Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Disease and THBD[original query] |
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| Genetic risk for restenosis after coronary balloon angioplasty. Atherosclerosis 2004 May 174 (1): 181-7. Horibe Hideki, Yamada Yoshiji, Ichihara Sahoko, Watarai Masato, Yanase Masanobu, Takemoto Kenji, Shimizu Seiji, Izawa Hideo, Takatsu Fumimaro, Yokota Mitsuhi |
| Combined effects of thrombosis pathway gene variants predict cardiovascular events. PLoS genetics 2007 Jul 3 (7): e120. Auro Kirsi, Alanne Mervi, Kristiansson Kati, Silander Kaisa, Kuulasmaa Kari, Salomaa Veikko, Peltonen Leena, Perola Mark |
| Association of polymorphisms in platelet and hemostasis system genes with acute myocardial infarction. American heart journal 2007 Dec 154 (6): 1052-8. Knowles Joshua W, Wang Huijan, Itakura Haruka, Southwick Audrey, Myers Richard M, Iribarren Carlos, Fortmann Stephen P, Go Alan S, Quertermous Thomas, Hlatky Mark |
| Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clinical journal of the American Society of Nephrology : CJASN 2010 Oct 5 (10): 1844-59. Noris Marina, Caprioli Jessica, Bresin Elena, Mossali Chiara, Pianetti Gaia, Gamba Sara, Daina Erica, Fenili Chiara, Castelletti Federica, Sorosina Annalisa, Piras Rossella, Donadelli Roberta, Maranta Ramona, van der Meer Irene, Conway Edward M, Zipfel Peter F, Goodship Timothy H, Remuzzi Giusep |
| Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Human mutation 2010 Jun 31 (6): E1445-60. Maga Tara K, Nishimura Carla J, Weaver Amy E, Frees Kathy L, Smith Richard J |
| Prevalence of thrombosis-related DNA polymorphisms in a healthy Greek population. In vivo (Athens, Greece) 0 26 (6): 1095-101. Yapijakis Christos, Serefoglou Zoe, Nixon Alexander M, Vylliotis Antonis, Ragos Vassilis, Vairaktaris Eleftheri |
| [Polymorphic markers Ala455Val of the THBD gene and Arg353Gln of the F7 gene and association with unfavorable outcomes of coronary atherosclerosis in patients with a history of acute ischemic heart disease]. Genetika 2011 Oct 47 (10): 1386-92. Pushkov A A, Blagodatskikh K A, Nikitin A G, Agapkina Iu V, Brovkin A N, Chudakova D A, Evdokimova M A, Ase?cheva O Iu, Osmolovskaia V S, Minushkina L O, Baklanova T N, Talyzin P A, Donetskaia O P, Tereshchenko S N, Dzhaiani N A, Akatova E A, Glezer M G, Galiavich A S, Zakirova V B, Koziolova N A, Iagoda A V, Boeva O I, Horolets E V, Shlyk S V, Volkova E G, Margarian M P, Guz' I O, Konstantinov V O, Sidorenko B A, Zate?shchikov D A, Nosikov V |
| Single-Nucleotide Polymorphisms Within the Thrombomodulin Gene (THBD) Predict Mortality in Patients With Graft-Versus-Host Disease. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2014 Oct 32 (30): 3421-7. Rachakonda Sivaramakrishna P, Penack Olaf, Dietrich Sascha, Blau Olga, Blau Igor Wolfgang, Radujkovic Aleksandar, Isermann Berend, Ho Anthony D, Uharek Lutz, Dreger Peter, Kumar Rajiv, Luft Thom |
| A donor thrombomodulin gene variation predicts graft-versus-host disease development and mortality after bone marrow transplantation. International journal of hematology 2015 Aug . Nomoto Haruka, Takami Akiyoshi, Espinoza J Luis, Matsuo Keitaro, Mizuno Shohei, Onizuka Makoto, Kashiwase Koichi, Morishima Yasuo, Fukuda Takahiro, Kodera Yoshihisa, Doki Noriko, Miyamura Koichi, Mori Takehiko, Nakao Shinji, Ohtake Shigeki, Morishita Eri |
| Thrombomodulin gene proximal promoter polymorphisms in premature acute coronary syndrome patients in Bahrain. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2015 Jul . Azme Aliaa Al, Shome Durjoy K, Salem Abdel Halim, Fadhli Suad Al, Bannay Rashed Al, Jaradat Ahm |
| [The preliminary research in paroxysmal nocturnal hemoglobinuria with thrombosis]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2016 Apr 37 (4): 318-23. Du Y L, Long Z B, Xie H Y, Zhuang J L, Han |
| Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome. Molecular immunology 2016 Feb 71 131-142. Iatropoulos Paraskevas, Noris Marina, Mele Caterina, Piras Rossella, Valoti Elisabetta, Bresin Elena, Curreri Manuela, Mondo Elena, Zito Anna, Gamba Sara, Bettoni Serena, Murer Luisa, Fremeaux-Bacchi Veronique, Vivarelli Marina, Emma Francesco, Daina Erica, Remuzzi Giusep |
Novel genetic predictors of venous thromboembolism risk in African Americans.
