Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants
about
Prdm1 functions in the mesoderm of the second heart field, where it interacts genetically with Tbx1, during outflow tract morphogenesis in the mouse embryoPartial rescue of the Tbx1 mutant heart phenotype by Fgf8: genetic evidence of impaired tissue response to Fgf8Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in miceMesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract developmentA Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesisEarly thyroid development requires a Tbx1-Fgf8 pathwaySignals and switches in Mammalian neural crest cell differentiationTbx1 controls the morphogenesis of pharyngeal pouch epithelia through mesodermal Wnt11r and Fgf8a.Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndromeGenetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome.Identification of a Tbx1/Tbx2/Tbx3 genetic pathway governing pharyngeal and arterial pole morphogenesisHeterogeneity in the Segmental Development of the Aortic Tree: Impact on Management of Genetically Triggered Aortic Aneurysms.Disruption of Smad4 in neural crest cells leads to mid-gestation death with pharyngeal arch, craniofacial and cardiac defectsT-box factors determine cardiac design.22q11.2 Deletion Syndrome: Laboratory Diagnosis and TBX1 and FGF8 Mutation Screening.Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndrome.Transcription factor TBX1 overexpression induces downregulation of proteins involved in retinoic acid metabolism: a comparative proteomic analysis.Tbx1, subpulmonary myocardium and conotruncal congenital heart defects.Frs2alpha-deficiency in cardiac progenitors disrupts a subset of FGF signals required for outflow tract morphogenesis.Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation.The Complex Genetic Basis of Congenital Heart Defects.Transforming growth factor β-mediated Sox10 suppression controls mesenchymal progenitor generation in neural crest stem cells.Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling.SDF1-CXCR4 signaling: A new player involved in DiGeorge/22q11-deletion syndrome.Pcsk5 is required in the early cranio-cardiac mesoderm for heart development.β-catenin promoter ChIP-chip reveals potential schizophrenia and bipolar disorder gene network.Copy number variants in Ebstein anomaly.Loss of Tbx1 induces bone phenotypes similar to cleidocranial dysplasia.Development of patient-specific neurons in schizophrenia using induced pluripotent stem cells.
P2860
Q28509491-06B37756-BCE7-4880-ADED-6418648B00CDQ28585923-FAB4119A-85E2-40F2-BE05-BA2029EC6C9CQ28586874-BA9BE9D8-1E97-48FF-B1AD-360F00946213Q28587491-23DD92F0-B4A6-4135-999B-47CF9AA61CFCQ28589314-DC60CEB7-26F9-4FC1-986D-8028F84CA83DQ28589620-0119E8B7-BB92-42F1-8A9E-1EFB6401CC0BQ28709598-2E8A049B-7C5D-4C7F-B23D-A262ED145385Q30592681-07AB9814-32FB-44CA-8CBA-B2174160B281Q33829670-DB9FB063-74BA-48C8-B036-BECA3AC47A86Q35916112-7D55042E-2876-411D-890F-21E23850FA03Q36379778-B4FC3AF2-6088-4C26-A53F-6CF735FDDB0CQ36391104-ED490187-AAB5-4A61-82E9-0CA041591867Q36618064-8B264512-2F70-4FB1-8032-F824C50618B7Q36767576-1F094F85-EDFD-4A35-BCAD-B41450B85D1BQ37000669-B66FEEF9-5245-4808-9310-5FE180D569D6Q37219657-A23F2420-F80C-426A-B2E6-A22BE30E9612Q37327760-A1234CE3-40F2-44E4-AC0B-5035F75C15EEQ37876851-940BEC31-B826-4BB7-884D-D721740D6780Q38498581-54050155-6B26-46D1-AA26-554E2D7B4867Q38803986-08C0AFF5-4FCE-4B7F-881D-7BE0C1879F68Q39223050-C8B651D3-4AE4-41A2-B626-6A17F6A24B7FQ39784476-3C62F3D2-7B21-4A20-81E0-95BF0312A6AFQ40416047-618EE96A-C0EB-4937-A5F9-23C341DF45C4Q41901850-C519EB7F-4AC1-47E3-BF31-2D75472BD946Q41910908-C7DBC247-08E7-4286-B5E4-FD042A41A34BQ42976183-D567B03E-244A-4CA7-9E71-988C957FCBDCQ46184553-280CED9F-0E34-47BF-8D5F-FBE56C26C6F9Q46549763-FF4B235A-0482-4ACD-B5F3-A1C3777BAED7Q47788549-CFE5B80F-E4A8-4269-88CD-A4C3D75333AC
P2860
Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants
description
2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2006
@ast
im Juli 2006 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2006/07/15)
@sk
vědecký článek publikovaný v roce 2006
@cs
wetenschappelijk artikel (gepubliceerd op 2006/07/15)
@nl
наукова стаття, опублікована в липні 2006
@uk
مقالة علمية (نشرت في 15-7-2006)
@ar
name
Fgf8 expression in the Tbx1 do ...... ract phenotype of Tbx1 mutants
@ast
Fgf8 expression in the Tbx1 do ...... ract phenotype of Tbx1 mutants
@en
Fgf8 expression in the Tbx1 do ...... ract phenotype of Tbx1 mutants
@nl
type
label
Fgf8 expression in the Tbx1 do ...... ract phenotype of Tbx1 mutants
@ast
Fgf8 expression in the Tbx1 do ...... ract phenotype of Tbx1 mutants
@en
Fgf8 expression in the Tbx1 do ...... ract phenotype of Tbx1 mutants
@nl
prefLabel
Fgf8 expression in the Tbx1 do ...... ract phenotype of Tbx1 mutants
@ast
Fgf8 expression in the Tbx1 do ...... ract phenotype of Tbx1 mutants
@en
Fgf8 expression in the Tbx1 do ...... ract phenotype of Tbx1 mutants
@nl
P2093
P2860
P3181
P1476
Fgf8 expression in the Tbx1 do ...... ract phenotype of Tbx1 mutants
@en
P2093
Angela Sobotka
Antonio Baldini
Francesca Vitelli
Tuong Huynh
P2860
P304
P3181
P356
10.1016/J.YDBIO.2006.03.044
P407
P577
2006-07-15T00:00:00Z