CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance (Q38307798)

2 September 2017

CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance (English)

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2 September 2017

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Gabriela Salinas-Riester

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Gabriela Salinas-Riester

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Lennart Opitz

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Ernie M H F Bongers

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Yvonne Schulz

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Peter Wehner

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Conny M A van Ravenswaaij-Arts

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Josephine Wincent

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Jacqueline Schoumans

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Jürgen Kohlhase

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Annette Borchers

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Silke Pauli

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997-1009

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https://scigraph.springernature.com/pub.10.1007/s00439-014-1444-2

2 September 2017

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cites work

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CHD7 cooperates with PBAF to control multipotent neural crest formation

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CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype.

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Multiple mutations in mouse Chd7 provide models for CHARGE syndrome

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Olfactory evaluation in children: application to the CHARGE syndrome.

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Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists

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Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

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Neural crest specification: migrating into genomics

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The neural crest as a fourth germ layer and vertebrates as quadroblastic not triploblastic

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SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome

21 January 2018

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Appendix G: In Situ Hybridization: An Improved Whole-Mount Method for Xenopus Embryos

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Two new mouse mutants with vestibular defects that map to the highly mutable locus on chromosome 4.

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CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

21 January 2018

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CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome

21 January 2018

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Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

21 January 2018

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Factors controlling cardiac neural crest cell migration

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Semaphorin and neuropilin expression during early morphogenesis of Xenopus laevis.

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Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation

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Ear-nose-throat abnormalities in the CHARGE association.

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Kallmann syndrome phenotype in a female patient with CHARGE syndrome and CHD7 mutation.

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Impact of RNA degradation on gene expression profiling.

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CHARGE syndrome includes hypogonadotropic hypogonadism and abnormal olfactory bulb development

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CHARGE syndrome: an update

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Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.

21 January 2018

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Origin of luteinizing hormone-releasing hormone neurons

21 January 2018

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Pathologic features of the CHARGE association: support for involvement of the neural crest.

21 January 2018

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Injected Xwnt-8 RNA acts early in Xenopus embryos to promote formation of a vegetal dorsalizing center

21 January 2018

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Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions

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Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

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CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome

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SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

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Oculo-auriculo-vertebral spectrum and the CHARGE association: clinical evidence for a common pathogenetic mechanism.

21 January 2018

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PubMed

12 December 2020

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12 December 2020

Xenopus cadherin-11 restrains cranial neural crest migration and influences neural crest specification.

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PubMed

12 December 2020

Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice

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PubMed

12 December 2020

10.1007/S00439-014-1444-2

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2 September 2017

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