Year |
Citation |
Score |
2023 |
Zlatanova I, Sun F, Wu RS, Chen X, Lau BH, Colombier P, Sinha T, Celona B, Xu SM, Materna SC, Huang GN, Black BL. An injury-responsive enhancer is required for heart regeneration. Science Advances. 9: eadh5313. PMID 38019918 DOI: 10.1126/sciadv.adh5313 |
0.339 |
|
2023 |
Krup AL, Winchester SAB, Ranade SS, Agrawal A, Devine WP, Sinha T, Choudhary K, Dominguez MH, Thomas R, Black BL, Srivastava D, Bruneau BG. A Mesp1-dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors. Development (Cambridge, England). PMID 36994838 DOI: 10.1242/dev.201229 |
0.388 |
|
2020 |
Galang G, Mandla R, Ruan H, Jung C, Sinha T, Stone NR, Wu RS, Mannion BJ, Allu PK, Chang K, Rammohan A, Shi MB, Pennacchio LA, Black BL, Vedantham V. ATAC-seq Reveals an Enhancer that Regulates Sinoatrial Node Development and Function. Circulation Research. PMID 33044128 DOI: 10.1161/CIRCRESAHA.120.317145 |
0.346 |
|
2020 |
van Eif VW, Protze S, Bosada FM, Yuan X, Sinha T, van Duijvenboden K, Ernault AC, Mohan RA, Wakker V, de Gier-de Vries C, Hooijkaas IB, Wison MD, Verkerk AO, Bakkers J, Boukens BJ, et al. Human Pacemaker Regulatory Element Analysis Identifies TBX3 Pacemaker Enhancer. Circulation Research. PMID 33040635 DOI: 10.1161/CIRCRESAHA.120.317054 |
0.381 |
|
2018 |
Materna SC, Sinha T, Barnes RM, Lammerts van Bueren K, Black BL. Cardiovascular development and survival require Mef2c function in the myocardial but not the endothelial lineage. Developmental Biology. PMID 30521808 DOI: 10.1016/J.Ydbio.2018.12.002 |
0.463 |
|
2016 |
Li D, Sinha T, Ajima R, Seo HS, Yamaguchi T, Wang J. Spatial regulation of cell cohesion by Wnt5a during second heart field progenitor deployment. Developmental Biology. PMID 26916252 DOI: 10.1016/J.Ydbio.2016.02.017 |
0.587 |
|
2016 |
Barnes RM, Harris IS, Jaehnig EJ, Sauls K, Sinha T, Rojas A, Schachterle W, McCulley DJ, Norris RA, Black BL. MEF2C regulates outflow tract alignment and transcriptional control of Tdgf1. Development (Cambridge, England). PMID 26811383 DOI: 10.1242/Dev.126383 |
0.463 |
|
2015 |
Sinha T, Lin L, Li D, Davis J, Evans S, Wynshaw-Boris A, Wang J. Mapping the dynamic expression of Wnt11 and the lineage contribution of Wnt11-expressing cells during early mouse development. Developmental Biology. 398: 177-92. PMID 25448697 DOI: 10.1016/J.Ydbio.2014.11.005 |
0.635 |
|
2015 |
Sinha T, Li D, Théveniau-Ruissy M, Hutson MR, Kelly RG, Wang J. Loss of Wnt5a disrupts second heart field cell deployment and may contribute to OFT malformations in DiGeorge syndrome. Human Molecular Genetics. 24: 1704-16. PMID 25410658 DOI: 10.1093/Hmg/Ddu584 |
0.594 |
|
2013 |
Agarwal M, Nitta R, Dovat S, Li G, Arita H, Narita Y, Fukushima S, Tateishi K, Matsushita Y, Yoshida A, Miyakita Y, Ohno M, Collins VP, Kawahara N, Shibui S, ... ... Sinha T, et al. CELL BIOLOGY AND SIGNALING Neuro-Oncology. 15: iii12-iii31. DOI: 10.1093/Neuonc/Not174 |
0.412 |
|
2012 |
Sinha T, Wang B, Evans S, Wynshaw-Boris A, Wang J. Disheveled mediated planar cell polarity signaling is required in the second heart field lineage for outflow tract morphogenesis. Developmental Biology. 370: 135-44. PMID 22841628 DOI: 10.1016/J.Ydbio.2012.07.023 |
0.652 |
|
2012 |
Wang J, Sinha T, Wynshaw-Boris A. Wnt signaling in mammalian development: lessons from mouse genetics. Cold Spring Harbor Perspectives in Biology. 4. PMID 22550229 DOI: 10.1101/Cshperspect.A007963 |
0.611 |
|
2011 |
Wang B, Sinha T, Jiao K, Serra R, Wang J. Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B. Human Molecular Genetics. 20: 271-85. PMID 20962035 DOI: 10.1093/Hmg/Ddq462 |
0.592 |
|
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