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Search results 101 to 200 out of 1277 for Tbx1

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Type Details Score
Publication
9268629 | J:42496
First Author: Chieffo C
Year: 1997
Journal: Genomics
Title: Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene.
Volume: 43
Issue: 3
Pages: 267-77
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Publication
28884822 | J:319604
First Author: Sutherland JM
Year: 2018
Journal: J Cell Physiol
Title: RNA binding protein Musashi-2 regulates PIWIL1 and TBX1 in mouse spermatogenesis.
Volume: 233
Issue: 4
Pages: 3262-3273
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Publication
19247433 | J:146769
First Author: Choi M
Year: 2009
Journal: PLoS Genet
Title: Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.
Volume: 5
Issue: 2
Pages: e1000395
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Publication
16600992 | J:109536
First Author: Arnold JS
Year: 2006
Journal: Hum Mol Genet
Title: Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients.
Volume: 15
Issue: 10
Pages: 1629-39
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Publication
29866044 | J:263025
First Author: Zoupa M
Year: 2018
Journal: BMC Genomics
Title: Gene expression profiling in the developing secondary palate in the absence of Tbx1 function.
Volume: 19
Issue: 1
Pages: 429
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Publication
30166330 | J:267181
 
First Author: Pane LS
Year: 2018
Journal: Dis Model Mech
Title: Tbx1 represses Mef2c gene expression and is correlated with histone 3 deacetylation of the anterior heart field enhancer.
Volume: 11
Issue: 9
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Publication
16399080 | J:105259
First Author: Guris DL
Year: 2006
Journal: Dev Cell
Title: Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome.
Volume: 10
Issue: 1
Pages: 81-92
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Publication
14975726 | J:88814
First Author: Brown CB
Year: 2004
Journal: Dev Biol
Title: Cre-mediated excision of Fgf8 in the Tbx1 expression domain reveals a critical role for Fgf8 in cardiovascular development in the mouse.
Volume: 267
Issue: 1
Pages: 190-202
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Publication
16684884 | J:110101
First Author: Paylor R
Year: 2006
Journal: Proc Natl Acad Sci U S A
Title: Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.
Volume: 103
Issue: 20
Pages: 7729-34
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Publication
18082678 | J:130823
First Author: Mitsiadis TA
Year: 2008
Journal: Dev Biol
Title: Deletion of the Pitx1 genomic locus affects mandibular tooth morphogenesis and expression of the Barx1 and Tbx1 genes.
Volume: 313
Issue: 2
Pages: 887-96
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Publication
22674535 | J:185606
First Author: Simrick S
Year: 2012
Journal: Dev Dyn
Title: Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling.
Volume: 241
Issue: 8
Pages: 1310-24
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Publication
20501333 | J:163487
First Author: Aggarwal VS
Year: 2010
Journal: Dev Biol
Title: Mesodermal Tbx1 is required for patterning the proximal mandible in mice.
Volume: 344
Issue: 2
Pages: 669-81
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Publication
15469978 | J:93588
First Author: Hu T
Year: 2004
Journal: Development
Title: Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors.
Volume: 131
Issue: 21
Pages: 5491-502
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Publication
25190705 | J:246236
First Author: Rana MS
Year: 2014
Journal: Circ Res
Title: Tbx1 coordinates addition of posterior second heart field progenitor cells to the arterial and venous poles of the heart.
Volume: 115
Issue: 9
Pages: 790-9
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Publication
37625409 | J:352505
First Author: Wang W
Year: 2023
Journal: Immunity
Title: Lymphatic endothelial transcription factor Tbx1 promotes an immunosuppressive microenvironment to facilitate post-myocardial infarction repair.
Volume: 56
Issue: 10
Pages: 2342-2357.e10
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Publication
15703190 | J:98074
First Author: Stoller JZ
Year: 2005
Journal: Hum Mol Genet
Title: Identification of a novel nuclear localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation.
Volume: 14
Issue: 7
Pages: 885-92
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Publication
15652707 | J:96463
First Author: Moraes F
Year: 2005
Journal: Mech Dev
Title: Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development.
Volume: 122
Issue: 2
Pages: 199-212
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Publication
23642587 | J:320857
First Author: Spruijt NE
Year: 2013
Journal: Int J Pediatr Otorhinolaryngol
