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Showing 1 to 8 of 8 for “"B-thalassemia"”.
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ELUCIDATING THE ROLE OF HET0016 IN AMELIORATING 20-HETE INDUCED OXIDATIVE STRESS AND LIVER INJURY IN B-THALASSEMIA: A NOVEL THERAPEUTIC TARGET
… main contributors to pathological outcomes in β-thalassemia, with their generation being a consequence of iron overload and abnormal red blood cell metabolism. We have previously shown that CYP450 mediates ROS production in the liver of a mouse model of β-thalassemia through an increase in …
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Utilizzo della tecnologia microchip per l'identificazione di geni candidati responsabili dell'aumento di HbF.
… as a cure for sickle cell disease (SCD) and b thalassemia, since formation of FS hybrids in SCD inhibits deoxy Hb S polymerization while increased fetal chain expression compensates partially for decreased adult b-globin chains in b thalassemia. Characterization and controlled manipulation of …
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ΤΟ ΕΠΙΠΕΔΟ ΤΟΥ 2,3-ΔΙΦΩΣΦΟΡΟΓΛΥΚΕΡΙΝΙΚΟΥ ΟΞΕΩΣ ΤΩΝ ΕΡΥΘΡΩΝ ΑΙΜΟΣΦΑΙΡΙΩΝ ΣΤΗΝ ΔΡΕΠΑΝΟΚΥΤΤΑΡΙΚΗ ΝΟΣΟ
… ANEMIA; III) IN 23 PATIENTS WITHSICKLE-THALASSEMIA; IV) IN 51 INDIVIDUALS WITH SICKLE-CELL TRAIT AND V) IN 18INDIVIDUALS WITH B-THALASSEMIA TRAIT. IN GROUP I, 2,3 DPG LEVEL WAS SIGNIFICANTLY HIGHER IN WOMEN THAN IN MEN AND A NEGATIVE LINEAR RELATIONSHIP WAS FOUND BETWEEN THE VALUES OF …
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ΠΡΟΓΕΝΝΗΤΙΚΗ ΔΙΑΓΝΩΣΗ Β-ΜΕΣΟΓΕΙΑΚΗΣ ΑΝΑΙΜΙΑΣ (COOLEY). ΜΕΛΕΤΗ ΤΩΝ ΑΝΑΛΟΓΙΩΝ ΤΩΝ ΓΛΟΒΙΝΙΚΩΝ ΑΛΥΣΕΩΝ ΤΗΣ ΑΙΜΟΣΦΑΙΡΙΝΗΣ ΚΑΤΑ ΤΗΝ ΠΡΟΓΕΝΝΗΤΙΚΗ ΚΑΙ ΠΕΡΙΓΕΝΝΗΤΙΚΗ ΠΕΡΙΟΔΟ
… WEEKS,WITH BOTH PARENTS BEING HETEROZYGOUS OF B-THALASSEMIA. DIAGNOSIS WAS ATTEMPTED BY USE OF THE B RATIOS OF GLOBIN CHAINS, SEPARATED BY Γ ELECTROPHORESIS. A STUDY ON THE SWITCH OF B- CΓ, AΓ, CHAINS DURING THE GESTATION. A MATHEMATIC APPROACH BY USE OF A CYBER 18 COMPUTER. GRAPHS OF THE CHANGES …
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Characterisation of two genetic loci involved in fetal haemoglobin production: BCLIIA and HBSIL-MYB intergenic region
… ameliorating factor in sickle cell disease and B-thalassemia. We have previously mapped two quantitative trait loci (QTLs) controlling HbF levels, one in intron 2 of BCL11A gene, and the other, an intergenic region on chromosome 6 between the genes HBS1L and MYB, known as HMIP. Histone …
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ΝΕΥΡΟΦΥΣΙΟΛΟΓΙΚΗ ΜΕΛΕΤΗ ΤΟΥ ΠΕΡΙΦΕΡΙΚΟΥ ΝΕΥΡΙΚΟΥ ΚΑΙ ΜΥΙΚΟΥ ΣΥΣΤΗΜΑΤΟΣ ΣΕ ΑΣΘΕΝΕΙΣ ΜΕ ΟΜΟΖΥΓΟ Β-ΘΑΛΑΣΣΑΙΜΙΑ
… DURING THE PAST FIVE YEARS IN A UNIVERSITY THALASSEMIA UNIT AND IN 29 CONTROLS OF THE SAME AGE RANGE (5 TO 35YEARS). WE STUDIED SEPARATELY SEVEN THALASEMIC PATIENTS WITH THE COMPLICATION OF DIABETES MELLITUS. FROM THE DETAIL CLINICAL EXAMINATION (MEDICAL HISTORY ANDPHYSICAL EXAMINATION) IT …
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Συχνότητα μόλυνσης με κυτταρομεγαλοϊό, yersinia enterocolitica και toxoplasma gondii, ασθενών με μεσογειακή αναιμία και οικείων τους
… and Yersinia Enterocolitica in patients with β-thalassemia and their household contacts. We studied a total of 503 individuals that is 123 β-thalassemic patients, 146 of their household contacts and 234 healthy control subjects of the same age. Antibodies to CMV (cytomegalovirus) and Toxoplasma …
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ΜΕΛΕΤΗ ΤΩΝ ΑΠΛΟΤΥΠΩΝ ΚΑΙ ΜΕΤΑΛΛΑΓΩΝ ΤΗΣ Β-ΘΑΛΑΣΣΑΙΜΙΑΣ ΣΤΗΝ ΕΛΛΑΔΑ
THE PRESENT THESIS AIMS TO STUDY THE DISTRIBUTION OF THE B-GENE CLUSTER HAPLOTYPES IN THE GREEK POPULATION. TO THIS EFFECT WE EXAMINED 316 NORMAL AND 219 THALASSEMIC CHROMOSOMES. IN ADDITION, WE IDENTIFIED THE MOLECULAR DEFECT WHICH CAUSES THE DECREASED B- CHAIN SYNTHESIS ON ALMOST ALL OF THE …