Results 111 to 120 of about 21,841,476 (331)

A Mechanism of crystallization process of hemoglobin S

open access: yesRevista Integración, 2009
It has been studied as the qualitative consequence of a proposed mechanism of reaction for the formation of HbS molecular aggregations, as well as the mathematical model associated with it, for the particular case that the process of crystallization ...
Carlos Cabal Mirabal, Ivan Ruiz Chaveco
doaj  

A framework for protein classification [PDF]

open access: yes, 2003
It is widely understood that protein functions can be exhaustively described in terms of no single parameter, whether this be amino acid sequence or the three-dimensional structure of the underlying protein molecule. This means that a number of
Kumar, Anand, Smith, Barry
core   +1 more source

Association Between Symptomatic Knee Osteoarthritis and Target Glycemic Control in Individuals With Type 2 Diabetes

open access: yesArthritis Care &Research, EarlyView.
Objective Knee osteoarthritis (OA) commonly affects individuals with type 2 diabetes (T2DM) and is associated with increased risk of diabetes‐related complications. To better understand potential mechanisms, we examined the association between symptomatic knee OA and glycemic control in individuals with T2DM.
Lauren K. King   +10 more
wiley   +1 more source

A “Split” Hemoglobin S Peak [PDF]

open access: yesClinical Chemistry, 2020
Jennifer M, Colby, Zahra, Shajani-Yi
openaire   +2 more sources

Marked Long‐Term Improvement in Lung Function in Melanoma Differentiation–Associated Protein 5 Antibody–Positive Dermatomyositis Patients: Experience of a Single‐Center Longitudinal Cohort in North America

open access: yesArthritis Care &Research, EarlyView.
Objective The objective of this study was to describe the longitudinal disease course and pulmonary outcomes of North American patients with melanoma differentiation–associated protein 5 (MDA5) antibody–associated dermatomyositis (DM). Methods Thirty patients with MDA5 antibody–associated DM were identified in a single‐center longitudinal cohort of 352
Jenice X. Cheah   +8 more
wiley   +1 more source

A Modification of the Spectrophotometric Method for Determining Oxyhemoglobin Affinity [PDF]

open access: yes, 1972
The role of hemoglobin as a carrier of oxygen in the blood was established in 1859 by Hoppe-Seyler. Bert, using whole blood, furnished experimental data whereby an oxyhemoglobin affinity curve could be plotted. In 1886, C. Bohr published data on purified
Burke, Jack D.
core   +1 more source

Redox Potential (E0′) of the β-Chain 93Cys of HbS Measured with the Equilibrium Technique in a Heterozygous Sickle Cell Carrier Subject

open access: yesMolecules
The hitherto unknown thiol-disulfide redox potential (E0′) of the β93Cys residue in the HbS (β6Glu→Val) variant of human hemoglobin was calculated by MALDI-ToF mass spectrometry, which analyzes blood from a heterozygous carrier.
Federico Maria Rubino   +9 more
doaj   +1 more source

Rheumatologic Manifestations of Patients With Type B Insulin Resistance

open access: yesArthritis Care &Research, EarlyView.
Objective The objectives of this study were to identify laboratory and clinical features associated with type B insulin resistance (TBIR), a rare condition caused by autoantibodies that inhibit the insulin receptor, most frequently occurring in the setting of systemic lupus erythematosus (SLE), and to increase awareness of this rare, life‐threatening ...
S. Amara Ogbonnaya   +4 more
wiley   +1 more source

Alpha chain hemoglobins with electrophoretic mobility similar to that of hemoglobin S in a newborn screening program

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2013
OBJECTIVE: To characterize alpha-chain variant hemoglobins with electric mobility similar to that of hemoglobin S in a newborn screening program. METHODS: βS allele and alpha-thalassemia deletions were investigated in 14 children who had undefined ...
Marcilene Rezende Silva   +4 more
doaj  

Cross sectional study on prevalence of sickle cell alleles S and C among patients with mild malaria in Ivory Coast

open access: yesBMC Research Notes, 2018
Objectives Sickle cell anemia is due to a mutations on the betaglobin gene, inducing abnormal hemoglobin. In West Africa the main mutations lead to S or C types of hemoglobin.
Stephane Koui Tossea   +8 more
doaj   +1 more source

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