FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation
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Congenital hypoplasia of the cerebellum: developmental causes and behavioral consequencesInferior cerebellar hypoplasia resembling a Dandy-Walker-like malformation in purebred Eurasier dogs with familial non-progressive ataxia: a retrospective and prospective clinical cohort studyZebrafish foxc1a drives appendage-specific neural circuit development.Forkhead box transcription factor FoxC1 preserves corneal transparency by regulating vascular growthIf the skull fits: magnetic resonance imaging and microcomputed tomography for combined analysis of brain and skull phenotypes in the mouseStudies on Axenfeld-Rieger syndrome patients and mice reveal Foxc1's role in corneal neovascularizationFOXC1 contributes to microvascular invasion in primary hepatocellular carcinoma via regulating epithelial-mesenchymal transitionComparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses of FOXC1 Mutations in Patients with Axenfeld-Rieger SyndromeAutosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation.Model organisms inform the search for the genes and developmental pathology underlying malformations of the human hindbrain.Blake's pouch cyst and Werdnig-Hoffmann disease: Report of a new association and review of the literature.Update on neuroimaging phenotypes of mid-hindbrain malformations.The genetics of cerebellar malformationsNovel approaches to studying the genetic basis of cerebellar developmentAnomalous development of brain structure and function in spina bifida myelomeningocele.Tumor Hypoxia Regulates Forkhead Box C1 to Promote Lung Cancer ProgressionDigital expression profiling of the compartmentalized translatome of Purkinje neuronsThe developmental trajectory of brain-scalp distance from birth through childhood: implications for functional neuroimagingPurkinje cell compartmentalization in the cerebellum of the spontaneous mutant mouse dreherPolymicrogyria: pathology, fetal origins and mechanisms.MYOC and FOXC1 gene analysis in primary congenital glaucoma.Primary cellular meningeal defects cause neocortical dysplasia and dyslamination.A comprehensive volumetric analysis of the cerebellum in children and adolescents with autism spectrum disorderDifferential effects of intraventricular hemorrhage and white matter injury on preterm cerebellar growth.Multiple developmental programs are altered by loss of Zic1 and Zic4 to cause Dandy-Walker malformation cerebellar pathogenesis.Foxc1 dependent mesenchymal signalling drives embryonic cerebellar growth.Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyriaWe have got you 'covered': how the meninges control brain development.Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.Integrating diverse datasets improves developmental enhancer predictionGenomic imbalances detected by array-CGH in patients with syndromal ocular developmental anomalies.Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity.Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disordersFOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25.Disruptions in a cluster of computationally identified enhancers near FOXC1 and GMDS may influence brain development.Perturbations of the cerebrovascular matrisome: A convergent mechanism in small vessel disease of the brain?Yap and Taz play a crucial role in neural crest-derived craniofacial development.Foxc1 controls the growth of the murine frontal bone rudiment by direct regulation of a Bmp response threshold of Msx2.Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVsMolecular characterization of a novel ring 6 chromosome using next generation sequencing.
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P2860
FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation
description
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
articolo scientifico
@it
artículu científicu espublizáu en 2009
@ast
im September 2009 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
wetenschappelijk artikel (gepubliceerd op 2009/09/01)
@nl
наукова стаття, опублікована у вересні 2009
@uk
مقالة علمية (نشرت في سبتمبر 2009)
@ar
name
FOXC1 is required for normal c ...... 25.3 Dandy-Walker malformation
@ast
FOXC1 is required for normal c ...... 25.3 Dandy-Walker malformation
@en
type
label
FOXC1 is required for normal c ...... 25.3 Dandy-Walker malformation
@ast
FOXC1 is required for normal c ...... 25.3 Dandy-Walker malformation
@en
prefLabel
FOXC1 is required for normal c ...... 25.3 Dandy-Walker malformation
@ast
FOXC1 is required for normal c ...... 25.3 Dandy-Walker malformation
@en
P2093
P2860
P3181
P356
P1433
P1476
FOXC1 is required for normal c ...... 25.3 Dandy-Walker malformation
@en
P2093
Alexander G. Bassuk
Ian D. Krantz
Kathleen J. Millen
Kimberly A. Aldinger
Lesley C. Ades
Louanne Hudgins
Ordan J. Lehmann
Victor V. Chizhikov
William B. Dobyns
P2860
P2888
P304
P3181
P356
10.1038/NG.422
P407
P577
2009-09-01T00:00:00Z
P5875
P6179
1030356828