Title: Exploring a neurogenic basis of velopharyngeal dysfunction in Tbx1 mutant mice: no difference in volumes of the nucleus ambiguus.
Volume: 77
Issue: 6
Pages: 1002-7
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Publication
28346476 | J:242314
First Author: Racedo SE
Year: 2017
Journal: PLoS Genet
Title: Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome.
Volume: 13
Issue: 3
Pages: e1006687
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Publication
24356861 | J:208359
First Author: Mc Laughlin D
Year: 2014
Journal: Pediatr Surg Int
Title: Altered Tbx1 gene expression is associated with abnormal oesophageal development in the adriamycin mouse model of oesophageal atresia/tracheo-oesophageal fistula.
Volume: 30
Issue: 2
Pages: 143-9
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Publication
32107392 | J:292863
First Author: Tejedor G
Year: 2020
Journal: Sci Rep
Title: Whole embryo culture, transcriptomics and RNA interference identify TBX1 and FGF11 as novel regulators of limb development in the mouse.
Volume: 10
Issue: 1
Pages: 3597
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Publication
26689739 | J:317609
First Author: Brock LJ
Year: 2016
Journal: J Anat
Title: Mapping cellular processes in the mesenchyme during palatal development in the absence of Tbx1 reveals complex proliferation changes and perturbed cell packing and polarity.
Volume: 228
Issue: 3
Pages: 464-73
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Publication
20122914 | J:160266
First Author: van Bueren KL
Year: 2010
Journal: Dev Biol
Title: Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome.
Volume: 340
Issue: 2
Pages: 369-80
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Publication
17047027 | J:117754
First Author: Roberts C
Year: 2006
Journal: Hum Mol Genet
Title: 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.
Volume: 15
Issue: 23
Pages: 3394-410
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GXD Expression
GXD Expression
Probe: MGI:7430772
Assay Type: Immunohistochemistry
Annotation Date: 2023-01-31
Strength: Trace
Sex: Not Specified
Emaps: EMAPS:1612817
Pattern: Regionally restricted
Stage: TS17
Assay Id: MGI:7430778
Age: embryonic day 10.5
Image: 2U
Note: The labeled cell population was severely reduced in size, and the level of Tbx1 expression was only barely detectable.
Specimen Label: 2U
Detected: true
Specimen Num: 2
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Publication
8853987 | J:34541
First Author: Chapman DL
Year: 1996
Journal: Dev Dyn
Title: Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.
Volume: 206
Issue: 4
Pages: 379-90
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Publication
28838968 | J:247916
First Author: Macchiarulo S
Year: 2017
Journal: Biol Open
Title: Tbx1 and Jag1 act in concert to modulate the fate of neurosensory cells of the mouse otic vesicle.
Volume: 6
Issue: 10
Pages: 1472-1482
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Publication
7920656 | J:18978
First Author: Bollag RJ
Year: 1994
Journal: Nat Genet
Title: An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locus.
Volume: 7
Issue: 3
Pages: 383-9
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Publication
28105375 | J:244462
 
First Author: Chen J
Year: 2016
Journal: Neural Plast
Title: Identification of a Novel ENU-Induced Mutation in Mouse Tbx1 Linked to Human DiGeorge Syndrome.
Volume: 2016
Pages: 5836143
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Publication
31444215 | J:284143
 
First Author: Phillips HM
Year: 2019
Journal: Development
Title: Pax9 is required for cardiovascular development and interacts with Tbx1 in the pharyngeal endoderm to control 4th pharyngeal arch artery morphogenesis.
Volume: 146
Issue: 18
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Publication
34552467 | J:311152
 
First Author: Favicchia I
Year: 2021
Journal: Front Mol Neurosci
Title: Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome.
Volume: 14
Pages: 663598
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Publication
8878690 | J:35709
First Author: Agulnik SI
Year: 1996
Journal: Genetics
Title: Evolution of mouse T-box genes by tandem duplication and cluster dispersion.
Volume: 144
Issue: 1
Pages: 249-54
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Strain
MGI:5471795 | FVB.Cg-Tbx1<tm1Bem>/Mmucd
Attribute String: congenic, mutant strain, targeted mutation
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UniProt Feature
UniProt Feature
Begin: 1
Description: T-box transcription factor TBX1
Type: chain
End: 479
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Publication
34789765 | J:315702
First Author: Nomaru H
Year: 2021
Journal: Nat Commun
Title: Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm.
Volume: 12
Issue: 1
Pages: 6645
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Publication
35946435 | J:330214
 
