Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 38 Records) |
Query Trace: EGLN1[original query] |
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[Association between six single nucleotide polymorphisms of EGLN1 gene and adaptation to high-altitude hypoxia]. Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji 2013 Aug 35 (8): 992-8. Li Qian, Liu Shu-Yuan, Lin Ke-Qin, Sun Hao, Yu Liang, Huang Xiao-Qin, Chu Jia-You, Yang Zhao-Qi |
Identification of a Tibetan-specific mutation in the hypoxic gene EGLN1 and its contribution to high-altitude adaptation. Molecular biology and evolution 2013 Aug 30 (8): 1889-98. Xiang Kun, Ouzhuluobu , Peng Yi, Yang Zhaohui, Zhang Xiaoming, Cui Chaoying, Zhang Hui, Li Ming, Zhang Yanfeng, Bianba , Gonggalanzi , Basang , Ciwangsangbu , Wu Tianyi, Chen Hua, Shi Hong, Qi Xuebin, Su Bi |
Andean and Tibetan patterns of adaptation to high altitude. American journal of human biology : the official journal of the Human Biology Council 2013 Jan . Bigham AW, Wilson MJ, Julian CG, Kiyamu M, Vargas E, Leon-Velarde F, Rivera-Chira M, Rodriquez C, Browne VA, Parra E, Brutsaert TD, Moore LG, Shriver MD |
Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma. The Journal of clinical endocrinology and metabolism 2014 Jul 99 (7): E1352-60. Welander Jenny, Andreasson Adam, Juhlin C Christofer, Wiseman Roger W, Bäckdahl Martin, Höög Anders, Larsson Catharina, Gimm Oliver, Söderkvist Pet |
Variants of the low oxygen sensors EGLN1 and HIF-1AN associated with acute mountain sickness. International journal of molecular sciences 2014 15 (12): 21777-87. Zhang Enhao, Zhang Jihang, Jin Jun, Qin Jun, Li Huijie, Huang L |
Combined genetic effects of EGLN1 and VWF modulate thrombotic outcome in hypoxia revealed by Ayurgenomics approach. Journal of translational medicine 2015 13 184. Aggarwal Shilpi, Gheware Atish, Agrawal Anurag, Ghosh Saurabh, Prasher Bhavana, Mukerji Mitali, |
Correlation between single nucleotide polymorphisms in hypoxia-related genes and susceptibility to acute high-altitude pulmonary edema. Genetics and molecular research : GMR 2015 14 (3): 11562-72. Wu A L, Xiong Y S, Li Z Q, Liu Y G, Quan Q, Wu L |
Hypoxia inducible factor-1 alpha and prolinhydroxlase 2 polymorphisms in patients with severe sepsis: a prospective observational trial. BMC anesthesiology 2016 16 (1): 61. Höcker Annika, Rabeling Miriam, Bick Alexandra, Cox Linda, Kreuzer Maximiliane, Engler Andrea, Walstein Kai, Bachmann Hagen S, Jöckel Karl-Heinz, Eisele Lewin, Adamzik Michael, Peters Jürgen, Schäfer Simon |
Raised HIF1a during normoxia in high altitude pulmonary edema susceptible non-mountaineers. Scientific reports 2016 6 26468. Soree Poonam, Gupta Rajinder K, Singh Krishan, Desiraju Koundinya, Agrawal Anurag, Vats Praveen, Bharadwaj Abhishek, Baburaj T P, Chaudhary Pooja, Singh Vijay K, Verma Saroj, Bajaj Amir Chand, Singh Shashi Ba |
[Hereditary pheochromocytoma-associated syndromes. Part 2]. Terapevticheskii arkhiv 2017 6 87 (10): 115-119. Yukina M Yu, Troshina E A, Beltsevich D |
