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Search results 101 to 200 out of 1262 for Tbx1

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Type Details Score
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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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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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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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Publication
32014863 | J:284172
 
First Author: Adachi N
Year: 2020
Journal: Development
Title: Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx.
Volume: 147
Issue: 3
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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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Protein Coding Gene
MGP_CAROLIEiJ_G0020549 | -
Type: protein_coding_gene
Organism: Mus caroli
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Protein Coding Gene
MGP_129S1SvImJ_G0022614 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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•
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•
•
Protein Coding Gene
MGP_AJ_G0022575 | -
Type: protein_coding_gene
Organism: mouse, laboratory
•
•
•
•
•
Protein Coding Gene
MGP_AKRJ_G0022552 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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