Rozprawy doktorskie na temat „Epidermolysis bullosa”
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Kemp, Matthew W. St George Clinical School UNSW. "Gene studies in epidermolysis bullosa". Awarded by:University of New South Wales. St. George Clinical School, 2005. http://handle.unsw.edu.au/1959.4/23439.
Pełny tekst źródłaMcKenna, Kevin Eamon. "Molecular analysis of epidermolysis bullosa". Thesis, Queen's University Belfast, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.357463.
Pełny tekst źródłaWinship, Ingrid M. "Epidermolysis bullosa in South Africa". Doctoral thesis, University of Cape Town, 1986. http://hdl.handle.net/11427/25674.
Pełny tekst źródłaMallipeddi, Rajeev. "Understanding squamous cell carcinoma in epidermolysis bullosa". Thesis, King's College London (University of London), 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.416097.
Pełny tekst źródłaAl, Maani Noor Walid Salem. "Refining genotype-phenotype correlation in epidermolysis bullosa". Thesis, King's College London (University of London), 2017. https://kclpure.kcl.ac.uk/portal/en/theses/refining-genotypephenotype-correlation-in-epidermolysis-bullosa(0efb4606-e7eb-422c-9402-28c29de6ebfc).html.
Pełny tekst źródłaJones, S. M. "The ocular complications in children with epidermolysis bullosa". Thesis, University College London (University of London), 2012. http://discovery.ucl.ac.uk/1338582/.
Pełny tekst źródłaPetrova, Anastasia. "Towards hES cell-based therapy of epidermolysis bullosa". Thesis, King's College London (University of London), 2012. https://kclpure.kcl.ac.uk/portal/en/theses/towards-hes-cellbased-therapy-of-epidermolysis-bullosa(79901c47-3f09-41be-b737-fab3127af800).html.
Pełny tekst źródłaKühl, Tobias Hans-Jürgen [Verfasser], i Leena [Akademischer Betreuer] Bruckner-Tuderman. "Mesenchymal stromal cell therapy for dystrophic epidermolysis bullosa". Freiburg : Universität, 2016. http://d-nb.info/1119452716/34.
Pełny tekst źródłaMacDonnell, Samuel. "Recreating Epidermolysis Bullosa Simplex in Zebrafish with Transgenesis". Thesis, Université d'Ottawa / University of Ottawa, 2018. http://hdl.handle.net/10393/38249.
Pełny tekst źródłaSmith, Frances J. D. "Studies of the molecular basis of epidermolysis bullosa simplex". Thesis, University of Edinburgh, 1994. http://hdl.handle.net/1842/20795.
Pełny tekst źródłaVorobyev, Artem [Verfasser]. "Diagnosis and models of epidermolysis bullosa acquisita / Artem Vorobyev". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2017. http://d-nb.info/1126468878/34.
Pełny tekst źródłaSchlüter, Ulrich. "Zur Frage der Vernarbung bei Epidermolysis bullosa dystrophica : eine vergleichende histologische und immunhistochemische Untersuchung /". Marburg : Görich und Weiershäuser, 2004. http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&doc_number=013209178&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA.
Pełny tekst źródłaTitman, Penelope Susan. "The psychological impact of skin disorders on children and their families". Thesis, University College London (University of London), 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270496.
Pełny tekst źródłaCompton, Sarah. "Developing ex vivo gene therapy for recessive dystrophic epidermolysis bullosa". Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.393399.
Pełny tekst źródłaWessagowit, Vasarat. "Keratinocyte gene expression profile in recessive dystrophic epidermolysis bullosa wounds". Thesis, King's College London (University of London), 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.408868.
Pełny tekst źródłaAbdul, Wahab Alya Omar. "The development of gene therapy for recessive dystrophic epidermolysis bullosa". Thesis, King's College London (University of London), 2017. https://kclpure.kcl.ac.uk/portal/en/theses/the-development-of-gene-therapy-for-recessive-dystrophic-epidermolysis-bullosa(4a405332-0065-448f-b62c-4977ca0d8bf0).html.
Pełny tekst źródłaHuilaja, L. (Laura). "Collagen XVII and pathomechanisms of junctional epidermolysis bullosa and gestational pemphigoid". Doctoral thesis, University of Oulu, 2008. http://urn.fi/urn:isbn:9789514287749.
Pełny tekst źródłaHorn, Helen M. "The prevalence, clinical features and genetics of epidermolysis bullosa in Scotland". Thesis, University of Edinburgh, 2003. http://hdl.handle.net/1842/24711.
Pełny tekst źródłaPetrof, Gampriela. "Allogeneic cell-based therapies for individuals with recessive dystrophic epidermolysis bullosa". Thesis, King's College London (University of London), 2017. https://kclpure.kcl.ac.uk/portal/en/theses/allogeneic-cellbased-therapies-for-individuals-with-recessive-dystrophic-epidermolysis-bullosa(7e30bed8-6252-45b4-b5f3-cbe70b6a8d81).html.
Pełny tekst źródłaKasprick, Anika [Verfasser]. "Die Beteiligung von Mastzellen in der Autoimmunerkrankung Epidermolysis bullosa acquisita / Anika Kasprick". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2014. http://d-nb.info/1046712403/34.
Pełny tekst źródłaMcGrath, John Alexander. "Abnormalities of wound healing and basement membrane zone composition in dystrophic epidermolysis bullosa". Thesis, King's College London (University of London), 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343791.
Pełny tekst źródłaProudfoot, Laura Erin. "The characterisation of cellular and tissue chronic inflammation in recessive dystrophic epidermolysis bullosa". Thesis, King's College London (University of London), 2015. https://kclpure.kcl.ac.uk/portal/en/theses/the-characterisation-of-cellular-and-tissue-chronic-inflammation-in-recessive-dystrophic-epidermolysis-bullosa(ebd52ed7-020a-48cb-9f75-4110ed7d9117).html.
Pełny tekst źródłaSitaru, Cassian. "Pathogenicity of autoantibodies to type VII collagen from patients with epidermolysis bullosa acquisita". Doctoral thesis, [S.l.] : [s.n.], 2002. https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-3982.
Pełny tekst źródłaEpidermolysis bullosa acquisita (EBA) is an autoimmune subepidermal blistering disease associated with autoantibodies to type VII collagen, the major constituent of anchoring fibrils. Previous attempts to demonstrate the blister inducing potential of autoantibodies to this protein have failed. To address this question, we used an in vitro model involving cryosections of human skin incubated with patients’ autoantibodies and leukocytes from healthy donors. We show that sera from 14 out of 16 EBA patients, in contrast to sera from healthy controls, induced dermal-epidermal separation in the cryosections. The level of the experimentally induced split localizes to the lamina lucida of the dermal-epidermal junction. Recruitment and activation of neutrophils at the dermal-epidermal junction was necessary for split induction, whereas mononuclear cells were not required. Importantly, patients’ autoantibodies affinity-purified against a recombinant form of the non-collagenous 1 (NC1) domain of type VII collagen retained their blister-inducing capacity, while patients’ IgG that was depleted of reactivity to type VII collagen lost this ability. Monoclonal antibody LH7.2 to the NC1 domain of type VII collagen also induced subepidermal splits in the cryosections; F(ab’)2 fragments of autoantibodies to type VII collagen were not pathogenic. These findings demonstrate the capacity of autoantibodies to type VII collagen to trigger an Fcg-dependent inflammation leading to split formation in cryosections of human skin
Ellebrecht, Christoph Thomas [Verfasser]. "In-vivo-Untersuchung zur Vorhersagbarkeit der Epidermolysis bullosa acquisita im Tiermodell / Christoph Thomas Ellebrecht". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2013. http://d-nb.info/103059578X/34.
Pełny tekst źródłaWilliams, Felicity. "A qualitative study of the experiences of children and young people with Epidermolysis Bullosa". Thesis, University of East London, 2008. http://roar.uel.ac.uk/3667/.
Pełny tekst źródłaSrinivas, Girish [Verfasser]. "Genome-wide mapping of gene-microbiota interactions in susceptibility to epidermolysis bullosa acquisita / Girish Srinivas". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2013. http://d-nb.info/1045769339/34.
Pełny tekst źródłaMöckel, Nicole [Verfasser]. "Neue Therapieoptionen des bullösen Pemphigoids und der Epidermolysis bullosa acquisita: Untersuchungen am Gefrierschnittmodell / Nicole Möckel". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2014. http://d-nb.info/1052241867/34.
Pełny tekst źródłaMarx, Jennifer. "In vitro modelling of recessive dystrophic epidermolysis bullosa (RDEB) using stem cells and genome editing". Thesis, Högskolan i Skövde, Institutionen för hälsa och lärande, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-17333.
Pełny tekst źródłaSamavedam, Unni Krishna Sri Rama Lingeswar [Verfasser]. "Contribution of cytokines to the pathogenesis of epidermolysis bullosa acquisita / Unni Krishna Sri Rama Lingeswar Samavedam". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2014. http://d-nb.info/104671256X/34.
Pełny tekst źródłaGhorbanalipoor, Saeedeh [Verfasser], Ralf J. [Akademischer Betreuer] Ludwig i Rudolf [Gutachter] Manz. "Drug repurposing for epidermolysis bullosa acquisita / Saeedeh Ghorbanalipoor ; Gutachter: Rudolf Manz ; Akademischer Betreuer: Ralf J. Ludwig". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2020. http://d-nb.info/1209091186/34.