First Author: Lania G
Year: 2022
Journal: Dis Model Mech
Title: A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome.
Volume: 15
Issue: 9
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Publication
34050709 | J:314464
First Author: Cheung MY
Year: 2021
Journal: Genesis
Title: Setd5 is required in cardiopharyngeal mesoderm for heart development and its haploinsufficiency is associated with outflow tract defects in mouse.
Volume: 59
Issue: 7-8
Pages: e23421
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Publication
33608392 | J:304609
     
First Author: Caprio C
Year: 2021
Journal: Dis Model Mech
Title: EZH2 is required for parathyroid and thymic development through differentiation of the third pharyngeal pouch endoderm.
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Publication
38048357 | J:343546
First Author: Huang Z
Year: 2023
Journal: PLoS Biol
Title: Supraclavicular brown adipocytes originate from Tbx1+ myoprogenitors.
Volume: 21
Issue: 12
Pages: e3002413
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Publication
23971992 | J:204435
 
First Author: Freyer L
Year: 2013
Journal: BMC Dev Biol
Title: Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice.
Volume: 13
Pages: 33
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Publication
28438970 | J:242227
First Author: Antoine MW
Year: 2017
Journal: J Neurosci
Title: The Severity of Vestibular Dysfunction in Deafness as a Determinant of Comorbid Hyperactivity or Anxiety.
Volume: 37
Issue: 20
Pages: 5144-5154
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Publication
19389367 | J:149463
First Author: Lania G
Year: 2009
Journal: Dev Biol
Title: Early thyroid development requires a Tbx1-Fgf8 pathway.
Volume: 328
Issue: 1
Pages: 109-17
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Publication
16258075 | J:102846
First Author: Stennard FA
Year: 2005
Journal: Development
Title: T-box transcription factors and their roles in regulatory hierarchies in the developing heart.
Volume: 132
Issue: 22
Pages: 4897-910
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Publication
16365290 | J:104695
First Author: Hiroi N
Year: 2005
Journal: Proc Natl Acad Sci U S A
Title: A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice.
Volume: 102
Issue: 52
Pages: 19132-7
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Publication
28173146 | J:238654
First Author: Lania G
Year: 2016
Journal: Hum Mol Genet
Title: Vitamin B12 ameliorates the phenotype of a mouse model of DiGeorge syndrome.
Volume: 25
Issue: 20
Pages: 4369-4375
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Publication
12617845 | J:81319
First Author: Sauka-Spengler T
Year: 2002
Journal: Gene Expr Patterns
Title: Embryonic expression of Tbx1, a DiGeorge syndrome candidate gene, in the lamprey Lampetra fluviatilis.
Volume: 2
Issue: 1-2
Pages: 99-103
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Publication
21173260 | J:169004
First Author: Bok J
Year: 2011
Journal: Proc Natl Acad Sci U S A
Title: Transient retinoic acid signaling confers anterior-posterior polarity to the inner ear.
Volume: 108
Issue: 1
Pages: 161-6
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Publication
11242110 | J:70730
First Author: Jerome LA
Year: 2001
Journal: Nat Genet
Title: DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1.
Volume: 27
Issue: 3
Pages: 286-91
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Publication
35620058 | J:325041
 
First Author: Anderson RH
Year: 2022
Journal: Front Cell Dev Biol
Title: Morphogenesis of the Mammalian Aortic Arch Arteries.
Volume: 10
Pages: 892900
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Publication
21908517 | J:177772
First Author: Hiramoto T
Year: 2011
Journal: Hum Mol Genet
Title: Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model.
Volume: 20
Issue: 24
Pages: 4775-85
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Publication
15789410 | J:97317
First Author: Vincentz JW
Year: 2005
Journal: Genesis
Title: Fgf15 is required for proper morphogenesis of the mouse cardiac outflow tract.
Volume: 41
Issue: 4
Pages: 192-201
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Publication
33348080 | J:306135
 
