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International Journal of Food Sciences and Nutrition|June 15, 2007
Antioxidant activity of commonly consumed plant foods of India: contribution of their phenolic contentRita Saxena, K Venkaiah, P Anitha, 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.
Clinical Genetics|June 7, 2003
A cluster of autosomal recessive spondylocostal dysostosis caused by three newly identified DLL3 mutations segregating in a small villageL Bonafé, C Giunta, M Gassner, et al.
European Journal of Pediatrics|May 1, 1985
Anomalous eosinophil granulocytes in blood and bone marrow: a diagnostic marker for infantile GM1-gangliosidosis?R Gitzelmann, M A Spycher, S Adank, et al.
The Journal of Biological Chemistry|January 25, 1989
Decreased thermal denaturation temperature of osteogenesis imperfecta mutant collagen is independent of post-translational overmodifications of lysine and hydroxylysineV H Rao, B Steinmann, W de Wet, et al.
Indian Journal of Experimental Biology|September 8, 2007
Chronic maternal dietary iodine deficiency but not thiocyanate feeding affects maternal reproduction and postnatal performance of the ratS Bala Tripura Sundari, L Venu, Y Sunita, et al.
Klinische Monatsblatter Fur Augenheilkunde|December 1, 1986
[Infantile cataract, hypertrophic cardiomyopathy and lactic acidosis following minor muscular exertion--a little known metabolic disease]S Lalive d'Epinay, S Rampini, U Arbenz, et al.
Nature Genetics|November 14, 1997
Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndromeR Santer, R Schneppenheim, A Dombrowski, et al.
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