نتایج جستجو برای: hemoglobin f

تعداد نتایج: 360598  

2010

Hemoglobin is the iron-containing oxygen-transport metalloproteins in the red cells of the blood in mammals and other animals. A spheroidal heme protein having four subunits each consisting of a globular protein non-covalently bound, with an embedded heme group. Hb has a molecular weight of about 64456. The globular protein units of Hb is made up of two identical pairs of polypeptide chains, i....

Journal: :Blood 1974
P T Rowley R A Doherty C Rosecrans E Cernichiari

For the quantitation of hemoglobin S, a radioimm unoassay has been developed which is specific and highly sensitive. Hemoglobin S was purified by column chromatography and injected with complete Freund’s adjuvant into goats. Each goat serum was tested for reactivity against hemoglobins A and S by immunodiffusion and by quantitative precipitation. Hemoglobin A reactivity was removed by absorptio...

2012
A. Agapidou S. Theodoridou K. Tegos E. Mandala E. Leukou O. Karakasidou B. Aletra A. Sevastidou M. Alemayehou E. Voskaridou

records, she was known to be a carrier of 5PN deficiency. The proposita’s hematological parameters were as follows: Hb: 10.7 g dL—1; Hct: 34%; RBC: 4.35 x 106; MCV: 77 fL; MCH: 24.7 pg; RDW: 16.2%; reticulocytes: 3.97%; ferritin: 30 (normal range=20-81ngr/Ml). Microscopic examination of a stained peripheral blood smear showed severe anisocytosis, microcytosis, and basophilic stippling. Biochemi...

Journal: :Clinical chemistry 1975
L G Morin

Hemoglobin A2 is batch fractionated with diethylaminoethyl Bio-Gel A (Bio-Rad Laboratories) equilibrated with a tris(hydroxymethyl)aminomethane HCl buffer (pH 7.68, 8.75 mmol/liter, 6.36 mmol of CL- per liter). Hemoglobin A1 and F become bound to the resin, allowing the separation and quantitation of A1. Hemoglobin S alters the equilibrium condition, but adjustments are easily made so that A2 c...

2015
Amanda J. Grieco Henny H. Billett Nancy S. Green M. Catherine Driscoll Eric E. Bouhassira Andrew C. Wilber

The molecular mechanisms governing γ-globin expression in a subset of fetal hemoglobin (α2γ2: HbF) expressing red blood cells (F-cells) and the mechanisms underlying the variability of response to hydroxyurea induced γ-globin expression in the treatment of sickle cell disease are not completely understood. Here we analyzed intra-person clonal populations of basophilic erythroblasts (baso-Es) de...

2017
Takashi Yamada Mamoru Morikawa Takahiro Yamada Ryutaro Nishida Masamitsu Takeda Satoshi Kawaguchi Hisanori Minakami

Complete automation of high-performance liquid chromatography (HPLC) for determination of hemoglobin F (%Hb F) and hemoglobin A1c (%Hb A1c) levels has made this procedure available in many clinical laboratories. However, the physiological changes in %Hb F during pregnancy and the effects of physiological and supraphysiological levels of %Hb A1c on measurement of %Hb F have not been studied exte...

Journal: :Blood 2007
Stephan Menzel Jie Jiang Nicholas Silver Joy Gallagher Juliette Cunningham Gabriela Surdulescu Mark Lathrop Martin Farrall Tim D Spector Swee Lay Thein

Common sequence variants situated between the HBS1L and MYB genes on chromosome 6q23.3 (HMIP) influence the proportion of F cells (erythrocytes that carry measurable amounts of fetal hemoglobin). Since the physiological processes underlying the F-cell variability are thought to be linked to kinetics of erythrocyte maturation and differentiation, we have investigated the influence of the HMIP lo...

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