About: Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome

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About: Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	artículu científicu espublizáu en 2006 (ast) wetenschappelijk artikel (gepubliceerd op 2006/01/01) (nl) vedecký článok (publikovaný 2006/01/01) (sk) vědecký článek publikovaný v roce 2006 (cs) مقالة علمية (نشرت عام 2006) (ar) 2006 թվականի հունվարին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в січні 2006 (uk) 2006 թուականի Յունուարին հրատարակուած գիտական յօդուած (hyw) scientific journal article (en) im Januar 2006 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28508893-34AE7012-6D90-4B3E-B186-48CD40E7FDEE
publication date	2006-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28508893-3F501DF3-F13C-4CB8-82CB-3A8F6545D15F
language of work or name	English
author name string	wds:Q28508893-A6ACEF0F-ADD3-44FE-A920-42086EF778A9 wds:Q28508893-F8979396-6116-49C7-AC4F-A3EA245E6639
OpenCitations bibliographic resource ID	wds:Q28508893-B634AEEC-73BF-4499-8F2C-8C460065DCDD
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/3251654
author name string	Akira Imamoto Deborah L Guris
OpenCitations bibliographic resource ID	3251654
rdfs:label	Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome (en) Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome (nl) Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome (ast)
skos:prefLabel	Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome (en) Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome (nl) Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome (ast)
name	Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome (en) Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome (nl) Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome (ast)
author	wds:Q28508893-74F82D57-048C-4B29-A7F4-63E1444C2450 wds:Q28508893-B053C8A4-B55F-4CFB-AE3F-29553367B24E
author	Gregg Duester Virginia E Papaioannou
title	wds:Q28508893-FE1F27E9-9705-410D-AFC6-DA0DB3195F2D
title	Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome (en)
page(s)	wds:Q28508893-47CEC6A3-D4FD-48CD-A161-11ADFF9A5A36
page(s)	81-92
instance of	wds:Q28508893-E1469FB6-28FE-4688-85D5-92D0D3B5BAC2
instance of	scholarly article
main subject	wds:Q28508893-C2989D6A-1FAB-46CE-AEE6-43A75872A10B wds:Q28508893-CDF551C1-415F-4266-B8ED-1F6B4E8FCB89
main subject	V-crk avian sarcoma virus CT10 oncogene homolog-like T-box 1
PubMed ID	wds:Q28508893-B59E30B9-156F-4EDD-A9CB-A47BC1B45908
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16399080
PubMed ID	16399080
published in	wds:Q28508893-8A7E5654-66AF-47F6-879B-21F5B87F33FD
published in	Developmental Cell
issue	wds:Q28508893-F99D06DE-A7CC-4A74-B9A5-CE68B930E061
volume	wds:Q28508893-20201803-D12F-4423-86D2-43C9825193FC
issue	1
volume	10
number of pages	wds:Q28508893-516AA698-51BE-4749-AFE6-23D21D26BDA6
number of pages	12 (xsd:decimal)
DOI	wds:Q28508893-31428272-BE4B-4EDE-ACA7-3BB02726CB03
DOI	http://dx.doi.org/10.1016/J.DEVCEL.2005.12.002
DOI	10.1016/J.DEVCEL.2005.12.002
ResearchGate publication ID	wds:Q28508893-EE8BD413-CB76-423D-9939-63B493816FFF
ResearchGate publication ID	7372880
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28508893
is cites work of	Myocardial lineage development Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome How to make a heart: the origin and regulation of cardiac progenitor cells 22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome DiGeorge syndrome, Tbx1, and retinoic acid signaling come full circle The developmental genetics of congenital heart disease. Definitive endoderm of the mouse embryo: formation, cell fates, and morphogenetic function Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome The adaptor protein Crk in immune response Crk and CrkL adaptor proteins: networks for physiological and pathological signaling Identification of putative retinoic acid target genes downstream of mesenchymal Tbx1 during inner ear development Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation. The neural crest in cardiac congenital anomalies Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm. Phenotypic impact of genomic structural variation: insights from and for human disease Retinoic acid controls heart anteroposterior patterning by down-regulating Isl1 through the Fgf8 pathway The mammalian doublesex homolog DMRT1 is a transcriptional gatekeeper that controls the mitosis versus meiosis decision in male germ cells Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick. Retinoic acid signaling organizes endodermal organ specification along the entire antero-posterior axis Schizophrenia and 22q11.2 deletion syndrome Model systems for the study of heart development and disease. Cardiac neural crest and conotruncal malformations Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndrome Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia Global control regions and regulatory landscapes in vertebrate development and evolution Beta-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1. Endothelial neuropilin disruption in mice causes DiGeorge syndrome-like malformations via mechanisms distinct to those caused by loss of Tbx1 Canonical Wnt signaling modulates Tbx1, Eya1, and Six1 expression, restricting neurogenesis in the otic vesicle Retracted: Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm Identification of downstream genetic pathways of Tbx1 in the second heart field Focal adhesion kinase is required for neural crest cell morphogenesis during mouse cardiovascular development. MAP'ing CNS development and cognition: an ERKsome process Identification of a Tbx1/Tbx2/Tbx3 genetic pathway governing pharyngeal and arterial pole morphogenesis

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