Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Keri Oxendine, Harp"'
Autor:
Justin J. Thomas, Keri Oxendine Harp, Alaijah Bashi, Joshua L. Hood, Felix Botchway, Michael D. Wilson, Winston E. Thompson, Jonathan K. Stiles, Adel Driss
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Hemolysis is associated with many pathologies, including trauma, sepsis, hemorrhagic stroke, malaria, and genetic disorders such as sickle cell disease (SCD). When hemolysis occurs, free-heme drives vascular inflammation, resulting in oxidative tissu
Externí odkaz:
https://doaj.org/article/e8c37e4f126b4229a63da5b737918a56
Autor:
Adriana Harbuzariu, Annette Nti, Keri Oxendine Harp, Juan C. Cespedes, Adel Driss, Jonathan K. Stiles
Publikováno v:
iScience, Vol 25, Iss 6, Pp 104407- (2022)
Summary: Human cerebral malaria (HCM) is a severe complication of Plasmodium falciparum (P.f.) infection that is characterized by capillary occlusions, rupture of the blood-brain barrier (BBB), perivascular cellular injury, and brain swelling. P.f.hi
Externí odkaz:
https://doaj.org/article/614beb3c118f4e97a27a715fe28270a5
Autor:
Keri Oxendine Harp, Felix Botchway, Yvonne Dei-Adomakoh, Michael D. Wilson, Mohamed Mubasher, Andrew A. Adjei, Winston E. Thompson, Jonathan K. Stiles, Adel Driss
Publikováno v:
EClinicalMedicine, Vol 39, Iss , Pp 101045- (2021)
Background: Sickle cell anemia (SCA) is a severe monogenic disorder, caused by single nucleotide mutations in the hemoglobin (Hb) gene, that is prevalent in malaria endemic regions of the world. Sickle cell trait (SCT) individuals carry only one of t
Externí odkaz:
https://doaj.org/article/4a6811c384ed4a8c988f1a1a159402f8
Autor:
Christopher Chambliss, Tatayana Richardson, John Onyekaba, Juan Cespedes, Annette Nti, Keri Oxendine Harp, Iris Buchanan-Perry, Jonathan K. Stiles, Beatrice E. Gee
Publikováno v:
Endocrine and Metabolic Science, Vol 3, Iss , Pp 100088- (2021)
ABSTRACT: Stroke, or cerebral infarction, is one of the most serious complications of sickle cell anemia (SCA) in childhood, potentially leading to impaired development and life-long physical and cognitive disabilities. About one in ten children with
Externí odkaz:
https://doaj.org/article/c8fd888f066c4a0ea969398e6965fd8c
Autor:
Keri Oxendine Harp, Felix Botchway, Yvonne Dei-Adomakoh, Michael D. Wilson, Joshua L. Hood, Andrew A. Adjei, Jonathan K. Stiles, Adel Driss
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
In 2018, 228 million cases and 405,000 malaria-associated deaths were reported worldwide with a majority being in Africa. A wide range of factors, including parasitemia, host immunity, inflammatory responses to infection, and host hemoglobin genotype
Externí odkaz:
https://doaj.org/article/8ff6d80ac58d4010bc679e1f43218877
Autor:
Christopher, Chambliss, Tatayana, Richardson, John, Onyekaba, Juan, Cespedes, Annette, Nti, Keri Oxendine, Harp, Iris, Buchanan-Perry, Jonathan K, Stiles, Beatrice E, Gee
Publikováno v:
Endocrine and metabolic science. 3
Stroke, or cerebral infarction, is one of the most serious complications of sickle cell anemia (SCA) in childhood, potentially leading to impaired development and life-long physical and cognitive disabilities. About one in ten children with SCA are a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::166e3c7b8ce0b54040fe333953a1311b
https://pubmed.ncbi.nlm.nih.gov/35935682
https://pubmed.ncbi.nlm.nih.gov/35935682
Autor:
Keri Oxendine Harp, Alaijah Bashi, Felix Botchway, Yvonne Dei-Adomakoh, Shareen A. Iqbal, Michael D. Wilson, Andrew A. Adjei, Jonathan K. Stiles, Adel Driss
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 500, p 500 (2022)
Journal of Clinical Medicine; Volume 11; Issue 3; Pages: 500
Journal of Clinical Medicine; Volume 11; Issue 3; Pages: 500
Sickle cell disease (SCD) occurs when two alleles of mutated hemoglobin (HbS or HbC) are inherited (HbSS and HbSC) rather than one (HbAS or HbAC), which indicates a person carries the sickle cell trait. The high prevalence of these two alleles in Afr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8396da83279560c46225fb72dcde9cfd
https://pubmed.ncbi.nlm.nih.gov/35159951
https://pubmed.ncbi.nlm.nih.gov/35159951
Autor:
Andrew A. Adjei, Michael D. Wilson, Jonathan K. Stiles, Winston E. Thompson, Yvonne Dei-Adomakoh, Felix Botchway, Keri Oxendine Harp, Mohamed Mubasher, Adel Driss
Publikováno v:
EClinicalMedicine
EClinicalMedicine, Vol 39, Iss, Pp 101045-(2021)
EClinicalMedicine, Vol 39, Iss, Pp 101045-(2021)
Background: Sickle cell anemia (SCA) is a severe monogenic disorder, caused by single nucleotide mutations in the hemoglobin (Hb) gene, that is prevalent in malaria endemic regions of the world. Sickle cell trait (SCT) individuals carry only one of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0158cf7f526f3eefb09b11ccca8d107a
http://europepmc.org/articles/PMC8342910
http://europepmc.org/articles/PMC8342910
Autor:
Juan Carlos Cespedes, Keri Oxendine Harp, Christopher Chambliss, Iris Buchanan-Perry, Jonathan K. Stiles, Beatrice E. Gee, Annette Nti, Tatayana Richardson, John Onyekaba
Publikováno v:
Endocrine and Metabolic Science, Vol 3, Iss, Pp 100088-(2021)
Stroke, or cerebral infarction, is one of the most serious complications of sickle cell anemia (SCA) in childhood, potentially leading to impaired development and life-long physical and cognitive disabilities. About one in ten children with SCA are a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a15a6930820d0fe47736f06c1106d739
http://www.sciencedirect.com/science/article/pii/S266639612100011X
http://www.sciencedirect.com/science/article/pii/S266639612100011X
Autor:
Adriana, Harbuzariu, Annette, Nti, Keri Oxendine, Harp, Juan C, Cespedes, Adel, Driss, Jonathan K, Stiles
Publikováno v:
iScience. 25(6)
Human cerebral malaria (HCM) is a severe complication of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f0e8d06a30c9921d6b59922c8035d33b
https://pubmed.ncbi.nlm.nih.gov/35663028
https://pubmed.ncbi.nlm.nih.gov/35663028