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Items: 1 to 20 of 84

1.
TBX5 genetic variants and SCD-CAD susceptibility: insights from Chinese Han cohorts
Yukun Rui, Ju Zhou, Xiaoyuan Zhen, Jianhua Zhang, Shiquan Liu, Yuzhen Gao
PeerJ. 2024; 12: e17139. Published online 2024 Mar 19. doi: 10.7717/peerj.17139
PMCID:
PMC10959103
AbstractArticlePDF–3.7M
2.
Prioritizing cardiovascular disease-associated variants altering NKX2-5 and TBX5 binding through an integrative computational approach
Edwin G. Peña-Martínez, Diego A. Pomales-Matos, Alejandro Rivera-Madera, Jean L. Messon-Bird, Joshua G. Medina-Feliciano, Leandro Sanabria-Alberto, Adriana C. Barreiro-Rosario, Jeancarlos Rivera-Del Valle, Jessica M. Rodríguez-Ríos, José A. Rodríguez-Martínez
J Biol Chem. 2023 Dec; 299(12): 105423. Published online 2023 Nov 4. doi: 10.1016/j.jbc.2023.105423
PMCID:
PMC10750078
AbstractArticlePDF–1.8M
3.
CircTBX5 knockdown modulates the miR-558/MyD88 axis to alleviate IL-1β-induced inflammation, apoptosis and extracellular matrix degradation in chondrocytes via inactivating the NF-κB signaling
Wei Wei, Hongjie Mu, Qiaoyi Cui, Peng Yu, Tong Liu, Tao Wang, Lin Sheng
J Orthop Surg Res. 2023; 18: 477. Published online 2023 Jul 1. doi: 10.1186/s13018-023-03949-5
PMCID:
PMC10314403
AbstractArticlePDF–5.0M
4.
Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves
Melanie MY Chan, Omid Sadeghi-Alavijeh, Filipa M Lopes, Alina C Hilger, Horia C Stanescu, Catalin D Voinescu, Glenda M Beaman, William G Newman, Marcin Zaniew, Stefanie Weber, Yee Mang Ho, John O Connolly, Dan Wood, Carlo Maj, Alexander Stuckey, Athanasios Kousathanas, Genomics England Research Consortium, Robert Kleta, Adrian S Woolf, Detlef Bockenhauer, Adam P Levine, Daniel P Gale
eLife. 2022; 11: e74777. Published online 2022 Sep 20. doi: 10.7554/eLife.74777
PMCID:
PMC9512401
AbstractArticlePDF–5.7M
5.
Identification of a novel TBX5 c.755 + 1 G > A variant and related pathogenesis in a family with Holt–Oram syndrome
De‐Gang Wang, Xing‐Sheng Dong, Yi Xiong, Zhi‐Ming Li, Ying‐Jun Xie, Shu‐Hua Liang, Tian‐Hua Huang
Am J Med Genet A. 2022 Jan; 188(1): 58–70. Published online 2021 Sep 6. doi: 10.1002/ajmg.a.62488
PMCID:
PMC9290998
AbstractArticlePDF–2.5M
6.
TBX5 variant with the novel phenotype of mixed-type total anomalous pulmonary venous return in Holt-Oram Syndrome and variable intrafamilial heart defects
Bilal Azab, Dunia Aburizeg, Weizhen Ji, Lauren Jeffries, Nooredeen Jamal Isbeih, Amal Saleh Al-Akily, Hashim Mohammad, Yousef Abu Osba, Mohammad A. Shahin, Zain Dardas, Ma'mon M. Hatmal, Iyad Al-Ammouri, Saquib Lakhani
Mol Med Rep. 2022 Jun; 25(6): 210. Published online 2022 May 4. doi: 10.3892/mmr.2022.12726
PMCID:
PMC9133962
AbstractArticlePDF–2.2M
7.
Transcription Factor Protein Interactomes Reveal Genetic Determinants in Heart Disease
Barbara Gonzalez-Teran, Maureen Pittman, Franco Felix, Reuben Thomas, Desmond Richmond-Buccola, Ruth Hüttenhain, Krishna Choudhary, Elisabetta Moroni, Mauro W. Costa, Yu Huang, Arun Padmanabhan, Michael Alexanian, Clara Youngna Lee, Bonnie E. J. Maven, Kaitlen Samse-Knapp, Sarah U. Morton, Michael McGregor, Casey A. Gifford, J. G. Seidman, Christine E. Seidman, Bruce D. Gelb, Giorgio Colombo, Bruce R. Conklin, Brian L. Black, Benoit G. Bruneau, Nevan J. Krogan, Katherine S. Pollard, Deepak Srivastava
Cell. Author manuscript; available in PMC 2023 Mar 3.
