Human Genome Epidemiology Literature Finder
|
Records 1 - 25 (of 25 Records) |
| Query Trace: Disease and HBA2[original query] |
|---|
| Relative protection from ischaemic heart disease in beta-thalassaemia carriers. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2010 Oct 20 (10): 653-6. Bozdar Manzar, Ahmed Suhaib, Anwar Jale |
| A novel HBA2 gene conversion in cis or trans: "a12 allele" in a Saudi population. Blood cells, molecules & diseases 2014 Dec 53 (4): 199-203. Borgio J Francis, AbdulAzeez S, Al-Nafie Awatif N, Naserullah Zaki A, Al-Jarrash Sana, Al-Madan Mohammed S, Al-Muhanna Fahad, Steinberg Martin H, Al-Ali Amein |
| Changes in hematological parameters in a-thalassemia individuals co-inherited with erythroid Krüppel-like factor mutations. Clinical genetics 2015 Jul 88 (1): 56-61. Yu L-H, Liu D, Cai R, Shang X, Zhang X-H, Ma X-X, Yan S-H, Fang P, Zheng C-G, Wei X-F, Liu Y-H, Zhou T-B, Xu X |
| Molecular Epidemiological Investigation of Thalassemia in the Chengdu Region, Sichuan Province, Southwest China. Hemoglobin 2015 Aug 1-5. Yu Xia, Yang Li-Ye, Yang Hui-Tian, Liu Cheng-Gui, Cao Deng-Cheng, Shen Wei, Yang Hui, Zhan Xiao-Fen, Li Jian, Xue Bing-Rong, Lin M |
| Multi-allele DNA biosensor for the rapid genotyping of 'nondeletion' alpha thalassaemia mutations in HBA1 and HBA2 genes by means of multiplex primer extension reaction. Clinica chimica acta; international journal of clinical chemistry 2015 Jun 446 241-7. Petropoulou Margarita, Poula Amalia, Traeger-Synodinos Jan, Kanavakis Emmanuel, Christopoulos Theodore K, Ioannou Penelope |
| Hb Dapu (HBA2: c.52G?>?T): A Novel Nondeletional a-Thalassemia Mutation. Hemoglobin 2016 Jun 1-3. Yang Yu, Li Dong-Zhi, He Pi |
| Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon. British journal of haematology 2017 May . Geard Amy, Pule Gift D, Chetcha Chemegni Bernard, Ngo Bitoungui Valentina J, Kengne Andre P, Chimusa Emile R, Wonkam Ambroi |
| A Comprehensive Molecular Investigation of a-Thalassemia in an Iranian Cohort from Different Provinces of North Iran. Hemoglobin 2017 Jan 41 (1): 32-37. Eftekhari Hajar, Tamaddoni Ahmad, Mahmoudi Nesheli Hassan, Vakili Mohsen, Sedaghat Sadegh, Banihashemi Ali, Azizi Mandana, Youssefi Kamangar Reza, Akhavan-Niaki Hal |
| Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in Cameroon. British journal of haematology 2017 Dec . Wonkam Ambroise, Mnika Khuthala, Ngo Bitoungui Valentina J, Chetcha Chemegni Bernard, Chimusa Emile R, Dandara Collet, Kengne Andre |
| Two ?1-Globin Gene Point Mutations Causing Severe Hb H Disease. Hemoglobin 2017 11 41 (4-6): 293-296. Jiang Hua, Huang Lv-Yin, Zhen Li, Jiang Fan, Li Dong-Z |
| Shine & Lal index as a predictor for early detection of ?-thalassemia carriers in a limited resource area in Bandung, Indonesia. BMC medical genetics 2019 8 20 (1): 136. Maskoen Ani Melani, Reniarti Lelani, Sahiratmadja Edhyana, Sisca Joice, Effendi Sjarif Hidaj |
| A Novel Mutation at HBB: c.91delA (Codon 30, -A) Causing ?-Thalassemia in a Chinese Family. Acta haematologica 2019 5 142 (4): 249-252. Jia Wenguang, Wang Weidong, Zhu Hengying, Chen Pi |
| Krüppel-Like Factor 1 Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with ?-Thalassemia Intermedia. Hemoglobin 2019 2 43 (1): 12-17. Tamaddoni Ahmad, Khabaz Astaneh Sahar, Tabaripour Reza, Akhavan-Niaki Hal |
| Molecular Genetic Analysis of ?-Thalassemia in Hamadan Province, West Iran. Hemoglobin 2020 9 44 (5): 319-324. Moradi Keivan, Aznab Mozaffar, Biglari Mostafa, Shafieenia Samaneh, Azimi Azam, Bijari Nushin, Alibakhshi Re |
