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Showing 1 to 20 of 27 for “"HBF"”.

  1. Determinanti genetici dell’espressione dell’emoglobina HbF

    Background: Increased levels of fetal hemoglobin (HbF, α2γ2) may reduce beta thalassemia severity. We have investigated the influence of three known major loci on the HbF trait (HBG2, rs7482144; BCL11A, rs1427407; HBS1L-MYB, rs9399137), prevalent Sardinian mutations in human Kruppel-like factor 1 …

    cagliari Repository record for Determinanti genetici dell’espressione dell’emoglobina HbF (opens in a new tab)

  2. Bakterielle Kontamination von HbF-Erythrozytenkonzentraten aus Plazentarestblut

    Plazentablut kann unter anderem zur autologen Transfusion von Frühgeborenen verwendet werden. Dabei ist die Kontamination von Plazentablut ein wichtiger limitierender Faktor für die klinische Verwendung. In dieser Studie wurde die Kontaminationsrate von Plazentablutentnahmen untersucht, wobei die …

    lmu-germany Repository record for Bakterielle Kontamination von HbF-Erythrozytenkonzentraten aus Plazentarestblut (opens in a new tab)

  3. Utilizzo della tecnologia microchip per l'identificazione di geni candidati responsabili dell'aumento di HbF.

    Expression of fetal globin is silenced normally in adult life; however, determinants linked and/or unlinked to the globin-gene clusters could modify Hb F expression so it persists into adults. Increased expression in adults offers hope as a cure for sickle cell disease (SCD) and b thalassemia, …

    cagliari Repository record for Utilizzo della tecnologia microchip per l'identificazione di geni candidati responsabili dell'aumento di HbF. (opens in a new tab)

  4. New predictive and diagnostic biomarkers for preeclampsia

    … of the genes coding for fetal hemoglobin (HbF) in preeclamptic placentas. The cell-free HbF protein was shown to be accumulating in the vascular lumen, to induce oxidative stress, which damages the blood-placenta-barrier, causing a leak into the maternal blood circulation. Unbound cell-free …

    lund Repository record for New predictive and diagnostic biomarkers for preeclampsia (opens in a new tab)

  5. Genetic basis of hereditary persistence of fetal haemoglobin

    … the variations observed in fetal haemoglobin (HbF) levels. This is important as it is known that an elevated HbF level can ameliorate the symptoms of many of the haemoglobinopathies. The frequency and range of hereditary persistence of fetal haemoglobin (HPFH) in the UK population was …

    oxford-brookes Repository record for Genetic basis of hereditary persistence of fetal haemoglobin (opens in a new tab)

  6. Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease

    … since been associated with fetal hemoglobin (HbF), the disease-ameliorating globin protein, including variants at three principal loci; BCL11A, HBS1L-MYB intergenic polymorphisms (HMIP1/2) and the β-globin gene cluster, which together account for 10 - 20% HbF variance in SCD patients. …

    cape-town Repository record for Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease (opens in a new tab)

  7. Characterisation of two genetic loci involved in fetal haemoglobin production: BCLIIA and HBSIL-MYB intergenic region

    The continuous production of fetal haemoglobin (HbF, a2Ya) into adulthood is an 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 …

    kings Repository record for Characterisation of two genetic loci involved in fetal haemoglobin production: BCLIIA and HBSIL-MYB intergenic region (opens in a new tab)

  8. Análise funcional do gene FOXO3 na indução de hemoglobina fetal em células K562

    … com o aumento dos níveis de hemoglobina fetal (HbF; α2γ2). O único fármaco autorizado pelo Food and Drug Administration (FDA) é a hidroxiureia, que mesmo sendo eficiente para manutenção e controle do desenvolvimento das principais manifestações clínicas destes pacientes, necessita de …

    brazil-ufpe Repository record for Análise funcional do gene FOXO3 na indução de hemoglobina fetal em células K562 (opens in a new tab)

