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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 28, 2001
Plasma levels of soluble CD30 are increased in children with chronic renal failure and with primary growth deficiency and decrease during treatment with recombination human growth hormoneG Barbano, F Cappa, I Prigione, et al.Human Genetics|June 1, 1993
SSCP detection of a Gly565Val substitution in the pro alpha 1(I) collagen chain resulting in osteogenesis imperfecta type IIK Mackay, A M Lund, M Raghunath, et al.Helvetica Paediatrica Acta|January 1, 1979
Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathologyE R Baumgartner, H Wick, R Maurer, et al.Archives of Biochemistry and Biophysics|October 15, 1983
Ascorbate deficiency results in decreased collagen production: under-hydroxylation of proline leads to increased intracellular degradationR A Berg, B Steinmann, S I Rennard, et al.The Journal of Biological Chemistry|November 15, 1988
The structure of human collagen type IX and its organization in fetal and infant cartilage fibrilsP Bruckner, M Mendler, B Steinmann, et al.Journal of Thrombosis and Haemostasis : JTH|March 26, 2011
Circulating matrix γ-carboxyglutamate protein (MGP) species are refractory to vitamin K treatment in a new case of Keutel syndromeE C M Cranenburg, K Y VAN Spaendonck-Zwarts, L Bonafe, et al.European Journal of Pediatrics|April 1, 1990
Brittle cornea syndrome: an heritable connective tissue disorder distinct from Ehlers-Danlos syndrome type VI and fragilitas oculi, with spontaneous perforations of the eye, blue sclerae, red hair, and normal collagen lysyl hydroxylationP M Royce, B Steinmann, A Vogel, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1986
Lethal osteogenesis imperfecta resulting from a single nucleotide change in one human pro alpha 1(I) collagen alleleD H Cohn, P H Byers, B Steinmann, et al.The Journal of Biological Chemistry|July 25, 1993
Ehlers-Danlos syndrome type VIIB. Morphology of type I collagen fibrils formed in vivo and in vitro is determined by the conformation of the retained N-propeptideD F Holmes, R B Watson, B Steinmann, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Gly802Asp substitution in the pro alpha 2(I) collagen chain in a family with recurrent osteogenesis imperfecta due to paternal mosaicismA M Lund, M Schwartz, M Raghunath, et al.Pageof 31