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The Global ETD Search service is a free service for researchers
to find electronic theses and dissertations. This service is
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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.
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Showing 1 to 10 of 63 (0.063 seconds)Spelling suggestions: "subject:"osteogenesis imperfect."" "subject:"osteogenesis imperfection.""
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Identifizierung, Genkartierung, und Charakterisierung von ENU-induzierten mutanten Mauslinien für Knochenkrankheiten des MenschenLisse, Thomas Stephen, January 2007 (has links)
Stuttgart, Univ., Diss., 2008.
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| 2 |
Klinik der Osteogenesis imperfecta tarda Einzelbeobachtungen an 35 Patienten /Werner, Karl Christoph, January 1979 (has links)
Thesis (doctoral)--Ludwig Maximilians-Universität zu München, 1979.
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Mama, ich bin nicht anders : Leben mit einem behinderten Kind ; am Beispiel der Osteogenesis imperfecta - Glasknochen /Mittelberg, Petra. January 1999 (has links)
Zugl.: Diplomarbeit.
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The effects of ascorbic acid treatment for Osteogenesis imperfecta /Winterfeldt, Esther A. January 1970 (has links)
Thesis (Ph. D.)--Ohio State University, 1970. / Includes vita. Includes bibliographical references (leaves 67-77). Available online via OhioLINK's ETD Center.
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Collagen metabolism by fibroblasts from normals and individuals with Osteogenesis ImperfectaFraser, Judith. January 1980 (has links)
Collagen production by skin fibroblast cell strains from normal subjects and age-matched patients with the mendelian disorder--Osteogenesis Imperfecta (OI)--was studied in culture. / Number of generations in culture, phase of growth, labelling times, and site of biopsy did not influence collagen production by normal skin fibroblasts. / OI cell strains from patients with dominantly inherited OI have abnormal morphology and growth in culture. The ratio of Type I to protype III collagen is reduced in OI Types I, II and IV (Sillence classification). Type III OI could not be distinguished from normal strains by the analysis used. From the collagen phenotype (biochemical parameters) we were able to distinguish different OI phenotypes and to correlate these with clinical phenotypes. One form of OI Type I produces an unstable collagen that is degraded to small peptides in culture.
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The role of genetic background on the phenotypic severity of the osteogensis imperfecta murine (oim) COLIA2 gene mutation throughout postnatal developmentCarleton, Stephanie M., January 2006 (has links)
Thesis (Ph.D.)--University of Missouri-Columbia, 2006. / The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Title from title screen of research.pdf file (viewed on May 1, 2009) Vita. Includes bibliographical references.
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Collagen metabolism by fibroblasts from normals and individuals with Osteogenesis ImperfectaFraser, Judith. January 1980 (has links)
No description available.
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Quality control of type I procollagen folding and assembly in the secretory pathway /Pace, James M., January 2001 (has links)
Thesis (Ph. D.)--University of Washington, 2001. / Vita. Includes bibliographical references (leaves 113-123).
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Molekulargenetische Untersuchungen zur Heterogenität der Osteogenesis imperfectaTrummer, Tatjana. January 2001 (has links)
Ulm, Univ., Diss., 2001.
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| 10 |
Students with osteogenesis imperfecta a comparative intergenerational study of inclusive participation in New Zealand schools /Holmes, Heather J. January 2007 (has links)
Thesis (M.Ed.)--University of Waikato, 2007. / Title from PDF cover (viewed May 1, 2008) Includes bibliographical references (p. 124-133)
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