Rough Joints
Mostrando 1-6 de 6 artigos, teses e dissertações.
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1. Avaliação comparativa de propriedades geradas pelos processos de soldagem TIG e brasagem em uma liga odontológica à base de Ni-Cr / Comparative assessment of properties generated by the process of TIG welding and brazing in a Ni-Cr dental alloy
The purpose of this study was to compare, by means of microhardness testing and metallurgical characterization techniques as metallography, optical microscopy, scanning electron microscopy (SEM) and energy dispersion spectroscopy (EDS), mechanical and metallurgical properties of welded joints by TIG and brazing methods in a dental alloy based on Ni-Cr (FIT-C
Publicado em: 2009
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2. Propagação de fraturas em juntas rugosas não-persistentes / Fracture propagation on rough non-persistent joints
O presente trabalho foi realizado para estudar o efeito sobre a propagação de fraturas em juntas não-persistentes quando existe uma variação da rugosidade nas juntas. Para esta abordagem, foram analisados os modos de coalescência, o ângulo de início das fraturas, a resistência à compressão e deformação de modelos de argamassa contendo juntas nã
Publicado em: 2005
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3. Lubrication and cartilage.
Mechanisms of lubrication of human synovial joints have been analysed in terms of the operating conditions of the joint, the synovial fluid and articular cartilage. In the hip and knee during a walking cycle the load may rise up to four times body weight. In the knee on dropping one metre the load may go up to 25 time body weight. The elastic modulus of cart
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4. An inbred line of transgenic mice expressing an internally deleted gene for type II procollagen (COL2A1). Young mice have a variable phenotype of a chondrodysplasia and older mice have osteoarthritic changes in joints.
Studies were carried out on a line of transgenic mice that expressed an internally deleted COL2A1 gene and developed a phenotype resembling human chondrodysplasias (Vandenberg et al. 1991. Proc. Natl. Acad. Sci. USA. 88:7640-7644. Marked differences in phenotype were observed with propagation of the mutated gene in an inbred strain of mice in that approximat
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5. A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy
Multiple epiphyseal dysplasia (MED) is a degenerative cartilage condition shown in some cases to be caused by mutations in genes encoding cartilage oligomeric matrix protein or type IX collagen. We studied a family with autosomal dominant MED affecting predominantly the knee joints and a mild proximal myopathy. Genetic linkage to the COL9A3 locus on chromoso
The National Academy of Sciences.
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6. Human epidermal growth factor for the stratification of synovial lining layer and neovascularisation in rheumatoid arthritis.
Immunohistochemical study showed selective localisation of human epidermal growth factor (hEGF) to the synovial lining layer. Although the synovial lining layer of the rheumatoid, osteoarthritic, and traumatic joints was hEGF positive, hEGF staining was especially dense at the rheumatoid synovial lining layer; the staining increasing linearly according to th