Zobrazeno 1 - 10
of 4 719
pro vyhledávání: '"β–thalassemia"'
Publikováno v:
Arab Gulf Journal of Scientific Research, 2023, Vol. 42, Issue 3, pp. 714-721.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/AGJSR-01-2023-0016
Publikováno v:
Jichu yixue yu linchuang, Vol 44, Iss 12, Pp 1633-1637 (2024)
Objective To investigate the differential expression of miR-124-3p in peripheral blood and clinical significance of patients with β-thalassemia. Methods Peripheral blood samples were collected from 33 patients with β-thalassemia and 30 healthy cont
Externí odkaz:
https://doaj.org/article/3785bf868d9f4edd8e0928e64c8ce214
Publikováno v:
Therapeutics and Clinical Risk Management, Vol Volume 20, Pp 799-809 (2024)
Wei-Jia Yang,1,* Lian-dong Shi,2,* Ye Liang,3,* Li-ming Liang,4,* Hao Zhang,5 Li Wang,2 Qian Zhou1 1Department of Eugenics and Genetics, Guilin People’s Hospital, Guilin, Guangxi Zhuang Autonomous Region, 541002, People’s Republic
Externí odkaz:
https://doaj.org/article/bc16cbb0d0d64b23a8bbf1243a6fe2fe
Autor:
Diana Hanna, Mervat Atfy, Ashraf Bor’i, Marwa Elsayed, Eman Mohamed Abd el-Sattar, Dalia Gameil
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-10 (2024)
Abstract Background Beta thalassemia major is an inherited blood disorder due to a mutation of the β globin chain gene. Ocular complications have increasingly been reported in β-thalassemia patients with a negative influence on the health related q
Externí odkaz:
https://doaj.org/article/5c74fa2b7901454abc35b34f4a22e848
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
Autor:
Shirui Chen, Yueyue Liu, Xiaolin Yin, Quanyi Lu, Xiangzhou Du, Rong Huang, Yu Jia, Xin Wang, Xiaoyu Xi
Publikováno v:
BMC Health Services Research, Vol 24, Iss 1, Pp 1-13 (2024)
Abstract Background Transfusion-dependent β-thalassemia (TDT) is one of the global public health concerns highlighted by the World Health Organization. Patients with TDT require regular blood transfusion to survive. However, the availability of bloo
Externí odkaz:
https://doaj.org/article/713f67c258c7459a93439ac088d7de3b
Publikováno v:
Frontiers in Nutrition, Vol 11 (2024)
BackgroundTransfusion-dependent β-thalassemia (TDT) is a hereditary blood disorder that often leads to complications affecting growth, nutritional status, and muscle mass in children. This study aims to investigate the associations between age, nutr
Externí odkaz:
https://doaj.org/article/75e268cbdb4a48679db8492194ca0303
Publikováno v:
Molecular Medicine, Vol 30, Iss 1, Pp 1-14 (2024)
Abstract The oncofetal mRNA-binding protein IGF2BP1 belongs to a conserved family of RNA-binding proteins. It primarily promotes RNA stability, regulates translation and RNA localization, and mediates gene expression through its downstream effectors.
Externí odkaz:
https://doaj.org/article/e433a9fdbc244d6881f7ad5489603a5f
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-5 (2024)
Abstract Background Posterior reversible encephalopathy syndrome (PRES) is a neurotoxic condition associated with a distinctive brain imaging pattern which typically occur in some complex clinical conditions. However, the leading offender to this con
Externí odkaz:
https://doaj.org/article/fe6dacad1c924641956d0a07dcc211ac
Publikováno v:
Thalassemia Reports, Vol 14, Iss 3, Pp 49-59 (2024)
β-thalassemia, a life-threatening inheritable hemoglobin disorder caused by mutations in the HBB gene, poses a significant public health challenge in the world. Although no comprehensive work has been carried out in Bangladesh, the world prevalence
Externí odkaz:
https://doaj.org/article/551d73b7344643069c5712c3c306e954