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M J Econs

Showing results (21-30 of 57) with videos related to

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 1991
Uremic tumoral calcinosis: preliminary observations suggesting an association with aberrant vitamin D homeostasisL D Quarles, G Murphy, M J Econs, et al.
Genomics|January 1, 1994
Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35C H Kos, F Tihy, M J Econs, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Locus heterogeneity of autosomal dominant osteopetrosis (ADO)K E White, D L Koller, I Takacs, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1995
Phosphate transport in immortalized cell cultures from the renal proximal tubule of normal and Hyp mice: evidence that the HYP gene locus product is an extrarenal factorT Nesbitt, M J Econs, J K Byun, et al.
Gene|April 18, 2000
Molecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) geneK E White, B Lorenz, W E Evans, et al.
Human Molecular Genetics|February 1, 1997
Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemiaT M Strom, F Francis, B Lorenz, et al.
Kidney International|December 12, 2001
Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23K E White, G Carn, B Lorenz-Depiereux, et al.
Genomics|July 1, 1990
The human glycine receptor: a new probe that is linked to the X-linked hypophosphatemic rickets geneM J Econs, M A Pericak-Vance, H Betz, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1992
Multilocus mapping of the X-linked hypophosphatemic rickets geneM J Econs, D F Barker, M C Speer, et al.
Human Molecular Genetics|April 1, 1994
Dinucleotide repeat polymorphism at the DXS1683 locusM J Econs, F Francis, P S Rowe, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 1991
Uremic tumoral calcinosis: preliminary observations suggesting an association with aberrant vitamin D homeostasisL D Quarles, G Murphy, M J Econs, et al.
Genomics|January 1, 1994
Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35C H Kos, F Tihy, M J Econs, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Locus heterogeneity of autosomal dominant osteopetrosis (ADO)K E White, D L Koller, I Takacs, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1995
Phosphate transport in immortalized cell cultures from the renal proximal tubule of normal and Hyp mice: evidence that the HYP gene locus product is an extrarenal factorT Nesbitt, M J Econs, J K Byun, et al.
Gene|April 18, 2000
Molecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) geneK E White, B Lorenz, W E Evans, et al.
Human Molecular Genetics|February 1, 1997
Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemiaT M Strom, F Francis, B Lorenz, et al.
Kidney International|December 12, 2001
Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23K E White, G Carn, B Lorenz-Depiereux, et al.
Genomics|July 1, 1990
The human glycine receptor: a new probe that is linked to the X-linked hypophosphatemic rickets geneM J Econs, M A Pericak-Vance, H Betz, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1992
Multilocus mapping of the X-linked hypophosphatemic rickets geneM J Econs, D F Barker, M C Speer, et al.
Human Molecular Genetics|April 1, 1994
Dinucleotide repeat polymorphism at the DXS1683 locusM J Econs, F Francis, P S Rowe, et al.
Pageof 6