Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: TUBB1[original query] |
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The TUBB1 Q43P functional polymorphism reduces the risk of cardiovascular disease in men by modulating platelet function and structure. Blood 2005 Oct 106 (7): 2356-62. Freson Kathleen, De Vos Rita, Wittevrongel Christine, Thys Chantal, Defoor Johan, Vanhees Luc, Vermylen Jos, Peerlinck Kathelijne, Van Geet Chr |
The association of the beta1-tubulin Q43P polymorphism with intracerebral hemorrhage in men. Haematologica 2007 Apr 92 (4): 513-8. Navarro-Núñez Leyre, Lozano María L, Rivera José, Corral Javier, Roldán Vanessa, González-Conejero Rocío, Iniesta Juan A, Montaner Joan, Vicente Vicente, Martínez Constanti |
Genotype-phenotype relationship for six common polymorphisms in genes affecting platelet function from 286 healthy subjects and 160 patients with mucocutaneous bleeding of unknown cause. British journal of haematology 2009 Jun 146 (1): 95-103. Martínez Constantino, Antón Ana Isabel, Corral Javier, Quiroga Teresa, Panes Olga, Lozano María Luisa, González-Conejero Rocío, Teruel Raúl, Navarro-Núñez Leyre, Pereira Jaime, Mezzano Diego, Vicente Vicente, Rivera Jo |
TUBB1 Q43P polymorphism does not protect against acute coronary syndrome and premature myocardial infarction. Thrombosis and haemostasis 2008 Dec 100 (6): 1211-3. Navarro-Núñez Leyre, Roldán Vanessa, Lozano María Luisa, Rivera José, Marin Francisco, Vicente Vicente, Martínez Constanti |
Polymorphisms of the vincristine pathway and response to treatment in children with childhood acute lymphoblastic leukemia. Pharmacogenomics 2014 Jun 15 (8): 1105-16. Ceppi Francesco, Langlois-Pelletier Chloé, Gagné Vincent, Rousseau Julie, Ciolino Claire, De Lorenzo Samanta, Kevin Kojok M, Cijov Diana, Sallan Stephen E, Silverman Lewis B, Neuberg Donna, Kutok Jeffery L, Sinnett Daniel, Laverdière Caroline, Krajinovic Ma |
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
Nature genetics 2014 Jun 46 (6): 629-34. Auer Paul L, Teumer Alexander, Schick Ursula, O'Shaughnessy Andrew, Lo Ken Sin, Chami Nathalie, Carlson Chris, de Denus Simon, Dubé Marie-Pierre, Haessler Jeff, Jackson Rebecca D, Kooperberg Charles, Perreault Louis-Philippe Lemieux, Nauck Matthias, Peters Ulrike, Rioux John D, Schmidt Frank, Turcot Valérie, Völker Uwe, Völzke Henry, Greinacher Andreas, Hsu Li, Tardif Jean-Claude, Diaz George A, Reiner Alexander P, Lettre Guillau |
SNPs associated with activity and toxicity of cabazitaxel in patients with advanced urothelial cell carcinoma. Pharmacogenomics 2016 Mar . Duran Ignacio, Hagen Carlos, Arranz José Ángel, Apellaniz-Ruiz María, Pérez-Valderrama Begoña, Sala Nuria, Lainez Nuria, García-Del Muro Xavier, Noguerón Esther, Climent Miguel Ángel, Maroto Pablo, Font Albert, García-Donas Jesús, Gallardo Enrique, López-Criado Pilar, González Del Alba Aránzazu, Sáez María Isabel, Vázquez Sergio, Luque Raquel, Rodríguez-Antona Cristi |
Variants in vincristine pharmacodynamic genes involved in neurotoxicity at induction phase in the therapy of pediatric acute lymphoblastic leukemia. The pharmacogenomics journal 2019 Feb . Martin-Guerrero Idoia, Gutierrez-Camino Angela, Echebarria-Barona Aizpea, Astigarraga Itziar, Garcia de Andoin Nagore, Navajas Aurora, Garcia-Orad Afri |
[TUBB1 mutation in children with congenital hypothyroidism and thyroid dysgenesis in Shandong, China]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2019 10 21 (10): 972-976. Sun Chun-Hui, Liu Wen-Miao, Li Miao-Miao, Zou Hui, Liu Shi-Guo, Wang Fa |
