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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2001 | 1 |
2002 | 1 |
2003 | 2 |
2005 | 1 |
2016 | 1 |
2024 | 0 |
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Page 1
Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation.
Nat Genet. 2001 Jul;28(3):276-80. doi: 10.1038/90123.
Nat Genet. 2001.
PMID: 11431700
Functional analysis of TBX5 missense mutations associated with Holt-Oram syndrome.
Fan C, Liu M, Wang Q.
Fan C, et al.
J Biol Chem. 2003 Mar 7;278(10):8780-5. doi: 10.1074/jbc.M208120200. Epub 2002 Dec 23.
J Biol Chem. 2003.
PMID: 12499378
Free PMC article.
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GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
Garg V, Kathiriya IS, Barnes R, Schluterman MK, King IN, Butler CA, Rothrock CR, Eapen RS, Hirayama-Yamada K, Joo K, Matsuoka R, Cohen JC, Srivastava D.
Garg V, et al.
Nature. 2003 Jul 24;424(6947):443-7. doi: 10.1038/nature01827. Epub 2003 Jul 6.
Nature. 2003.
PMID: 12845333
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A WW domain protein TAZ is a critical coactivator for TBX5, a transcription factor implicated in Holt-Oram syndrome.
Murakami M, Nakagawa M, Olson EN, Nakagawa O.
Murakami M, et al.
Proc Natl Acad Sci U S A. 2005 Dec 13;102(50):18034-9. doi: 10.1073/pnas.0509109102. Epub 2005 Dec 6.
Proc Natl Acad Sci U S A. 2005.
PMID: 16332960
Free PMC article.
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TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.
Guo DF, Li RG, Yuan F, Shi HY, Hou XM, Qu XK, Xu YJ, Zhang M, Liu X, Jiang JQ, Yang YQ, Qiu XB.
Guo DF, et al.
Mol Med Rep. 2016 May;13(5):4349-56. doi: 10.3892/mmr.2016.5043. Epub 2016 Mar 24.
Mol Med Rep. 2016.
PMID: 27035640
Clinical Trial.
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