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Gastric autoimmunity in Addisonian pernicious anemia and studies of human intrinsic factor secretion.Strickland, Robert Geoffrey. January 1970 (has links)
Degree awarded by the University of Adelaide. / 223 leaves : / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (M.D. 1971)--Stanford University School of Medicine California, Dept. of Medicine, 1970
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Studies in the reproductive Physiology of the AmphibiaBerk, Lionel 16 April 2020 (has links)
The changes occurring in the red blood cells in infective illness are amongst the least carefully studied problems of haematology. In spite of the fact that these anamias are extremely common, it is difficult to find adequate literature to make possible even a clear description of the blood picture under these circumstances. Part of the difficulty is due to the fact that anaemias in infections are grouped together with other anaemia, in which many mechanisms undoubtedly active. Another major source of confusion is the fact that in many of the cases in which "secondary anaemia" occurs, complicating factors such as haemorrhage and liver disease are not adequately dealt with.
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Red cell membrane abnormalities in hereditary spherocytosis patients of KwaZulu-Natal.Bridgemohan, Roshini. January 2006 (has links)
Hereditary Spherocytosis (HS) is a common inherited haemolytic anaemia with variable clinical expression. Fifty subjects with HS from KwaZulu-Natal were studied with the aim of providing further information on the protein abnormalities of the red blood cell (RBC) membrane and their relationship with clinical presentations. Haematological and biochemical tests were performed by routine procedures. Mean Corpuscular Haemoglobin Concentration ( MCHC) in the HS group was 35.1g /dl. This was significantly higher than in normal control subjects (33.6g /dl) (p value < 0.001); indicating its usefulness for the screening of HS. Mean Red Cell Distribution Width (RDW) was also significantly higher in subjects with HS (p<0.001); thus providing an additional screening tool. Erythrocyte membrane proteins from 21 subjects were analysed by SDS - polyacrylamide gel electrophoresis (SDS-PAGE) using the Laemmli and Fairbanks methods. The most common abnormality was a deficiency of band 3 (10 subjects), followed by a combined spectrin and ankyrin deficiency in five subjects. One subject had increased band 6 and in five cases no abnormality was detected. A decreased ratio of protein 4.1a / 4.1b on the Laemmli SDS PAGE correlated with an increased reticulocyte count. The degree of haemolysis and clinical findings did not correlate with the type of red cell membrane protein defect. In this study red cell membrane analysis did not contribute further to the initial laboratory diagnosis. In addition it did not influence clinical management. The presence of red cell membrane abnormalities, either single or multiple, did not correlate with disease severity. Red cell membrane analysis, however, will play an important role for future management such as gene therapy. Red cell membrane analysis is also useful as a research tool to determine the underlying molecular defect and to assess racial or ethnic differences. It is also of value as a differential diagnostic tool in cases where the clinical and laboratory findings are not conclusive for HS. / Thesis (M.Med.Sci)-University of KwaZulu-Natal, Durban, 2006.
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Anaemia in experimental chronic renal failureMason, C. January 1987 (has links)
No description available.
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William Bosworth Castle: Pioneer of Haematological Clinical InvestigationElrod, Jeffrey M., Karnad, Anand B. 01 May 2003 (has links)
No description available.
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Studies on the structure and mechanisms of methylmalonyl-CoA mutaseKeep, Nicholas herbert January 1992 (has links)
No description available.
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KCI cotransport regulation in mammalian erythrocyctesGodart, Helene January 1996 (has links)
No description available.
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Potassium transport in human red blood cellsKhan, Asif Iqbal January 2000 (has links)
No description available.
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Phytochemical and anti-drepanocytosis studies of Cajanus cajan, Callistemon viminalis, Melaleuca bracteata var. Revolution Gold and Syzygium guineense.Tshibangu, Damien Sha-Tshibey. January 2010 (has links)
All over Africa, traditional healers use medicinal plants to prepare medicines to treat a
wide range of illnesses. One of these illnesses is sickle cell anaemia or drepanocytosis
or sicklemia. This disease is particularly common among sub-Saharan Africans with a
clear predominance in equatorial Africa. However, it also exists in North Africa,
Greece, Turkey, Saudi Arabia and India. An estimated 50 million people are affected
worldwide. A literature review on sickle cell anaemia revealed that a number of plants
have anti-drepanocytosic activity. The availability and frequency of ethnobotanic use of
plants were taken into account when selecting the plants investigated in this study.
