| scholarly article | Q13442814 |
| P2093 | author name string | H Scott Baldwin | |
| Christopher Brown | |||
| Amy Law | |||
| Steven Goudy | |||
| Gabriela Sanchez | |||
| P2860 | cites work | Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6) | Q24675845 |
| DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1 | Q28204282 | ||
| Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch | Q28268504 | ||
| Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways | Q28511687 | ||
| Conditional inactivation of Tgfbr2 in cranial neural crest causes cleft palate and calvaria defects | Q28512647 | ||
| TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome | Q28512803 | ||
| Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy | Q28586089 | ||
| Defects in limb, craniofacial, and thymic development in Jagged2 mutant mice | Q28586431 | ||
| Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate | Q28587665 | ||
| Expression and requirement of T-box transcription factors Tbx2 and Tbx3 during secondary palate development in the mouse | Q28587760 | ||
| Gli3-deficient mice exhibit cleft palate associated with abnormal tongue development | Q28587791 | ||
| Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development | Q28589109 | ||
| The many faces and factors of orofacial clefts | Q33724077 | ||
| Palatal fusion - where do the midline cells go? A review on cleft palate, a major human birth defect | Q34564875 | ||
| Specification and patterning of neural crest cells during craniofacial development. | Q36299299 | ||
| Recent advances in craniofacial morphogenesis | Q36471176 | ||
| Molecular control of secondary palate development | Q36581780 | ||
| Palatal seam disintegration: to die or not to die? that is no longer the question | Q37137587 | ||
| Integration of IRF6 and Jagged2 signalling is essential for controlling palatal adhesion and fusion competence. | Q37239895 | ||
| An extracellular matrix infrastructure provides support for murine secondary palatal shelf remodelling | Q38484994 | ||
| Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse. | Q44132458 | ||
| Cre-mediated excision of Fgf8 in the Tbx1 expression domain reveals a critical role for Fgf8 in cardiovascular development in the mouse | Q47194311 | ||
| Tbx1 is expressed at multiple sites of epithelial-mesenchymal interaction during early development of the facial complex. | Q52021572 | ||
| The cellular and molecular etiology of the cleft secondary palate in Fgf10 mutant mice. | Q52085311 | ||
| Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development. | Q52200425 | ||
| Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations. | Q52568551 | ||
| P433 | issue | 5-6 | |
| P304 | page(s) | 292-300 | |
| P577 | publication date | 2010-03-07 | |
| P1433 | published in | Mechanisms of Development | Q6804657 |
| P1476 | title | Tbx1 is necessary for palatal elongation and elevation | |
| P478 | volume | 127 |
| Q64926091 | Cellular and molecular mechanisms of cleft palate development. |
| Q36891185 | Contribution of polymorphisms in genes associated with craniofacial development to the risk of nonsyndromic cleft lip and/or palate in the Brazilian population. |
| Q28255041 | Cranial neural crest ablation of Jagged1 recapitulates the craniofacial phenotype of Alagille syndrome patients |
| Q41249705 | Cranial neural crest deletion of VEGFa causes cleft palate with aberrant vascular and bone development |
| Q37845412 | Disintegration of the medial epithelial seam: is cell death important in palatogenesis? |
| Q34187192 | Endothelial neuropilin disruption in mice causes DiGeorge syndrome-like malformations via mechanisms distinct to those caused by loss of Tbx1 |
| Q55306118 | Gene expression profiling in the developing secondary palate in the absence of Tbx1 function. |
| Q42316991 | Genetic interactions between the hedgehog co-receptors Gas1 and Boc regulate cell proliferation during murine palatogenesis. |
| Q54372898 | Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome. |
| Q49834334 | Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans. |
| Q35878640 | Implications of TGFβ on Transcriptome and Cellular Biofunctions of Palatal Mesenchyme |
| Q57186379 | Loss of Tbx3 in murine neural crest reduces enteric glia and causes cleft palate, but does not influence heart development or bowel transit |
| Q40186459 | Mapping cellular processes in the mesenchyme during palatal development in the absence of Tbx1 reveals complex proliferation changes and perturbed cell packing and polarity. |
| Q37736023 | MicroRNAs in Palatogenesis and Cleft Palate |
| Q28081179 | Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development |
| Q36247698 | Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice |
| Q35085547 | Neural crest-specific deletion of Ldb1 leads to cleft secondary palate with impaired palatal shelf elevation |
| Q38199181 | Roles of retinoic acid signaling in normal and abnormal development of the palate and tongue |
| Q35234113 | TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome |
| Q35040180 | Tak1, Smad4 and Trim33 redundantly mediate TGF-β3 signaling during palate development |
| Q39271331 | Tbx1 regulates oral epithelial adhesion and palatal development. |
| Q48613114 | The regulation of endogenous retinoic acid level through CYP26B1 is required for elevation of palatal shelves |
| Q28592403 | Type III transforming growth factor beta receptor regulates vascular and osteoblast development during palatogenesis |
| Q37341674 | Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndrome |
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