| scholarly article | Q13442814 |
| P50 | author | Gregg Duester | Q28805328 |
| Virginia E Papaioannou | Q38326748 | ||
| P2093 | author name string | Akira Imamoto | |
| Deborah L Guris | |||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | T-box 1 | Q21980210 |
| V-crk avian sarcoma virus CT10 oncogene homolog-like | Q21981293 | ||
| P1104 | number of pages | 12 | |
| P304 | page(s) | 81-92 | |
| P577 | publication date | 2006-01-01 | |
| P1433 | published in | Developmental Cell | Q1524277 |
| P1476 | title | Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome | |
| P478 | volume | 10 |
| Q36477668 | 22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development. |
| Q37669766 | 22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development |
| Q36988231 | 22q11.2 deletion syndrome |
| Q35163449 | A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome |
| Q38072446 | A molecular and genetic outline of cardiac morphogenesis. |
| Q34800084 | A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development. |
| Q41760688 | A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case report |
| Q30008856 | A pre-metazoan origin of the CRK gene family and co-opted signaling network |
| Q33714238 | Beta-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1. |
| Q40416047 | Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling |
| Q41729839 | Canonical Wnt signaling modulates Tbx1, Eya1, and Six1 expression, restricting neurogenesis in the otic vesicle |
| Q91655227 | Characterization and function of the T-box 1 gene in Chinese giant salamander Andrias davidianus |
| Q33413046 | Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse |
| Q48318063 | Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development |
| Q54531000 | Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1. |
| Q37089619 | Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome |
| Q54241827 | Crk Adaptor Proteins Regulate NK Cell Expansion and Differentiation during Mouse Cytomegalovirus Infection. |
| Q41942048 | Crk and CrkL adaptor proteins: networks for physiological and pathological signaling |
| Q35606917 | Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes. |
| Q52574335 | 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. |
| Q33829670 | Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome |
| Q36496880 | Definitive endoderm of the mouse embryo: formation, cell fates, and morphogenetic function |
| Q42862708 | DiGeorge syndrome, Tbx1, and retinoic acid signaling come full circle |
| Q37566124 | Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome |
| Q50420674 | Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome |
| Q34187192 | Endothelial neuropilin disruption in mice causes DiGeorge syndrome-like malformations via mechanisms distinct to those caused by loss of Tbx1 |
| Q89636629 | Essential role of the Crk family-dosage in DiGeorge-like anomaly and metabolic homeostasis |
| Q28652450 | Evolutionary and developmental origins of the cardiac neural crest: building a divided outflow tract |
| Q35123153 | Expression in the human brain of retinoic acid induced 1, a protein associated with neurobehavioural disorders |
| Q28513912 | Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants |
| Q37286661 | Focal adhesion kinase is required for neural crest cell morphogenesis during mouse cardiovascular development. |
| Q34745253 | Functional zebrafish studies based on human genotyping point to netrin-1 as a link between aberrant cardiovascular development and thyroid dysgenesis |
| Q37219657 | Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndrome |
| Q35916112 | Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome |
| Q35388414 | Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients |
| Q34514307 | Genotype-phenotype correlation in 22q11.2 deletion syndrome |
| Q37087585 | Global control regions and regulatory landscapes in vertebrate development and evolution |
| Q36494895 | Hard to swallow: Developmental biological insights into pediatric dysphagia |
| Q34130162 | How to make a heart: the origin and regulation of cardiac progenitor cells |
| Q36379778 | Identification of a Tbx1/Tbx2/Tbx3 genetic pathway governing pharyngeal and arterial pole morphogenesis |
| Q54353492 | Identification of copy number variants on human chromosome 22 in patients with a variety of clinical findings. |
| Q41272218 | Identification of downstream genetic pathways of Tbx1 in the second heart field |
| Q30505432 | Identification of putative retinoic acid target genes downstream of mesenchymal Tbx1 during inner ear development |
| Q38160483 | Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia |
| Q37943798 | Immunological aspects of 22q11.2 deletion syndrome |
| Q64890460 | In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects? |
| Q24621710 | MAP'ing CNS development and cognition: an ERKsome process |
