• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 2
  • 1
  • Tagged with
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Congenital Dyserythropoietic Anemia type III (CDA III) : diagnostics, genetics and morbidity

Liljeholm, Maria January 2016 (has links)
The Congenital Dyserythropoietic Anemias (CDA) are rare hereditary hemolytic disorders with large bi- to multi-nucleated erythroblasts in the bone marrow. Hemolysis is negative in a direct antiglobulin test (DAT). Based on morphology and clinical picture, three major forms of CDAs, type I, II, and III have been defined. CDA III, dominantly inherited, constitutes the rarest type with a majority of cases belonging to a family in Västerbotten, Sweden. The genetic background of CDA I and CDA II has been linked to mutations in CDAN1 and SEC23B respectively. The mutation of CDA III has been linked to 15q22 in earlier studies. In this project we have defined the causative genetic lesion in two families with CDA III. The novel mutation KIF23 c.2747C>G (p.P916R) was shown to segregate with CDA III in the Swedish and American CDA III families and was absent in 356 healthy controls. KIF23 encodes mitotic kinesin-like protein 1 (MKLP1), which plays a central role in the last step of cytokinesis. RNAi-based knock-down and rescue experiments demonstrated that the p.P916R mutation causes cytokinesis failure in HeLa cells, resulting in increasing number of bi-nuclear cells, consistent with appearance of large multinucleated erythroblasts in CDA III patients. We conclude that CDA III is caused by a mutation in KIF23, encoding MKLP1, a conserved mitotic kinesin crucial for cytokinesis. Flow cytometry with eosin-5´-maleimide (EMA), anti-CD55 and anti-CD59 is commonly used when investigating non-autoimmune hemolytic anemias. Reduced fluorescence of EMA, typically detected in hereditary spherocytosis, is also seen in CDA II, while reduction of CD55 and CD59 characterizes paroxysmal nocturnal hemoglobinuria (PNH). We studied the flow cytometric profile of EMA, CD55, and CD59 on erythrocytes in CDA III. We found no abnormality of the erythrocyte membrane in CDA III and concluded that standard flow cytometry cannot be used to discriminate between CDA III and normal controls. In CDA I and CDA II a majority of patients, including those who are not transfusion dependent, suffer from iron overload, which, according to earlier studies, is not the case in CDA III. We found that individuals of the Västerbotten CDA III family carry mutations in the hemochromatosis (HFE) gene. Three CDA III patients with heterozygous or compound HFE mutations need treatment with phlebotomy due to iron overload. One of them carries heterozygous H63D mutation, which is not reported to lead to iron overload by itself in otherwise healthy individuals. We propose that molecular genetic testing of the HFE gene is indicated in all patients with CDA, including CDA III.
2

KIF23 expression in congenital dyserythropoietic anemia type III / Undersökningav uttrycket av KIF23 vid kongenitaldyserytropoetisk anemi typ III.

Ulander, Anna Karin January 2012 (has links)
No description available.
3

Transkriptionsregulation von TMPO- und KIF23-Genen im Zellzyklus und deren Repression durch den Tumorsuppressor p53

Girmay, Inga 11 November 2019 (has links)
p53 ist das wichtigste bisher bekannte Tumorsuppressorprotein. Es kann den Zellzyklusarrest vermitteln und die Korrektur von DNA-Schäden ermöglichen beziehungsweise in irreversibel geschädigten Zellen den programmierten Zelltod einleiten. Seine Inaktivierung spielt eine wesentliche Rolle bei der Tumorentstehung, intaktes p53 ist für den Zellzyklusarrest und die Seneszenz von Zellen von wesentlicher Bedeutung. Der Tumorsuppressor p53 übt seine Funktion hauptsächlich als Transkriptionsfaktor aus. Zahlreiche Zielgene von p53 sind inzwischen bekannt und detailliert charakterisiert worden. Besonders interessant sind die regulierten Zellzyklusgene, die die Verknüpfung der p53-Funktion bei Tumorsuppression und Alterungsprozessen der Zellenseneszenz darstellen. Zwei dieser Gene wurden in der vorliegenden Arbeit ausführlich charakterisiert und damit neue p53-Signalwege der Zellzyklusregulation demonstriert.

Page generated in 0.0133 seconds