Zobrazeno 1 - 10
of 639
pro vyhledávání: '"β-globin gene"'
Publikováno v:
Hematology, Vol 27, Iss 1, Pp 150-156 (2022)
Objectives Shaokwan is one of the inhabitant regions of Hakka population in Guangdong province of southern China. Previous survey has reported that a higher prevalence of abnormal hemoglobin (Hb) in this region. However, large-scale survey on the mol
Externí odkaz:
https://doaj.org/article/ad3758ef68fc462aa8a25c31aedcacff
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
BackgroundThalassemia is a common inherited hemoglobin disorder caused by a deficiency of one or more globin subunits. Substitution variants and deletions in the HBB gene are the major causes of β-thalassemia, of which large fragment deletions are r
Externí odkaz:
https://doaj.org/article/5d066a138d3d4ab4a83a8ee6763a5bfb
Akademický článek
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Autor:
Anna He, Cheng Fang, Yue Ming, He Tan, Mengyi Zhang, Ruiqing Zhang, Jingyi Li, Mingzhu Nie, Fengyu Li, Yaxin Hu, Xinxin Shen, Xiuge Rong, Xuejun Ma
Publikováno v:
Heliyon, Vol 8, Iss 11, Pp e11323- (2022)
Objective: Human papillomavirus (HPV) 6 and 11 are the two most common low-risk HPV subtypes, accounting for more than 90% of condyloma acuminatum. A simple, accurate and rapid screening method to be applied in community-level hospitals is in high de
Externí odkaz:
https://doaj.org/article/f92346cc7b474d139077f0f481a75948
Autor:
Guoxing Zhong, Zeyan Zhong, Zhiyang Guan, Dina Chen, Zhiyong Wu, Kunxiang Yang, Dan Chen, Yinyin Liu, Ruofan Xu, Jianhong Chen
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Thalassemia was the most common monogenic diseases worldwide, which was caused by mutations, deletions or duplications in human globin genes which disturbed the synthesis balance between α- and β-globin chains of hemoglobin. There were
Externí odkaz:
https://doaj.org/article/0563b26d05db44d38b669767cc815ab8
Autor:
Luis J. Sánchez-Martínez, Candela L. Hernández, Juan N. Rodríguez, Jean M. Dugoujon, Andrea Novelletto, Paloma Ropero, Luisa Pereira, Rosario Calderón
Publikováno v:
Annals of Human Biology, Vol 48, Iss 5, Pp 406-417 (2021)
Background Analyses of the genomic variation in the western Mediterranean population are being used to reveal its evolutionary history and to understand the molecular basis of particular diseases. Aim To observe the β-thalassemia mutational spectrum
Externí odkaz:
https://doaj.org/article/4a80fa9b0d5d48e4a36b6c12f85b3449
Autor:
Hanan Kamel M. Saad, Wan Rohani Wan Taib, Azly Sumanty Ab Ghani, Imilia Ismail, Futoon Abedrabbu Al-Rawashde, Belal Almajali, Maysa Alhawamdeh, Alawiyah Awang Abd Rahman, Abdullah Saleh Al-wajeeh, Hamid Ali Nagi Al-Jamal
Publikováno v:
Diagnostics, Vol 13, Iss 7, p 1247 (2023)
Background: β-thalassaemia is a disorder caused by mutations in the β-globin gene, leading to defective production of haemoglobins (Hb) and red blood cells (RBCs). It is characterised by anaemia, ineffective erythropoiesis, and iron overload. Patie
Externí odkaz:
https://doaj.org/article/02a0af964a2a4d96b6915aaf84db6309
Autor:
Korntip Srewaradachpisal, Wanicha Tepakhan, Sataron Kanjanaopas, Chawadee Nopparatana, Malai Wongchanchailert, Chamnong Nopparatana
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 38, Iss 3, Pp 221-229 (2020)
Objective: The aim of this study was to characterize unknown β-globin gene mutations in individuals who attended Songklanagarind Hospital for thalassemia screening and genetic counseling. Material and Methods: β-thalassemia mutations in individuals
Externí odkaz:
https://doaj.org/article/4026707a92314b8299dcca2669e741ce
Akademický článek
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Akademický článek
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