Analysis of polymorphisms in the colchicine binding site of tubulin in colchicine-resistant familial Mediterranean fever patients. Molecular biology reports 2020 Nov . Akbaba Tayfun Hilmi, Ustabas Gizem, Kasap-Cuceloglu Muserref, Ozen Seza, Balci-Peynircioglu Ba |
The influence of single-nucleotide polymorphisms on overall survival and toxicity in cabazitaxel-treated patients with metastatic castration-resistant prostate cancer. Cancer chemotherapy and pharmacology 2020 Jan . Belderbos Bodine P S, de With Mirjam, Singh Rajbir K, Agema Bram C, El Bouazzaoui Samira, Oomen-de Hoop Esther, de Wit Ronald, van Schaik Ron H N, Mathijssen Ron H J, Bins Sand |
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
Human molecular genetics 2021 9 31 (3): 347-361. Little Amarise, Hu Yao, Sun Quan, Jain Deepti, Broome Jai, Chen Ming-Huei, Thibord Florian, McHugh Caitlin, Surendran Praveen, Blackwell Thomas W, Brody Jennifer A, Bhan Arunoday, Chami Nathalie, de Vries Paul S, Ekunwe Lynette, Heard-Costa Nancy, Hobbs Brian D, Manichaikul Ani, Moon Jee-Young, Preuss Michael H, Ryan Kathleen, Wang Zhe, Wheeler Marsha, Yanek Lisa R, Abecasis Goncalo R, Almasy Laura, Beaty Terri H, Becker Lewis C, Blangero John, Boerwinkle Eric, Butterworth Adam S, Choquet Hélène, Correa Adolfo, Curran Joanne E, Faraday Nauder, Fornage Myriam, Glahn David C, Hou Lifang, Jorgenson Eric, Kooperberg Charles, Lewis Joshua P, Lloyd-Jones Donald M, Loos Ruth J F, Min Yuan-I, Mitchell Braxton D, Morrison Alanna C, Nickerson Deborah A, North Kari E, O'Connell Jeffrey R, Pankratz Nathan, Psaty Bruce M, Vasan Ramachandran S, Rich Stephen S, Rotter Jerome I, Smith Albert V, Smith Nicholas L, Tang Hua, Tracy Russell P, Conomos Matthew P, Laurie Cecelia A, Mathias Rasika A, Li Yun, Auer Paul L, , Thornton Timothy, Reiner Alexander P, Johnson Andrew D, Raffield Laura |
Mutation screening of eight genes and comparison of the clinical data in a Chinese cohort with congenital hypothyroidism. Endocrine 2022 9 79 (1): 125-134. Li Liangshan, Li Xiaole, Wang Xiaoyu, Han Mengmeng, Zhao Dehua, Wang Fang, Liu Shig |
Transcriptome and genome sequencing investigating the molecular characteristics of patients with varicocele infertility. Andrologia 2022 Aug e14542. Zhang Chenming, Li Xun, Chen Jianshe, Zhao Lina, Wei Xiao, Dong Yazhou, Sicheng Ma, Sun Zix |
The effects of pathogenic variants for inherited hemostasis disorders in 140,214 UK Biobank participants. Blood 2023 8 . Luca Stefanucci, Janine H Collins, Matthew Christopher Sims, Iñigo Barrio-Hernandez, Luanluan Sun, Oliver Burren, Livia Perfetto, Isobel Bender, Tiffany J Callahan, Kathryn Fleming, Jose Antonio Guerrero, Henning Hermjakob, Maria J Martin, James David Stephenson, Kalpana Paneerselvam, Slavé Petrovski, Pablo Porras, Peter N Robinson, Quanli Wang, Xavier Watkins, Mattia Frontini, Roman A Laskowski, Pedro Beltrao, Emanuele Di Angelantonio, Keith Gomez, Michael Laffan, Willem H Ouwehand, Andrew D Mumford, Kathleen Freson, Keren Jacqueline Carss, Kate Downes, Nicholas S Gleadall, Karyn Megy, Elspeth Bruford, Dragana Vuckov |
Evaluating the prevalence of inborn errors of immunity in adults with chronic immune thrombocytopenia or Evans syndrome. Blood advances 2023 10 . Debbie Jiang, Kira Maria Rosenlind, Sarah K Baxter, Terry Gernsheimer, Suleyman Gulsuner, Eric Allenspach, Sioban B Ke |
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- Page last updated:Apr 22, 2024
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