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Summary Expression Phenotypes Gene Literature (44) GO Terms (13) Nucleotides (139) Proteins (46) Interactants (772) Wiki
XB--478083

Papers associated with tbx1



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8 paper(s) referencing morpholinos

Results 1 - 44 of 44 results

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Modeling human congenital disorders with neural crest developmental defects using patient-derived induced pluripotent stem cells., Okuno H, Okano H., Regen Ther. December 1, 2021; 18 275-280.      


Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease., Coppenrath K, Tavares ALP, Shaidani NI, Wlizla M, Moody SA, Horb M., Genesis. January 1, 2021; 59 (12): e23453.        


Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development., Shah AM, Krohn P, Baxi AB, Tavares ALP, Sullivan CH, Chillakuru YR, Majumdar HD, Neilson KM, Moody SA., Dis Model Mech. January 1, 2020; 13 (3):                                               


Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R, Ververi A, Beleza-Meireles A, Ji W, Mis E, Patterson QT, Griffin JN, Bhujel N, Chang CA, Dixit A, Konstantino M, Healy C, Hannan S, Neo N, Cash A, Li D, Bhoj E, Zackai EH, Cleaver R, Baralle D, McEntagart M, Newbury-Ecob R, Scott R, Hurst JA, Au PYB, Hosey MT, Khokha M, Marciano DK, Lakhani SA, Liu KJ, Liu KJ., Hum Mol Genet. January 1, 2020; 29 (11): 1900-1921.                  


The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis., Guo Y, Dorn T, Kühl SJ, Linnemann A, Rothe M, Pfister AS, Vainio S, Laugwitz KL, Moretti A, Kühl M., Dev Biol. January 1, 2019; 449 (1): 1-13.                                  


Timing is everything: Reiterative Wnt, BMP and RA signaling regulate developmental competence during endoderm organogenesis., Rankin SA, Rankin SA, McCracken KW, Luedeke DM, Han L, Wells JM, Shannon JM, Zorn AM., Dev Biol. January 1, 2018; 434 (1): 121-132.          


Conservatism and variability of gene expression profiles among homeologous transcription factors in Xenopus laevis., Watanabe M, Yasuoka Y, Mawaribuchi S, Kuretani A, Ito M, Kondo M, Ochi H, Ogino H, Fukui A, Taira M, Kinoshita T., Dev Biol. June 15, 2017; 426 (2): 301-324.                          


Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development., Neilson KM, Abbruzzesse G, Kenyon K, Bartolo V, Krohn P, Alfandari D, Alfandari D, Moody SA., Dev Biol. January 15, 2017; 421 (2): 171-182.                    


Genomic integration of Wnt/β-catenin and BMP/Smad1 signaling coordinates foregut and hindgut transcriptional programs., Stevens ML, Chaturvedi P, Rankin SA, Rankin SA, Macdonald M, Jagannathan S, Yukawa M, Barski A, Zorn AM., Development. January 1, 2017; 144 (7): 1283-1295.                            


Crystal structure of the DNA binding domain of the transcription factor T-bet suggests simultaneous recognition of distant genome sites., Liu CF, Brandt GS, Hoang QQ, Naumova N, Lazarevic V, Hwang ES, Dekker J, Glimcher LH, Ringe D, Petsko GA., Proc Natl Acad Sci U S A. January 1, 2016; 113 (43): E6572-E6581.            


RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance., Ramírez-Gordillo D, Powers TR, van Velkinburgh JC, Trujillo-Provencio C, Schilkey F, Serrano EE., BMC Res Notes. November 18, 2015; 8 691.      


A calixpyrrole derivative acts as an antagonist to GPER, a G-protein coupled receptor: mechanisms and models., Lappano R, Rosano C, Pisano A, Santolla MF, De Francesco EM, De Marco P, Dolce V, Ponassi M, Felli L, Cafeo G, Kohnke FH, Abonante S, Maggiolini M., Dis Model Mech. October 1, 2015; 8 (10): 1237-46.              


The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development., Nogueira JM, Hawrot K, Sharpe C, Noble A, Wood WM, Jorge EC, Goldhamer DJ, Kardon G, Dietrich S., Front Aging Neurosci. January 1, 2015; 7 62.                                            


On the origin of vertebrate somites., Onai T, Aramaki T, Inomata H, Hirai T, Kuratani S., Zoological Lett. January 1, 2015; 1 33.              


Predicting Variabilities in Cardiac Gene Expression with a Boolean Network Incorporating Uncertainty., Grieb M, Burkovski A, Sträng JE, Kraus JM, Groß A, Palm G, Kühl M, Kestler HA., PLoS One. January 1, 2015; 10 (7): e0131832.        


Sp8 regulates inner ear development., Chung HA, Medina-Ruiz S, Harland RM., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.                                                    


Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome., Karpinski BA, Maynard TM, Fralish MS, Nuwayhid S, Zohn IE, Moody SA, LaMantia AS., Dis Model Mech. February 1, 2014; 7 (2): 245-57.                


Comparative analysis reveals distinct and overlapping functions of Mef2c and Mef2d during cardiogenesis in Xenopus laevis., Guo Y, Kühl SJ, Pfister AS, Cizelsky W, Denk S, Beer-Molz L, Kühl M., PLoS One. January 1, 2014; 9 (1): e87294.                


Transcriptional regulation of mesoderm genes by MEF2D during early Xenopus development., Kolpakova A, Katz S, Keren A, Rojtblat A, Bengal E., PLoS One. January 1, 2013; 8 (7): e69693.                  


New developments in the second heart field., Zaffran S, Kelly RG., Differentiation. July 1, 2012; 84 (1): 17-24.


