Dysregulation of FOXG1 pathway in a 14q12 microdeletion case-Reference-Cited by-同舟云学术

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Dysregulation of FOXG1 pathway in a 14q12 microdeletion case

Published:2013-08-16 Issue:12 Volume:161 Page:3072-3077
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Perche Olivier¹²³,Haddad Georges⁴,Menuet Arnaud¹²,Callier Patrick⁵,Marcos Mélanie¹²,Briault Sylvain¹²³,Laudier Béatrice¹²³

Affiliation:

1. UMR7355; CNRS; Orleans France

2. Experimental and Molecular Immunology and Neurogenetics; University of Orleans; Orleans France

3. Genetic Department; Regional Hospital; Orleans France

4. Genetic Department; Hospital of Blois; Mail Pierre Charlot; Blois France

5. Cytogenetics Department; CHU de Dijon; Plateau technique de biologie; Dijon Cedex France

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36170/fullpdf

Reference20 articles.

1. FOXG1 is responsible for the congenital variant of Rett syndrome;Ariani;Am J Hum Genet,2008

2. Mutations in BMP4 cause eye, brain, and digit developmental anomalies: Overlap between the BMP4 and hedgehog signaling pathways;Bakrania;Am J Hum Genet,2008

3. TCF and Groucho-related genes influence pituitary growth and development;Brinkmeier;Mol Endocrinol,2003

4. 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype;Ellaway;Eur J Hum Genet,2012

5. The role of Pax6 in forebrain development;Georgala;Dev Neurobiol,2011

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1. Dietary Supplement Enriched in Antioxidants and Omega-3 Promotes Glutamine Synthesis in Müller Cells: A Key Process against Oxidative Stress in Retina;Nutrients;2021-09-16

2. Conditional Deletion of Foxg1 Alleviates Demyelination and Facilitates Remyelination via the Wnt Signaling Pathway in Cuprizone-Induced Demyelinated Mice;Neuroscience Bulletin;2020-10-05

3. Diagnosis of FOXG1 syndrome caused by recurrent balanced chromosomal rearrangements: case study and literature review;Molecular Cytogenetics;2020-09-03

4. A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network;The Journal of Pediatrics;2018-05

5. Síndrome de West secundario a duplicación patogénica en la citobanda 14q12;Revista de Neurología;2017

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