  9. ΕΠΙ ΤΗΣ ΕΝΕΡΓΟΠΟΙΗΣΕΩΣ ΤΗΣ ΕΜΒΡΥΙΚΗΣ ΑΙΜΟΣΦΑΙΡΙΝΗΣ ΕΙΣ ΤΟΝ ΕΝΗΛΙΚΟΝ

    … MECHANISMS RESPONSIBLE FOR THE ACTIVATION OF HBF IN THE ADULT AND B) THE CHARACTERIZATION OF FACTORS THAT STIMULATE THE PRODUCTION OF HBFIN THE ADULT. TWO MAJOR PARTS OF EXPERIMENTS ARE DESCRIBED: 1) PHARMACOLOGIC STIMULATION OF HBF IN VIVO IN BABOONS AND MICE USING CYTOTOXIC DRUGS, …

    greece Repository record for ΕΠΙ ΤΗΣ ΕΝΕΡΓΟΠΟΙΗΣΕΩΣ ΤΗΣ ΕΜΒΡΥΙΚΗΣ ΑΙΜΟΣΦΑΙΡΙΝΗΣ ΕΙΣ ΤΟΝ ΕΝΗΛΙΚΟΝ (opens in a new tab)

  10. Genomic Characterization of Sickle Cell Mouse Models for Therapeutic Genome Editing Applications

    … resulting in a shift from fetal hemoglobin (HbF, α2γ2) to adult hemoglobin (HbA, α2β2). Some individuals harbor rare genetic variants in the extended β-globin gene cluster that cause constitutively elevated postnatal HbF, a benign condition known as hereditary persistence of fetal hemoglobin …

    tenn-hsc Repository record for Genomic Characterization of Sickle Cell Mouse Models for Therapeutic Genome Editing Applications (opens in a new tab)

  11. Genomics of sickle cell disease and fetal hemoglobin in African populations

    … is therefore an imperative. Fetal hemoglobin (HbF) has long been recognized to ameliorate SCD severity whereby patients harboring natural genetic variations that lead to the persistence of high HbF levels in their blood tend to live longer with fewer complications. The HbF quantitative trait is …

    cape-town Repository record for Genomics of sickle cell disease and fetal hemoglobin in African populations (opens in a new tab)

  12. Συσχέτιση γονιδιωματικών βιοδεικτών σε γονίδια της οικογένειας KLF με τα επίπεδα της εμβρυικής αιμοσφαιρίνης στον άνθρωπο : προεκτάσεις στην εξατομίκευση της θεραπείας με υδροξυουρία ασθενών με β-τύπου αιμοσφαιρινοπάθειες

    … αύξηση των επιπέδων της εμβρυικής αιμοσφαιρίνης HbF, προς βελτίωση της κλινικής εικόνας των ασθενών. Η μοναδική φαρμακευτική ουσία που έχει λάβει την έγκριση του Οργανισμού Τροφίμων και Φαρμάκων των Ηνωμένων Πολιτειών Αμερικής (FDA) για την επαγωγή της HbF σε δρεπανοκυτταρικούς ασθενείς είναι η …

    patras-thes Repository record for Συσχέτιση γονιδιωματικών βιοδεικτών σε γονίδια της οικογένειας KLF με τα επίπεδα της εμβρυικής αιμοσφαιρίνης στον άνθρωπο : προεκτάσεις στην εξατομίκευση της θεραπείας με υδροξυουρία ασθενών με β-τύπου αιμοσφαιρινοπάθειες (opens in a new tab)

  13. Caratterizzazione strutturale e funzionale dei sistemi emoglobinici di due specie di pesci (Mugil cephalus e Ophisurus serpens) e di due varianti emoglobiniche umane (HbRoma e HbF-SS-Monserrato)

