coloboma: a reassessment in the age of molecular neuroscience.An Orthologous Epigenetic Gene Expression Signature Derived from Differentiating Embryonic Stem Cells Identifies Regulators of CardiogenesisDlx1&2-dependent expression of Zfhx1b (Sip1, Zeb2) regulates the fate switch between cortical and striatal interneuronsAnaesthetic management of Mowat-Wilson syndromeMutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locusZeb2 recruits HDAC-NuRD to inhibit Notch and controls Schwann cell differentiation and remyelinationHighly conserved upstream sequences for transcription factor genes and implications for the regulatory network.Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.Hirschsprung's disease and the brain.Chromosomal and related Mendelian syndromes associated with Hirschsprung's disease.Clinical utility gene card for: Mowat-Wilson syndromeMowat-Wilson syndrome: deafness in the first Egyptian case who was conceived by intracytoplasmic sperm injection.A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson Syndrome.Mowat-Wilson syndrome: neurological and molecular study in seven patients.Pc2-mediated sumoylation of Smad-interacting protein 1 attenuates transcriptional repression of E-cadherin.ZEB2 gene mutation and duplication of 22q11.23 in Mowat-Wilson syndrome.Supernumerary intestinal muscle coat in a patient with Hirschsprung disease/Mowat-Wilson syndrome.A cascade of morphogenic signaling initiated by the meninges controls corpus callosum formation.Zfh1 promotes survival of a peripheral glia subtype by antagonizing a Jun N-terminal kinase-dependent apoptotic pathway.ZEB2, a new candidate gene for asplenia.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Mowat-Wilson syndrome
@ast
Mowat-Wilson syndrome
@en
Mowat-Wilson syndrome
@nl
type
label
Mowat-Wilson syndrome
@ast
Mowat-Wilson syndrome
@en
Mowat-Wilson syndrome
@nl
prefLabel
Mowat-Wilson syndrome
@ast
Mowat-Wilson syndrome
@en
Mowat-Wilson syndrome
@nl
P2093
P2860
P3181
P356
P1476
Mowat-Wilson syndrome
@en
P2093
P2860
P304
P3181
P356
10.1136/JMG.40.5.305
P407
P577
2003-05-01T00:00:00Z