First Author: Shimizu R
Year: 2021
Journal: Biochem Biophys Res Commun
Title: Decrease in the T-box1 gene expression in embryonic brain and adult hippocampus of down syndrome mouse models.
Volume: 535
Pages: 87-92
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Publication
12539040 | J:81698
First Author: Stalmans I
Year: 2003
Journal: Nat Med
Title: VEGF: a modifier of the del22q11 (DiGeorge) syndrome?
Volume: 9
Issue: 2
Pages: 173-82
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Publication
12810603 | J:83662
First Author: Bachiller D
Year: 2003
Journal: Development
Title: The role of chordin/Bmp signals in mammalian pharyngeal development and DiGeorge syndrome.
Volume: 130
Issue: 15
Pages: 3567-78
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Publication
22982415 | J:190655
First Author: Yee KK
Year: 2012
Journal: Gene
Title: Transrepression activity of T-box1 in a gene regulation network in mouse cells.
Volume: 510
Issue: 2
Pages: 162-70
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Publication
20215350 | J:158677
First Author: Huh SH
Year: 2010
Journal: Development
Title: Beta-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1.
Volume: 137
Issue: 7
Pages: 1137-47
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Publication
15084464 | J:89188
First Author: Raft S
Year: 2004
Journal: Development
Title: Suppression of neural fate and control of inner ear morphogenesis by Tbx1.
Volume: 131
Issue: 8
Pages: 1801-12
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Publication
26387456 | J:225351
First Author: Gopalakrishnan S
Year: 2015
Journal: Dev Cell
Title: A Cranial Mesoderm Origin for Esophagus Striated Muscles.
Volume: 34
Issue: 6
Pages: 694-704
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Publication
31535973 | J:283675
   
First Author: Comai G
Year: 2019
Journal: Elife
Title: A distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle.
Volume: 8
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Publication
21145505 | J:169047
First Author: Wang J
Year: 2010
Journal: Dev Cell
Title: Bmp signaling regulates myocardial differentiation from cardiac progenitors through a MicroRNA-mediated mechanism.
Volume: 19
Issue: 6
Pages: 903-12
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Publication
19531352 | J:150130
First Author: Sambasivan R
Year: 2009
Journal: Dev Cell
Title: Distinct regulatory cascades govern extraocular and pharyngeal arch muscle progenitor cell fates.
Volume: 16
Issue: 6
Pages: 810-21
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Publication
22219655 | J:196547
 
First Author: Liu X
Year: 2011
Journal: J Biomed Biotechnol
Title: ENU mutagenesis screen to establish motor phenotypes in wild-type mice and modifiers of a pre-existing motor phenotype in tau mutant mice.
Volume: 2011
Pages: 130947
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Publication
30016433 | J:266570
First Author: De Bono C
Year: 2018
Journal: Hum Mol Genet
Title: T-box genes and retinoic acid signaling regulate the segregation of arterial and venous pole progenitor cells in the murine second heart field.
Volume: 27
Issue: 21
Pages: 3747-3760
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Publication
11709542 | J:72986
First Author: Funke B
Year: 2001
Journal: Hum Mol Genet
Title: Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects.
Volume: 10
Issue: 22
Pages: 2549-56
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Publication
17321697 | J:120112
First Author: Amati F
Year: 2007
Journal: Gene
Title: Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development.
Volume: 391
Issue: 1-2
Pages: 91-102
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Publication
27256596 | J:239907
 
First Author: Fulcoli FG
Year: 2016
Journal: Nat Commun
Title: Rebalancing gene haploinsufficiency in vivo by targeting chromatin.
Volume: 7
Pages: 11688
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Publication
30087351 | J:266263
First Author: Andersen P
Year: 2018
Journal: Nat Commun
Title: Precardiac organoids form two heart fields via Bmp/Wnt signaling.
Volume: 9
Issue: 1
Pages: 3140
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Publication
25605943 | J:217656
First Author: Lescroart F
Year: 2015
Journal: Proc Natl Acad Sci U S A
Title: Clonal analysis reveals a common origin between nonsomite-derived neck muscles and heart myocardium.
Volume: 112
Issue: 5
Pages: 1446-51
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Publication
26755698 | J:229008
First Author: Escot S
Year: 2016
Journal: Development
Title: Disruption of CXCR4 signaling in pharyngeal neural crest cells causes DiGeorge syndrome-like malformations.
Volume: 143
Issue: 4
Pages: 582-8
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Publication
32041892 | J:283745
 
