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C R Scriver

Showing results (251-260 of 317) with videos related to

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Lancet (London, England)|August 11, 1973
X-linked hypophosphataemic rickets: Inadequate therapeutic response to 1,25-dihydroxycholecalciferolF H Glorieux, M F Holick, C R Scriver, et al.
Pediatric Research|February 1, 1975
Dominantly inherited osteogenesis imperfecta in man: an examination of collagen biosynthesisG Lancaster, H Goldman, C R Scriver, et al.
Pediatrics|December 1, 1970
Vitamin D dependency: an inherited postnatal syndrome with secondary hyperparathyroidismC Arnaud, R Maijer, T Reade, et al.
Lancet (London, England)|December 11, 1971
A "new" disorder of isoleucine catabolismR S Daum, P H Lamm, O A Mamer, et al.
American Journal of Human Genetics|May 1, 1990
Recurrent mutation, gene conversion, or recombination at the human phenylalanine hydroxylase locus: evidence in French-Canadians and a catalog of mutationsS W John, R Rozen, C R Scriver, et al.
Molecular Genetics and Metabolism|August 15, 1998
Different clinical forms of hereditary tyrosinemia (type I) in patients with identical genotypesJ Poudrier, F Lettre, C R Scriver, et al.
American Journal of Human Genetics|December 1, 1989
Novel PKU mutation on haplotype 2 in French-CanadiansS W John, R Rozen, R Laframboise, et al.
Molecular Genetics and Metabolism|March 18, 2000
Characterization of phenylketonuria missense substitutions, distant from the phenylalanine hydroxylase active site, illustrates a paradigm for mechanism and potential modulation of phenotypeP J Waters, M A Parniak, B R Akerman, et al.
Molecular Genetics and Metabolism|April 18, 2000
A heteroallelic mutant mouse model: A new orthologue for human hyperphenylalaninemiaC N Sarkissian, D M Boulais, J D McDonald, et al.
Kidney International|September 1, 1978
Renal handling of phosphate in vivo and in vitro by the X-linked hypophosphatemic male mouse: evidence for a defect in the brush border membraneH S Tenenhouse, C R Scriver, R R McInnes, et al.
Pageof 32

Showing results (251-260 of 317) with videos related to

Sort By:
Pageof 32
Lancet (London, England)|August 11, 1973
X-linked hypophosphataemic rickets: Inadequate therapeutic response to 1,25-dihydroxycholecalciferolF H Glorieux, M F Holick, C R Scriver, et al.
Pediatric Research|February 1, 1975
Dominantly inherited osteogenesis imperfecta in man: an examination of collagen biosynthesisG Lancaster, H Goldman, C R Scriver, et al.
Pediatrics|December 1, 1970
Vitamin D dependency: an inherited postnatal syndrome with secondary hyperparathyroidismC Arnaud, R Maijer, T Reade, et al.
Lancet (London, England)|December 11, 1971
A "new" disorder of isoleucine catabolismR S Daum, P H Lamm, O A Mamer, et al.
American Journal of Human Genetics|May 1, 1990
Recurrent mutation, gene conversion, or recombination at the human phenylalanine hydroxylase locus: evidence in French-Canadians and a catalog of mutationsS W John, R Rozen, C R Scriver, et al.
Molecular Genetics and Metabolism|August 15, 1998
Different clinical forms of hereditary tyrosinemia (type I) in patients with identical genotypesJ Poudrier, F Lettre, C R Scriver, et al.
American Journal of Human Genetics|December 1, 1989
Novel PKU mutation on haplotype 2 in French-CanadiansS W John, R Rozen, R Laframboise, et al.
Molecular Genetics and Metabolism|March 18, 2000
Characterization of phenylketonuria missense substitutions, distant from the phenylalanine hydroxylase active site, illustrates a paradigm for mechanism and potential modulation of phenotypeP J Waters, M A Parniak, B R Akerman, et al.
Molecular Genetics and Metabolism|April 18, 2000
A heteroallelic mutant mouse model: A new orthologue for human hyperphenylalaninemiaC N Sarkissian, D M Boulais, J D McDonald, et al.
Kidney International|September 1, 1978
Renal handling of phosphate in vivo and in vitro by the X-linked hypophosphatemic male mouse: evidence for a defect in the brush border membraneH S Tenenhouse, C R Scriver, R R McInnes, et al.
Pageof 32