Sherpas share genetic variations with Tibetans for high-altitude adaptation. Molecular genetics & genomic medicine 2017 Jan 5 (1): 76-84. Bhandari Sushil, Zhang Xiaoming, Cui Chaoying, Yangla , Liu Lan, Ouzhuluobu , Baimakangzhuo , Gonggalanzi , Bai Caijuan, Bianba , Peng Yi, Zhang Hui, Xiang Kun, Shi Hong, Liu Shiming, Gengdeng , Wu Tianyi, Qi Xuebin, Su Bi |
Association of EGLN1 genetic polymorphisms with SpO responses to acute hypobaric hypoxia in a Japanese cohort. Journal of physiological anthropology 2018 Apr 37 (1): 9. Yasukochi Yoshiki, Nishimura Takayuki, Motoi Midori, Watanuki Shige |
Genetic basis of unexplained erythrocytosis in Indian patients. European journal of haematology 2019 May . Mallik Nabhajit, Sharma Prashant, Kaur Hira Jasbir, Chhabra Sanjeev, Sreedharanunni Sreejesh, Kumar Narender, Naseem Shano, Sachdeva Man Updesh Singh, Ahluwalia Jasmina, Malhotra Pankaj, Varma Neelam, Varma Subhash, Das Ree |
Novel association of SNP rs479200 in EGLN1 gene with predisposition to preeclampsia. Gene 2019 4 705 1-4. Kumar K S Praveen, Arcot Madhuri, Munisamaiah Munikrishna, Balakrishna Shara |
An EGLN1 mutation may regulate hypoxic response in cyanotic congenital heart disease through the PHD2/HIF-1A pathway. Genes & diseases 2019 3 6 (1): 35-42. Zhou Yuanlin, Ouyang Na, Liu Lingjuan, Tian Jie, Huang Xupei, Lu Tiew |
Genetic variants at the EGLN1 locus associated with high-altitude adaptation in Tibetans are absent or found at low frequency in highland Andeans. Annals of human genetics 2019 Feb . Heinrich Erica C, Wu Lu, Lawrence Elijah S, Cole Amy M, Anza-Ramirez Cecilia, Villafuerte Francisco C, Simonson Tatum |
Association Between Single Nucleotide Polymorphisms in PPARA and EPAS1 Genes and High-Altitude Appetite Loss in Chinese Young Men. Frontiers in physiology 2019 10 59. Pan Wenxu, Liu Chuan, Zhang Jihang, Gao Xubin, Yu Shiyong, Tan Hu, Yu Jie, Qian Dehui, Li Jiabei, Bian Shizhu, Yang Jie, Zhang Chen, Huang Lan, Jin J |
Association of EGLN1 gene with high aerobic capacity of Peruvian Quechua at high altitude. Proceedings of the National Academy of Sciences of the United States of America 2019 11 116 (48): 24006-24011. Brutsaert Tom D, Kiyamu Melisa, Elias Revollendo Gianpietro, Isherwood Jenna L, Lee Frank S, Rivera-Ch Maria, Leon-Velarde Fabiola, Ghosh Sudipta, Bigham Abigail |
Juvenile erythrocytosis in children after liver transplantation: prevalence, risk factors and outcome. Scientific reports 2020 6 10 (1): 9683. Casale Maddalena, Roberti Domenico, Mandato Claudia, Iorio Raffaele, Caropreso Maria, Scianguetta Saverio, Picariello Stefania, Perrotta Silverio, Vajro Piet |
Genetic Analysis of EGLN1 C127S Variant in Taiwanese Parkinson's Disease. Parkinson's disease 2020 5 2020 9582317. Chiang Han-Lin, Chen Chiung Mei, Chen Yi-Chun, Chao Chih-Ying, Wu Yih-Ru, Lee-Chen Guey-J |
Hypoxia responsiveness linked variant in EGLN1 gene is enriched in oral cancer patients. Archives of oral biology 2020 May 116 104767. Francis Immaculate, Arcot Madhuri, Mohiyuddin S M Azeem, Balakrishna Shara |