First Author: Imamoto A
Year: 2020
Journal: Life Sci Alliance
Title: Essential role of the Crk family-dosage in DiGeorge-like anomaly and metabolic homeostasis.
Volume: 3
Issue: 2
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Publication
32466118 | J:320909
 
First Author: Stothard CA
Year: 2020
Journal: J Cardiovasc Dev Dis
Title: Pax9 and Gbx2 Interact in the Pharyngeal Endoderm to Control Cardiovascular Development.
Volume: 7
Issue: 2
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Publication
25410658 | J:219374
First Author: Sinha T
Year: 2015
Journal: Hum Mol Genet
Title: Loss of Wnt5a disrupts second heart field cell deployment and may contribute to OFT malformations in DiGeorge syndrome.
Volume: 24
Issue: 6
Pages: 1704-16
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Publication
20939858 | J:171024
First Author: Calmont A
Year: 2011
Journal: Neurogastroenterol Motil
Title: Absence of the vagus nerve in the stomach of Tbx1-/- mutant mice.
Volume: 23
Issue: 2
Pages: 125-30
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Publication
25197075 | J:216364
First Author: Caprio C
Year: 2014
Journal: Proc Natl Acad Sci U S A
Title: p53 Suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome.
Volume: 111
Issue: 37
Pages: 13385-90
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Publication
22495305 | J:183832
First Author: Chen T
Year: 2012
Journal: Nature
Title: An RNA interference screen uncovers a new molecule in stem cell self-renewal and long-term regeneration.
Volume: 485
Issue: 7396
Pages: 104-8
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Publication
25912687 | J:221397
First Author: Vanyai HK
Year: 2015
Journal: Dev Biol
Title: Mesodermal expression of Moz is necessary for cardiac septum development.
Volume: 403
Issue: 1
Pages: 22-9
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Publication
17825816 | J:128008
First Author: Xu H
Year: 2007
Journal: Dev Biol
Title: In vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea.
Volume: 310
Issue: 2
Pages: 329-40
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Publication
22396765 | J:186857
First Author: Zhou J
Year: 2012
Journal: PLoS One
Title: Endothelial neuropilin disruption in mice causes DiGeorge syndrome-like malformations via mechanisms distinct to those caused by loss of Tbx1.
Volume: 7
Issue: 3
Pages: e32429
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Publication
20685737 | J:164590
First Author: Mitsiadis TA
Year: 2010
Journal: Development
Title: BMPs and FGFs target Notch signalling via jagged 2 to regulate tooth morphogenesis and cytodifferentiation.
Volume: 137
Issue: 18
Pages: 3025-35
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Publication
24068957 | J:202467
First Author: Wang J
Year: 2013
Journal: PLoS Genet
Title: MicroRNA-17-92, a direct Ap-2α transcriptional target, modulates T-box factor activity in orofacial clefting.
Volume: 9
Issue: 9
Pages: e1003785
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Publication
20736290 | J:164582
First Author: Hurd EA
Year: 2010
Journal: Development
Title: The ATP-dependent chromatin remodeling enzyme CHD7 regulates pro-neural gene expression and neurogenesis in the inner ear.
Volume: 137
Issue: 18
Pages: 3139-50
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Publication
20110535 | J:170865
First Author: Ryckebüsch L
Year: 2010
Journal: Circ Res
Title: Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome.
Volume: 106
Issue: 4
Pages: 686-94
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Publication
31758944 | J:285717
First Author: Ishizaki-Asami R
Year: 2020
Journal: Dev Biol
Title: Inositol 1,4,5-trisphosphate receptor 2 as a novel marker of vasculature to delineate processes of cardiopulmonary development.
Volume: 458
Issue: 2
Pages: 237-245
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Publication
24821700 | J:213584
First Author: Vincent SD
Year: 2014
Journal: Hum Mol Genet
Title: Prdm1 functions in the mesoderm of the second heart field, where it interacts genetically with Tbx1, during outflow tract morphogenesis in the mouse embryo.
Volume: 23
Issue: 19
Pages: 5087-101
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Publication
25997579 | J:223933
First Author: Okubo T
Year: 2015
Journal: Dev Dyn
Title: Pharyngeal arch deficiencies affect taste bud development in the circumvallate papilla with aberrant glossopharyngeal nerve formation.
Volume: 244
Issue: 7
Pages: 874-87
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Publication
19805316 | J:153232
First Author: Meechan DW
Year: 2009
Journal: Proc Natl Acad Sci U S A
Title: Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome.
Volume: 106
Issue: 38
Pages: 16434-45
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Publication
27633995 | J:237523
First Author: Bain VE
Year: 2016
Journal: Development
Title: Tissue-specific roles for sonic hedgehog signaling in establishing thymus and parathyroid organ fate.
Volume: 143
Issue: 21
Pages: 4027-4037
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Publication
30121012 | J:270507
 