    … never described before, that we have named HbF-Monserrato-Sassari [Gγ93(F9) Cys Arg] and Hb Roma [β115(G17)Ala Val], and the hemoblobin systems of two species of fish, Mugil cephalus and Ophisurus serpens. HbF-Monserrato-Sassari [Gγ93(F9) Cys Arg] is an abnormal fetal hemoglobin observed in …

    cagliari Repository record for Caratterizzazione strutturale e funzionale dei sistemi emoglobinici di due specie di pesci (Mugil cephalus e Ophisurus serpens) e di due varianti emoglobiniche umane (HbRoma e HbF-SS-Monserrato) (opens in a new tab)

  14. Pentamethylcyclopentadienyl Osmium Chemistry: An Approach to Transition Metal Alkane Complexes

    … of $\rm(C\sb5Me\sb5)Os(PMe\sb3)\sb2Me$ with $\rm HBF\sb4{\cdot}Et\sb2O$ at room temperature affords the Os$\sp{\rm IV}$ alkyl hydride complex $\lbrack\rm(C\sb5Me\sb5)Os(PMe\sb3)\sb2Me(H)\rbrack\lbrack BF\sb4\rbrack.$ Protonation of $\rm(C\sb5Me\sb5)Os(dmpm)Me$ at ${-}120\sp\circ$C with …

    uiuc Repository record for Pentamethylcyclopentadienyl Osmium Chemistry: An Approach to Transition Metal Alkane Complexes (opens in a new tab)

  15. Identificazione e analisi funzionale di fattori regolatori dei geni globinici

    … cluster associated with fetal hemoglobin (HbF) levels, number of F cell and β-thalassemia severity: the HBS1L-MYB intergenic region and the BCL11A gene. In order to understand the functional role of the associated variants at these loci we applied “Genome Wide Chromosome Conformation …

    cagliari Repository record for Identificazione e analisi funzionale di fattori regolatori dei geni globinici (opens in a new tab)

  16. Pharmacogenomics of sickle cell disease therapeutics: pain and drug metabolism associated gene variants and hydroxyurea-induced post-transcriptional expression of miRNAs

    … of disease severity, such as fetal hemoglobin (HbF) levels and αthalassemia, other genetic variants might influence specific sub-phenotypes. New treatments and management strategies accounting for these genetic and nongenetic factors could substantially and rapidly improve the quality of life …

    cape-town Repository record for Pharmacogenomics of sickle cell disease therapeutics: pain and drug metabolism associated gene variants and hydroxyurea-induced post-transcriptional expression of miRNAs (opens in a new tab)

  17. On new allotropes and nanostructures of carbon nitrides

    … process to yield the heptazine based frameworks, HBF-1 and HBF-2. Due to the structural motifs of their molecular precursors, individual sheets of HBF-1 and HBF-2 span cavities of 14.2 Å and 23.0 Å respectively which makes both materials attractive as potential organic zeolites. Crystallographic …

    potsdam-diss Repository record for On new allotropes and nanostructures of carbon nitrides (opens in a new tab)

  18. Synthesis and characterization of novel polyaniline/metal composites

    … for the doped PANI/Au composite relative to PANI/HBF4 without Au particles. In the case of the PANI/Pt composite, the polymer is found to exist as an amine salt leading to diminished conductance for the doped PANI/Pt composite relative to PANI/HBF 4 without Pt particles. Most importantly, the data …

    unlv Repository record for Synthesis and characterization of novel polyaniline/metal composites (opens in a new tab)

  19. Steric and Electronic Effects Induced by Ancillary Ligand Substitutions on Cyclopentadienyl Osmium Complexes

    … (C5H5)Os(dmpm)H, which can be protonated with HBF 4·Et2O to afford [(C5H5)Os(dmpm)H 2][BF4]. Comparison of the X-ray crystal structures of (C 5H5)Os(dmpm)H and (C5Me5)Os(dmpm)H revealed no significant differences. In contrast, comparison of the structures of [(C5H5)Os(dmpm)H2+] and …

    uiuc Repository record for Steric and Electronic Effects Induced by Ancillary Ligand Substitutions on Cyclopentadienyl Osmium Complexes (opens in a new tab)

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