| Hb Westmead (HBA2: c.369C>G): Hematological Characteristics in Heterozygotes with and without ?-Thalassemia. Hemoglobin 2020 5 44 (3): 153-155. Jiang Fan, Ju Ai-Ping, Li Jian, Chen Gui-Lan, Zhou Jian-Ying, Tang Xue-Wei, Zuo Lian-Dong, Li Dong-Z |
| Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland China. Hemoglobin 2020 4 44 (2): 86-88. Jiang Fan, Xu Li-Li, Chen Gui-Lan, Zhou Jian-Ying, Li Jian, Tang Xue-Wei, Zuo Lian-Dong, Li Dong-Z |
| Haemoglobin switching modulator SNPs rs5006884 is associated with increased HbA in ?-thalassaemia carriers. Archives of medical science : AMS 2021 8 17 (4): 1064-1074. Cyrus Cyril, Vatte Chittibabu, Chathoth Shahanas, Sayed Abdul Azeez, Borgio J Francis, Alrubaish Mohammed Abdullah, Alfalah Rawan, Alsaikhan Jana, Al Ali Amein |
Multiple-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
The Journal of clinical investigation 2021 May . Page Grier P, Kanias Tamir, Guo Yuelong J, Lanteri Marion C, Zhang Xu, Mast Alan E, Cable Ritchard G, Spencer Bryan R, Kiss Joseph E, Fang Fang, Endres-Dighe Stacy M, Brambilla Donald, Nouraie Mehdi, Gordeuk Victor R, Kleinman Steve, Busch Michael P, Gladwin Mark T, |
| Molecular Determination of Vascular Endothelial Growth Factor, miRNA-423 Gene Abnormalities by Utilizing ARMS-PCR and Their Association with Fetal Hemoglobin Expression in the Patients with Sickle Cell Disease. Current issues in molecular biology 2022 6 44 (6): 2569-2582. Hamadi Abdullah, Mir Rashid, Mahzari Ali, Hakami Abdulrahim, Almotairi Reema, Dobie Gasim, Hamdi Fawaz, Nahari Mohammed Hassan, Alhefzi Razan, Alasseiri Mohammed, Hakami Nora Y, Al Sadoun Hadeel, Al-Amer Osama M, Barnawi Jameel, Madkhali Hassan |
| Detecting rare thalassemia in children with anemia using third-generation sequencing. Hematology (Amsterdam, Netherlands) 2023 8 28 (1): 2241226. Zhen-Min Ren, Wu-Jiao Li, Zhi-Hao Xing, Xiao-Ying Fu, Ju-Yan Zhang, Yun-Sheng Chen, De-Fa |
| Clinical significance of mutational variants in beta and alpha genes in patients with hemoglobinopathies from two large Greek centers: a complex interplay between genotype and phenotype. Journal of molecular medicine (Berlin, Germany) 2023 7 . Michael D Diamantidis, Rebecca-Anastasia Karanikola, Chrysoula Polyzoudi, Sophia Delicou, Achilles Manafas, Helen Savera, Aikaterini Xydaki, Angeliki Kotsiafti, Evangelos Tsangalas, Georgia Ikonomou, Eirini Mani, Konstantinos Ntoulas, Evangelos Alexiou, Ioanna Argyrakouli, John Koskinas, Paraskevi Foti |
| Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot. Translational pediatrics 2023 11 12 (10): 1835-1841. Yu Pan, Manli Liu, Songsong Zhang, Huaxian Mei, Jing |
| Prevalence and Impact of HMOX1 Polymorphism (rs2071746: A?>?T) in Indian Sickle Cell Disease Patients. Journal of laboratory physicians 2023 10 15 (4): 583-589. Hareram Pandey, Kanwaljeet Singh, Ravi Ranjan, Jasmita Dass, Seema Tyagi, Tulika Seth, Renu Saxena, Manoranjan Mahapat |
| A large cohort of Hb H disease in northeast Thailand: A molecular revisited, diverse genetic interactions and identification of a novel mutation. Clinica chimica acta; international journal of clinical chemistry 2024 6 561 119830. Kritsada Singha, Wanicha Tepakhan, Supawadee Yamsri, Attawut Chaibunruang, Hataichanok Srivorakun, Anupong Pansuwan, Goonnapa Fucharoen, Supan Fucharo |
| First clinical and pedigree study of rare HBB: c.316-90 A?>?G variant in ?-globin gene in Chinese population using third-generation sequencing. Annals of hematology 2024 12 . Jianlong Zhuang, Nan Huang, Yu Zheng, Na Zhang, Chunnuan Ch |
- Page last reviewed:Feb 1, 2024
- Content source: