Human Genome Epidemiology Literature Finder
Records 1 - 24 (of 24 Records) |
Query Trace: TAZ[original query] |
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Improved survival in women with BRCA-associated ovarian carcinoma. Cancer 2003 May 97 (9): 2187-95. Cass Ilana, Baldwin Rae Lynn, Varkey Taz, Moslehi Roxana, Narod Steven A, Karlan Beth |
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 |
Germline polymorphisms in genes involved in the Hippo pathway as recurrence biomarkers in stages II/III colon cancer. The pharmacogenomics journal 2015 Sep . Sebio A, Matsusaka S, Zhang W, Yang D, Ning Y, Stremitzer S, Stintzing S, Sunakawa Y, Yamauchi S, Fujimoto Y, Ueno M, Lenz H |
Genetic variations in the Hippo signaling pathway and breast cancer risk in African American women in the AMBER Consortium. Carcinogenesis 2016 Aug . Zhang Jianmin, Yao Song, Hu Qiang, Zhu Qianqian, Liu Song, Lunetta Kathryn L, Haddad Stephen A, Yang Nuo, Shen He, Hong Chi-Chen, Sucheston-Campbell Lara, Ruiz-Narvaez Edward A, Bensen Jeannette T, Troester Melissa A, Bandera Elisa V, Rosenberg Lynn, Haiman Christopher A, Olshan Andrew F, Palmer Julie R, Ambrosone Christine |
[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 |
A genetic variant in large tumor suppressor kinase 2 of Hippo signaling pathway contributes to prognosis of hepatocellular carcinoma. OncoTargets and therapy 2016 9 1945-51. Shen Lili, Wen Juan, Zhao Tingting, Hu Zhibin, Song Ci, Gu Dongying, He Mingliang, Lee Nikki P, Xu Zhi, Chen Jinf |
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 |
Association between the expression levels of TAZ, AXL and CTGF and clinicopathological parameters in patients with colon cancer. Oncology letters 2016 Feb 11 (2): 1223-1229. Zhang Shu-Dong, McCrudden Cian M, Yuen Hiu-Fung, Leung Ka Lai, Hong Wan-Jin, Kwok Hang F |
A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular Noncompaction. Journal of the American Heart Association 2017 Aug 6 (9): . Wang Ce, Hata Yukiko, Hirono Keiichi, Takasaki Asami, Ozawa Sayaka Watanabe, Nakaoka Hideyuki, Saito Kazuyoshi, Miyao Nariaki, Okabe Mako, Ibuki Keijiro, Nishida Naoki, Origasa Hideki, Yu Xianyi, Bowles Neil E, Ichida Fukiko, |
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 |
Comprehensive analysis of Reverse Phase Protein Array data reveals characteristic unique proteomic signatures for glioblastoma subtypes. Gene 2018 11 685 85-95. Patil Vikas, Mahalingam Kulandaive |
[The genetic diversity of burbot (Lota lota L., 1758) of Western Siberia (the analysis of the mtDNA control region polymorphism)]. Genetika 2018 1 53 (2): 214-22. Khrunyk Yu Ya, Bogdanov V D, Yalkovskaya L E, Koporikov A R, Rakitin S B, Sibiryakov P A, Borodin A |
[Genetic analysis of a family with recurrent hydrops fetalis and dilated cardiomyopathy]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 10 36 (10): 1028-1030. Wu Qinghua, Ma Xiyang, Shi Huirong, Kong Xiangdong, Ren Shumin, Jiao Zhih |
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 |
Targeting the YAP/TAZ Pathway in Uveal and Conjunctival Melanoma With Verteporfin. Investigative ophthalmology & visual science 2021 Apr 62 (4): 3. Brouwer Niels J, Konstantinou Eleni K, Gragoudas Evangelos S, Marinkovic Marina, Luyten Gregorius P M, Kim Ivana K, Jager Martine J, Vavvas Demetrios |
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 |
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 |
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 |
Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel. European journal of haematology 2024 4 . Lital Yeshareem, Joanne Yacobovich, Asaf Lebel, Sharon Noy-Lotan, Orly Dgany, Tanya Krasnov, Galit Berger Pinto, Nino Oniashvili, Jacques Mardoukh, Bella Bielorai, Ruth Laor, Noa Mandel-Shorer, Ayelet Ben Barak, Carina Levin, Mahdi Asleh, Hagit Miskin, Shoshana Revel-Vilk, Dror Levin, Marganit Benish, Tsila Zuckerman, Ofir Wolach, Idit Pazgal, Dafna Brik Simon, Oded Gilad, Asaf David Yanir, Tracie Alison Goldberg, Shai Izraeli, Hannah Tamary, Orna Steinberg-Shem |
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- Page last updated:Apr 16, 2024
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