Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: TCAP[original query] |
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Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy. Journal of the American College of Cardiology 2004 Dec 44 (11): 2192-201. Hayashi Takeharu, Arimura Takuro, Itoh-Satoh Manatsu, Ueda Kazuo, Hohda Shigeru, Inagaki Natsuko, Takahashi Megumi, Hori Hisae, Yasunami Michio, Nishi Hirofumi, Koga Yoshinori, Nakamura Hiroshi, Matsuzaki Masunori, Choi Bo Yoon, Bae Sung Won, You Cheol Woon, Han Kyung Hoon, Park Jeong Euy, Knöll Ralph, Hoshijima Masahiko, Chien Kenneth R, Kimura Akino |
HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer. British journal of cancer 2006 Dec 95 (12): 1689-95. Benusiglio P R, Pharoah P D, Smith P L, Lesueur F, Conroy D, Luben R N, Dew G, Jordan C, Dunning A, Easton D F, Ponder B A |
Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives. Human mutation 2009 Mar 30 (3): 363-70. Andersen Paal Skytt, Havndrup Ole, Hougs Lotte, Sørensen Karina M, Jensen Morten, Larsen Lars Allan, Hedley Paula, Thomsen Alex Rojas Bie, Moolman-Smook Johanna, Christiansen Michael, Bundgaard Henni |
Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy. Clinical and translational science 2008 May 1 (1): 21-6. Hershberger Ray E, Parks Sharie B, Kushner Jessica D, Li Duanxiang, Ludwigsen Susan, Jakobs Petra, Nauman Deirdre, Burgess Donna, Partain Julie, Litt Micha |
Common susceptibility variants examined for association with dilated cardiomyopathy. Annals of human genetics 2010 Mar 74 (2): 110-6. Rampersaud Evadnie, Kinnamon Daniel D, Hamilton Kara, Khuri Sawsan, Hershberger Ray E, Martin Eden |
Rare variant mutations identified in pediatric patients with dilated cardiomyopathy. Progress in pediatric cardiology 2011 Jan 31 (1): 39-47. Rampersaud Evadnie, Siegfried Jill D, Norton Nadine, Li Duanxiang, Martin Eden, Hershberger Ray |
Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects. PloS one 2011 6 (12): 12. Posch MG, Waldmuller S, Müller M, Scheffold T, Fournier D, Andrade-Navarro MA, De Geeter B, Guillaumont S, Dauphin C, Yousseff D, Schmitt KR, Perrot A, Berger F, Hetzer R, Bouvagnet P, Ozcelik C |
Association analysis of ERBB2 amplicon genetic polymorphisms and STARD3 expression with risk of gastric cancer in the Chinese population. Gene 2014 Feb 535 (2): 225-32. Qiu Yue, Zhang Zuo-Yang, Du Wei-Dong, Ye Lei, Xu Song, Zuo Xian-Bo, Zhou Fu-Sheng, Chen Gang, Ma Xue-Ling, Schneider Marion E, Xia Hong-Zhen, Zhou Yuan, Wu Ji-Feng, Yuan-Hong Xu, Zhang Xue-J |
Detection of Variants in Patients with Idiopathic Ventricular Fibrillation by Whole-exome Sequencing. Annals of clinical and laboratory science 2018 8 48 (4): 427-434. Chang Ya-Sian, Lee Chien-Chin, Huang Hsi-Yuan, Lin Kuo-Hung, Chen Jan-Yow, Chang Kuan-Cheng, Chang Jan-Gow |
Breast Cancer Clinical Trial of Chemotherapy and Trastuzumab: Potential Tool to Identify Cardiac Modifying Variants of Dilated Cardiomyopathy. Journal of cardiovascular development and disease 2018 1 4 (2): . Serie Daniel J, Crook Julia E, Necela Brian M, Axenfeld Bianca C, Dockter Travis J, Colon-Otero Gerardo, Perez Edith A, Thompson E Aubrey, Norton Nadi |
Clinical, pathological, imaging, and genetic characterization in a Taiwanese cohort with limb-girdle muscular dystrophy. Orphanet journal of rare diseases 2020 6 15 (1): 160. Liang Wen-Chen, Jong Yuh-Jyh, Wang Chien-Hua, Wang Chen-Hua, Tian Xia, Chen Wan-Zi, Kan Tzu-Min, Minami Narihiro, Nishino Ichizo, Wong Lee-Jun |
Identification of a novel titin-cap/telethonin mutation in a Portuguese family with hypertrophic cardiomyopathy. Revista portuguesa de cardiologia 2020 6 39 (6): 317-327. Toste Alexandra, Perrot Andreas, Özcelik Cemil, Cardim Nu |
Genetic Determinants and Genotype-Phenotype Correlations in Vietnamese Patients With Dilated Cardiomyopathy. Circulation journal : official journal of the Japanese Circulation Society 2021 5 85 (9): 1469-1478. Nguyen Thuy Vy, Tran Vu Minh Thu, Do Thi Nam Phuong, Tran Thi Huynh Nga, Do Thi Hao, Nguyen Thi My Hanh, Tran Huynh Bao Nam, Le Lan Anh, Nguyen Pham Ngoc Thieu, Nguyen Thi Dieu Ai, Nguyen Thi My Nuong, Le Ngoc Hong Phuong, Pham Nguyen Vinh, Ho Huynh Thuy Duo |
Genetic variants in Chinese patients with sporadic dilated cardiomyopathy: a cross-sectional study. Annals of translational medicine 2022 3 10 (3): 129. Shen Cheng, Xu Lei, Sun Xiaoning, Sun Aijun, Ge Jun |
TCAP gene is not a common cause of cardiomyopathy in Iranian patients. European journal of medical research 2023 9 28 (1): 376. Zahra Alaei, Nasrin Zamani, Bahareh Rabbani, Nejat Mahdi |
The clinical features and TCAP mutation Spectrum in a Chinese cohort of patients with limb-girdle muscular dystrophy R7. Human molecular genetics 2023 5 . Xiaoqing Lv, Feng Lin, Wenjing Wu, Hui Wang, Yuebei Luo, Zhiqiang Wang, Chuanzhu Yan, He Lv, Sushan Luo, Pengfei L |
Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients. Orphanet journal of rare diseases 2023 11 18 (1): 356. Feng Lin, Kang Yang, Xin Lin, Ming Jin, Long Chen, Fu-Ze Zheng, Liang-Liang Qiu, Zhi-Xian Ye, Hai-Zhu Chen, Min-Ting Lin, Ning Wang, Zhi-Qiang Wa |
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- Page last updated:Apr 22, 2024
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