Myogenic waves and myogenic programs during Xenopus embryonic myogenesis., Della Gaspera B, Armand AS, Sequeira I, Chesneau A, Mazabraud A, Lécolle S, Charbonnier F, Chanoine C., Dev Dyn. May 1, 2012; 241 (5): 995-1007.                                    


RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm., Janesick A, Shiotsugu J, Taketani M, Blumberg B., Development. March 1, 2012; 139 (6): 1213-24.                        


ARVCF depletion cooperates with Tbx1 deficiency in the development of 22q11.2DS-like phenotypes in Xenopus., Tran HT, Delvaeye M, Verschuere V, Descamps E, Crabbe E, Van Hoorebeke L, McCrea P, Adriaens D, Van Roy F, Vleminckx K, Vleminckx K., Dev Dyn. December 1, 2011; 240 (12): 2680-7.                


Tbx5 overexpression favors a first heart field lineage in murine embryonic stem cells and in Xenopus laevis embryos., Herrmann F, Bundschu K, Kühl SJ, Kühl M., Dev Dyn. December 1, 2011; 240 (12): 2634-45.  


PAPC and the Wnt5a/Ror2 pathway control the invagination of the otic placode in Xenopus., Jung B, Köhler A, Schambony A, Wedlich D., BMC Dev Biol. June 10, 2011; 11 36.                          


Characterization of new otic enhancers of the pou3f4 gene reveal distinct signaling pathway regulation and spatio-temporal patterns., Robert-Moreno À, Naranjo S, de la Calle-Mustienes E, Gómez-Skarmeta JL, Alsina B., PLoS One. December 17, 2010; 5 (12): e15907.              


Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis., Tazumi S, Yabe S, Uchiyama H., Dev Biol. October 15, 2010; 346 (2): 170-80.                                


Polypyrimidine tract-binding protein is required for the repression of gene expression by all-trans retinoic acid., Tamanoue Y, Yamagishi M, Hongo I, Okamoto H., Dev Growth Differ. June 1, 2010; 52 (5): 469-79.                    


Comparative gene expression analysis and fate mapping studies suggest an early segregation of cardiogenic lineages in Xenopus laevis., Gessert S, Kühl M., Dev Biol. October 15, 2009; 334 (2): 395-408.          


The Xenopus Bowline/Ripply family proteins negatively regulate the transcriptional activity of T-box transcription factors., Hitachi K, Danno H, Tazumi S, Aihara Y, Uchiyama H, Okabayashi K, Kondow A, Asashima M., Int J Dev Biol. January 1, 2009; 53 (4): 631-9.                    


The mych gene is required for neural crest survival during zebrafish development., Hong SK, Tsang M, Dawid IB., PLoS One. April 30, 2008; 3 (4): e2029.                


SHP-2 is required for the maintenance of cardiac progenitors., Langdon YG, Goetz SC, Berg AE, Swanik JT, Conlon FL., Development. November 1, 2007; 134 (22): 4119-30.    


Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm., Dastjerdi A, Robson L, Walker R, Hadley J, Zhang Z, Rodriguez-Niedenführ M, Ataliotis P, Baldini A, Scambler P, Francis-West P., Dev Dyn. February 1, 2007; 236 (2): 353-63.


Developmental expression patterns of Tbx1, Tbx2, Tbx5, and Tbx20 in Xenopus tropicalis., Showell C, Christine KS, Mandel EM, Conlon FL., Dev Dyn. June 1, 2006; 235 (6): 1623-30.                      


Xtbx6r, a novel T-box gene expressed in the paraxial mesoderm, has anterior neural-inducing activity., Yabe S, Tazumi S, Yokoyama J, Uchiyama H., Int J Dev Biol. January 1, 2006; 50 (8): 681-9.                        


XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis., Ataliotis P, Ivins S, Mohun TJ, Scambler PJ., Dev Dyn. April 1, 2005; 232 (4): 979-91.                  


The MLC1v gene provides a transgenic marker of myocardium formation within developing chambers of the Xenopus heart., Smith SJ, Ataliotis P, Kotecha S, Towers N, Sparrow DB, Mohun TJ., Dev Dyn. April 1, 2005; 232 (4): 1003-12.            


Structure of the DNA-bound T-box domain of human TBX3, a transcription factor responsible for ulnar-mammary syndrome., Coll M, Seidman JG, Müller CW., Structure. March 1, 2002; 10 (3): 343-56.


Requirement of CDC45 for postimplantation mouse development., Yoshida K, Kuo F, George EL, Sharpe AH, Dutta A., Mol Cell Biol. July 1, 2001; 21 (14): 4598-603.


Differential DNA binding and transcription modulation by three T-box proteins, T, TBX1 and TBX2., Sinha S, Abraham S, Gronostajski RM, Campbell CE., Gene. November 27, 2000; 258 (1-2): 15-29.


Regulation of the early expression of the Xenopus nodal-related 1 gene, Xnr1., Hyde CE, Old RW., Development. March 1, 2000; 127 (6): 1221-9.            


Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19., Yi CH, Terrett JA, Li QY, Ellington K, Packham EA, Armstrong-Buisseret L, McClure P, Slingsby T, Brook JD., Genomics. January 1, 1999; 55 (1): 10-20.


The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome., Sperandeo MP, Borsani G, Incerti B, Zollo M, Rossi E, Zuffardi O, Castaldo P, Taglialatela M, Andria G, Sebastio G., Genomics. April 15, 1998; 49 (2): 230-6.


Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene., Chieffo C, Garvey N, Gong W, Roe B, Zhang G, Silver L, Emanuel BS, Budarf ML., Genomics. August 1, 1997; 43 (3): 267-77.

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