First Author: Funato N
Year: 2018
Journal: Arch Oral Biol
Title: Deletion of the T-box transcription factor gene, Tbx1, in mice induces differential expression of genes associated with cleft palate in humans.
Volume: 95
Pages: 149-155
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Publication
22116936 | J:181153
First Author: Mesbah K
Year: 2012
Journal: Hum Mol Genet
Title: Identification of a Tbx1/Tbx2/Tbx3 genetic pathway governing pharyngeal and arterial pole morphogenesis.
Volume: 21
Issue: 6
Pages: 1217-29
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Publication
21831920 | J:180898
First Author: Brown AS
Year: 2011
Journal: Development
Title: Otic ablation of smoothened reveals direct and indirect requirements for Hedgehog signaling in inner ear development.
Volume: 138
Issue: 18
Pages: 3967-76
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Publication
23077214 | J:191130
First Author: Maynard TM
Year: 2013
Journal: Hum Mol Genet
Title: 22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development.
Volume: 22
Issue: 2
Pages: 300-12
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Publication
30787001 | J:273025
 
First Author: Moreau JLM
Year: 2019
Journal: Development
Title: Gene-environment interaction impacts on heart development and embryo survival.
Volume: 146
Issue: 4
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Publication
27005988 | J:241099
First Author: Flore G
Year: 2017
Journal: Cereb Cortex
Title: Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome.
Volume: 27
Issue: 3
Pages: 2210-2225
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Publication
16109395 | J:101263
First Author: Ivins S
Year: 2005
Journal: Dev Biol
Title: Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1.
Volume: 285
Issue: 2
Pages: 554-69
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Publication
16839542 | J:119303
First Author: Seo S
Year: 2006
Journal: Dev Biol
Title: Forkhead transcription factors, Foxc1 and Foxc2, are required for the morphogenesis of the cardiac outflow tract.
Volume: 296
Issue: 2
Pages: 421-36
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Publication
15778864 | J:98850
First Author: Prescott K
Year: 2005
Journal: Hum Genet
Title: Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome.
Volume: 116
Issue: 6
Pages: 486-96
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Publication
29534062 | J:258739
First Author: Antoine MW
Year: 2018
Journal: PLoS Biol
Title: Early uneven ear input induces long-lasting differences in left-right motor function.
Volume: 16
Issue: 3
Pages: e2002988
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HT Experiment
E-GEOD-33064 | Expression data from a Tbx1 gene allelic series
Series Id: GSE33064
Experiment Type: transcription profiling by array
Study Type: WT vs. Mutant
Source: ArrayExpress
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Publication
36649430 | J:333562
First Author: Miyamoto M
Year: 2023
Journal: Proc Natl Acad Sci U S A
Title: Cardiac progenitors instruct second heart field fate through Wnts.
Volume: 120
Issue: 4
Pages: e2217687120
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Publication
24009395 | J:201156
First Author: Antoine MW
Year: 2013
Journal: Science
Title: A causative link between inner ear defects and long-term striatal dysfunction.
Volume: 341
Issue: 6150
Pages: 1120-3
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