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ArticlesPeer ReviewedFull Text
Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population
Author / Creator:Zhang, Rongfeng ; Tian, Xiaochen ; Gao, Lianjun ; Li, Huihua ; Yin, Xiaomeng ; Dong, Yingxue ; Yang, Yanzong ; Xia, Yunlong
Publisher:United States: Public Library of Science
Journal title:PloS one, 2016-08, Vol.11 (8), p.e0160467-e0160467
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DNA Methylation Levels of the TBX5 Gene Promoter Are Associated with Congenital Septal Defects in Mexican Paediatric Patients
Author / Creator:García-Flores, Esbeidy ; Rodríguez-Pérez, José Manuel ; Borgonio-Cuadra, Verónica Marusa ; Vargas-Alarcón, Gilberto ; Calderón-Colmenero, Juan ; Sandoval, Juan Pablo ; García-Montes, José Antonio ; Espinoza-Gutiérrez, Víctor Manuel ; Reyes-García, Juan Gerardo ; Cazarín-Santos, Benny Giovanni ; Miranda-Duarte, Antonio ; Gamboa-Domínguez, Armando ; Pérez-Hernández, Nonanzit
Publisher:Switzerland: MDPI AG
Journal title:Biology (Basel, Switzerland), 2022-01, Vol.11 (1), p.96
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Identification and functional analysis of genetic variants in TBX5 gene promoter in patients with acute myocardial infarction
Author / Creator:Wang, Shuai ; Zhang, Jie ; He, Xiaohui ; Zhang, Yexin ; Chen, Jing ; Su, Qiang ; Pang, Shuchao ; Zhang, Shufang ; Cui, Yinghua ; Yan, Bo
Publisher:England: BioMed Central Ltd
Journal title:BMC cardiovascular disorders, 2019-11, Vol.19 (1), p.265-265, Article 265
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Tbx4 and Tbx5 gene expression associated with appendage development and its relationship with the absence of the pelvic fin in Pampus argenteus
Author / Creator:Zhang, Shun ; Zhu, Xiaojing ; Hu, Lingzhu ; Liao, Kai ; Xu, Shanliang ; Wang, Danli ; Guo, Chunyang
Publisher:Heidelberg: Science Press
Journal title:Journal of oceanology and limnology, 2024-03, Vol.42 (2), p.580-593
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Reconstruction and in vivo analysis of the extinct tbx5 gene from ancient wingless moa (Aves: Dinornithiformes)
Author / Creator:Huynen, Leon ; Suzuki, Takayuki ; Ogura, Toshihiko ; Watanabe, Yusuke ; Millar, Craig D ; Hofreiter, Michael ; Smith, Craig ; Mirmoeini, Sara ; Lambert, David M
Publisher:England: BioMed Central Ltd
Journal title:BMC evolutionary biology, 2014-05, Vol.14 (1), p.75-75, Article 75
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The human TBX5 gene mutation database
Author / Creator:Heinritz, Wolfram ; Shou, Lin ; Moschik, Andre ; Froster, Ursula G.
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2005-10, Vol.26 (4), p.397-397
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A novel missense mutation in the TBX5 gene in a Saudi infant with Holt-Oram syndrome
Author / Creator:Qattan, Mohammad M. Al ; Shaar, Hussam Abou Al
Publisher:Saudi Arabia: Saudi Medical Journal
Journal title:Saudi medical journal, 2015-08, Vol.36 (8), p.980-982
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Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects
Author / Creator:Khatami, Mehri ; Heidari, Mohammad Mehdi ; Kazeminasab, Fatemeh ; Zare Bidaki, Razieh
Publisher:Iran: Tabriz University of Medical Sciences
Journal title:Journal of cardiovascular and thoracic research, 2018-01, Vol.10 (1), p.41-45
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SNP RS3825214 IN THE TBX5 GENE IS ASSOCIATED WITH LONE ATRIAL FIBRILLATION IN CHINESE HAN POPULATION
Author / Creator:Xiaobiao, Zang ; Wang, Qing K
Publisher:London: BMJ Publishing Group Ltd and British Cardiovascular Society
Journal title:Heart (British Cardiac Society), 2012-10, Vol.98 (Suppl 2), p.E33-E33
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Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndrome
Author / Creator:Heinritz, W ; Moschik, A ; Kujat, A ; Spranger, S ; Heilbronner, H ; Demuth, S ; Bier, A ; Tihanyi, M ; Mundlos, S ; Gruenauer-Kloevekorn, C ; Froster, U G
Publisher:London: BMJ Publishing Group Ltd and British Cardiovascular Society
Journal title:Heart (British Cardiac Society), 2005-03, Vol.91 (3), p.383-384
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A Boy with Holt-Oram Syndrome Caused by Novel Mutation c.1304delT in the TBX5 Gene
Author / Creator:Muru, K. ; Kalev, I. ; Teek, R. ; Sõnajalg, M. ; Kuuse, K. ; Reimand, T. ; Õunap, K.
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Molecular syndromology, 2011-09, Vol.1 (6), p.307-310
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When the heart and hands tell a story: an intriguing case of Holt–Oram syndrome
Author / Creator:Atlas, Ilyas ; Zagdan, Soukaina ; Megzari, Mohamed ; Arous, Salim ; Drighil, Abdenasser
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:The Egyptian heart journal, 2024-09, Vol.76 (1), p.117-6, Article 117
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Screening and identification of miRNAs regulating Tbx4/5 genes of Pampus argenteus
Author / Creator:Zhang, Cheng ; Zhang, Shun ; Liu, Mengdi ; Wang, Yajun ; Wang, Danli ; Xu, Shanliang
Publisher:United States: PeerJ, Inc
Journal title:PeerJ (San Francisco, CA), 2022-10, Vol.10, p.e14300-e14300, Article e14300
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Gene-Specific Assessment of Guanine Oxidation as an Epigenetic Modulator for Cardiac Specification of Mouse Embryonic Stem Cells
Author / Creator:Park, Joonghoon ; Park, Jong Woo ; Oh, Hawmok ; Maria, Fernanda S ; Kang, Jaeku ; Tian, Xiuchun
Publisher:United States: Public Library of Science
Journal title:PloS one, 2016-06, Vol.11 (6), p.e0155792-e0155792
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University of Development Alternative Researchers Target Biochemistry and Biophysics [Identification of deleterious single nucleotide polymorphism (SNP)s in the human TBX5 gene prediction of their str...
Publisher:NewsRX LLC
Journal title:Obesity, fitness, & wellness week, 2021-12, p.4622
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A Case Report on Holt Oram Syndrome
Author / Creator:Khan, Ali Nawaz ; Malik, Erum Shahzadi ; Anwar, Syed Onaiz ; Mahmood, Amjad ; Khan, Jamal Azfar
Publisher:Rawalpindi: Knowledge Bylanes
Journal title:Pakistan Armed Forces medical journal, 2022-10, Vol.72 (SUPPL-3), p.S645-47
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Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation
Author / Creator:Hiroi, Yukio ; Kudoh, Sumiyo ; Monzen, Koshiro ; Ikeda, Yuichi ; Yazaki, Yoshio ; Nagai, Ryozo ; Komuro, Issei
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2001-07, Vol.28 (3), p.276-280
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MicroRNA 19a replacement partially rescues fin and cardiac defects in zebrafish model of Holt Oram syndrome
Author / Creator:Chiavacci, Elena ; D’Aurizio, Romina ; Guzzolino, Elena ; Russo, Francesco ; Baumgart, Mario ; Groth, Marco ; Mariani, Laura ; D’Onofrio, Mara ; Arisi, Ivan ; Pellegrini, Marco ; Cellerino, Alessandro ; Cremisi, Federico ; Pitto, Letizia
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2015-12, Vol.5 (1), p.18240-18240, Article 18240
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Identification of deleterious single nucleotide polymorphism (SNP)s on the human TBX5 gene & prediction of their structural & functional consequences: An in silico approach
Author / Creator:A M U B Mahfuz ; Khan, Md Arif
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2021-07
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Identification of deleterious single nucleotide polymorphism (SNP)s on the human TBX5 gene prediction of their structural functional consequences: An in silico approach (Updated July 29, 2021)
Publisher:NewsRX LLC
Journal title:Obesity, fitness, & wellness week, 2021-08, p.1653
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Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population

