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M P Whyte

Showing results (141-150 of 166) with videos related to

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The Journal of Clinical Investigation|April 1, 1995
Alkaline phosphatase: placental and tissue-nonspecific isoenzymes hydrolyze phosphoethanolamine, inorganic pyrophosphate, and pyridoxal 5'-phosphate. Substrate accumulation in carriers of hypophosphatasia corrects during pregnancyM P Whyte, M Landt, L M Ryan, et al.
Journal of Dental Research|January 8, 2011
Enzyme replacement therapy prevents dental defects in a model of hypophosphatasiaM D McKee, Y Nakano, D L Masica, et al.
Journal of the American Veterinary Medical Association|October 1, 1994
Periarticular hyperostosis and renal disease in six black lemurs of two family groupsR E Junge, K G Mehren, T P Meehan, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1995
Pseudohypoparathyroidism type Ib is not caused by mutations in the coding exons of the human parathyroid hormone (PTH)/PTH-related peptide receptor geneE Schipani, L S Weinstein, C Bergwitz, et al.
Human Genetics|July 1, 1993
New markers for linkage analysis of X-linked hypophosphataemic ricketsP S Rowe, J Goulding, A Read, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 29, 2000
Expansile skeletal hyperphosphatasia: a new familial metabolic bone diseaseM P Whyte, B G Mills, W R Reinus, et al.
The American Journal of Medicine|September 1, 1992
Significant developmental elevation in serum parathyroid hormone levels in a large kindred with familial benign (hypocalciuric) hypercalcemiaC T McMurtry, F W Schranck, D A Walkenhorst, et al.
Human Genetics|January 1, 1996
Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1D Trump, G Pilia, P H Dixon, et al.
Journal of Medical Genetics|December 1, 1987
Bridging markers defining the map position of X linked hypophosphataemic ricketsR V Thakker, A P Read, K E Davies, et al.
American Journal of Medical Genetics|October 6, 1999
Mild autosomal dominant hypophosphatasia: in utero presentation in two familiesC A Moore, C J Curry, P S Henthorn, et al.
Pageof 17

Showing results (141-150 of 166) with videos related to

Sort By:
Pageof 17
The Journal of Clinical Investigation|April 1, 1995
Alkaline phosphatase: placental and tissue-nonspecific isoenzymes hydrolyze phosphoethanolamine, inorganic pyrophosphate, and pyridoxal 5'-phosphate. Substrate accumulation in carriers of hypophosphatasia corrects during pregnancyM P Whyte, M Landt, L M Ryan, et al.
Journal of Dental Research|January 8, 2011
Enzyme replacement therapy prevents dental defects in a model of hypophosphatasiaM D McKee, Y Nakano, D L Masica, et al.
Journal of the American Veterinary Medical Association|October 1, 1994
Periarticular hyperostosis and renal disease in six black lemurs of two family groupsR E Junge, K G Mehren, T P Meehan, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1995
Pseudohypoparathyroidism type Ib is not caused by mutations in the coding exons of the human parathyroid hormone (PTH)/PTH-related peptide receptor geneE Schipani, L S Weinstein, C Bergwitz, et al.
Human Genetics|July 1, 1993
New markers for linkage analysis of X-linked hypophosphataemic ricketsP S Rowe, J Goulding, A Read, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 29, 2000
Expansile skeletal hyperphosphatasia: a new familial metabolic bone diseaseM P Whyte, B G Mills, W R Reinus, et al.
The American Journal of Medicine|September 1, 1992
Significant developmental elevation in serum parathyroid hormone levels in a large kindred with familial benign (hypocalciuric) hypercalcemiaC T McMurtry, F W Schranck, D A Walkenhorst, et al.
Human Genetics|January 1, 1996
Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1D Trump, G Pilia, P H Dixon, et al.
Journal of Medical Genetics|December 1, 1987
Bridging markers defining the map position of X linked hypophosphataemic ricketsR V Thakker, A P Read, K E Davies, et al.
American Journal of Medical Genetics|October 6, 1999
Mild autosomal dominant hypophosphatasia: in utero presentation in two familiesC A Moore, C J Curry, P S Henthorn, et al.
Pageof 17