Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: Hypertension and ACVRL1[original query] |
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Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease. Blood 2008 Jun 111 (12): 5721-6. Ashley-Koch Allison E, Elliott Laine, Kail Melanie E, De Castro Laura M, Jonassaint Jude, Jackson Terry L, Price Jennifer, Ataga Kenneth I, Levesque Marc C, Weinberg J Brice, Orringer Eugene P, Collins Ann, Vance Jeffery M, Telen Marilyn |
Clinical outcomes of pulmonary arterial hypertension in patients carrying an ACVRL1 (ALK1) mutation. American journal of respiratory and critical care medicine 2010 Jan . Girerd Barbara, Montani David, Coulet Florence, Sztrymf Benjamin, Yaici Azzeddine, Jaïs Xavier, Tregouet David, Reis Abilio, Drouin-Garraud Valérie, Fraisse Alain, Sitbon Olivier, O'Callaghan Dermot S, Simonneau Gérald, Soubrier Florent, Humbert Ma |
Hemodynamic and genetic analysis in children with idiopathic, heritable, and congenital heart disease associated pulmonary arterial hypertension. Respiratory research 2013 14 (1): 3. Pfarr Nicole, Fischer Christine, Ehlken Nicola, Becker-Grünig Tabea, López-González Vanesa, Gorenflo Matthias, Hager Alfred, Hinderhofer Katrin, Miera Oliver, Nagel Christian, Schranz Dietmar, Grünig Ekkeha |
Novel mutations in BMPR2, ACVRL1 and KCNA5 genes and hemodynamic parameters in patients with pulmonary arterial hypertension. PloS one 2014 9 (6): e100261. Pousada Guillermo, Baloira Adolfo, Vilariño Carlos, Cifrian Jose Manuel, Valverde Dia |
Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects. Human mutation 2015 Sep . Machado Rajiv D, Southgate Laura, Eichstaedt Christina A, Aldred Micheala A, Austin Eric D, Best D Hunter, Chung Wendy K, Benjamin Nicola, Elliott C Gregory, Eyries Mélanie, Fischer Christine, Gräf Stefan, Hinderhofer Katrin, Humbert Marc, Keiles Steven B, Loyd James E, Morrell Nicholas W, Newman John H, Soubrier Florent, Trembath Richard C, Viales Rebecca Rodríguez, Grünig Ekkeha |
Accurate genetic diagnosis of Finnish pulmonary arterial hypertension patients using oligonucleotide-selective sequencing. Molecular genetics & genomic medicine 2015 Jul 3 (4): 354-62. Vattulainen Sanna, Aho Joonas, Salmenperä Pertteli, Bruce Siina, Tallila Jonna, Gentile Massimiliano, Sankelo Marja, Laitinen Tarja, Koskenvuo Juha W, Alastalo Tero-Pekka, Myllykangas Samu |
Genetic analyses in a cohort of children with pulmonary hypertension. The European respiratory journal 2016 Sep . Levy Marilyne, Eyries Mélanie, Szezepanski Isabelle, Ladouceur Magalie, Nadaud Sophie, Bonnet Damien, Soubrier Flore |
Complex inheritance in Pulmonary Arterial Hypertension patients with several mutations. Scientific reports 2016 6 33570. Pousada Guillermo, Baloira Adolfo, Valverde Dia |
Mutational and clinical analysis of the ENG gene in patients with pulmonary arterial hypertension. BMC genetics 2016 17 (1): 72. Pousada Guillermo, Baloira Adolfo, Fontán Diego, Núñez Marta, Valverde Dia |
High Frequency of Pulmonary Hypertension-Causing Gene Mutation in Chinese Patients with Chronic Thromboembolic Pulmonary Hypertension. PloS one 2016 11 (1): e0147396. Xi Qunying, Liu Zhihong, Zhao Zhihui, Luo Qin, Huang Zhiw |
