The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans - Wikidata - wikimedia - TriplyDB

The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans

The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans

http://www.wikidata.org/entity/Q28312215

about

A symphony of inner ear developmental control genes.A zebrafish screen for craniofacial mutants identifies wdr68 as a highly conserved gene required for endothelin-1 expression Identification of a novel nuclear localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation mef2ca is required in cranial neural crest to effect Endothelin1 signaling in zebrafish An integrin-dependent role of pouch endoderm in hyoid cartilage development Segregating neural and mechanosensory fates in the developing ear: patterning, signaling, and transcriptional control.Reproductive and developmental toxicity of dioxin in fish RUNX3, EGR1 and SOX9B form a regulatory cascade required to modulate BMP-signaling during cranial cartilage development in zebrafish Semicircular canal morphogenesis in the zebrafish inner ear requires the function of gpr126 (lauscher), an adhesion class G protein-coupled receptor gene The mych gene is required for neural crest survival during zebrafish development The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development Evolutionary and developmental origins of the cardiac neural crest: building a divided outflow tract Developmental expression patterns of Tbx1, Tbx2, Tbx5, and Tbx20 in Xenopus tropicalis A zebrafish model for Waardenburg syndrome type IV reveals diverse roles for Sox10 in the otic vesicle Tbx1 controls the morphogenesis of pharyngeal pouch epithelia through mesodermal Wnt11r and Fgf8a.The old and new face of craniofacial research: How animal models inform human craniofacial genetic and clinical data The zebrafish as a tool to identify novel therapies for human cardiovascular disease.A divergent Tbx6-related gene and Tbx6 are both required for neural crest and intermediate mesoderm development in Xenopus In vivo tracking of T cell development, ablation, and engraftment in transgenic zebrafish.Development and evolution of the pharyngeal apparatus RA and FGF signalling are required in the zebrafish otic vesicle to pattern and maintain ventral otic identities Retinoic acid signaling and the evolution of chordates.DiGeorge syndrome gene tbx1 functions through wnt11r to regulate heart looping and differentiation Distinct functional and temporal requirements for zebrafish Hdac1 during neural crest-derived craniofacial and peripheral neuron development.Zebrafish cardiac development requires a conserved secondary heart field Tbx2a is required for specification of endodermal pouches during development of the pharyngeal arches A perspective on the value of aquatic models in biomedical research.The zebrafish: a new model of T-cell and thymic development.How insights from cardiovascular developmental biology have impacted the care of infants and children with congenital heart disease.Endoderm development in vertebrates: fate mapping, induction and regional specification.Cellular and molecular events during early thymus development.Zebrafish Craniofacial Development: A Window into Early Patterning Tbx1 is required for second heart field proliferation in zebrafish PCB126 exposure disrupts zebrafish ventricular and branchial but not early neural crest development.lessen encodes a zebrafish trap100 required for enteric nervous system development.Zebrafish as a developmental model organism for pediatric research.Normal function of Myf5 during gastrulation is required for pharyngeal arch cartilage development in zebrafish embryos Zebrafish models to study hypoxia-induced pathological angiogenesis in malignant and nonmalignant diseases.

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The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans

http://www.wikidata.org/entity/Q28312215

description

2003 nî lūn-bûn

@nan

2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2003年の論文

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2003年論文

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2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

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2003年論文

@zh-tw

2003年论文

@wuu

name

The zebrafish van gogh mutatio ...... ge deletion syndrome in humans

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The zebrafish van gogh mutatio ...... ge deletion syndrome in humans

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The zebrafish van gogh mutatio ...... ge deletion syndrome in humans

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type

label

The zebrafish van gogh mutatio ...... ge deletion syndrome in humans

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The zebrafish van gogh mutatio ...... ge deletion syndrome in humans

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The zebrafish van gogh mutatio ...... ge deletion syndrome in humans

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prefLabel

The zebrafish van gogh mutatio ...... ge deletion syndrome in humans

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The zebrafish van gogh mutatio ...... ge deletion syndrome in humans

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The zebrafish van gogh mutatio ...... ge deletion syndrome in humans

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The zebrafish van gogh mutatio ...... ge deletion syndrome in humans

@en

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Dae-gwon Ahn

http://www.w3.org/2001/XMLSchema#string

Helen Foott

http://www.w3.org/2001/XMLSchema#string

Ilya Ruvinsky

http://www.w3.org/2001/XMLSchema#string

Leonard I Zon

http://www.w3.org/2001/XMLSchema#string

Robert Geisler

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Robert K Ho

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Sreelaja Nair

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Tatjana Piotrowski

http://www.w3.org/2001/XMLSchema#string

Thomas F Schilling

http://www.w3.org/2001/XMLSchema#string

Yi Zhou

http://www.w3.org/2001/XMLSchema#string

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5043-52

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scholarly article

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4441729

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10.1242/DEV.00704

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20

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130

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Gerd-Jörg Rauch

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2003-10-01T00:00:00Z

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10585007

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12952905

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