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Wyszukujesz frazę ""Sickle cell trait"" wg kryterium: Temat


Tytuł :
Membrane protein carbonylation of Plasmodium falciparum infected erythrocytes under conditions of sickle cell trait and G6PD deficiency.
Autorzy :
Contreras-Puentes N; Analytical Chemistry and Biomedicine Group, Exact and Natural Sciences Faculty, University of Cartagena, Cartagena, Colombia.
Rodríguez-Cavallo E; Analytical Chemistry and Biomedicine Group, Pharmaceutical Sciences Faculty, University of Cartagena, Cartagena, Colombia.
Méndez-Cuadro D; Analytical Chemistry and Biomedicine Group, Exact and Natural Sciences Faculty, University of Cartagena, Cartagena, Colombia. Electronic address: .
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Źródło :
Molecular and biochemical parasitology [Mol Biochem Parasitol] 2019 Jan; Vol. 227, pp. 5-14. Date of Electronic Publication: 2018 Nov 22.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Erythrocytes/*parasitology
Glucosephosphate Dehydrogenase Deficiency/*blood
Malaria, Falciparum/*blood
Membrane Proteins/*metabolism
Plasmodium falciparum/*metabolism
Sickle Cell Trait/*blood
Erythrocyte Membrane/metabolism ; Erythrocyte Membrane/parasitology ; Erythrocytes/enzymology ; Erythrocytes/metabolism ; Glucosephosphate Dehydrogenase Deficiency/metabolism ; Glucosephosphate Dehydrogenase Deficiency/parasitology ; Humans ; Malaria, Falciparum/metabolism ; Malaria, Falciparum/parasitology ; Oxidation-Reduction ; Oxidative Stress ; Plasmodium falciparum/genetics ; Protein Carbonylation ; Sickle Cell Trait/metabolism ; Sickle Cell Trait/parasitology
Czasopismo naukowe
Tytuł :
Sickle Cell Trait Induces Oxidative Damage on Plasmodium falciparum Proteome at Erythrocyte Stages.
Autorzy :
Díaz-Castillo A; Analytical Chemistry and Biomedicine Group, Exacts and Natural Sciences Faculty, University of Cartagena, 130015 Cartagena, Colombia.
Contreras-Puentes N; Analytical Chemistry and Biomedicine Group, Pharmaceuticals Sciences Faculty, University of Cartagena, 130015 Cartagena, Colombia.
Alvear-Sedán C; Biochemistry and disease Group, Medicine School, University of Cartagena, 130015 Cartagena, Colombia.
Moneriz-Pretell C; Biochemistry and disease Group, Medicine School, University of Cartagena, 130015 Cartagena, Colombia.
Rodríguez-Cavallo E; Analytical Chemistry and Biomedicine Group, Pharmaceuticals Sciences Faculty, University of Cartagena, 130015 Cartagena, Colombia.
Mendez-Cuadro D; Analytical Chemistry and Biomedicine Group, Exacts and Natural Sciences Faculty, University of Cartagena, 130015 Cartagena, Colombia.
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Źródło :
International journal of molecular sciences [Int J Mol Sci] 2019 Nov 16; Vol. 20 (22). Date of Electronic Publication: 2019 Nov 16.
Typ publikacji :
Journal Article
MeSH Terms :
Erythrocytes/*metabolism
Plasmodium falciparum/*growth & development
Proteome/*analysis
Sickle Cell Trait/*pathology
Electrophoresis, Polyacrylamide Gel ; Erythrocytes/parasitology ; Hemoglobin A/chemistry ; Hemoglobin A/metabolism ; Hemoglobin, Sickle/chemistry ; Hemoglobin, Sickle/metabolism ; Humans ; Life Cycle Stages ; Oxidative Stress ; Plasmodium falciparum/metabolism ; Plasmodium falciparum/pathogenicity ; Protein Carbonylation ; Proteome/metabolism ; Protozoan Proteins/analysis ; Protozoan Proteins/metabolism ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Czasopismo naukowe
Tytuł :
The rationale for abandoning sickle trait screening of red blood cell units for patients with sickle cell disease.
Autorzy :
Aneke J; Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.; Faculty of Medicine, Nnamdi Azikiwe University, Awka, Nigeria.
Barth D; Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Ward R; Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Pendergrast J; Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Kuo K; Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Cserti-Gazdewich C; Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
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Źródło :
Transfusion medicine (Oxford, England) [Transfus Med] 2019 Dec; Vol. 29 (6), pp. 466-467. Date of Electronic Publication: 2019 May 16.
Typ publikacji :
Letter
MeSH Terms :
Donor Selection*
Erythrocytes*
Mass Screening*
Sickle Cell Trait/*blood
Commission on Professional and Hospital Activities ; Female ; Humans ; Male ; Ontario
Opinia redakcyjna
Tytuł :
Atomic force microscopy: From red blood cells to immunohaematology.
Autorzy :
Yeow N; Bioresource Processing Research Institute Australia (BioPRIA), Department of Chemical Engineering, Monash University, Clayton, VIC 3800, Australia.
Tabor RF; School of Chemistry, Monash University, Clayton, VIC 3800, Australia.. Electronic address: .
Garnier G; Bioresource Processing Research Institute Australia (BioPRIA), Department of Chemical Engineering, Monash University, Clayton, VIC 3800, Australia. Electronic address: .
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Źródło :
Advances in colloid and interface science [Adv Colloid Interface Sci] 2017 Nov; Vol. 249, pp. 149-162. Date of Electronic Publication: 2017 May 11.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Coronary Artery Disease/*pathology
Diabetes Mellitus/*pathology
Erythrocytes/*ultrastructure
Hypertension/*pathology
Malaria, Falciparum/*pathology
Sickle Cell Trait/*pathology
Antibodies/metabolism ; Blood Group Antigens/analysis ; Blood Proteins/immunology ; Blood Proteins/metabolism ; Cell Shape ; Coronary Artery Disease/diagnosis ; Coronary Artery Disease/immunology ; Diabetes Mellitus/diagnosis ; Diabetes Mellitus/immunology ; Elasticity ; Humans ; Hypertension/diagnosis ; Hypertension/immunology ; Malaria, Falciparum/diagnosis ; Malaria, Falciparum/immunology ; Malaria, Falciparum/parasitology ; Microscopy, Atomic Force ; Protein Binding ; Sickle Cell Trait/diagnosis ; Sickle Cell Trait/immunology ; Surface Properties
Czasopismo naukowe
Tytuł :
Human red blood cell polymorphisms prevalent in Colombian population and its protective role against malaria.
Autorzy :
Contreras N; University of Cartagena, Zaragocilla Campus, Cartagena, Colombia; Corporation Universitary Rafael Nuñez, Faculty of Medicine. Centro Clle de la Soledad, Cartagena, Colombia. Electronic address: .
Alvíz A; University of Cartagena, Zaragocilla Campus, Cartagena, Colombia. Electronic address: .
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Źródło :
Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine [Transfus Clin Biol] 2019 Feb; Vol. 26 (1), pp. 60-68. Date of Electronic Publication: 2018 Aug 10.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Erythrocytes/*parasitology
Glucosephosphate Dehydrogenase Deficiency/*genetics
Malaria/*epidemiology
Sickle Cell Trait/*genetics
Adaptation, Physiological/genetics ; Colombia/epidemiology ; Humans ; Malaria/genetics ; Mutation ; Polymorphism, Genetic ; Prevalence
Czasopismo naukowe
Tytuł :
Anemia Offers Stronger Protection Than Sickle Cell Trait Against the Erythrocytic Stage of Falciparum Malaria and This Protection Is Reversed by Iron Supplementation.
Autorzy :
Goheen MM; Department of Microbiology and Immunology, University of North Carolina School of Medicine, CB# 7435, Chapel Hill, NC 27599-7435, USA. Electronic address: .
Wegmüller R; MRC Unit The Gambia, MRC International Nutrition Group, Keneba, P.O. Box 273, Banjul, Gambia.
Bah A; MRC Unit The Gambia, MRC International Nutrition Group, Keneba, P.O. Box 273, Banjul, Gambia.
Darboe B; MRC Unit The Gambia, MRC International Nutrition Group, Keneba, P.O. Box 273, Banjul, Gambia.
Danso E; MRC Unit The Gambia, MRC International Nutrition Group, Keneba, P.O. Box 273, Banjul, Gambia.
Affara M; MRC Unit The Gambia, MRC International Nutrition Group, Keneba, P.O. Box 273, Banjul, Gambia.
