Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Sickled erythrocytes"'
Autor:
Allan Doctor, Jin-Moo Lee, Konstantin Maslov, Michael M. Binkley, Hsun-Chia Hsu, Lihong V. Wang, Stephen C. Rogers, Toru Imai, Andria L. Ford
Publikováno v:
Am J Hematol
Individuals with sickle cell disease (SCD) face ongoing risk of multi-organ ischemia resulting in chronic disability, frequent hospitalizations, and early mortality. The relationship between hemoglobin (Hb) S polymerization, erythrocyte sickling, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70e8d549ea25c0ed7628983b4de8b46a
https://resolver.caltech.edu/CaltechAUTHORS:20211201-171925356
https://resolver.caltech.edu/CaltechAUTHORS:20211201-171925356
Autor:
Adam R. Metwalli, Pamela Coleman, Chukwuka Ibecheozor, Geeta Ahuja, Nnaemeka C. Okorie, Anish Jain, Jeremy B. Tonkin
Publikováno v:
Urology. 156
Sickle cell disease (SCD) is an inherited medical condition where sickled red blood cells cause vaso-occlusive crisis. One major complication of SCD is priapism, defined as an erection of the penis lasting over four hours beyond sexual stimulation or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12efe30301dd286dbbccf0bbd188e21f
https://pubmed.ncbi.nlm.nih.gov/34181970
https://pubmed.ncbi.nlm.nih.gov/34181970
Publikováno v:
In vitro cellulardevelopmental biology. Animal. 56(9)
Sickle cell disease is a group of diseases inherited through the gene and it affects the haemoglobin in the red blood cell. This study investigated the methanol seed extract of Buchholzia coriacea for possible in vitro anti-sickling effects and also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0ac299decd31f54c8e9ac37f04cac63
https://pubmed.ncbi.nlm.nih.gov/33025340
https://pubmed.ncbi.nlm.nih.gov/33025340
Autor:
G O Asieba, Parvesh Singh, Neha Manhas, John A. Ajiboye, Ochuko L. Erukainure, Md. Shahidul Islam, Solomon A. Mamuru, Moses Z. Zaruwa, U A Abbah
Publikováno v:
Human & Experimental Toxicology. 37:458-467
The antioxidative effect of Monodora myristica seed acetone extract and its effect on chemical functional groups were investigated in sickled erythrocytes as well as molecular modeling of the antisickling potentials of its secondary metabolites. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd3bc475f2d5193d000cf84e5787c1b4
https://doi.org/10.1177/0960327117712385
https://doi.org/10.1177/0960327117712385
Autor:
Melina de Barros Pinheiro, Sílvia Letícia de Oliveira Toledo, Danyelle Romana Alves Rios, João Victor Marques Guedes, Patrícia Nessralla Alpoim
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 493
Sickle cell disease, the most common genetic blood disorder in the world, has high clinical variability, negatively impacts quality of life and contributes to early mortality. Sickled erythrocytes cause blood flow obstruction, hemolysis, and several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::071f134a77f2593b40fb5fdeadd90a97
https://pubmed.ncbi.nlm.nih.gov/30825426
https://pubmed.ncbi.nlm.nih.gov/30825426
Autor:
Laurel Mendelsohn, J. Philip McCoy, Kleber Yotsumoto Fertrin, Christine A. Brantner, James S. Nichols, Rehan Saiyed, Mathew P. Daniels, Leigh Samsel, Eduard J. van Beers, Gregory J. Kato
Publikováno v:
American Journal of Hematology. 89:598-603
In preclinical and early phase pharmacologic trials in sickle cell disease, the percentage of sickled erythrocytes after deoxygenation, an ex vivo functional sickling assay, has been used as a measure of a patient's disease outcome. We developed a ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3953cf810830ff1b8f2a8ff466145f9f
https://doi.org/10.1002/ajh.23699
https://doi.org/10.1002/ajh.23699
Publikováno v:
Bayero Journal of Pure and Applied Sciences. 11:255
Sickle cell anaemia is a hereditary disease affecting the red blood cells as a result of acquisition of a mutant β-globin gene, one from each parent. One of the pathophysiology of sickle cell anaemia is abnormally high concentration of methaemoglobi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e06e7817ea9318d5483210b3ca93442f
https://doi.org/10.4314/bajopas.v11i1.42s
https://doi.org/10.4314/bajopas.v11i1.42s
Akademický článek
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Publikováno v:
Scientifica
Scientifica, Vol 2016 (2016)
Scientifica, Vol 2016 (2016)
Background and Purpose. Traditional management of sickle cell disease (SCD) is ubiquitous in Africa. In south-eastern Nigeria,Telfairia occidentalis (T. occidentalis)is strongly recommended for consumption by SCD patients, owing to its presumed thera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::112906f2e0005d26d22aca5c3fa10fb9
http://europepmc.org/articles/PMC4940565
http://europepmc.org/articles/PMC4940565
Autor:
Nikisha Kothari, Amir Mohsenin
Publikováno v:
Manual of Retinal Diseases ISBN: 9783319204598
Mutations in the β-globin gene result in erythrocytes that undergo sickling in response to hypoxic, acidotic, and hyperosmolar conditions. Sickled erythrocytes are not pliable thereby resulting in mechanical occlusion of arterioles. Arteriolar occlu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::707d255e8afcbfd5db03be3e1a184a20
https://doi.org/10.1007/978-3-319-20460-4_69
https://doi.org/10.1007/978-3-319-20460-4_69