Zobrazeno 1 - 10
of 33 896
pro vyhledávání: '"hb"'
Autor:
Rosnah Bahar, Vasuhi Kalimuthu, Muhammad Farid Johan, Siti Zubaidah Mustapha, Zefarina Zulkafli
Publikováno v:
Liaquat National Journal of Primary Care, Vol 6, Iss 3, Pp 232-239 (2024)
Background: To date, more than 70 variants of non-deletional mutations associated with α-thalassaemia have been recognized and recorded, showcasing the diverse genetic manifestations of the condition. Objective: This study is to provide data on th
Externí odkaz:
https://doaj.org/article/27c141626c3a46919d0d28d5fed63840
Autor:
Gorwa, Robert, author
Publikováno v:
The Politics of Platform Regulation : How Governments Shape Online Content Moderation, 2024.
Externí odkaz:
https://doi.org/10.1093/oso/9780197692851.003.0007
Autor:
Maha Abubakr Feissal Rabie, Sanaa A. El Benhawy, Inas M. Masoud, Amal R. R. Arab, Sally A. M. Saleh
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Transfusion dependent β-thalassemia is a genetic blood disorder characterized by chronic anaemia. Blood transfusion is lifesaving but comes at a cost. Iron overload emerges as a prime culprit as a free radicals damage endothelial cells. Chr
Externí odkaz:
https://doaj.org/article/eeba722e55094f11bc777d3ae0974f89
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Background Third-generation sequencing (TGS) based on long-read technology has been gradually used in identifying thalassemia and hemoglobin (Hb) variants. The aim of the present study was to explore genotype varieties of thalassemia and Hb
Externí odkaz:
https://doaj.org/article/6cd02a5d73b14364846fb5cb66220500
Publikováno v:
Journal of Blood Medicine, Vol Volume 15, Pp 255-264 (2024)
Roszymah Hamzah,1 Ahmad Sabry Mohamad,2 Norafiza Mohd Yasin,3 Ezalia Esa,3 Guo Chen,4 Veena Selvaratnam1 1Hematology Department, Ampang Hospital, Ampang, Selangor, Malaysia; 2Medical Engineering, Universiti Kuala Lumpur-British Malaysian Institute, G
Externí odkaz:
https://doaj.org/article/bf98c391d1a44d00a78bdf1d0d364e63
Autor:
Ajia Sha, Bingliang Liu, Changying Liu, Qizhong Sun, Mingxing Chen, Lianxin Peng, Liang Zou, Changsong Zhao, Qiang Li
Publikováno v:
Ecotoxicology and Environmental Safety, Vol 288, Iss , Pp 117379- (2024)
This study is the first to use highland barley (HB) to study the toxic effects of Cr (VI) on seedlings and the response mechanism of HELNs to Cr (VI) stress. The outcomes indicated that the germination rate of HB seeds, plant height, root length, wat
Externí odkaz:
https://doaj.org/article/6355af0616554908bd0eefe484cf5b4d
Autor:
Jian-lian Liang, Yi-yuan Ge, Jing-wei Situ, Jin-xiu Yao, Jin-ling Chen, Long-xu Xie, Li-ye Yang
Publikováno v:
Hematology, Vol 29, Iss 1 (2024)
Objective To summarize and analyze the clinical characteristics of the Hb Phnom Penh (HBA1:c.354_355insATC) variant in the Chinese population, and to guide clinical diagnosis and genetic counseling for hemoglobin disorders.Methods Peripheral blood sa
Externí odkaz:
https://doaj.org/article/6895606d791a43cdb7fa553a0c13a0ba
Autor:
Rawand P. Shamoon, Amir Charkaneh, Elena Di Pierro, Milena Irrera, Cristina Curcio, Ahmed Yassin, Rozhgar A. Khailany
Publikováno v:
Hematology, Vol 29, Iss 1 (2024)
Background Thalassemias are genetic disorders of globin chain synthesis. In Iraq, β-thalassemia is more prevalent than α-thalassemia. This study identifies two unpredicted globin gene mutations, a rare α-globin gene mutation (Hb SKMC) and a novel
Externí odkaz:
https://doaj.org/article/cb6c7b1af1674f8286969f500083ff2d
Publikováno v:
Physiological Reports, Vol 12, Iss 22, Pp n/a-n/a (2024)
Abstract This study investigates hemoglobin (Hb)‐induced kidney injury and the protective role of the ApoHemoglobin‐Haptoglobin (ApoHb‐Hp) complex against heme and Hb damage. Hb facilitates oxygen (O2) delivery but poses challenges outside red
Externí odkaz:
https://doaj.org/article/9f7741f53fdc49e38b4b17e08f1ac500
Publikováno v:
Practical Laboratory Medicine, Vol 42, Iss , Pp e00438- (2024)
Objective: Presentation of a novel case of a patient with Hb Bart's hydrops fetalis, which was accurately identified by SMRT sequencing leading to expand the mutation spectrum of α-thalassemia. Case report: A 26-year-old pregnant woman and her husba
Externí odkaz:
https://doaj.org/article/d64ab6c93ca84aa586d00b520edd0837