Ampliando el fenotipo del síndrome FOXG1

Ampliando el fenotipo del síndrome FOXG1

Bibliographic Details
Main Authors:	E. Candelo, G. Caicedo, H. Pachajoa
Format:	Article
Language:	Spanish
Published:	Elsevier España 2020-04-01
Series:	Neurología
Online Access:	http://www.sciencedirect.com/science/article/pii/S0213485317303201

Similar Items

Expanding FOXG1 syndrome phenotype
by: E. Candelo, et al.
Published: (2020-04-01)

FOXG1 Dose in Brain Development
by: Nuwan C. Hettige, et al.
Published: (2019-11-01)

The Role of FoxG1 in the Inner Ear
by: Yanyan Ding, et al.
Published: (2020-12-01)

Foxg1 deletion impairs the development of the epithalamus
by: Bin Liu, et al.
Published: (2018-02-01)

El síndrome X frágil: identificación del fenotipo y propuestas educativas
by: Begoña Medina Gómez
Published: (2014-12-01)

Elucidating the pathogenic and biomarker potentials of FOXG1 in glioblastoma
by: Seidu A. Richard, et al.
Published: (2020-04-01)

Foxg1 : a pleiotropic regulator of telencephalic development
by: Martynoga, Ben
Published: (2007)

Fenotipos clínicos en el síndrome de apnea obstructiva del sueño
by: Jorge Jorquera, et al.
Published: (2021-09-01)

Cognition and Evolution of Movement Disorders of FOXG1-Related Syndrome
by: Lee-Chin Wong, et al.
Published: (2019-06-01)

The role of Foxg1 in retinal axon divergence at the optic chiasm
by: Tian, Natasha
Published: (2008)

Transcription and Beyond: Delineating FOXG1 Function in Cortical Development and Disorders
by: Pei-Shan Hou, et al.
Published: (2020-02-01)

Ampliando as perspectivas
by: Ângela Tonietto, et al.
Published: (2015-08-01)

Síndrome X frágil: detección e intervención en el fenotipo conductual
by: Begoña Medina Gómez, et al.
Published: (2014-09-01)

Síndrome de Williams-Beuren. Enfoque diagnóstico a través del fenotipo
by: María Angelina Lacruz-Rengel, et al.
Published: (2015-10-01)

Correlación fenotipo neuroanatómico y neurocognitivo en el síndrome de Williams
by: Cristiana Vasconcelos, et al.
Published: (2013-06-01)

Evolutionary analysis and functional characterization of the forkhead transcription factor FoxG1
by: Bredenkamp, Nicholas
Published: (2014)

Phenotypic overlap between pyruvate dehydrogenase complex deficiency and FOXG1 syndrome
by: Yuichi Akaba, et al.
Published: (2021-03-01)

Characterization of a FOXG1:TLE1 transcriptional network in glioblastoma‐initiating cells
by: Rola Dali, et al.
Published: (2018-06-01)

Ampliando la visión
by: Ana María Fernández, et al.
Published: (1999-01-01)

Ampliando la visión
by: Ana María Fernández, et al.
Published: (1999-01-01)

Ampliando la visión
by: Ana María Fernández, et al.
Published: (2009-11-01)

Ampliando o debate
by: Maria do Carmo Leal, et al.
Published: (2014-08-01)

Doble aneuploidía en un niño Colombiano: síndrome de Down–Klinefelter, con fenotipo de síndrome de Down = Double aneuploidy in a Colombian child: Down-Klinefelter syndrome with Down syndrome phenotype
by: Pachajoa Londoño, Harry, et al.
Published: (2011-03-01)

Collagen-derived dipeptide prolyl-hydroxyproline promotes osteogenic differentiation through Foxg1
by: Yoshifumi Kimira, et al.
Published: (2017-12-01)

Disruption of Foxg1 impairs neural plasticity leading to social and cognitive behavioral defects
by: Baocong Yu, et al.
Published: (2019-06-01)

REBEn: ampliando a contribuição REBEn: ampliando la contribución REBEn: increasing the contribution
by: Jussara Gue Martini
Published: (2009-02-01)

Mutação EPCAM e sindrome de Lynch: genótipo e fenótipo
by: Tiago José Monteiro Pais
Published: (2019)

The generation of an induced pluripotent stem cell line (DCGi001-A) from an individual with FOXG1 syndrome carrying the c.460dupG (p.Glu154fs) variation in the FOXG1 gene
by: Adrian J. Waite, et al.
Published: (2020-12-01)

Phänotyp-Analyse und Genotyp-Phänotyp-Assoziationen bei 83 mit FOXG1-Syndrom
by: Plümacher, Kim Sarah
Published: (2019)

Precisely controlling endogenous protein dosage in hPSCs and derivatives to model FOXG1 syndrome
by: Wenliang Zhu, et al.
Published: (2019-02-01)

<i>FOXG1</i>-Related Syndrome: From Clinical to Molecular Genetics and Pathogenic Mechanisms
by: Lee-Chin Wong, et al.
Published: (2019-08-01)

FoxG1 Directly Represses Dentate Granule Cell Fate During Forebrain Development
by: Xiao Han, et al.
Published: (2018-11-01)

Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation
by: Qingping Zhang, et al.
Published: (2017-08-01)

Microcephaly in Colombia before the Zika outbreak: A systematic literature review
by: Estephania Candelo, et al.
Published: (2018-08-01)

Síndrome dos ovários policísticos: correlação dos fenótipos com as manifestações metabólicas
by: Neves, Erika Mendonça das
Published: (2013)

Síndrome dos ovários policísticos: correlação dos fenótipos com as manifestações metabólicas
by: Erika Mendonça das Neves
Published: (2013)

Foxg specifies sensory neurons in the anterior neural plate border of the ascidian embryo
by: Boqi Liu, et al.
Published: (2019-10-01)

GDF-5 promotes epidermal stem cells proliferation via Foxg1-cyclin D1 signaling
by: Xiaohong Zhao, et al.
Published: (2021-01-01)

A case of congenital Rett variant in a Chinese patient caused by a FOXG1 mutation
by: Yan Niu, et al.
Published: (2020-07-01)

Diagnosis of FOXG1 syndrome caused by recurrent balanced chromosomal rearrangements: case study and literature review
by: Connor P. Craig, et al.
Published: (2020-09-01)

Cannot write session to /tmp/vufind_sessions/sess_1kghnoqlfuplkce3kkpmushr42