Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 100 Records) |
| Query Trace: HBA2[original query] |
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| [The value of combined detection of HbA2 and HbF for the screening of thalassemia among individuals of childbearing ages]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 12 39 (1): 16-20. Zhuang Qianmei, Wang Geng, Wang Yuanbai, Zhuang Jianlong, Jiang Yuying, Huang Hailong, Xu Liang |
| Hemoglobinopathy gone astray-three novel forms of ?-thalassemia in Norwegian patients characterized by quantitative real-time PCR and DNA sequencing. Scandinavian journal of clinical and laboratory investigation 2021 11 81 (8): 670-678. Grimholt Runa M, Fjeld Bente, Klingenberg Ol |
| Analysis of genotype-phenotype correlation in patients with ?-thalassemia from Fujian province, Southeastern China. Journal of clinical laboratory analysis 2022 9 36 (10): e24696. Pan Yali, Chen Meihuan, Zhang YanHong, Zhang Min, Chen Lingji, Lin Na, Xu Liangpu, Huang Hailo |
| Combined Gap-Polymerase Chain Reaction and Targeted Next-Generation Sequencing Improve ?- and ?-Thalassemia Carrier Screening in Pregnant Women in Vietnam. Hemoglobin 2022 8 46 (4): 233-239. Lam Tuan-Thanh, Nguyen Doan-Tu, Le Quang Thanh, Nguyen Duy-Anh, Hoang Diem-Tuyet Thi, Nguyen Huu Du, Nguyen Canh Chuong, Doan Kim Phuong Thi, Tran Nhat-Thang, Ha Thi Minh Thi, Trinh Thu Huong Nhat, Nguyen Van Thong, Lam Duc Tam, Le Minh Tam, Nguyen Xuan Thao, Ho Thu-Hang Thi, Tran Trung Hoanh, Ho Viet Thang, Bui Thanh Van, Nguyen Van Trong, Hoang Phuoc Ba, Nguyen Hoai Thanh, Nguyen Manh Hoan, Vo Thanh-Binh, Le Duy-Khang Nguyen, Truong Thao Ngoc, Dao Hong-Thuy Thi, Vo Phuong-Anh Ngoc, Nguyen Thien-Chi Van, Tran Ngoc-Nhu Thi, Tran Quynh-Nhu Thi, Van Yen-Linh Thi, Nguyen Thanh-Thanh Thi, Huynh Bich-Ngoc Thi, Nguyen Thanh-Phuong Thi, Tran Kim-Van Thi, Nguyen Cong-Trai, Doan Phuoc-Loc, Nguyen Thanh-Dat, Do Thanh-Thuy Thi, Truong Dinh-Kiet, Tang Hung Sang, Cao Ngoc-Phuong Thi, Phan Minh-Duy, Giang Hoa, Nguyen Hoai-Ngh |
| RS12574989 and haplotype associated with ?/?-chain imbalance and population HbA2 reduction. BMC medical genomics 2022 8 15 (1): 179. Lin Qiyin, Xie Yingjun, Zhong Xuan, Sun Xiaofang, Wang Di |
| [Genotypic and hematological characteristics of 83 ?-thalassemia mutation carriers and patients from Henan Province]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 7 39 (7): 674-679. Wang Weilin, Zhao Xiaoming, Bai Songting, Wang Lu, Wang Chunmei, Yao Qianghua, Li Bai, Wang D |
| 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 |
| Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare ?- and ?-Globin Gene Variants in Thalassemia Alleles in the Chinese Population. Archives of pathology & laboratory medicine 2022 5 147 (2): 208-214. Zhuang Jianlong, Chen Chunnuan, Fu Wanyu, Wang Yuanbai, Zhuang Qianmei, Lu Yulin, Xie Tiantian, Xu Ruofan, Zeng Shuhong, Jiang Yuying, Xie Yingjun, Wang Gaoxio |
| Effects of Senegal haplotype (Xmn1-rs7412844), alpha-thalassemia (3.7kb HBA1/HBA2 deletion), NPRL3-rs11248850 and BCL11A-rs4671393 variants on sickle cell nephropathy. International journal of biochemistry and molecular biology 2022 5 13 (2): 5-16. Ndour El Hadji Malick, Mnika Khuthala, Guèye Tall Fatou, Seck Moussa, Dème Ly Indou, Nembaware Victoria, Sagna-Bassène Hélène Ange Thérèse, Dione Rokhaya, Ndongo Aliou Abdoulaye, Diop Jean Pascal Demba, Barry Nènè Oumou Kesso, Djité Moustapha, Ndiaye Diallo Rokhaya, Guèye Papa Madièye, Diop Saliou, Diagne Ibrahima, Cissé Aynina, Wonkam Ambroise, Lopez Sall Philomè |
| Molecular prevalence of HBB-associated hemoglobinopathy among reproductive-age adults and the prenatal diagnosis in Jiangxi Province, southern central China. Frontiers in genetics 2022 10 13 992073. Luo Haiyan, Huang Ting, Lu Qing, Zhang Liuyang, Xu Yonghua, Yang Yan, Guo Zhen, Yuan Huizhen, Shen Yinqin, Huang Shuhui, Yang Bicheng, Zou Yongyi, Liu Yanq |