Gardner D; University of North Carolina School of Medicine, CB# 9535, Chapel Hill, NC 27599-9535, USA.
Patel JC; Department of Epidemiology, University of North Carolina Gillings School of Global Public Health, CB# 7435, Chapel Hill, NC 27599-7435, USA.
Prentice AM; MRC Unit The Gambia, MRC International Nutrition Group, Keneba, P.O. Box 273, Banjul, Gambia; London School of Hygiene & Tropical Medicine, Keppel Street, WC1E 7HT London, UK.
Cerami C; MRC Unit The Gambia, MRC International Nutrition Group, Keneba, P.O. Box 273, Banjul, Gambia.
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Źródło :
EBioMedicine [EBioMedicine] 2016 Dec; Vol. 14, pp. 123-130. Date of Electronic Publication: 2016 Nov 09.
Typ publikacji :
Journal Article
MeSH Terms :
Dietary Supplements*
Anemia/*complications
Anemia/*drug therapy
Erythrocytes/*parasitology
Iron/*administration & dosage
Malaria, Falciparum/*etiology
Malaria, Falciparum/*prevention & control
Sickle Cell Trait/*complications
Anemia/etiology ; Anemia/metabolism ; Biomarkers ; Child, Preschool ; Disease Susceptibility ; Female ; Genotype ; Humans ; Infant ; Iron/metabolism ; Malaria, Falciparum/epidemiology ; Malaria, Falciparum/metabolism ; Male ; Plasmodium falciparum/growth & development ; Population Surveillance ; Sickle Cell Trait/genetics ; Sickle Cell Trait/metabolism
Czasopismo naukowe
Tytuł :
Sickle Cell Trait Increases Red Blood Cell Storage Hemolysis and Post-Transfusion Clearance in Mice.
Autorzy :
Osei-Hwedieh DO; Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA, United States; Department of Molecular Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, PA, United States.
Kanias T; Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA, United States.
Croix CS; Center for Biologic Imaging, University of Pittsburgh, Pittsburgh, PA, United States.
Jessup M; Center for Biologic Imaging, University of Pittsburgh, Pittsburgh, PA, United States.
Xiong Z; Division of Pulmonary, Allergy and Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Sinchar D; Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA, United States.
Franks J; Center for Biologic Imaging, University of Pittsburgh, Pittsburgh, PA, United States.
Xu Q; Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA, United States.
M Novelli E; Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA, United States.
Sertorio JT; Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA, United States.
Potoka K; Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA, United States.
Binder RJ; Department of Immunology, University of Pittsburgh, Pittsburgh, PA, United States.
Basu S; Department of Physics, Wake Forest University, Winston-Salem, NC, United States.
Belanger AM; Department of Physics, Wake Forest University, Winston-Salem, NC, United States.
Kim-Shapiro DB; Department of Physics, Wake Forest University, Winston-Salem, NC, United States.
Triulzi D; Institute for Transfusion Medicine, ITxM, Pittsburgh, PA, United States.
Lee JS; Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA, United States; Division of Pulmonary, Allergy and Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, United States. Electronic address: .
Gladwin MT; Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA, United States; Division of Pulmonary, Allergy and Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, United States; Department of Molecular Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, PA, United States. Electronic address: .
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Źródło :
EBioMedicine [EBioMedicine] 2016 Sep; Vol. 11, pp. 239-248. Date of Electronic Publication: 2016 Aug 04.
Typ publikacji :
Journal Article
MeSH Terms :
Blood Preservation*/adverse effects
Erythrocyte Transfusion*
Hemolysis*
Erythrocytes/*metabolism
Sickle Cell Trait/*blood
Animals ; Clodronic Acid/pharmacology ; Clodronic Acid/therapeutic use ; Disease Models, Animal ; Erythrocytes/pathology ; Erythrocytes/ultrastructure ; Erythrocytes, Abnormal/ultrastructure ; Female ; Hemoglobin A/genetics ; Hemoglobin A/metabolism ; Humans ; Male ; Mice ; Mice, Transgenic ; Osmotic Fragility/genetics ; Sickle Cell Trait/mortality ; Sickle Cell Trait/therapy ; Splenectomy
Czasopismo naukowe
Tytuł :
Associations between erythrocyte polymorphisms and risks of uncomplicated and severe malaria in Ugandan children: A case control study.