Association of Transforming Growth Factor-ß Superfamily Genes with Non-Regression of Pulmonary Artery Hypertension Following Balloon Mitral Valvotomy: A Pilot Study. The Journal of heart valve disease 2016 Nov 25 (6): 708-715. Prabhu Mukund A, Ismael Saifudeen, Remani Konnottil, Nair Renuka, Koshy Linda, Pillai Harikrishn |
Genetic analyses in a cohort of 191 pulmonary arterial hypertension patients. Respiratory research 2018 05 19 (1): 87. Yang Hang, Zeng Qixian, Ma Yanyun, Liu Bingyang, Chen Qianlong, Li Wenke, Xiong Changming, Zhou Zh |
Pulmonary arterial hypertension associated to systemic erythematosus lupus: molecular characterization of 3 cases. Medicina clinica 2018 3 151 (3): 111-115. Pousada Guillermo, Lago-Docampo Mauro, Baloira Adolfo, Valverde Dia |
Functional analysis of a novel ENG variant in a patient with hereditary hemorrhagic telangiectasia (HHT) identifies a new Sp1 binding-site. Gene 2018 1 647 85-92. Plumitallo Sara, Ruiz-Llorente Lidia, Langa Carmen, Morini Jacopo, Babini Gabriele, Cappelletti Donata, Scelsi Laura, Greco Alessandra, Danesino Cesare, Bernabeu Carmelo, Olivieri Car |
Pulmonary Hypertension and Hereditary Hemorrhagic Telangiectasia Related to an ACVRL1 Mutation. Internal medicine (Tokyo, Japan) 2019 9 59 (2): 221-227. Yokokawa Tetsuro, Sugimoto Koichi, Kimishima Yusuke, Misaka Tomofumi, Yoshihisa Akiomi, Morisaki Hiroko, Yamada Osamu, Nakazato Kazuhiko, Ishida Takafumi, Takeishi Yasuchi |
Genotypes and Phenotypes of Chinese Pediatric Patients With Idiopathic and Heritable Pulmonary Arterial Hypertension-A Single-Center Study. The Canadian journal of cardiology 2019 12 35 (12): 1851-1856. Zhang Hong-Sheng, Liu Qian, Piao Chun-Mei, Zhu Yan, Li Qiang-Qiang, Du Jie, Gu Ho |
Association of the gene polymorphisms of BMPR2, ACVRL1, SMAD9 and their interactions with the risk of essential hypertension in the Chinese Han population. Bioscience reports 2019 1 39 (1): . Chen Yunpeng, Ye Chenxi, Chen Jingwen, Lin Dongming, Wang Hao, Wang Sh |
The Genetic Epidemiology of Pediatric Pulmonary Arterial Hypertension. The Journal of pediatrics 2020 Jun . Haarman Meindina G, Kerstjens-Frederikse Wilhelmina S, Vissia-Kazemier Theresia R, Breeman Karel T N, Timens Wim, Vos Yvonne J, Roofthooft Marc T R, Hillege Hans L, Berger Rolf M |
Clinical characteristics and prognosis analysis of idiopathic and hereditary pulmonary hypertension patients with ACVRL1 gene mutations. Pulmonary circulation 2021 12 11 (4): 20458940211044577. Zhang Xinyu, Zhang Chen, Li Qiangqiang, Piao Chunmei, Zhang Hongsheng, Gu Ho |
Possible association between a polymorphism of EPAS1 gene and persistent pulmonary hypertension of the newborn: a case-control study. Jornal de pediatria 2021 Oct . Nakwan Narongsak, Mahasirimongkol Surakameth, Satproedprai Nusara, Chaiyasung Tassamonwan, Kunhapan Punna, Charoenlap Cheep, Singkhamanan Kamonnut, Charalsawadi Chariyaw |
Whole Exome Sequencing of Patients With Heritable and Idiopathic Pulmonary Arterial Hypertension in Central Taiwan. Frontiers in cardiovascular medicine 2022 9 911649. Liang Kae-Woei, Chang Sheng-Kai, Chen Yu-Wei, Lin Wei-Wen, Tsai Wan-Jane, Wang Kuo-Ya |
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