FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish. - Wikidata - awgldk - TriplyDB

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

http://www.wikidata.org/entity/Q34560870

about

Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate Epidemiology, Etiology, and Treatment of Isolated Cleft Palate Overlap of Patau and Pierre Robin syndromes along with abnormal metabolism: an interesting case study 500,000 fish phenotypes: The new informatics landscape for evolutionary and developmental biology of the vertebrate skeleton Palatogenesis: morphogenetic and molecular mechanisms of secondary palate development PDGFRa mutations in humans with isolated cleft palate.Zebrafish Craniofacial Development: A Window into Early Patterning A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.Diabetes mellitus and drug abuse during pregnancy and the risk for orofacial clefts and related abnormalities Genetic variants in fas signaling pathway genes and risk of gastric cancer.Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence.Developmental and genetic perspectives on Pierre Robin sequence.Analysis of the Relationship Between Micrognathia and Cleft Palate: A Systematic Review.Zebrafish models of orofacial clefts.The Role of Noncoding Genetic Variation in Isolated Orofacial Clefts.Dysregulation of Wnt-Signaling and a Candidate Set of miRNAs Underlie the Effect of Metformin on Neural Crest Cell Development.Examination of a palatogenic gene program in zebrafish.Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate.A novel inducible mutagenesis screen enables to isolate and clone both embryonic and adult zebrafish mutants.Genetics and management of the patient with orofacial cleft.Defective neural crest migration revealed by a Zebrafish model of Alx1-related frontonasal dysplasia.Early Craniofacial Defects in Zebrafish That Have Reduced Function of a Wnt-Interacting Extracellular Matrix Protein, Tinagl1.Update on 13 Syndromes Affecting Craniofacial and Dental Structures.Using Zebrafish to Test the Genetic Basis of Human Craniofacial Diseases.Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate.GWAS reveals loci associated with velopharyngeal dysfunction.

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P2860

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

http://www.wikidata.org/entity/Q34560870

description

2011 nî lūn-bûn

@nan

2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

@ast

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

@en

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

@nl

type

label

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

@ast

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

@en

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

@nl

prefLabel

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

@ast

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

@en

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

@nl

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P356

J.AJHG.2011.01.003

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American Journal of Human Genetics

P1476

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.

@en

P2093

Bénédicte Bayet

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Carlotta Baluardo

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Elisabeth Mangold

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Filip Claes

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Geneviève François

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Hélène A Poirel

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Jacqueline Hecht

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Jeffrey Murray

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Joris R Vermeesch

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Karlien Hermans

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P2860

p53 activation by knockdown technologies

Fas-associated factor-1 inhibits nuclear factor-kappaB (NF-kappaB) activity by interfering with nuclear translocation of the RelA (p65) subunit of NF-kappaB

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

IKK1-deficient mice exhibit abnormal development of skin and skeleton

Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome

Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)

Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

The genetic basis of the Pierre Robin Sequence

Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization

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2

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88

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Peter Carmeliet

Michella Ghassibe-Sabbagh

Mieke Dewerchin

Markus M Nöthen

Melissa Ferrian

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2011-02-03T00:00:00Z

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