Autorzy :
Mpimbaza A; Child Health and Development Centre, Makerere University-College of Health Sciences, Kampala, Uganda.
Walakira A; Infectious Diseases Research Collaboration, Kampala, Uganda.
Ndeezi G; Department of Pediatrics and Child Health, Makerere University-College of Health Sciences, Kampala, Uganda.
Katahoire A; Child Health and Development Centre, Makerere University-College of Health Sciences, Kampala, Uganda.
Karamagi C; Department of Pediatrics and Child Health, Makerere University-College of Health Sciences, Kampala, Uganda.; Clinical Epidemiology Unit, Department of Medicine, Makerere University-College of Health Sciences, Kampala, Uganda.
Nsobya SL; Infectious Diseases Research Collaboration, Kampala, Uganda.
Tukwasibwe S; Infectious Diseases Research Collaboration, Kampala, Uganda.
Asua V; Infectious Diseases Research Collaboration, Kampala, Uganda.
Rosenthal PJ; Department of Medicine, University of California, San Francisco, CA, United States of America.
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Źródło :
PloS one [PLoS One] 2018 Sep 17; Vol. 13 (9), pp. e0203229. Date of Electronic Publication: 2018 Sep 17 (Print Publication: 2018).
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Erythrocytes/*metabolism
Erythrocytes/*pathology
Malaria/*blood
Malaria/*complications
Case-Control Studies ; Child ; Child, Preschool ; Female ; Genotype ; Glucosephosphate Dehydrogenase Deficiency/blood ; Glucosephosphate Dehydrogenase Deficiency/complications ; Glucosephosphate Dehydrogenase Deficiency/genetics ; Hemoglobins, Abnormal/genetics ; Humans ; Infant ; Malaria/genetics ; Male ; Phenotype ; Polymorphism, Genetic ; Risk Factors ; Sickle Cell Trait/blood ; Sickle Cell Trait/complications ; Sickle Cell Trait/genetics ; Uganda ; alpha-Thalassemia/blood ; alpha-Thalassemia/complications ; alpha-Thalassemia/genetics
Czasopismo naukowe
Tytuł :
Cellular function reinstitution of offspring red blood cells cloned from the sickle cell disease patient blood post CRISPR genome editing.
Autorzy :
Wen J; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Tao W; Department of Leukemia, The University of Texas M.D. Anderson Cancer Center, Houston, TX, 77030, USA.
Hao S; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Zu Y; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston Methodist Research Institute, Houston, TX, 77030, USA. .
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Źródło :
Journal of hematology & oncology [J Hematol Oncol] 2017 Jun 13; Vol. 10 (1), pp. 119. Date of Electronic Publication: 2017 Jun 13.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
CRISPR-Cas Systems*
Anemia, Sickle Cell/*genetics
Anemia, Sickle Cell/*therapy
Erythrocytes/*metabolism
Gene Editing/*methods
Hematopoietic Stem Cells/*metabolism
Anemia, Sickle Cell/pathology ; Antigens, CD34/analysis ; Cell Line ; Cells, Cultured ; Clustered Regularly Interspaced Short Palindromic Repeats ; Erythrocytes/cytology ; Erythrocytes/pathology ; Erythroid Cells/cytology ; Erythroid Cells/metabolism ; Erythroid Cells/pathology ; Erythropoiesis ; Genetic Therapy/methods ; Genotype ; Hematopoietic Stem Cells/cytology ; Hematopoietic Stem Cells/pathology ; Hemoglobin, Sickle/analysis ; Hemoglobin, Sickle/genetics ; Hemoglobins/analysis ; Hemoglobins/genetics ; Humans ; Sickle Cell Trait/genetics ; Sickle Cell Trait/pathology
Czasopismo naukowe
Tytuł :
Individual variability in response to a single sickling event for normal, sickle cell, and sickle trait erythrocytes.
Autorzy :
Tarasev M; Blaze Medical Devices, Ann Arbor, Mich. Electronic address: .
Muchnik M; Blaze Medical Devices, Ann Arbor, Mich.
Light L; Ontario HIV Treatment Network, Toronto, Ontario, Canada.
Alfano K; Blaze Medical Devices, Ann Arbor, Mich.
Chakraborty S; Blaze Medical Devices, Ann Arbor, Mich.
