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1
Physical interaction between TBX5 and MEF2C is required for early heart development.
Mol Cell Biol. 2009 Apr;29(8):2205-18. doi: 10.1128/MCB.01923-08. Epub 2009 Feb 9.
2
Mutation in myosin heavy chain 6 causes atrial septal defect.
Nat Genet. 2005 Apr;37(4):423-8. doi: 10.1038/ng1526. Epub 2005 Feb 27.
3
Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndrome.
Hum Mol Genet. 2001 Sep 1;10(18):1983-94. doi: 10.1093/hmg/10.18.1983.
4
Synergistic activation of cardiac genes by myocardin and Tbx5.
PLoS One. 2011;6(8):e24242. doi: 10.1371/journal.pone.0024242. Epub 2011 Aug 29.
5
Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.
Circ Arrhythm Electrophysiol. 2015 Apr;8(2):400-8. doi: 10.1161/CIRCEP.114.002534. Epub 2015 Feb 25.
8
Functional analysis of TBX5 missense mutations associated with Holt-Oram syndrome.
J Biol Chem. 2003 Mar 7;278(10):8780-5. doi: 10.1074/jbc.M208120200. Epub 2002 Dec 23.
10
Ventricular expression of tbx5 inhibits normal heart chamber development.
Dev Biol. 2000 Jul 1;223(1):169-80. doi: 10.1006/dbio.2000.9748.

引用本文的文献

1
Transcriptomic profiling of skeletal muscle in the DMD rat model of Duchenne muscular dystrophy.
Sci Rep. 2025 Aug 11;15(1):29312. doi: 10.1038/s41598-025-14756-9.
4
Stage-specific DNA methylation dynamics in mammalian heart development.
Epigenomics. 2025 Apr;17(5):359-371. doi: 10.1080/17501911.2025.2467024. Epub 2025 Feb 21.
5
Decoding the epigenetic and transcriptional basis of direct cardiac reprogramming.
Stem Cells. 2025 Mar 10;43(3). doi: 10.1093/stmcls/sxaf002.
6
The molecular mechanisms of cardiac development and related diseases.
Signal Transduct Target Ther. 2024 Dec 23;9(1):368. doi: 10.1038/s41392-024-02069-8.
7
Context-dependent T-BOX transcription factor family: from biology to targeted therapy.
Cell Commun Signal. 2024 Jul 4;22(1):350. doi: 10.1186/s12964-024-01719-2.
8
Cardiac Transcription Factors and Regulatory Networks.
Adv Exp Med Biol. 2024;1441:295-311. doi: 10.1007/978-3-031-44087-8_16.
9
Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heart.
J Anat. 2024 Jul;245(1):70-83. doi: 10.1111/joa.14033. Epub 2024 Feb 28.

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3
Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart.
Nat Genet. 2006 Feb;38(2):175-83. doi: 10.1038/ng1707. Epub 2005 Dec 25.
4
A WW domain protein TAZ is a critical coactivator for TBX5, a transcription factor implicated in Holt-Oram syndrome.
Proc Natl Acad Sci U S A. 2005 Dec 13;102(50):18034-9. doi: 10.1073/pnas.0509109102. Epub 2005 Dec 6.
5
Mutation in myosin heavy chain 6 causes atrial septal defect.
Nat Genet. 2005 Apr;37(4):423-8. doi: 10.1038/ng1526. Epub 2005 Feb 27.
6
Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis.
Development. 2005 Feb;132(3):553-63. doi: 10.1242/dev.01596. Epub 2005 Jan 5.
9
Mutations in the human TBX4 gene cause small patella syndrome.
Am J Hum Genet. 2004 Jun;74(6):1239-48. doi: 10.1086/421331. Epub 2004 Apr 21.
10
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
Nature. 2003 Jul 24;424(6947):443-7. doi: 10.1038/nature01827. Epub 2003 Jul 6.

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