Cajanus cajan, Callistemon viminalis, Melaleuca bracteata var. Revolution Gold and
Syzygium guineense (from DRC and South Africa) were selected for study. The selected
plants were subjected to modern phytochemical analysis. A total of 8 compounds were
isolated from the plants’ extracts and their structures determined by modern
spectroscopic techniques (1D and 2D NMR, FT-IR and MS). S. guineense from DRC
(Democratic Republic of Congo) yielded flavanonoid glycoside (A) as its major
chemical constituent. The South African S. guineense afforded 4 compounds namely
betulinic acid (B), sitosterol (C), friedelan-3-one (D) and a betulinic acid derivative (E).
Cajanus cajan showed the presence of fatty acids, one of them was characterized as an
unsaturated fatty acid (I). Callistemon viminalis afforded one compound, betulic acid
(F) and Melaleuca bracteata afforded two compounds which were characterized as
betulinic acid acetate (G) and ursolic acid acetate (H).
CH3-(CH2)n-CH2-CH=CH-CH2-CH=CH-(CH2)n-CH2-CH2-COOH
The investigation of the anti-drepanocytosis activities of the extractives and their crude
extracts showed in vitro antisickling activity.
Ethyl acetate crude extracts of Callistemon viminalis and Melaleuca bracteata; hexane,
dichloromethane and ethyl acetate crude extracts of Syzygium guineense of DRC,
betulinic acid, betulinic acid acetate and maslinic acid showed a high antisickling
activity, more than 70% of normalization. The compound BF4, a fatty acid, from
Melaleuca bracteata was found to have a medium activity, between 50 and 70% of
normalization and oleanolic acid showed the weakest activity, between 10 and 50 % of
normalization.
Maslinic acid and oleanolic acid which were used for anti-sickling bioassay were
isolated and characterized from Syzygium cordatum by my supervisor, Professor Shode.
Others crude extracts and pure isolated compounds were found to be non-active antisickling
agents. These included crude hexane and methanol extracts of Cajanus cajan;
crude dichloromethane extract of Callistemon viminalis; crude dichloromethane,
methanol and 80% aqueous methanol extracts of Melaleuca bracteata; crude hexane,
dichloromethane, ethyl acetate, and methanol extracts of Syzygium guineense (South
Africa); ursolic acid from Melaleuca bracteata and flavanone glycoside from Syzygium
guineense of DRC.
This is the first report of the in vitro anti-sickling activity of betunilic acid, betulinic
acid acetate, oleanolic acid, and maslinic acid. / Thesis (M.Sc.)-University of KwaZulu-Natal, Westville, 2010.
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The Fanconi Anaemia Protein FANCJ is Involved in the Alternative Lengthening of Telomeres (ALT) Mechanism in Human CellsKomosa, Martin 25 August 2011 (has links)
Approximately 15% of human cancers utilize a recombination-based mechanism termed Alternative Lengthening of Telomeres (ALT) to maintain the lengths of their telomeres. The Fanconi anaemia protein FANCJ localizes to telomeric foci in human ALT cells, but not in telomerase-positive or primary cells. Telomere-associated FANCJ frequently localizes with FANCD2 and BRCA1, and primarily localizes to ALT-associated PML nuclear bodies. Depletion of FANCJ in human ALT cells causes the loss of BRCA1 at telomeric foci and a decrease in telomeric repeat DNA content primarily as a result of the loss of the brightest telomeric repeat DNA foci. In contrast, depletion of the FANCD2 results in increased telomeric repeat DNA synthesis and this is suppressed upon the codepletion of FANCJ. Together, data from this study suggest that FANCJ is required for telomeric repeat DNA synthesis in human ALT cells, which may or may not be dependent on BRCA1, and FANCD2 restrains this synthesis.
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