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Źródło :
Translational research : the journal of laboratory and clinical medicine [Transl Res] 2017 Mar; Vol. 181, pp. 96-107. Date of Electronic Publication: 2016 Sep 23.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Anemia, Sickle Cell/*pathology
Erythrocytes/*pathology
Sickle Cell Trait/*pathology
Adult ; Area Under Curve ; Cell Hypoxia ; Female ; Humans ; Male
Czasopismo naukowe
Tytuł :
α-Thalassemia does not seem to influence erythrocyte deformability in sickle cell trait carriers.
Autorzy :
Vayá A; Haemorheology and Haemostasis Unit, Service of Clinical Pathology, La Fe University Hospital , Valencia , Spain .
Collado S
Alis R
Vera B
Romagnoli M
Barragán E
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Źródło :
Hemoglobin [Hemoglobin] 2014; Vol. 38 (3), pp. 165-8. Date of Electronic Publication: 2014 Mar 07.
Typ publikacji :
Clinical Trial; Comparative Study; Journal Article
MeSH Terms :
Erythrocyte Deformability*
Erythrocytes/*metabolism
Sickle Cell Trait/*metabolism
alpha-Thalassemia/*metabolism
Adult ; Amino Acid Substitution ; Erythrocyte Indices ; Erythrocytes/pathology ; Female ; Hemoglobin, Sickle/genetics ; Hemoglobin, Sickle/metabolism ; Humans ; Male ; Middle Aged ; Mutation, Missense ; Sickle Cell Trait/genetics ; Sickle Cell Trait/pathology ; alpha-Thalassemia/genetics ; alpha-Thalassemia/pathology
Czasopismo naukowe
Tytuł :
Mechanical differences of sickle cell trait (SCT) and normal red blood cells.
Autorzy :
Zheng Y; Department of Mechanical and Industrial Engineering, University of Toronto, Toronto, ON, Canada. .
Cachia MA
Ge J
Xu Z
Wang C
Sun Y
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Źródło :
Lab on a chip [Lab Chip] 2015 Aug 07; Vol. 15 (15), pp. 3138-46.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Erythrocytes/*physiology
Sickle Cell Trait/*physiopathology
Humans ; Microfluidic Analytical Techniques/instrumentation ; Shear Strength ; Viscosity
Czasopismo naukowe
Tytuł :
Prevalence of classic erythrocyte polymorphisms among 749 children in southern highland Rwanda.
Autorzy :
Gahutu JB; Butare University Teaching Hospital, Faculty of Medicine, National University of Rwanda, P. O. Box 264, Butare, Rwanda.
Musemakweri A
Harms G
Mockenhaupt FP
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Źródło :
Transactions of the Royal Society of Tropical Medicine and Hygiene [Trans R Soc Trop Med Hyg] 2012 Jan; Vol. 106 (1), pp. 63-5. Date of Electronic Publication: 2011 Oct 20.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Erythrocytes*
Polymorphism, Genetic*
Glucosephosphate Dehydrogenase Deficiency/*genetics
Malaria/*genetics
Sickle Cell Trait/*genetics
alpha-Thalassemia/*genetics
Altitude ; Anemia/genetics ; Child, Preschool ; Female ; Glucosephosphate Dehydrogenase Deficiency/epidemiology ; Humans ; Infant ; Infant, Newborn ; Malaria/epidemiology ; Male ; Prevalence ; Rwanda/epidemiology ; Sickle Cell Trait/epidemiology ; alpha-Thalassemia/epidemiology
Czasopismo naukowe
Tytuł :
F-cell levels are altered with erythrocyte density in sickle cell disease.
Autorzy :
Basu S; Structural Genomics Division, Saha Institute of Nuclear Physics, Kolkata, India.
Dash BP
Patel DK
Chakravarty S
Chakravarty A
Banerjee D
Chakrabarti A
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Źródło :
Blood cells, molecules & diseases [Blood Cells Mol Dis] 2011 Aug 15; Vol. 47 (2), pp. 117-9. Date of Electronic Publication: 2011 May 17.
