Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.
about
The neural crest in cardiac congenital anomaliesTbx1 regulates the BMP-Smad1 pathway in a transcription independent manner.Strain-specific modifier genes governing craniofacial phenotypes.Pitx2-dependent occupancy by histone deacetylases is associated with T-box gene regulation in mammalian abdominal tissue.A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients.Endothelial neuropilin disruption in mice causes DiGeorge syndrome-like malformations via mechanisms distinct to those caused by loss of Tbx1Phenotypic impact of genomic structural variation: insights from and for human disease.Multiple tissue-specific requirements for the BMP antagonist Noggin in development of the mammalian craniofacial skeleton.Functional interactions between Fat family cadherins in tissue morphogenesis and planar polarity.Bmp signaling mediates endoderm pouch morphogenesis by regulating Fgf signaling in zebrafish.An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature.Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndromeGenetics of Cleft Palate and Velopharyngeal Insufficiency.Morphological and molecular evolution of the ultimobranchial gland of nonmammalian vertebrates, with special reference to the chicken C cells.Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling.Crossveinless-2 is required for the relocalization of Chordin protein within the vertebral field in mouse embryos.Functional interaction between Foxd3 and Pax3 in cardiac neural crest development.Penetrance for copy number variants associated with schizophrenia.The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1.Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions.22q11.2 Deletion Syndrome
P2860
Q27024385-22FC3176-CD4A-4E11-BDEE-1199E21576C8Q27863405-FA7F144B-4BF6-46AD-AC4C-3CCA0EE26A0DQ30457692-2A464F4A-E01C-4B49-88BE-CE41D93FC6FAQ33799595-F305352F-7894-4D16-ADD3-DACF4AB337FEQ33903341-3C5421DF-B719-486A-953A-4D2E65132024Q34187192-91A447FA-B4FD-4CD4-AAEB-0DC4248FD28EQ34323221-21944C1B-8E61-4E1B-8D3C-D9C4FF995BB6Q35446042-6D521877-B498-4D2F-BB5A-8303366562EEQ35893646-F8289193-6D29-4F46-848F-D0F7A559354AQ37036174-8743C97E-4C8B-44ED-AD37-87B78AAABDCCQ37153544-C38B636E-E4C6-4097-AE49-9DD14DF75E09Q37341674-316465C2-01E0-42C4-8046-FBAC82644302Q38951651-D7AC9606-9D17-47A8-A5F8-E67569EEE0BDQ39368791-FFC49DCB-8C6E-4975-9334-47D9D3D40C6CQ40416047-A733332B-0C31-4781-838A-AEF059545481Q42377350-DA281B45-98BF-45FA-ABB9-BF409AEDC05EQ42722333-4F5E07EC-15B0-4A87-A25C-74CCD66469D9Q50303296-6338B347-3FA1-4BFF-A0F2-0FFC73F4A97CQ50737118-716AA7DE-D60B-4246-AFA5-7675AD7C132DQ52652397-62AC2F21-F0FA-4426-A3F8-C684522F3D82Q67131076-AD03F663-6BC1-43FA-A874-69CDAED99022
P2860
Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.
description
2009 nî lūn-bûn
@nan
2009 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Chordin is a modifier of tbx1 ...... syndrome phenotypes in mouse.
@ast
Chordin is a modifier of tbx1 ...... syndrome phenotypes in mouse.
@en
type
label
Chordin is a modifier of tbx1 ...... syndrome phenotypes in mouse.
@ast
Chordin is a modifier of tbx1 ...... syndrome phenotypes in mouse.
@en
prefLabel
Chordin is a modifier of tbx1 ...... syndrome phenotypes in mouse.
@ast
Chordin is a modifier of tbx1 ...... syndrome phenotypes in mouse.
@en
P2860
P1433
P1476
Chordin is a modifier of tbx1 ...... syndrome phenotypes in mouse.
@en
P2093
John Klingensmith
P2860
P304
P356
10.1371/JOURNAL.PGEN.1000395
P50
P577
2009-02-27T00:00:00Z