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DNA Methylation Levels of the TBX5 Gene Promoter Are Associated with Congenital Septal Defects in Mexican Paediatric Patients

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Identification and functional analysis of genetic variants in TBX5 gene promoter in patients with acute myocardial infarction

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Tbx4 and Tbx5 gene expression associated with appendage development and its relationship with the absence of the pelvic fin in Pampus argenteus

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Reconstruction and in vivo analysis of the extinct tbx5 gene from ancient wingless moa (Aves: Dinornithiformes)

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The human TBX5 gene mutation database

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A novel missense mutation in the TBX5 gene in a Saudi infant with Holt-Oram syndrome

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Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects

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SNP RS3825214 IN THE TBX5 GENE IS ASSOCIATED WITH LONE ATRIAL FIBRILLATION IN CHINESE HAN POPULATION

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Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndrome

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A Boy with Holt-Oram Syndrome Caused by Novel Mutation c.1304delT in the TBX5 Gene

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When the heart and hands tell a story: an intriguing case of Holt–Oram syndrome

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Screening and identification of miRNAs regulating Tbx4/5 genes of Pampus argenteus

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Gene-Specific Assessment of Guanine Oxidation as an Epigenetic Modulator for Cardiac Specification of Mouse Embryonic Stem Cells

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University of Development Alternative Researchers Target Biochemistry and Biophysics [Identification of deleterious single nucleotide polymorphism (SNP)s in the human TBX5 gene prediction of their str...

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A Case Report on Holt Oram Syndrome

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Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation

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MicroRNA 19a replacement partially rescues fin and cardiac defects in zebrafish model of Holt Oram syndrome

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Identification of deleterious single nucleotide polymorphism (SNP)s on the human TBX5 gene & prediction of their structural & functional consequences: An in silico approach

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Identification of deleterious single nucleotide polymorphism (SNP)s on the human TBX5 gene prediction of their structural functional consequences: An in silico approach (Updated July 29, 2021)

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