| Differential Effects on HbA1c Detection by HPLC and Capillary Electrophoresis in Five Types of Hb Variants in China. Laboratory medicine 2022 10 . Wei Luo, Weifeng Zhang, Zuoliang Do |
| 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 |
| 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 |
| 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 |
| Hematological and molecular characteristics of a novel ?-globin variant Hb Liangqing (HBA2:c.224A>G). Hematology (Amsterdam, Netherlands) 2023 5 28 (1): 2213545. Youqiong Li, Shulin Liang, Liang Liang, Lihong Zheng, Xiaocai |
| The frequency of HK?? allele in silent deletional ?-thalassemia carriers in the Yulin region of southern China using the third-generation sequencing. Gene 2023 5 875 147505. Sisi Ning, Yunrong Qin, Yunning Liang, Yi Liang, Yuling Xie, Yinghong Lu, Guanghong Wei, Ruofan Xu, Yinyin Liu, Jihui |
| Gene Mutation Spectrum among Alpha-Thalassaemia Patients in Northeast Peninsular Malaysia. Diagnostics (Basel, Switzerland) 2023 3 13 (5): . Vijian Divashini, Wan Ab Rahman Wan Suriana, Ponnuraj Kannan Thirumulu, Zulkafli Zefarina, Bahar Rosnah, Yasin Norafiza, Hassan Syahzuwan, Esa Ezal |
| Mutation spectrum of thalassemia among pre-pregnant adults in the Jiangsu Province by capillary electrophoresis-based multiplex PCR assay. Molecular genetics & genomic medicine 2023 12 e2344. Binbin Shao, Yuguo Wang, Jingjing Zhang, Yan Wang, Juan Tan, Lulu Wang, Ping Hu, Jianxin Tan, Zhengfeng |
| 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 |
| [Effects of Hemoglobin Variants on Glycosylated Hemoglobin Testing]. Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition 2023 10 54 (5): 1019-1023. Dan Ye, Yan Tang, Mei Zha |
| 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 |
| HbA2 levels in children with ?-thalassemia trait associated with iron deficiency: A perspective for pediatricians. American journal of clinical pathology 2024 7 . ?eyda De?ermenci, Deniz Asl |
| [Molecular Diagnosis and Pedigree Analysis of Rare Mutations in Non-coding Region of HBA2 Gene]. Zhongguo shi yan xue ye xue za zhi 2024 6 32 (3): 940-944. Li-Zhu Chen, Ti-Zhen Yan, Jun Huang, Qing-Yan Zhong, Xue Qin, Ning Tang, Shi-Qiang L |
| 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 |
| [Analysis of rare mutations associated with Thalassemia and their hematological characteristics in Chenzhou region of Hunan Province]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 5 41 (6): 708-714. Caiyun Li, Jian Zhang, Yingli Cao, Haoqing Zhang, Dongqun Huang, Jufang Tan, Shuai Hou, Dongzhu L |
| Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing. Scientific reports 2024 5 14 (1): 9966. Jianlong Zhuang, Na Zhang, Yu Zheng, Yuying Jiang, Yu'e Chen, Aiping Mao, Chunnuan Ch |
| Screening for thalassemia carriers among the Han population of childbearing age in Southwestern of China. Frontiers in genetics 2024 4 15 1356068. Yepei Du, Cong Zhou, Jing Wang, Yanting Yang, Hui L |
| Molecular epidemiology and hematological profiles of hemoglobin variants in southern Thailand. Scientific reports 2024 4 14 (1): 9255. Wanicha Tepakhan, Sataron Kanjanaopas, Korntip Sreworadechpisal, Tipparat Penglong, Pornpun Sripornsawan, Chaowanee Wangchauy, Chadaporn Nokkong, Chulalak Kongkan, Saristha Buatho |
| [Study of the types of mutations of Thalassemia in Shanghai area]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 4 41 (4): 385-392. Yanying Gu, Beiying Wu, Yiyi Lu, Mingmin Gu, Jiafei L |
| Clinical, laboratory, and molecular characteristics of a cohort of children with hemoglobinopathy S/beta-thalassemia. Hematology, transfusion and cell therapy 2024 1 . Érica Louback Oliveira, André Rolim Belisário, Natiely Pereira Silva, Paulo Val Rezende, Maristela Braga Muniz, Larissa Maira Moura Oliveira, Cibele Velloso-Rodrigues, Marcos Borato Via |
- Page last reviewed:Feb 1, 2024
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