Blood 2016 Feb . Hernandez Wenndy, Gamazon Eric R, Smithberger Erin, O'Brien Travis J, Harralson Arthur F, Tuck Matthew, Barbour April, Kittles Rick A, Cavallari Larisa H, Perera Minoli |
| Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathies. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2017 7 30 (12): 1739-1747. Gaut Joseph P, Jain Sanjay, Pfeifer John D, Vigh-Conrad Katinka A, Corliss Meagan, Sharma Mukesh K, Heusel Jonathan W, Cottrell Catherine |
| A Prothrombotic Score Based on Genetic Polymorphisms of the Hemostatic System Differs in Patients with Ischemic Stroke, Myocardial Infarction, or Peripheral Arterial Occlusive Disease. Frontiers in cardiovascular medicine 2017 4 39. Herm Juliane, Hoppe Berthold, Siegerink Bob, Nolte Christian H, Koscielny Jürgen, Haeusler Karl Geo |
| THBD sequence variants potentially related to recurrent pregnancy loss. Reproductive biology and endocrinology : RB&E 2017 Dec 15 (1): 92. Quintero-Ronderos Paula, Mercier Eric, Gris Jean-Christophe, Esteban-Perez Clara, Moreno-Ortiz Harold, Fonseca Dora Janeth, Lucena Elkin, Vaiman Daniel, Laissue Pa |
| Single Nucleotide Polymorphisms in CD40L Predict Endothelial Complications and Mortality After Allogeneic Stem-Cell Transplantation. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2018 03 36 (8): 789-800. Rachakonda Sivaramakrishna P, Dai Hao, Penack Olaf, Blau Olga, Blau Igor Wolfgang, Radujkovic Aleksandar, Müller-Tidow Carsten, Kumar Rajiv, Dreger Peter, Luft Thom |
| Clinical, laboratory, and genetic risk factors for thrombosis in sickle cell disease. Blood advances 2020 May 4 (9): 1978-1986. Srisuwananukorn Andrew, Raslan Rasha, Zhang Xu, Shah Binal N, Han Jin, Gowhari Michel, Molokie Robert E, Gordeuk Victor R, Saraf Santosh |
| Thrombomodulin in patients with mild to moderate bleeding tendency. Haemophilia : the official journal of the World Federation of Hemophilia 2021 10 27 (6): 1028-1036. Mehic Dino, Tolios Alexander, Hofer Stefanie, Ay Cihan, Haslacher Helmuth, Downes Kate, Haimel Matthias, Pabinger Ingrid, Gebhart Johan |
| Association of SNP (rs1042579) in thrombomodulin gene and plasma thrombomodulin level in North Indian children with Kawasaki disease. Molecular biology reports 2022 May . Singh Ankita, Rawat Amit, Kaur Anit, Kaur Anupriya, Kumrah Rajni, Johnson Nameirakpam, Chaudhary Himanshi, Pilania Rakesh Kumar, Srivastava Priyanka, Singh Surj |
| Association study of polymorphism in Thrombomodulin gene [rs1042579] with cardiovascular disease. Acta bio-medica : Atenei Parmensis 2022 01 92 (6): e2021282. Khosravi Elham, Sadeghian Ladan, Mohamadynejad Parisa, Dianatkhah Minoo, Hajizadeh Mahsa, Gharipour Mojg |
| The Impact of Cardiovascular Disease Gene Polymorphism and Interaction with Homocysteine on Deep Vein Thrombosis. ACS omega 2024 9 9 (38): 39836-39845. Lei-Lei Niu, Hao-Liang Fan, Jie Cao, Qiu-Xiang Du, Qian-Qian Jin, Ying-Yuan Wang, Jun-Hong S |
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