Pełny tekst źródłaMaguire, Claire Merewyn. "Proteoglycans of the dermal-epidermal junction : their role in maintenance of skin integrity and dystrophic epidermolysis bullosa". Thesis, Imperial College London, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267703.
Pełny tekst źródłaPipi, Eleni [Verfasser]. "Receptor-independent anti-inflammatory activities of IgG : investigations using models of epidermolysis bullosa acquisita (EBA) / Eleni Pipi". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2015. http://d-nb.info/1080281118/34.
Pełny tekst źródłaBanczyk, David Michael [Verfasser]. "Autoantikörper: Induktion durch polyklonal aktivierte T-Zellen und Modulation in der Epidermolysis bullosa acquisita / David Michael Banczyk". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2013. http://d-nb.info/104395323X/34.
Pełny tekst źródłaCole, Clare Louise. "Identification of OATP1B3 as a potential therapeutic target in Recessive Dystrophic Epidermolysis Bullosa Associated Squamous Cell Carcinoma". Thesis, University of Dundee, 2011. https://discovery.dundee.ac.uk/en/studentTheses/20729995-be96-4f29-80b8-53da131c6fd8.
Pełny tekst źródłaArmbrust, Mikko Maurizio [Verfasser]. "Untersuchungen zur Signaltransduktion in Granulozyten nach Bindung an Immunkomplexe am Beispiel der Epidermolysis bullosa acquisita / Mikko Maurizio Armbrust". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2019. http://d-nb.info/1175134171/34.
Pełny tekst źródłaNiebuhr, Markus Arnold [Verfasser]. "Assessment of the T-lymphocyte receptor repertoire in the experimental model of epidermolysis bullosa acquisita / Markus Arnold Niebuhr". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2019. http://d-nb.info/1193100186/34.
Pełny tekst źródłaMezger, Markus Torsten [Verfasser], i Rupert [Akademischer Betreuer] Handgretinger. "Entwicklung eines mRNA basierten Transkript Therapieansatzes zur Behandlung der Erkrankung Epidermolysis bullosa / Markus Torsten Mezger ; Betreuer: Rupert Handgretinger". Tübingen : Universitätsbibliothek Tübingen, 2015. http://d-nb.info/1197058060/34.
Pełny tekst źródłaScheuber, Jarno Till [Verfasser]. "Die Effekte einer Inhibition der Januskinase 2 in in vitro Modellen der Epidermolysis bullosa acquisita / Jarno Till Scheuber". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2016. http://d-nb.info/1121536360/34.
Pełny tekst źródłaMezger, Markus [Verfasser], i Rupert [Akademischer Betreuer] Handgretinger. "Entwicklung eines mRNA basierten Transkript Therapieansatzes zur Behandlung der Erkrankung Epidermolysis bullosa / Markus Torsten Mezger ; Betreuer: Rupert Handgretinger". Tübingen : Universitätsbibliothek Tübingen, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:21-dspace-639388.
Pełny tekst źródłaGrund, Nikolai Alexander [Verfasser]. "Inhibition des NF-kB-Signalweges durch CEP-18770 im in-vitro Modell von Epidermolysis bullosa acquisita / Nikolai Alexander Grund". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2018. http://d-nb.info/1171364172/34.
Pełny tekst źródłaLunz, Andre [Verfasser]. "Untersuchung über den Einfluss verschiedener Leukozytenpopulationen in der Pathogenese des bullösen Pemphigoids und der Epidermolysis bullosa acquisita / Andre Lunz". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2015. http://d-nb.info/1079011587/34.
Pełny tekst źródłaTurczynski, Sandrine. "Stratégie thérapeutique par saut d’exon pour les épidermolyses bulleuses dystrophiques". Thesis, Paris 5, 2013. http://www.theses.fr/2013PA05T085.
