Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and TAZ[original query] |
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| Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis. Journal of endocrinological investigation 2009 Mar 32 (3): 3. Ferrara AM, De Sanctis L, Rossi G, Capuano S, Del Prete G, Zampella E, Gianino P, Corrias A, Fenzi G, Zannini M, Macchia PE |
| Genetic testing for dilated cardiomyopathy in clinical practice. Journal of cardiac failure 2012 Apr 18 (4): 296-303. Lakdawala Neal K, Funke Birgit H, Baxter Samantha, Cirino Allison L, Roberts Amy E, Judge Daniel P, Johnson Nicole, Mendelsohn Nancy J, Morel Chantal, Care Melanie, Chung Wendy K, Jones Carolyn, Psychogios Apostolos, Duffy Elizabeth, Rehm Heidi L, White Emily, Seidman J G, Seidman Christine E, Ho Carolyn |
| A low prevalence of sarcomeric gene variants in a Chinese cohort with left ventricular non-compaction. Heart and vessels 2015 Mar 30 (2): 258-64. Tian Tao, Wang Jizheng, Wang Hu, Sun Kai, Wang Yilu, Jia Lei, Zou Yubao, Hui Rutai, Zhou Xianliang, Song L |
| [The pathogenic gene screening in a cardiomyopathy pedigree of Yunnan province]. Zhonghua xin xue guan bing za zhi 2016 May 44 (5): 416-20. Xiang H, Zhang J, Hao Y L, Fan J, Li F Y, Wang L L, Ding L Q, Zhang X, Kuang X H, Gao X |
| Prospective and Retrospective Diagnosis of Barth Syndrome Aided by Next-Generation Sequencing. American journal of clinical pathology 2016 Apr . Brión María, de Castro López María José, Santori Montserrat, Pérez Muñuzuri Alejandro, López Abel Bernardo, Baña Souto Ana María, Martínez Soto María Isabel, Couce María L |
| New targets for monitoring and therapy in Barth syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Feb . Thompson W Reid, DeCroes Brittany, McClellan Rebecca, Rubens Jessica, Vaz Frédéric M, Kristaponis Kara, Avramopoulos Dimitrios, Vernon Hilary |
| Autoimmunity/inflammation in a monogenic primary immunodeficiency cohort. Clinical & translational immunology 2017 10 6 (9): e155. Rae William, Ward Daniel, Mattocks Christopher J, Gao Yifang, Pengelly Reuben J, Patel Sanjay V, Ennis Sarah, Faust Saul N, Williams Anthony |
| Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A. Annals of laboratory medicine 2017 10 38 (1): 54-58. Seo Soo Hyun, Kim So Yeon, Cho Sung Im, Park Hyunwoong, Lee Seungjun, Choi Jong Moon, Kim Man Jin, Lee Jee Soo, Ahn Kyung Jin, Song Mi Kyoung, Bae Eun Jung, Park Sung Sup, Seong Moon W |
| Expression of the Hippo transducer TAZ in association with WNT pathway mutations impacts survival outcomes in advanced gastric cancer patients treated with first-line chemotherapy. Journal of translational medicine 2018 2 16 (1): 22. Melucci Elisa, Casini Beatrice, Ronchetti Livia, Pizzuti Laura, Sperati Francesca, Pallocca Matteo, De Nicola Francesca, Goeman Frauke, Gallo Enzo, Amoreo Carla Azzurra, Sergi Domenico, Terrenato Irene, Vici Patrizia, Di Lauro Luigi, Diodoro Maria Grazia, Pescarmona Edoardo, Barba Maddalena, Mazzotta Marco, Mottolese Marcella, Fanciulli Maurizio, Ciliberto Gennaro, De Maria Ruggero, Buglioni Simonetta, Maugeri-Saccà Marcel |
| Cardiomyopathy in children with mitochondrial disease: Prognosis and genetic background. International journal of cardiology 2019 1 279 115-121. Imai-Okazaki Atsuko, Kishita Yoshihito, Kohda Masakazu, Mizuno Yosuke, Fushimi Takuya, Matsunaga Ayako, Yatsuka Yukiko, Hirata Tomoko, Harashima Hiroko, Takeda Atsuhito, Nakaya Akihiro, Sakata Yasushi, Kogaki Shigetoyo, Ohtake Akira, Murayama Kei, Okazaki Yasus |
| X-linked genetic risk factors that promote autoimmunity and dampen remyelination are associated with multiple sclerosis susceptibility. Multiple sclerosis and related disorders 2022 7 66 104065. Borziak Kirill, Finkelstein Jose |
| Genomic Profiling of Metastatic Basal cell Carcinoma Reveals Candidate Drivers of Disease and Therapeutic Targets. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2023 2 36 (4): 100099. Vergara Ismael A, Aivazian Karina, Carlino Matteo S, Guminski Alexander D, Maher Nigel G, Shannon Kerwin F, Ch'ng Sydney, Saw Robyn P M, Long Georgina V, Wilmott James S, Scolyer Richard |
| Low MBOAT7 expression, a genetic risk for MASH, promotes a pro-fibrotic pathway involving hepatocyte TAZ upregulation. Hepatology (Baltimore, Md.) 2024 5 . Mary P Moore, Xiaobo Wang, John Paul Kennelly, Hongxue Shi, Yuki Ishino, Kuniyuki Kano, Junken Aoki, Alessandro Cherubini, Luisa Ronzoni, Xiuqing Guo, Naga P Chalasani, Shareef Khalid, Danish Saleheen, Mathew A Mitsche, Jerome I Rotter, Katherine P Yates, Luca Valenti, Nozomu Kono, Peter Tontonoz, Ira Tab |
- Page last reviewed:Feb 1, 2024
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