Published in final edited form as: Cell. 2022 Mar 3; 185(5): 794–814.e30. Published online 2022 Feb 18. doi: 10.1016/j.cell.2022.01.021
PMCID:
PMC8923057
AbstractArticlePDF–2.5M
8.
Patient-Specific TBX5-G125R Variant Induces Profound Transcriptional Deregulation and Atrial Dysfunction
Antoinette F. van Ouwerkerk, Fernanda M. Bosada, Karel van Duijvenboden, Arjan C. Houweling, Koen T. Scholman, Vincent Wakker, Cornelis P. Allaart, Jae-Sun Uhm, Inge B. Mathijssen, Ton Baartscheer, Alex V. Postma, Phil Barnett, Arie O. Verkerk, Bastiaan J. Boukens, Vincent M. Christoffels
Circulation. 2022 Feb 22; 145(8): 606–619. Published online 2022 Feb 3. doi: 10.1161/CIRCULATIONAHA.121.054347
PMCID:
PMC8860223
AbstractArticlePDF–2.2M
9.
MicroRNA-603 Promotes Progression of Cutaneous Melanoma by Regulating TBX5
Xianghua Dong, Ying Wang, Yan Qu, Junru Liu, Xien Feng, Xuechao Xu
Comput Math Methods Med. 2021; 2021: 1888501. Published online 2021 Dec 31. doi: 10.1155/2021/1888501
PMCID:
PMC8741382
AbstractArticlePDF–1.8M
10.
TBX5-AS1, an enhancer RNA, is a potential novel prognostic biomarker for lung adenocarcinoma
Lin Cheng, Tong Han, Bolin Chen, Kechao Nie, Weijun Peng
BMC Cancer. 2021; 21: 794. Published online 2021 Jul 9. doi: 10.1186/s12885-021-08517-w
PMCID:
PMC8268367
AbstractArticlePDF–1.6M
11.
TBX5-encoded T-box transcription factor 5 variant T223M is associated with long QT syndrome and pediatric sudden cardiac death
Alexandra M. Markunas, Perathu K. R. Manivannan, Jordan E. Ezekian, Agnim Agarwal, William Eisner, Katherina Alsina, Hugh D. Allen, Gregory A. Wray, Jeffrey J. Kim, Xander H. T. Wehrens, Andrew P. Landstrom
Am J Med Genet A. Author manuscript; available in PMC 2022 Mar 1.
Published in final edited form as: Am J Med Genet A. 2021 Mar; 185(3): 923–929. Published online 2020 Dec 23. doi: 10.1002/ajmg.a.62037
PMCID:
PMC7945047
AbstractArticlePDF–626K
12.
Modeling human TBX5 haploinsufficiency predicts regulatory networks for congenital heart disease
Irfan S. Kathiriya, Kavitha S. Rao, Giovanni Iacono, W. Patrick Devine, Andrew P. Blair, Swetansu K. Hota, Michael H. Lai, Bayardo I. Garay, Reuben Thomas, Henry Z. Gong, Lauren K. Wasson, Piyush Goyal, Tatyana Sukonnik, Kevin M. Hu, Gunes A. Akgun, Laure D. Bernard, Brynn N. Akerberg, Fei Gu, Kai Li, Matthew L. Speir, Maximilian Haeussler, William T. Pu, Joshua M. Stuart, Christine E. Seidman, J. G. Seidman, Holger Heyn, Benoit G. Bruneau
Dev Cell. Author manuscript; available in PMC 2022 Feb 8.
Published in final edited form as: Dev Cell. 2021 Feb 8; 56(3): 292–309.e9. Published online 2020 Dec 14. doi: 10.1016/j.devcel.2020.11.020
PMCID:
PMC7878434
AbstractArticlePDF–4.0M
13.
Overexpression of T-box Transcription Factor 5 (TBX5) Inhibits Proliferation and Invasion in Non-Small Cell Lung Carcinoma Cells
Ruoting Ma, Yu Yang, Qiuyun Tu, Ke Hu
Oncol Res. 2017; 25(9): 1495–1504. Published online 2017 Nov 2. doi: 10.3727/096504017X14883287513729
PMCID:
PMC7841191
AbstractArticlePDF–16M
14.
TBX5基因在肺癌中的研究进展
黄 伟嘉, 李 培玮, 邱 小明
Zhongguo Fei Ai Za Zhi. 2020 Oct 20; 23(10): 883–888. Chinese. doi: 10.3779/j.issn.1009-3419.2020.102.27
PMCID:
PMC7583881
AbstractArticlePDF–1.1M
15.