Typ publikacji :
Journal Article
MeSH Terms :
Anemia, Sickle Cell/*metabolism
Cell Membrane/*chemistry
Erythrocytes/*metabolism
Fetal Hemoglobin/*analysis
Sickle Cell Trait/*metabolism
Adult ; Anemia, Sickle Cell/pathology ; Annexin A5/analysis ; Cell Count ; Cell Membrane/metabolism ; Cell Separation ; Child ; Erythrocyte Aging ; Erythrocyte Count ; Erythrocytes/pathology ; Flow Cytometry ; Glycophorins/analysis ; Humans ; Phosphatidylserines/analysis ; Povidone ; Sickle Cell Trait/pathology ; Silicon Dioxide
Czasopismo naukowe
Tytuł :
Effect of red blood cell variants on childhood malaria in Mali: a prospective cohort study.
Autorzy :
Lopera-Mesa TM; Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Doumbia S; Malaria Research and Training Center, University of Bamako, Bamako, Mali.
Konaté D; Malaria Research and Training Center, University of Bamako, Bamako, Mali.
Anderson JM; Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Doumbouya M; Malaria Research and Training Center, University of Bamako, Bamako, Mali.
Keita AS; Malaria Research and Training Center, University of Bamako, Bamako, Mali.
Diakité SA; Malaria Research and Training Center, University of Bamako, Bamako, Mali.
Traoré K; Malaria Research and Training Center, University of Bamako, Bamako, Mali.
Krause MA; Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Diouf A; Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA; Kelly Scientific Resources, Rockville, MD, USA.
Moretz SE; Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA; Kelly Scientific Resources, Rockville, MD, USA.
Tullo GS; Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA; Kelly Scientific Resources, Rockville, MD, USA.
Miura K; Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA; Kelly Scientific Resources, Rockville, MD, USA.
Gu W; Clinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research Inc, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
Fay MP; Biostatistics Research Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Taylor SM; Division of Infectious Diseases and International Health and Duke Global Health Institute, Duke University Medical Center, Durham, NC, USA; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC, USA.
Long CA; Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Diakité M; Malaria Research and Training Center, University of Bamako, Bamako, Mali.
Fairhurst RM; Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA. Electronic address: .
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Źródło :
The Lancet. Haematology [Lancet Haematol] 2015 Apr; Vol. 2 (4), pp. e140-9. Date of Electronic Publication: 2015 Mar 24.
Typ publikacji :
Journal Article; Observational Study; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural
MeSH Terms :
Erythrocytes/*parasitology
Malaria/*genetics
ABO Blood-Group System/genetics ; Adolescent ; Child ; Child, Preschool ; Female ; Genotype ; Glucosephosphate Dehydrogenase/genetics ; Hemoglobin C/genetics ; Hemoglobin, Sickle/genetics ; Humans ; Infant ; Malaria/blood ; Malaria/epidemiology ; Male ; Mali/epidemiology ; Prospective Studies ; Sickle Cell Trait/genetics ; alpha-Thalassemia/genetics
Czasopismo naukowe
Tytuł :
Inborn defects in the antioxidant systems of human red blood cells.
Autorzy :
van Zwieten R; Laboratory of Red Blood Cell Diagnostics, Department of Blood Cell Research, Sanquin Blood Supply Organization, 1066 CX Amsterdam, The Netherlands. Electronic address: .
Verhoeven AJ; Department of Medical Biochemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Roos D; Laboratory of Red Blood Cell Diagnostics, Department of Blood Cell Research, Sanquin Blood Supply Organization, 1066 CX Amsterdam, The Netherlands.
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Źródło :
Free radical biology & medicine [Free Radic Biol Med] 2014 Feb; Vol. 67, pp. 377-86. Date of Electronic Publication: 2013 Dec 06.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Antioxidants/*metabolism
Erythrocytes/*metabolism
Glutathione/*metabolism
NADP/*metabolism
Reactive Oxygen Species/*metabolism
Anemia, Hemolytic/metabolism ; Anemia, Hemolytic/pathology ; Erythrocytes/pathology ; Erythropoiesis ; Glucosephosphate Dehydrogenase Deficiency/metabolism ; Glucosephosphate Dehydrogenase Deficiency/pathology ; Humans ; Malaria/metabolism ; Malaria/prevention & control ; Oxidation-Reduction ; Oxidative Stress ; Sickle Cell Trait/metabolism ; Sickle Cell Trait/pathology ; Thalassemia/metabolism ; Thalassemia/pathology
Czasopismo naukowe
Tytuł :
New insights provided by a comparison of impaired deformability with erythrocyte oxidative stress for sickle cell disease.