Genome-wide Screening Identifies SFMBT1 as an Oncogenic Driver in Cancer with VHL Loss. Molecular cell 2020 2 77 (6): 1294-1306.e5. Liu Xijuan, Simon Jeremy M, Xie Haibiao, Hu Lianxin, Wang Jun, Zurlo Giada, Fan Cheng, Ptacek Travis S, Herring Laura, Tan Xianming, Li Mingjie, Baldwin Albert S, Kim William Y, Wu Tao, Kirschner Marc W, Gong Kan, Zhang Qi |
Effect of EGLN1 Genetic Polymorphisms on Hemoglobin Concentration in Andean Highlanders. BioMed research international 2020 12 2020 3436581. Yasukochi Yoshiki, Nishimura Takayuki, Ugarte Juan, Ohnishi Mayumi, Nishihara Mika, Alvarez Guillermo, Fukuda Hideki, Mendoza Victor, Aoyagi Kiyos |
High-altitude pulmonary edema is aggravated by risk loci and associated transcription factors in HIF-prolyl hydroxylases. Human molecular genetics 2021 May . Sharma Kavita, Mishra Aastha, Singh Himanshu N, Parashar Deepak, Alam Perwez, Thinlas Tashi, Mohammad Ghulam, Kukreti Ritushree, Syed Mansoor Ali, Pasha M A Qad |
Novel Germline PHD2 Variant in a Metastatic Pheochromocytoma and Chronic Myeloid Leukemia, but in the Absence of Polycythemia. Medicina (Kaunas, Lithuania) 2022 Aug 58 (8): . Provenzano Aldesia, Chetta Massimiliano, De Filpo Giuseppina, Cantini Giulia, La Barbera Andrea, Nesi Gabriella, Santi Raffaella, Martinelli Serena, Rapizzi Elena, Luconi Michaela, Maggi Mario, Mannelli Massimo, Ercolino Tonino, Canu Letiz |
Novel mutations in EPO-R and oxygen-dependent degradation (ODD) domain of EPAS1 genes-a causative reason for Congenital Erythrocytosis. European journal of medical genetics 2022 4 65 (6): 104493. Echambadi Loganathan Samundeshwari, Kattaru Surekha, Chandrasekhar Chodimella, Vengamma B, Sarma Potukuchi Venkata Gurunadha Krish |
Prediction of High-Altitude Cardiorespiratory Fitness Impairment Using a Combination of Physiological Parameters During Exercise at Sea Level and Genetic Information in an Integrated Risk Model. Frontiers in cardiovascular medicine 2021 8 719776. Yang Jie, Tan Hu, Sun Mengjia, Chen Renzheng, Zhang Jihang, Liu Chuan, Yang Yuanqi, Ding Xiaohan, Yu Shiyong, Gu Wenzhu, Ke Jingbin, Shen Yang, Zhang Chen, Gao Xubin, Li Chun, Huang L |
Two Novel Genetic Variants Involved in the Oxygen Sensing Pathway in JAK2-unmutated Erythrocytosis. Biochemical genetics 2024 4 . Qiang Ma, Ronghua Hu, Wuhan Hui, Hong Zhao, Dongmei Zou, Yan Liu, Wanling S |
Association of the C allele of rs479200 in the EGLN1 gene with COVID-19 severity in Indian population: a novel finding. Human genomics 2024 1 18 (1): 7. Renuka Harit, Sajal De, Piyoosh Kumar Singh, Deepika Kashyap, Manish Kumar, Dibakar Sahu, Chander Prakash Yadav, Mradul Mohan, Vineeta Singh, Ram Singh Tomar, Kailash C Pandey, Kapil Vashis |
A Case-Control Study of the Associations between EGLN1 Gene Polymorphisms and COPD. Frontiers in bioscience (Landmark edition) 2024 1 29 (1): 18. Xin Li, Peng Zhang, Jing Yu, Chunyan Zhang, Yanli Shi, Xueyan Wei, Honge Li, Xuhui Zhang, Ao Lin, Zhen Yang, Yunchao Wang, Xinhua Wa |
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- Page last updated:Apr 22, 2024
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