NKX2.5基因和TBX5基因在先天性心脏病试管婴儿中的突变检测
杨 景晖, 许 小艳, 米 弘瑛, 姜 艳, 麻 新梅, 李 利
Zhongguo Dang Dai Er Ke Za Zhi. 2017 Jun 25; 19(6): 652–657. Chinese. doi: 10.7499/j.issn.1008-8830.2017.06.008
PMCID:
PMC7390306
AbstractArticlePDF–1.4M
16.
中国人群心脏转录因子的单核苷酸多态性与先天性心脏病关系的Meta分析
陈 乐陶, 杨 土保, 王 婷婷, 郑 赞, 赵 丽娟, 叶 子薇, 张 森茂, 秦 家碧
Zhongguo Dang Dai Er Ke Za Zhi. 2018 Jun 25; 20(6): 490–496. Chinese. doi: 10.7499/j.issn.1008-8830.2018.06.012
PMCID:
PMC7389953
AbstractArticlePDF–1.4M
17.
Hypermethylation‐mediated down‐regulation of lncRNA TBX5‐AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducing TBX5 expression
Jing Ma, Shiyu Chen, Lili Hao, Wei Sheng, WeiCheng Chen, Xiaojing Ma, Bowen Zhang, Duan Ma, Guoying Huang
J Cell Mol Med. 2020 Jun; 24(11): 6472–6484. Published online 2020 May 5. doi: 10.1111/jcmm.15298
PMCID:
PMC7294119
AbstractArticlePDF–968K
18.
Tbx5 inhibits hedgehog signaling in determination of digit identity
Huiting Xu, Menglan Xiang, Yushu Qin, Henghui Cheng, Duohua Chen, Qiang Fu, Ke K Zhang, Linglin Xie
Hum Mol Genet. 2020 Jun 3; 29(9): 1405–1416. Published online 2019 Aug 2. doi: 10.1093/hmg/ddz185
PMCID:
PMC7268785
AbstractArticlePDF–1.7M
19.
A reference map of the human binary protein interactome
Katja Luck, Dae-Kyum Kim, Luke Lambourne, Kerstin Spirohn, Bridget E. Begg, Wenting Bian, Ruth Brignall, Tiziana Cafarelli, Francisco J. Campos-Laborie, Benoit Charloteaux, Dongsic Choi, Atina G. Coté, Meaghan Daley, Steven Deimling, Alice Desbuleux, Amélie Dricot, Marinella Gebbia, Madeleine F. Hardy, Nishka Kishore, Jennifer J. Knapp, István A. Kovács, Irma Lemmens, Miles W. Mee, Joseph C. Mellor, Carl Pollis, Carles Pons, Aaron D. Richardson, Sadie Schlabach, Bridget Teeking, Anupama Yadav, Mariana Babor, Dawit Balcha, Omer Basha, Christian Bowman-Colin, Suet-Feung Chin, Soon Gang Choi, Claudia Colabella, Georges Coppin, Cassandra D’Amata, David De Ridder, Steffi De Rouck, Miquel Duran-Frigola, Hanane Ennajdaoui, Florian Goebels, Liana Goehring, Anjali Gopal, Ghazal Haddad, Elodie Hatchi, Mohamed Helmy, Yves Jacob, Yoseph Kassa, Serena Landini, Roujia Li, Natascha van Lieshout, Andrew MacWilliams, Dylan Markey, Joseph N. Paulson, Sudharshan Rangarajan, John Rasla, Ashyad Rayhan, Thomas Rolland, Adriana San-Miguel, Yun Shen, Dayag Sheykhkarimli, Gloria M. Sheynkman, Eyal Simonovsky, Murat Taşan, Alexander Tejeda, Vincent Tropepe, Jean-Claude Twizere, Yang Wang, Robert J. Weatheritt, Jochen Weile, Yu Xia, Xinping Yang, Esti Yeger-Lotem, Quan Zhong, Patrick Aloy, Gary D. Bader, Javier De Las Rivas, Suzanne Gaudet, Tong Hao, Janusz Rak, Jan Tavernier, David E. Hill, Marc Vidal, Frederick P. Roth, Michael A. Calderwood
Nature. Author manuscript; available in PMC 2020 Oct 8.
Published in final edited form as: Nature. 2020 Apr; 580(7803): 402–408. Published online 2020 Apr 8. doi: 10.1038/s41586-020-2188-x
PMCID:
PMC7169983
AbstractArticlePDF–5.4M
20.
Identification and analysis of KLF13 variants in patients with congenital heart disease
Wenjuan Li, Baolei Li, Tingting Li, Ergeng Zhang, Qingjie Wang, Sun Chen, Kun Sun
BMC Med Genet. 2020; 21: 78. Published online 2020 Apr 15. doi: 10.1186/s12881-020-01009-x
PMCID:
PMC7160950
AbstractArticlePDF–992K

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