Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rasiqh Wadud"'
Autor:
Md. Mahbubur Rahman, Rupali Rani Chakraborti, Md. Abdullah Potol, Ariful Haque Abir, Ozayra Sharmin, Mahabub Alam, Md. Fazlur Rahman Khan, Rownock Afrin, Humayra Jannat, Rasiqh Wadud, Zaki Farhad Habib
Publikováno v:
Animal Models and Experimental Medicine, Vol 3, Iss 1, Pp 9-21 (2020)
Abstract Background Parkinson's disease (PD) is a progressive neurodegenerative disorder affecting a large number of elderly people worldwide. The current therapies for PD are symptom‐based; they do not provide a cure but improve the quality of lif
Externí odkaz:
https://doaj.org/article/ba87921c01514a7ab01831c3448eacd2
Autor:
David C.-Y. Lu, Rasiqh Wadud, Anke Hannemann, David C. Rees, John N. Brewin, John Stanley Gibson
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Red cells from patients with sickle cell anaemia (SCA) contain the abnormal haemoglobin HbS. Under hypoxic conditions, HbS polymerises and causes red cell sickling, a rise in intracellular Ca2+ and exposure of phosphatidylserine (PS). These changes m
Externí odkaz:
https://doaj.org/article/ebe75d5e74ca4d73a1ce09566d93a87d
Autor:
A. F. M. Towheedur Rahman, Ariful Haque Abir, Jewel Banik, Nuzhat Tarannum, Abdullah Potol, Mahbubur Rahman, Ozayra Sharmin, Rasiqh Wadud, Zaki F. Habib, Mahabub Alam
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Pamoic acid is a potent ligand for G protein Coupled Receptor 35 (GPR35) and exhibits antinociceptive property. GPR35 activation leads to increased energy utilization and the expression of anti-inflammatory genes. However, its role in brain disorders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac0a4d8795750f5f53a8b131c4ce52e2
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Frontiers in Physiology
Frontiers in Physiology
Red cells from patients with sickle cell anaemia (SCA) contain the abnormal haemoglobin HbS. Under hypoxic conditions, HbS polymerises and causes red cell sickling, a rise in intracellular Ca2+ and exposure of phosphatidylserine (PS). These changes m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29d819691c4eaf9af195d22ab9c53435
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Scientific Reports
Scientific Reports
Phosphatidylserine (PS) exposure is increased in red cells from sickle cell anaemia (SCA) patients. Externalised PS is prothrombotic and attractive to phagocytes and activated endothelial cells and thus contributes to the anaemic and ischaemic compli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d43151d39b627508d9769313d1f8d393
Autor:
John S. Gibson, Anke Hannemann, Rasiqh Wadud, David C. Rees, David C.-Y. Lu, John N. Brewin, Philip S. Low
Publikováno v:
Pflugers Archiv
Abnormal activity of red cell KCl cotransport (KCC) is involved in pathogenesis of sickle cell anaemia (SCA). KCC-mediated solute loss causes shrinkage, concentrates HbS, and promotes HbS polymerisation. Red cell KCC also responds to various stimuli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04dc52fd818626a922f33e9c3987a921