Autorzy :
Barodka VM; Department of Anesthesiology/Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Nagababu E; Molecular Dynamics Section, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
Mohanty JG; Molecular Dynamics Section, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
Nyhan D; Department of Anesthesiology/Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Berkowitz DE; Department of Anesthesiology/Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Rifkind JM; Molecular Dynamics Section, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States. Electronic address: .
Strouse JJ; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
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Źródło :
Blood cells, molecules & diseases [Blood Cells Mol Dis] 2014 Apr; Vol. 52 (4), pp. 230-5. Date of Electronic Publication: 2013 Nov 15.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Erythrocyte Deformability*
Oxidative Stress*
Anemia, Sickle Cell/*metabolism
Anemia, Sickle Cell/*pathology
Erythrocytes/*metabolism
Erythrocytes/*pathology
Erythrocytes, Abnormal/*metabolism
Adolescent ; Adult ; Anemia, Sickle Cell/diagnosis ; Child ; Female ; Fetal Hemoglobin/metabolism ; Heme/metabolism ; Hemoglobin, Sickle/metabolism ; Hemoglobins/metabolism ; Humans ; Male ; Proteolysis ; Sickle Cell Trait/diagnosis ; Sickle Cell Trait/metabolism ; Sickle Cell Trait/pathology ; Young Adult
Czasopismo naukowe
Tytuł :
Filter failures with sickling hemoglobin.
Autorzy :
Jacob EK; Department of Laboratory Medicine and Pathology, Division of Transfusion Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
Emery RL
Orrock JM
van Buskirk CM
Gandhi MJ
Pokaż więcej
Źródło :
Transfusion [Transfusion] 2009 Aug; Vol. 49 (8), pp. 1535-6.
Typ publikacji :
Journal Article
MeSH Terms :
Blood Donors*
Equipment Failure*
Erythrocytes*
Hemoglobin, Sickle*
Sickle Cell Trait*
Leukapheresis/*instrumentation
Humans ; Leukapheresis/methods
Czasopismo naukowe
Tytuł :
Counterpoint: Sickle cell trait should not be considered asymptomatic and as a benign condition during physical activity.
Autorzy :
Connes P; Laboratoire ACTES (EA 3596), Département de Physiologie, Université des Antilles et de la Guyane. />Hardy-Dessources MD
Hue O
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Źródło :
Journal of applied physiology (Bethesda, Md. : 1985) [J Appl Physiol (1985)] 2007 Dec; Vol. 103 (6), pp. 2138-40; discussion 2140-1.
Typ publikacji :
Journal Article
MeSH Terms :
Physical Exertion*
Erythrocytes/*metabolism
Hemoglobin, Sickle/*metabolism
Sickle Cell Trait/*physiopathology
Athletic Performance ; Energy Metabolism ; Exercise Tolerance ; Hemoglobin, Sickle/genetics ; Hemorheology ; Humans ; Lactic Acid/blood ; Mutation ; Oxygen Consumption ; Respiratory Mechanics ; Sickle Cell Trait/blood ; Sickle Cell Trait/genetics ; Sickle Cell Trait/mortality
Czasopismo naukowe
Tytuł :
Re: Point:Counterpoint: Sickle cell trait should/should not be considered asymptomatic and as a benign condition during physical activity.
Autorzy :
Baskurt OK
Meiselman HJ
Bergeron MF
Pokaż więcej
Źródło :
Journal of applied physiology (Bethesda, Md. : 1985) [J Appl Physiol (1985)] 2007 Dec; Vol. 103 (6), pp. 2142; author reply 2143-4.
Typ publikacji :
Comment; Letter
MeSH Terms :
Mutation*
Physical Exertion*
Erythrocytes/*metabolism
Hemoglobin, Sickle/*metabolism
Sickle Cell Trait/*physiopathology
Animals ; Athletic Performance ; Energy Metabolism ; Exercise Tolerance ; Hemoglobin, Sickle/genetics ; Hemorheology ; Humans ; Lactic Acid/blood ; Oxygen Consumption ; Respiratory Mechanics ; Sickle Cell Trait/blood ; Sickle Cell Trait/genetics ; Sickle Cell Trait/mortality
Opinia redakcyjna

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