Pełny tekst źródłaDystrophic Epidermolysis Bullosa (DEB) is a group of rare and severe genetic skin disorders, inherited in a dominant (DDEB) or recessive (RDEB) manner, and characterised by loss of adhesion between the epidermis and the underlying dermis. DEB patients suffer from severe blistering of the skin and mucosae after mild traumas, and in the most severe forms, DEB can be life-threatening. DEB is caused by mutations in the COL7A1 gene encoding type VII collagen that assembles into anchoring fibrils forming key dermo-epidermal adhesion structures. To date, there is no specific treatment for DEB. The first part of my thesis was to develop exon skipping as a therapeutic approach for RDEB. In this work, exon skipping strategy consists in modulating the splicing of a premessenger RNA to induce the skipping of a mutated exon and lead to the synthesis of a shorter but functional protein. Exons 73 and 80 of COL7A1 are of particular interest since they carry many recurrent mutations and their excision preserves the open reading frame. In first instance, we have demonstrated the dispensability of these exons for type VII collagen function in an in vivo xenograft model using RDEB cells transduced with retroviral vectors containing COL7A1 cDNAs, deleted of the sequences of exon 73 or 80. I have subsequently transfected primary RDEB keratinocytes and fibroblasts with antisense oligoribonucleotides (AONs) targeting key splicing regulatory elements of these exons, and achieved efficient skipping of these exons (up to 90%). Western blot and immunocytofluorescence experiments demonstrated significant type VII collagen re-expression (up to 25% of the normal amount) in cells from three RDEB patients. Finally, I have generated skin equivalents with cells of these patients, grafted them on immunodeficient mice and injected different doses of AONs in the grafts, and I have demonstrated type VII collagen re-expression in vivo. In the second part of my thesis, I have studied the case of a particular DEB family, in which two affected children presented a DEB much more severe than their mother and maternal grandfather, suffering from a mild form of DDEB. Sequencing of the 118 exons ofCOL7A1 and of their flanking splice sites, lead to the identification of a single dominant mutation c.6698G>A (p.Gly2233Asp) in exon 84, at the heterozygous state in the four individuals. By carrying out analyses on the paternal transcripts, I have identified a novel c.2587+40G>A recessive mutation in intron 19, which activates a cryptic donor splice site in this intron, leading to its partial retention and to the formation of a premature termination codon. I confirmed the presence of this second, recessive, mutation in the DNA of the two affected children, thus providing an explanation for the observed intrafamilial phenotypic variability: the two affected offsprings being compound heterozygotes for a dominant mutation and a recessive mutation in COL7A1. This novel mutation is the deepest intronic mutation found in COL7A1 so far, and emphasizes the importance of studying COL7A1 at the transcripts level to unravel intronic mutations, understand their molecular consequences and their involvement in the development of the disease. In the last part of my thesis, I have started the characterisation of a knock-in murine model of RDEB generated by our laboratory, which mimics some of the phenotypic characteristics of RDEB patients. My thesis work provided the in vivo demonstration of the feasibility of an exon skipping therapeutic approach for COL7A1. This first important step leads to development of proof of concept studies and toxicological studies in different animal models, with the aim of a clinical translation. It also illustrates the pathological splicing alterations that could benefit from similar approaches
Lieto, Louis D. "Characterization of Epitheliogenesis Imperfecta in Equus caballus". UKnowledge, 2001. http://uknowledge.uky.edu/gradschool_diss/475.
Pełny tekst źródłaSolimani, Farzan [Verfasser], i Michael [Akademischer Betreuer] Hertl. "Development and validation of serological immunoassays in laminin γ-1 pemphigoid and epidermolysis bullosa acquisita / Farzan Solimani ; Betreuer: Michael Hertl". Marburg : Philipps-Universität Marburg, 2019. http://d-nb.info/1191368696/34.
Pełny tekst źródłaKlockemann, Martti [Verfasser], Jennifer [Akademischer Betreuer] Hundt i Marc [Akademischer Betreuer] Ehlers. "Pharmakologische Inhibition des Komplement-5a-Rezeptors bei Antikörpertransfer-induzierter Epidermolysis bullosa acquisita / Martti Klockemann ; Akademische Betreuer: Jennifer Hundt, Marc Ehlers". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2020. http://d-nb.info/1217499172/34.
Pełny tekst źródłaUppalapati, Sai Kailash [Verfasser]. "Immune privilege collapse and epithelial stem cell damage during hair follicle inflammation in murine epidermolysis bullosa acquisita (EBA) / Sai Kailash Uppalapati". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2014. http://d-nb.info/1063210437/34.
Pełny tekst źródłaFründt, Thorben Wilhelm [Verfasser]. "Entwicklung eines ELISA zum Nachweis zirkulierender Antikörper gegen Kollagen Typ VII im aktiven Mausmodell der Epidermolysis bullosa acquisita / Thorben Wilhelm Fründt". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2011. http://d-nb.info/1010454161/34.
Pełny tekst źródłaRisteli, M. (Maija). "Substrate specificity of lysyl hydroxylase isoforms and multifunctionality of lysyl hydroxylase 3". Doctoral thesis, University of Oulu, 2008. http://urn.fi/urn:isbn:9789514288296.
Pełny tekst źródłaDures, Emma K. "An exploration of the psychosocial impact of epidermolysis bullosa on the daily lives of affected adults and identification of associated support needs". Thesis, University of the West of England, Bristol, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.522538.
Pełny tekst źródłaSadeghi, Hengameh [Verfasser]. "The contribution of interleukin-1 and retinoid acid receptor-related orphan receptor alpha to the pathogenesis of epidermolysis bullosa acquisita / Hengameh Sadeghi". Lübeck : Zentrale Hochschulbibliothek Lübeck, 2015. http://d-nb.info/1075027160/34.
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