| Q45338231 | Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene. |
| Q28587491 | Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development |
| Q36708506 | Model systems for the study of heart development and disease. Cardiac neural crest and conotruncal malformations |
| Q28081179 | Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development |
| Q35115385 | Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome |
| Q58124159 | Molecular genetics of 22q11.2 deletion syndrome |
| Q41212865 | Molecular mechanisms of functional natural killer deficiency in patients with partial DiGeorge syndrome |
| Q43136777 | Mouse and human CRKL is dosage sensitive for cardiac outflow tract formation |
| Q38510348 | Mouse models for investigating the developmental basis of human birth defects |
| Q37383073 | Mouse models of congenital cardiovascular disease |
| Q51905604 | Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation. |
| Q37819523 | Myocardial lineage development |
| Q37145622 | No evidence for parental imprinting of mouse 22q11 gene orthologs |
| Q33905027 | Novel TBX1 loss-of-function mutation causes isolated conotruncal heart defects in Chinese patients without 22q11.2 deletion |
| Q26995476 | Of mice and men: molecular genetics of congenital heart disease |
| Q28585923 | Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: genetic evidence of impaired tissue response to Fgf8 |
| Q50303296 | Penetrance for copy number variants associated with schizophrenia |
| Q34323221 | Phenotypic impact of genomic structural variation: insights from and for human disease |
| Q28509491 | Prdm1 functions in the mesoderm of the second heart field, where it interacts genetically with Tbx1, during outflow tract morphogenesis in the mouse embryo |
| Q50628160 | Prenatal diagnosis of 24 cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations. |
| Q35768103 | RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm |
| Q91829490 | Reduced maternal vitamin A status increases the incidence of normal aortic arch variants |
| Q90163058 | Regulating Retinoic Acid Availability during Development and Regeneration: The Role of the CYP26 Enzymes |
| Q92445859 | Reiterative Mechanisms of Retinoic Acid Signaling during Vertebrate Heart Development |
| Q37038354 | Retinoic acid controls heart anteroposterior patterning by down-regulating Isl1 through the Fgf8 pathway |
| Q28511599 | Retinoic acid down-regulates Tbx1 expression and induces abnormal differentiation of tongue muscles in fetal mice |
| Q90297521 | Retinoic acid signaling in heart development |
| Q33466026 | Retinoic acid signaling organizes endodermal organ specification along the entire antero-posterior axis |
| Q27863405 | Retracted: Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner |
| Q38569361 | Role of the translational repressor 4E-BP1 in the regulation of p21(Waf1/Cip1) expression by retinoids |
| Q31155236 | Schizophrenia and 22q11.2 deletion syndrome |
| Q37108404 | Signature MicroRNA expression patterns identified in humans with 22q11.2 deletion/DiGeorge syndrome |
| Q37191990 | Structural and functional basis of a role for CRKL in a fibroblast growth factor 8-induced feed-forward loop |
| Q33455008 | Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis |
| Q28588434 | Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm |
| Q33788869 | Tbx1 modulates endodermal and mesodermal differentiation from mouse induced pluripotent stem cells |
| Q50918494 | Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm. |
| Q37876851 | Tbx1, subpulmonary myocardium and conotruncal congenital heart defects. |
| Q50737118 | The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1. |
| Q39223050 | The Complex Genetic Basis of Congenital Heart Defects |
| Q26849320 | The adaptor protein Crk in immune response |
| Q37089736 | The developmental genetics of congenital heart disease. |
| Q46780624 | The duplicated rainbow trout (Oncorhynchus mykiss) T-box transcription factors 1, tbx1a and tbx1b, are up-regulated during testicular development. |
| Q90696674 | The fragile X mutation impairs homeostatic plasticity in human neurons by blocking synaptic retinoic acid signaling |
| Q28588842 | The mammalian doublesex homolog DMRT1 is a transcriptional gatekeeper that controls the mitosis versus meiosis decision in male germ cells |
| Q27024385 | The neural crest in cardiac congenital anomalies |
| Q37782137 | The outflow tract of the heart in fishes: anatomy, genes and evolution |
| Q28593890 | The retinaldehyde reductase DHRS3 is essential for preventing the formation of excess retinoic acid during embryonic development |
| Q37327760 | Transcription factor TBX1 overexpression induces downregulation of proteins involved in retinoic acid metabolism: a comparative proteomic analysis. |
| Q37341674 | Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndrome |
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