HuGE Literature Finder
Heart, Lung, Blood, and Sleep Disorders
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| Endothelin-1 gene polymorphism (G8002A) and endothelial monocyte-activating polypeptide II: Role in vascular dysfunction in pediatric patients with ?-thalassemia major. Cytokine 2022 Oct 161 156048. Tantawy Azza Abdel Gawad, Tadros Mourad Alfy Ramzy, Adly Amira Abdel Moneam, Ismail Eman Abdel Rahman, Ibrahim Fatma A, Salah Eldin Nanis Mohammed, Hussein Mahitab Morsy, Alfeky Mervat Abdalhameed, Ibrahim Sarah Mohammed, Hashem Marwa Adel, Ebeid Fatma Soliman Elsay |
| Endothelin-1 gene and endothelin receptor A gene polymorphisms in severe pulmonary hypertension associated with rheumatic mitral valve disease. Archives of medical science : AMS 2022 18 (1): 260-266. Mehra Pratishtha, Mehta Vimal, Yusuf Jamal, Sukhija Rishi, Aronow Wilbert |
Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function.
Nature genetics 2022 6 54 (6): 783-791. Aung Nay, Vargas Jose D, Yang Chaojie, Fung Kenneth, Sanghvi Mihir M, Piechnik Stefan K, Neubauer Stefan, Manichaikul Ani, Rotter Jerome I, Taylor Kent D, Lima Joao A C, Bluemke David A, Kawut Steven M, Petersen Steffen E, Munroe Patricia |
| 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 |
| 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 |
| In vivo assessment of a single adenine mutation in 5'UTR of Endothelin-1 gene in paediatric cases with severe pulmonary hypertension: an observational study. BMC research notes 2021 May 14 (1): 194. Kumar Abhishek, Choudhury Minati, Batra Sakshi Dhingra, Sikri Kriti, Gupta Anushr |
| Association between genetic variations in carbamoyl-phosphate synthetase gene and persistent neonatal pulmonary hypertension. European journal of pediatrics 2021 Mar . El-Khazragy Nashwa, El Barbary Mohamed, Fouad Hala, Abdelgawad Abdallah, Rabie Di |
| Incidence of alveolar capillary dysplasia with misalignment of pulmonary veins in infants with unexplained severe pulmonary hypertension: The roles of clinical, pathological, and genetic testing. Early human development 2021 Jan 155 105323. Onda Tetsuo, Manabe Atsushi, Akimoto Takuma, Hayasaka Itaru, Ikeda Masahiko, Furuse Yuta, Ando Akiko, Nakamura Yuichi, Honjo Ryota, Furuta Itsuko, Cho Kazutos |
| 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 |
| TRPV1 genetic polymorphisms and risk of COPD or COPD combined with PH in the Han Chinese population. Cell cycle (Georgetown, Tex.) 2020 Oct 1-8. Xiong Mingmei, Guo Meihua, Huang Dongjian, Li Jing, Zhou Y |
| Estrogen Signaling and Portopulmonary Hypertension: The Pulmonary Vascular Complications of Liver Disease Study (PVCLD2). Hepatology (Baltimore, Md.) 2020 May . Al-Naamani Nadine, Krowka Michael J, Forde Kimberly A, Krok Karen L, Feng Rui, Heresi Gustavo A, Dweik Raed A, Bartolome Sonja, Bull Todd M, Roberts Kari E, Austin Eric D, Hemnes Anna R, Patel Mamta J, Oh Jae K, Lin Grace, Doyle Margaret F, Denver Nina, Andrew Ruth, MacLean Margaret R, Fallon Michael B, Kawut Steven M, |
| Myeloproliferative Diseases as Possible Risk Factor for Development of Chronic Thromboembolic Pulmonary Hypertension-A Genetic Study. International journal of molecular sciences 2020 May 21 (9): . Eichstaedt Christina A, Verweyen Jeremias, Halank Michael, Benjamin Nicola, Fischer Christine, Mayer Eckhard, Guth Stefan, Wiedenroth Christoph B, Egenlauf Benjamin, Harutyunova Satenik, Xanthouli Panagiota, Marra Alberto M, Wilkens Heinrike, Ewert Ralf, Hinderhofer Katrin, Grünig Ekkeha |
| Association of Rare PTGIS Variants With Susceptibility and Pulmonary Vascular Response in Patients With Idiopathic Pulmonary Arterial Hypertension. JAMA cardiology 2020 Apr . Wang Xiao-Jian, Xu Xi-Qi, Sun Kai, Liu Ke-Qiang, Li Su-Qi, Jiang Xin, Zhao Qin-Hua, Wang Lan, Peng Fu-Hua, Ye Jue, Wu Yan, Jiang Rui, Zhang Jin, Huang Wei, Wei Wen-Bin, Yan Yi, Li Jing-Hui, Liu Qian-Qian, Li Sheng, Wang Yong, Zhang Shu-Yang, Zhang Xue, Jing Zhi-Che |
| Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results from the Recipient Epidemiology and Donor Evaluation Study III Brazil Cohort Study.
The journal of sexual medicine 2019 Oct . Cintho Ozahata Mina, Page Grier P, Guo Yuelong, Ferreira João Eduardo, Dinardo Carla Luana, Carneiro-Proietti Anna Bárbara F, Loureiro Paula, Mota Rosimere Afonso, Rodrigues Daniela O W, Belisario André Rolim, Maximo Claudia, Flor-Park Miriam V, Custer Brian, Kelly Shannon, Sabino Ester Cerdeira, |
| Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates. Respiratory research 2019 Aug 20 (1): 174. Liu Xu, Mei Mei, Chen Xiang, Lu Yulan, Dong Xinran, Hu Liyuan, Hu Xiaojing, Cheng Guoqiang, Cao Yun, Yang Lin, Zhou Wenh |
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- Page last updated:Feb 01, 2023
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