Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: HBG1[original query] |
---|
Identification of candidate genes for Parkinson's disease through blood transcriptome analysis in LRRK2-G2019S carriers, idiopathic cases, and controls. Neurobiology of aging 2015 Feb 36 (2): 1105-9. Infante Jon, Prieto Carlos, Sierra María, Sánchez-Juan Pascual, González-Aramburu Isabel, Sánchez-Quintana Coro, Berciano José, Combarros Onofre, Sainz Jes |
Evolutionary context for the association of ?-globin, serum uric acid, and hypertension in African Americans. BMC medical genetics 2015 16 (1): 103. Shriner Daniel, Kumkhaek Chutima, Doumatey Ayo P, Chen Guanjie, Bentley Amy R, Charles Bashira A, Zhou Jie, Adeyemo Adebowale, Rodgers Griffin P, Rotimi Charles |
ARHGAP18 is a novel gene under positive natural selection that influences HbF levels in ß-thalassaemia. Molecular genetics and genomics : MGG 2018 Feb 293 (1): 207-216. He Yunyan, Luo Jianming, Chen Yang, Zhou Xiaoheng, Yu Shanjuan, Jin Ling, Xiao Xuan, Jia Siyuan, Liu Qia |
The relationship between the variations in G? and A? promotors and the Hereditary Persistence of Fetal Hemoglobin (HPFH). Cellular and molecular biology (Noisy-le-Grand, France) 2018 2 64 (1): 32-39. Aydin Muhsin, Rencuzogullari Eyyup, Dalyan Ayse, Bayram Suleyman, Genc Ahm |
Regulatory Single Nucleotide Polymorphism rs368698783 (G>A): a Genetic Modifier of Hb F Production Only under Erythropoietic Stress Characteristic for ?-Globin Chain Deficiency? Hemoglobin 2019 5 43 (1): 73-75. Jiang Fan, Li Jian, Zhou Jian-Ying, Liao Can, Li Dong-Z |
New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level. Journal of pediatric hematology/oncology 2019 11 42 (1): 20-22. Chaouch Leila, Sellami Houssem, Kalai Miniar, Darragi Imen, Boudrigua Imen, Chaouachi Dorra, Abbes Salem, Mnif Sam |
Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania. BMC medical genetics 2020 Jun 21 (1): 125. Nkya Siana, Mwita Liberata, Mgaya Josephine, Kumburu Happiness, van Zwetselaar Marco, Menzel Stephan, Mazandu Gaston Kuzamunu, Sangeda Raphael, Chimusa Emile, Makani Jul |
Association of polymorphisms in the HBG1-HBD intergenic region with HbF levels. Journal of clinical laboratory analysis 2020 Feb e23243. Hu Li, Huang Ling, Han Yuanyuan, Jin Tingting, Liu Juan, Jiang Minmin, Liu Xingmei, Li Yuanyuan, Han Wenping, An Bangquan, Huang Shengw |
The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation. Journal of human genetics 2021 Oct . Luo Shiqiang, Chen Xingyuan, Zeng Dingyuan, Tang Ning, Yuan Dejian, Zhong Qingyan, Mao Aiping, Xu Ruofan, Yan Tizh |
[Molecular Epidemiological Characteristics and Differential Diagnosis of Common ??-Thalassemia/HPFH]. Zhongguo shi yan xue ye xue za zhi 2022 8 30 (4): 1182-1187. Ju Ai-Ping, Li Na, Lin Keng, Huang Hui-Hui, Liu Shu-Xian, Jiang F |
Mutational analysis of hemoglobin genes and functional characterization of detected variants, through in-silico analysis, in Pakistani beta-thalassemia major patients. Scientific reports 2023 8 13 (1): 13236. Samina Ejaz, Iqra Abdullah, Muhammad Usman, Muhammad Arslan Iqbal, Sidra Munawar, Muhammad Irfan Khan, Nagina Imtiaz, Hanniah Tahir, Muhammad Ihsan Bari, Tayyaba Rasool, Aneeza Fatima, Ramsha Anwar, Ayman Durrani, Yasir Hame |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: