| Year |
Citation |
Score |
| 2011 |
Scriver CR, Tenenhouse HS. Mendelian Phenotypes as “Probes” of Renal Transport Systems for Amino Acids and Phosphate Comprehensive Physiology. 1977-2016. DOI: 10.1002/Cphy.Cp080242 |
0.346 |
|
| 2008 |
Iwaki T, Sandoval-Cooper MJ, Tenenhouse HS, Castellino FJ. A missense mutation in the sodium phosphate co-transporter Slc34a1 impairs phosphate homeostasis. Journal of the American Society of Nephrology : Jasn. 19: 1753-62. PMID 18550648 DOI: 10.1681/Asn.2007121360 |
0.467 |
|
| 2008 |
Nowik M, Picard N, Stange G, Capuano P, Tenenhouse HS, Biber J, Murer H, Wagner CA. Renal phosphaturia during metabolic acidosis revisited: molecular mechanisms for decreased renal phosphate reabsorption. Pflã¼Gers Archiv : European Journal of Physiology. 457: 539-49. PMID 18535837 DOI: 10.1007/S00424-008-0530-5 |
0.458 |
|
| 2007 |
Perwad F, Zhang MY, Tenenhouse HS, Portale AA. Fibroblast growth factor 23 impairs phosphorus and vitamin D metabolism in vivo and suppresses 25-hydroxyvitamin D-1alpha-hydroxylase expression in vitro. American Journal of Physiology. Renal Physiology. 293: F1577-83. PMID 17699549 DOI: 10.1152/Ajprenal.00463.2006 |
0.437 |
|
| 2007 |
Tenenhouse HS. Phosphate transport: molecular basis, regulation and pathophysiology. The Journal of Steroid Biochemistry and Molecular Biology. 103: 572-7. PMID 17270430 DOI: 10.1016/J.Jsbmb.2006.12.090 |
0.504 |
|
| 2006 |
Bergwitz C, Roslin NM, Tieder M, Loredo-Osti JC, Bastepe M, Abu-Zahra H, Frappier D, Burkett K, Carpenter TO, Anderson D, Garabedian M, Sermet I, Fujiwara TM, Morgan K, Tenenhouse HS, et al. SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis. American Journal of Human Genetics. 78: 179-92. PMID 16358214 DOI: 10.1086/499409 |
0.455 |
|
| 2005 |
Perwad F, Azam N, Zhang MY, Yamashita T, Tenenhouse HS, Portale AA. Dietary and serum phosphorus regulate fibroblast growth factor 23 expression and 1,25-dihydroxyvitamin D metabolism in mice. Endocrinology. 146: 5358-64. PMID 16123154 DOI: 10.1210/En.2005-0777 |
0.408 |
|
| 2005 |
Tenenhouse HS. Regulation of phosphorus homeostasis by the type iia na/phosphate cotransporter. Annual Review of Nutrition. 25: 197-214. PMID 16011465 DOI: 10.1146/Annurev.Nutr.25.050304.092642 |
0.503 |
|
| 2004 |
Larsson T, Marsell R, Schipani E, Ohlsson C, Ljunggren O, Tenenhouse HS, Jüppner H, Jonsson KB. Transgenic mice expressing fibroblast growth factor 23 under the control of the alpha1(I) collagen promoter exhibit growth retardation, osteomalacia, and disturbed phosphate homeostasis. Endocrinology. 145: 3087-94. PMID 14988389 DOI: 10.1210/En.2003-1768 |
0.451 |
|
| 2004 |
Qiu ZQ, Travers R, Rauch F, Glorieux FH, Scriver CR, Tenenhouse HS. Effect of gene dose and parental origin on bone histomorphometry in X-linked Hyp mice Bone. 34: 134-139. PMID 14751570 DOI: 10.1016/J.Bone.2003.09.004 |
0.388 |
|
| 2004 |
Brewer AJ, Canaff L, Hendy GN, Tenenhouse HS. Differential regulation of PHEX expression in bone and parathyroid gland by chronic renal insufficiency and 1,25-dihydroxyvitamin D3. American Journal of Physiology. Renal Physiology. 286: F739-48. PMID 14693675 DOI: 10.1152/Ajprenal.00321.2003 |
0.446 |
|
| 2004 |
Tenenhouse HS, Gauthier C, Chau H, St-Arnaud R. 1alpha-Hydroxylase gene ablation and Pi supplementation inhibit renal calcification in mice homozygous for the disrupted Npt2a gene. American Journal of Physiology. Renal Physiology. 286: F675-81. PMID 14656762 DOI: 10.1152/ajprenal.00362.2003 |
0.385 |
|
| 2003 |
Tenenhouse HS, Martel J, Gauthier C, Segawa H, Miyamoto K. Differential effects of Npt2a gene ablation and X-linked Hyp mutation on renal expression of Npt2c. American Journal of Physiology. Renal Physiology. 285: F1271-8. PMID 12952859 DOI: 10.1152/Ajprenal.00252.2003 |
0.521 |
|
| 2003 |
Azam N, Zhang MY, Wang X, Tenenhouse HS, Portale AA. Disordered regulation of renal 25-hydroxyvitamin D-1alpha-hydroxylase gene expression by phosphorus in X-linked hypophosphatemic (hyp) mice. Endocrinology. 144: 3463-8. PMID 12865326 DOI: 10.1210/En.2003-0255 |
0.476 |
|
| 2003 |
Sabbagh Y, Boileau G, Campos M, Carmona AK, Tenenhouse HS. Structure and function of disease-causing missense mutations in the PHEX gene. The Journal of Clinical Endocrinology and Metabolism. 88: 2213-22. PMID 12727977 DOI: 10.1210/Jc.2002-021809 |
0.689 |
|
| 2003 |
Chau H, El-Maadawy S, McKee MD, Tenenhouse HS. Renal calcification in mice homozygous for the disrupted type IIa Na/Pi cotransporter gene Npt2. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 644-57. PMID 12674325 DOI: 10.1359/Jbmr.2003.18.4.644 |
0.484 |
|
| 2003 |
Khadeer MA, Tang Z, Tenenhouse HS, Eiden MV, Murer H, Hernando N, Weinman EJ, Chellaiah MA, Gupta A. Na+-dependent phosphate transporters in the murine osteoclast: cellular distribution and protein interactions. American Journal of Physiology. Cell Physiology. 284: C1633-44. PMID 12606316 DOI: 10.1152/Ajpcell.00580.2002 |
0.352 |
|
| 2003 |
Tenenhouse HS, Murer H. Disorders of renal tubular phosphate transport. Journal of the American Society of Nephrology : Jasn. 14: 240-8. PMID 12506157 DOI: 10.1097/01.Asn.0000045045.47494.71 |
0.403 |
|
| 2002 |
Zhang MY, Wang X, Wang JT, Compagnone NA, Mellon SH, Olson JL, Tenenhouse HS, Miller WL, Portale AA. Dietary Phosphorus Transcriptionally Regulates 25-Hydroxyvitamin D-1α-Hydroxylase Gene Expression in the Proximal Renal Tubule. Endocrinology. 143: 587-595. PMID 28201490 DOI: 10.1210/endo.143.2.8627 |
0.311 |
|
| 2002 |
Sabbagh Y, Gauthier C, Tenenhouse HS. The X chromosome deletion in HYP mice extends into the intergenic region but does not include the SAT gene downstream from Phex. Cytogenetic and Genome Research. 99: 344-9. PMID 12900584 DOI: 10.1159/000071613 |
0.674 |
|
| 2002 |
Tenenhouse HS, Gauthier C, Martel J, Hoenderop JG, Hartog A, Meyer MH, Meyer RA, Bindels RJ. Na/P(i) cotransporter ( Npt2) gene disruption increases duodenal calcium absorption and expression of epithelial calcium channels 1 and 2. Pflã¼Gers Archiv : European Journal of Physiology. 444: 670-6. PMID 12194021 DOI: 10.1007/S00424-002-0865-2 |
0.349 |
|
| 2002 |
Tenenhouse HS, Sabbagh Y. Novel phosphate-regulating genes in the pathogenesis of renal phosphate wasting disorders. PflüGers Archiv : European Journal of Physiology. 444: 317-26. PMID 12111239 DOI: 10.1007/S00424-002-0839-4 |
0.729 |
|
| 2002 |
Thompson DL, Sabbagh Y, Tenenhouse HS, Roche PC, Drezner MK, Salisbury JL, Grande JP, Poeschla EM, Kumar R. Ontogeny of Phex/PHEX protein expression in mouse embryo and subcellular localization in osteoblasts Journal of Bone and Mineral Research. 17: 311-320. PMID 11811562 DOI: 10.1359/Jbmr.2002.17.2.311 |
0.7 |
|
| 2002 |
Zhang MY, Wang X, Wang JT, Compagnone NA, Mellon SH, Olson JL, Tenenhouse HS, Miller WL, Portale AA. Dietary phosphorus transcriptionally regulates 25-hydroxyvitamin D-1alpha-hydroxylase gene expression in the proximal renal tubule. Endocrinology. 143: 587-95. PMID 11796514 DOI: 10.1210/Endo.143.2.8627 |
0.464 |
|
| 2002 |
Gupta A, Tenenhouse HS, Hoag HM, Wang D, Khadeer MA, Namba N, Feng X, Hruska KA. Identification of the type II Na(+)-Pi cotransporter (Npt2) in the osteoclast and the skeletal phenotype of Npt2-/- mice. Bone. 29: 467-76. PMID 11704500 DOI: 10.1016/S8756-3282(01)00601-9 |
0.397 |
|
| 2001 |
Tenenhouse HS, Martel J, Gauthier C, Zhang MY, Portale AA. Renal Expression of the Sodium/Phosphate Cotransporter Gene, Npt2, Is Not Required for Regulation of Renal 1α-Hydroxylase by Phosphate. Endocrinology. 142: 1124-1129. PMID 28201265 DOI: 10.1210/Endo.142.3.8029 |
0.488 |
|
| 2001 |
Soumounou Y, Gauthier C, Tenenhouse HS. Murine and human type I Na-phosphate cotransporter genes: structure and promoter activity. American Journal of Physiology. Renal Physiology. 281: F1082-91. PMID 11704559 DOI: 10.1152/Ajprenal.0092.2001 |
0.373 |
|
| 2001 |
Sabbagh Y, Boileau G, DesGroseillers L, Tenenhouse HS. Disease-causing missense mutations in the PHEX gene interfere with membrane targeting of the recombinant protein. Human Molecular Genetics. 10: 1539-46. PMID 11468271 DOI: 10.1093/Hmg/10.15.1539 |
0.695 |
|
| 2001 |
Boileau G, Tenenhouse HS, Desgroseillers L, Crine P. Characterization of PHEX endopeptidase catalytic activity: Identification of parathyroid-hormone-related peptide107-139 as a substrate and osteocalcin, PPi and phosphate as inhibitors Biochemical Journal. 355: 707-713. PMID 11311133 DOI: 10.1042/Bj3550707 |
0.413 |
|
| 2001 |
Jones A, Tzenova J, Frappier D, Crumley M, Roslin N, Kos C, Tieder M, Langman C, Proesmans W, Carpenter T, Rice A, Anderson D, Morgan K, Fujiwara T, Tenenhouse H. Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene. Journal of the American Society of Nephrology : Jasn. 12: 507-14. PMID 11181798 |
0.349 |
|
| 2000 |
Ruchon AF, Tenenhouse HS, Marcinkiewicz M, Siegfried G, Aubin JE, DesGroseillers L, Crine P, Boileau G. Developmental expression and tissue distribution of Phex protein: effect of the Hyp mutation and relationship to bone markers. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 15: 1440-50. PMID 10934642 DOI: 10.1359/Jbmr.2000.15.8.1440 |
0.439 |
|
| 2000 |
Sabbagh Y, Jones AO, Tenenhouse HS. PHEXdb, a locus-specific database for mutations causing X-linked hypophosphatemia. Human Mutation. 16: 1-6. PMID 10874297 DOI: 10.1002/1098-1004(200007)16:1<1::Aid-Humu1>3.0.Co;2-J |
0.7 |
|
| 2000 |
Zhao N, Tenenhouse HS. Npt2 gene disruption confers resistance to the inhibitory action of parathyroid hormone on renal sodium-phosphate cotransport. Endocrinology. 141: 2159-65. PMID 10830304 DOI: 10.1210/Endo.141.6.7484 |
0.505 |
|
| 1999 |
Tenenhouse HS. Recent advances in epithelial sodium-coupled phosphate transport. Current Opinion in Nephrology and Hypertension. 8: 407-14. PMID 10491734 DOI: 10.1097/00041552-199907000-00003 |
0.422 |
|
| 1999 |
Hoag HM, Martel J, Gauthier C, Tenenhouse HS. Effects of Npt2 gene ablation and low-phosphate diet on renal Na(+)/phosphate cotransport and cotransporter gene expression. The Journal of Clinical Investigation. 104: 679-86. PMID 10491403 DOI: 10.1172/Jci7103 |
0.445 |
|
| 1999 |
Blydt-Hansen TD, Tenenhouse HS, Goodyer P. PHEX expression in parathyroid gland and parathyroid hormone dysregulation in X-linked hypophosphatemia. Pediatric Nephrology (Berlin, Germany). 13: 607-11. PMID 10460513 DOI: 10.1007/S004670050669 |
0.434 |
|
| 1999 |
Tenenhouse HS. X-linked hypophosphataemia: a homologous disorder in humans and mice. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 14: 333-41. PMID 10069185 DOI: 10.1093/Ndt/14.2.333 |
0.512 |
|
| 1999 |
Portale AA, Zhang MYH, Hoag HH, Tenenhouse HS. Dietary and Serum Phosphorus Regulate 25-hydroxyvitamin D-1α- and 24-hydroxylase Gene Expression in Mouse Kidney Pediatric Research. 45: 335A-335A. DOI: 10.1203/00006450-199904020-01995 |
0.4 |
|
| 1998 |
Tenenhouse HS, Roy S, Martel J, Gauthier C. Differential expression, abundance, and regulation of Na-phosphate cotransporter genes in murine kidney. American Journal of Physiology. Renal Physiology. 275: F527-F534. PMID 29586181 DOI: 10.1152/Ajprenal.1998.275.4.F527 |
0.434 |
|
| 1998 |
Beck L, Karaplis AC, Amizuka N, Hewson AS, Ozawa H, Tenenhouse HS. Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities. Proceedings of the National Academy of Sciences of the United States of America. 95: 5372-7. PMID 9560283 DOI: 10.1073/PNAS.95.9.5372 |
0.426 |
|
| 1998 |
Tenenhouse HS, Gauthier C, Martel J, Gesek FA, Coutermarsh BA, Friedman PA. Na+-phosphate cotransport in mouse distal convoluted tubule cells: Evidence for Glvr-1 and Ram-1 gene expression Journal of Bone and Mineral Research. 13: 590-597. PMID 9556059 DOI: 10.1359/Jbmr.1998.13.4.590 |
0.374 |
|
| 1998 |
Ruchon AF, Marcinkiewicz M, Siegfried G, Tenenhouse HS, DesGroseillers L, Crine P, Boileau G. Pex mRNA is localized in developing mouse osteoblasts and odontoblasts Journal of Histochemistry and Cytochemistry. 46: 459-468. PMID 9524191 DOI: 10.1177/002215549804600405 |
0.398 |
|
| 1998 |
Roy S, Martel J, Tenenhouse HS. Growth hormone normalizes renal 1,25-dihydroxyvitamin D3-24-hydroxylase gene expression but not Na+-phosphate cotransporter (Npt2) mRNA in phosphate-deprived Hyp mice. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 12: 1672-80. PMID 9333128 DOI: 10.1359/Jbmr.1997.12.10.1672 |
0.496 |
|
| 1997 |
McPherson JD, Krane MC, Wagner-McPherson CB, Kos CH, Tenenhouse HS. High resolution mapping of the renal sodium-phosphate cotransporter gene (NPT2) confirms its localization to human chromosome 5q35. Pediatric Research. 41: 632-4. PMID 9128283 DOI: 10.1203/00006450-199705000-00005 |
0.373 |
|
| 1997 |
Beck L, Soumounou Y, Martel J, Krishnamurthy G, Gauthier C, Goodyer CG, Tenenhouse HS. Pex/PEX tissue distribution and evidence for a deletion in the 3' region of the Pex gene in X-linked hypophosphatemic mice. The Journal of Clinical Investigation. 99: 1200-9. PMID 9077527 DOI: 10.1172/Jci119276 |
0.389 |
|
| 1997 |
Tenenhouse HS. Cellular and molecular mechanisms of renal phosphate transport. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 12: 159-64. PMID 9041046 DOI: 10.1359/Jbmr.1997.12.2.159 |
0.429 |
|
| 1996 |
Beck L, Tenenhouse HS, Meyer RA, Meyer MH, Biber J, Murer H. Renal expression of Na+-phosphate cotransporter mRNA and protein: effect of the Gy mutation and low phosphate diet. Pflã¼Gers Archiv : European Journal of Physiology. 431: 936-41. PMID 8927512 DOI: 10.1007/S004240050088 |
0.488 |
|
| 1996 |
Roy S, Tenenhouse HS. Transcriptional regulation and renal localization of 1,25-dihydroxyvitamin D3-24-hydroxylase gene expression: effects of the Hyp mutation and 1,25-dihydroxyvitamin D3. Endocrinology. 137: 2938-46. PMID 8770917 DOI: 10.1210/Endo.137.7.8770917 |
0.484 |
|
| 1996 |
Hartmann CM, Hewson AS, Kos CH, Hilfiker H, Soumounou Y, Murer H, Tenenhouse HS. Structure of murine and human renal type II Na+-phosphate cotransporter genes (Npt2 and NPT2). Proceedings of the National Academy of Sciences of the United States of America. 93: 7409-14. PMID 8693007 DOI: 10.1073/Pnas.93.14.7409 |
0.439 |
|
| 1996 |
Tenenhouse HS, Beck L. Renal Na(+)-phosphate cotransporter gene expression in X-linked Hyp and Gy mice. Kidney International. 49: 1027-32. PMID 8691720 DOI: 10.1038/Ki.1996.149 |
0.532 |
|
| 1996 |
Roy S, Martel J, Tenenhouse HS. Comparative effects of 1,25-dihydroxyvitamin D3 and EB 1089 on mouse renal and intestinal 25-hydroxyvitamin D3-24-hydroxylase. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 10: 1951-9. PMID 8619376 DOI: 10.1002/Jbmr.5650101215 |
0.356 |
|
| 1996 |
Nesbitt T, Econs MJ, Byun JK, Martel J, Tenenhouse HS, Drezner MK. 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 factor. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 10: 1327-33. PMID 7502704 DOI: 10.1002/Jbmr.5650100909 |
0.464 |
|
| 1996 |
Beck L, Tenenhouse HS, Meyer RA, Meyer MH, Biber J, Murer H. Renal expression of Na+- phosphate cotransporter mRNA and protein: Effect of theGy mutation and low phosphate diet PflüGers Archiv. 431: 936-941. DOI: 10.1007/BF02332180 |
0.34 |
|
| 1995 |
Tenenhouse HS, Martel J, Rubin J, Harvey N. Effect of phosphate supplementation on the expression of the mutant phenotype in murine X-linked hypophosphatemic rickets. Bone. 15: 677-83. PMID 7873297 DOI: 10.1016/8756-3282(94)90317-4 |
0.491 |
|
| 1995 |
Tenenhouse HS, Martel J, Biber J, Murer H. Effect of P(i) restriction on renal Na(+)-P(i) cotransporter mRNA and immunoreactive protein in X-linked Hyp mice. The American Journal of Physiology. 268: F1062-9. PMID 7611447 DOI: 10.1152/Ajprenal.1995.268.6.F1062 |
0.419 |
|
| 1994 |
Kos CH, Tihy F, Econs MJ, Murer H, Lemieux N, Tenenhouse HS. Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35. Genomics. 19: 176-7. PMID 8188224 DOI: 10.1006/Geno.1994.1034 |
0.473 |
|
| 1994 |
Thornton SW, Tenenhouse HS, Martel J, Bockian RW, Meyer MH, Meyer RA. X-linked hypophosphatemic Gy mice: renal tubular maximum for phosphate vs. brush-border transport after low-P diet. The American Journal of Physiology. 266: F309-15. PMID 8141332 DOI: 10.1152/ajprenal.1994.266.2.F309 |
0.345 |
|
| 1994 |
Roy S, Martel J, Ma S, Tenenhouse HS. Increased renal 25-hydroxyvitamin D3-24-hydroxylase messenger ribonucleic acid and immunoreactive protein in phosphate-deprived Hyp mice: a mechanism for accelerated 1,25-dihydroxyvitamin D3 catabolism in X-linked hypophosphatemic rickets. Endocrinology. 134: 1761-7. PMID 8137741 DOI: 10.1210/Endo.134.4.8137741 |
0.487 |
|
| 1994 |
Tenenhouse HS, Werner A, Biber J, Ma S, Martel J, Roy S, Murer H. Renal Na(+)-phosphate cotransport in murine X-linked hypophosphatemic rickets. Molecular characterization. The Journal of Clinical Investigation. 93: 671-6. PMID 8113402 DOI: 10.1172/Jci117019 |
0.493 |
|
| 1993 |
Tenenhouse HS, Martel J. Renal adaptation to phosphate deprivation: lessons from the X-linked Hyp mouse. Pediatric Nephrology (Berlin, Germany). 7: 312-8. PMID 8518105 DOI: 10.1007/Bf00853232 |
0.508 |
|
| 1993 |
Qiu ZQ, Tenenhouse HS, Scriver CR. Parental origin of mutant allele does not explain absence of gene dose in X-linked Hyp mice. Genetical Research. 62: 39-43. PMID 8405991 DOI: 10.1017/S0016672300031542 |
0.41 |
|
| 1993 |
Tenenhouse HS, Martel J. Na(+)-dependent sulfate transport in opossum kidney cells is DIDS sensitive. The American Journal of Physiology. 265: C54-61. PMID 8338138 DOI: 10.1152/Ajpcell.1993.265.1.C54 |
0.355 |
|
| 1992 |
Tenenhouse HS, Meyer RA, Mandla S, Meyer MH, Gray RW. Renal phosphate transport and vitamin D metabolism in X-linked hypophosphatemic Gy mice: responses to phosphate deprivation. Endocrinology. 131: 51-6. PMID 1612032 DOI: 10.1210/Endo.131.1.1612032 |
0.511 |
|
| 1992 |
Tenenhouse HS, Scriver CR. X-linked hypophosphatemia. A phenotype in search of a cause. The International Journal of Biochemistry. 24: 685-91. PMID 1592145 DOI: 10.1016/0020-711X(92)90001-H |
0.451 |
|
| 1992 |
Mandla S, Jones G, Tenenhouse HS. Normal 24-hydroxylation of vitamin D metabolites in patients with vitamin D-dependency rickets type I. Structural implications for the vitamin D hydroxylases. The Journal of Clinical Endocrinology and Metabolism. 74: 814-20. PMID 1548347 DOI: 10.1210/Jcem.74.4.1548347 |
0.392 |
|
| 1992 |
Scriver CR, Tenenhouse HS. X-linked hypophosphataemia: a homologous phenotype in humans and mice with unusual organ-specific gene dosage. Journal of Inherited Metabolic Disease. 15: 610-24. PMID 1528020 DOI: 10.1007/Bf01799618 |
0.43 |
|
| 1992 |
Harvey N, Tenenhouse HS. Renal Na(+)-phosphate cotransport in X-linked Hyp mice responds appropriately to Na+ gradient, membrane potential, and pH. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 7: 563-71. PMID 1319668 DOI: 10.1002/Jbmr.5650070513 |
0.407 |
|
| 1992 |
Mandla S, Tenenhouse HS. Inhibition of 25-hydroxyvitamin D3-24-hydroxylase by forskolin: evidence for a 3',5'-cyclic adenosine monophosphate-independent mechanism. Endocrinology. 130: 2145-51. PMID 1312447 DOI: 10.1210/Endo.130.4.1312447 |
0.39 |
|
| 1992 |
Tenenhouse H, Rubin J, Harvey N, Martel J. Effect of phosphate supplementation on expression of the mutant phenotype in murine X-linked hypophosphatemic rickets Bone and Mineral. 17: 208. DOI: 10.1016/0169-6009(92)92166-N |
0.367 |
|
| 1991 |
Scriver CR, Tenenhouse HS. Conserved loci on the X chromosome confer phosphate homeostasis in mice and humans. Genetical Research. 56: 141-52. PMID 2177024 DOI: 10.1017/S0016672300035229 |
0.522 |
|
| 1991 |
Mandla S, Boneh A, Tenenhouse HS. Evidence for protein kinase C involvement in the regulation of renal 25-hydroxyvitamin D3-24-hydroxylase. Endocrinology. 127: 2639-47. PMID 2174334 DOI: 10.1210/Endo-127-6-2639 |
0.414 |
|
| 1991 |
Tenenhouse HS, Lee J, Harvey N. Renal brush-border membrane Na(+)-sulfate cotransport: stimulation by thyroid hormone. The American Journal of Physiology. 261: F420-6. PMID 1832265 DOI: 10.1152/Ajprenal.1991.261.3.F420 |
0.374 |
|
| 1990 |
Tenenhouse HS. Vitamin D metabolism and phosphate transport in developing kidney: effect of diet and mutation. Pediatric Nephrology (Berlin, Germany). 2: 171-5. PMID 3152993 DOI: 10.1007/Bf00870400 |
0.509 |
|
| 1990 |
Tomon M, Tenenhouse HS, Jones G. Expression of 25-hydroxyvitamin D3-24-hydroxylase activity in Caco-2 cells. An in vitro model of intestinal vitamin D catabolism. Endocrinology. 126: 2868-75. PMID 2351099 DOI: 10.1210/Endo-126-6-2868 |
0.332 |
|
| 1990 |
Tenenhouse HS, Jones G. Abnormal regulation of renal vitamin D catabolism by dietary phosphate in murine X-linked hypophosphatemic rickets. The Journal of Clinical Investigation. 85: 1450-5. PMID 2332500 DOI: 10.1172/Jci114590 |
0.422 |
|
| 1990 |
Cunningham J, Coldwell RD, Jones G, Tenenhouse HS, Trafford DJ, Makin HL. Plasma 24,25-dihydroxyvitamin D3 concentrations in X-linked hypophosphatemic mice: studies using mass fragmentographic and radioreceptor assays. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 5: 173-7. PMID 2316405 DOI: 10.1002/Jbmr.5650050211 |
0.347 |
|
| 1990 |
Boneh A, Tenenhouse HS. Protein kinase C in mouse kidney: effect of the Hyp mutation and phosphate deprivation. Kidney International. 37: 682-8. PMID 2308258 DOI: 10.1038/ki.1990.34 |
0.343 |
|
| 1990 |
Tomon M, Tenenhouse HS, Jones G. 1,25-Dihydroxyvitamin D3-inducible catabolism of vitamin D metabolites in mouse intestine. The American Journal of Physiology. 258: G557-63. PMID 2159220 DOI: 10.1152/Ajpgi.1990.258.4.G557 |
0.337 |
|
| 1990 |
Béliveau R, Jetté M, Demeule M, Potier M, Lee J, Tenenhouse HS. Different molecular sizes for Na(+)-dependent phosphonoformic acid binding and phosphate transport in renal brush border membrane vesicles. Biochimica Et Biophysica Acta. 1028: 110-6. PMID 2145976 DOI: 10.1016/0005-2736(90)90146-F |
0.36 |
|
| 1990 |
Tenenhouse HS, Lee J, Harvey N, Potier M, Jette M, Beliveau R. Normal molecular size of the Na+-phosphate cotransporter and normal Na+-dependent binding of phosphonoformic acid in renal brush border membranes of X-linked Hyp mice Biochemical and Biophysical Research Communications. 170: 1288-1293. PMID 2143899 DOI: 10.1016/0006-291X(90)90533-S |
0.399 |
|
| 1990 |
Tenenhouse HS, Lee J. Sulfate inhibits [14C]phosphonoformic acid binding to renal brush-border membranes. The American Journal of Physiology. 259: F286-92. PMID 2143632 DOI: 10.1152/Ajprenal.1990.259.2.F286 |
0.334 |
|
| 1989 |
Meyer RA, Tenenhouse HS, Meyer MH, Klugerman AH. The renal phosphate transport defect in normal mice parabiosed to X-linked hypophosphatemic mice persists after parathyroidectomy. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 4: 523-32. PMID 2816501 DOI: 10.1002/Jbmr.5650040411 |
0.411 |
|
| 1989 |
Boneh A, Mandla S, Tenenhouse HS. Phorbol myristate acetate activates protein kinase C, stimulates the phosphorylation of endogenous proteins and inhibits phosphate transport in mouse renal tubules. Biochimica Et Biophysica Acta. 1012: 308-16. PMID 2758041 DOI: 10.1016/0167-4889(89)90113-4 |
0.391 |
|
| 1989 |
Tenenhouse HS, Klugerman AH, Neal JL. Effect of phosphonoformic acid, dietary phosphate and the Hyp mutation on kinetically distinct phosphate transport processes in mouse kidney. Biochimica Et Biophysica Acta. 984: 207-13. PMID 2527564 DOI: 10.1016/0005-2736(89)90218-6 |
0.416 |
|
| 1988 |
Boneh A, Tenenhouse HS. Protein kinase C in mouse kidney: subcellular distribution and endogenous substrates. Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire. 66: 262-72. PMID 3401377 DOI: 10.1139/O88-035 |
0.382 |
|
| 1988 |
Tenenhouse HS, Yip A, Jones G. Increased renal catabolism of 1,25-dihydroxyvitamin D3 in murine X-linked hypophosphatemic rickets Journal of Clinical Investigation. 81: 461-465. PMID 3339128 DOI: 10.1172/JCI113342 |
0.3 |
|
| 1988 |
Vizel EJ, Tenenhouse HS, Scriver CR. Effect of the X-linked Hyp mutation on N-ethylmaleimide labelling of proteins in renal brush border membrane. Journal of Inherited Metabolic Disease. 10: 243-52. PMID 3123782 DOI: 10.1007/BF01800070 |
0.412 |
|
| 1988 |
Bell CL, Tenenhouse HS, Scriver CR. Initiation and characterization of primary mouse kidney epithelial cultures. In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association. 24: 683-95. PMID 2840432 DOI: 10.1007/Bf02623606 |
0.389 |
|
| 1988 |
Mandla S, Scriver CR, Tenenhouse HS. Decreased transport in renal basolateral membrane vesicles from hypertaurinuric mice. The American Journal of Physiology. 255: F88-95. PMID 2456022 DOI: 10.1152/Ajprenal.1988.255.1.F88 |
0.405 |
|
| 1988 |
Tenenhouse HS, Klugerman AH, Gurd W, Lapointe M, Tannenbaum GS. Pituitary involvement in renal adaptation to phosphate deprivation American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 255: R373-R378. DOI: 10.1152/ajpregu.1988.255.3.R373 |
0.327 |
|
| 1987 |
Tenenhouse HS, Jones G. Effect of the X-linked Hyp mutation and vitamin D status on induction of renal 25-hydroxyvitamin D3-24-hydroxylase. Endocrinology. 120: 609-16. PMID 3803293 DOI: 10.1210/Endo-120-2-609 |
0.408 |
|
| 1987 |
Smith DW, Scriver CR, Tenenhouse HS, Simell O. Lysinuric protein intolerance mutation is expressed in the plasma membrane of cultured skin fibroblasts. Proceedings of the National Academy of Sciences of the United States of America. 84: 7711-5. PMID 3478720 DOI: 10.1073/Pnas.84.21.7711 |
0.39 |
|
| 1987 |
Jones G, Yip A, Tenenhouse HS. Side-chain oxidation of vitamin D3 in mouse kidney mitochondria: Effect of the Hyp mutation and 1,25-dihydroxyvitamin D3 treatment Biochemistry and Cell Biology. 65: 853-859. PMID 2833907 DOI: 10.1139/O87-111 |
0.366 |
|
| 1987 |
Simell O, Smith DW, Tenenhouse HS, Seriver CR. 8. LYSINURIC PROTEIN INTOLERANCE (LPI): THE DEFECT IN CATIONIC AMINO ACID TRANSPORT IS EXPRESSED IN PLASMA MEMBRANE OF CULTURED FIBROBLASTS Pediatric Research. 22: 97-97. DOI: 10.1203/00006450-198707000-00029 |
0.326 |
|
| 1986 |
Scriver CR, Tenenhouse HS. Genetics and mammalian transport systems. Annals of the New York Academy of Sciences. 456: 384-97. PMID 3911843 DOI: 10.1111/J.1749-6632.1985.Tb14889.X |
0.449 |
|
| 1986 |
Lyon MF, Scriver CR, Baker LR, Tenenhouse HS, Kronick J, Mandla S. The Gy mutation: another cause of X-linked hypophosphatemia in mouse. Proceedings of the National Academy of Sciences of the United States of America. 83: 4899-903. PMID 3460077 DOI: 10.1073/Pnas.83.13.4899 |
0.482 |
|
| 1986 |
Tenenhouse HS, Veksler A. Effect of the Hyp mutation and diet-induced hyperparathyroidism on renal parathyroid hormone- and forskolin-stimulated adenosine 3',5'-monophosphate production and brush border membrane phosphate transport. Endocrinology. 118: 1047-53. PMID 3004890 DOI: 10.1210/Endo-118-3-1047 |
0.49 |
|
| 1985 |
Bell CL, Tenenhouse HS, Scriver CR. Isolation and culture of murine renal proximal tubule cells: a system to study solute transport in mutants. Annals of the New York Academy of Sciences. 456: 398-400. PMID 3004298 DOI: 10.1111/J.1749-6632.1985.Tb14890.X |
0.374 |
|
| 1985 |
Tenenhouse HS, Henry HL. Protein kinase activity and protein kinase inhibitor in mouse kidney: Effect of the X-linked Hyp mutation and vitamin D status Endocrinology. 117: 1719-1726. PMID 2994997 DOI: 10.1210/Endo-117-5-1719 |
0.455 |
|
| 1985 |
Tenenhouse HS. Effect of age and the X-linked Hyp mutation on renal adaptation to vitamin D and calcium deficiency. Comparative Biochemistry and Physiology. a, Comparative Physiology. 81: 367-71. PMID 2864180 DOI: 10.1016/0300-9629(85)90149-5 |
0.42 |
|
| 1984 |
Tenenhouse HS. Metabolism of 25-hydroxyvitamin D3 in renal slices from the X-linked hypophosphatemic (Hyp) mouse: abnormal response to fall in serum calcium. Cell Calcium. 5: 43-55. PMID 6608994 DOI: 10.1016/0143-4160(84)90153-2 |
0.431 |
|
| 1984 |
Tenenhouse HS. Investigation of the mechanism for abnormal renal 25-hydroxyvitamin D3-1-hydroxylase activity in the X-linked Hyp mouse. Endocrinology. 115: 634-9. PMID 6086274 DOI: 10.1210/Endo-115-2-634 |
0.472 |
|
| 1983 |
Tenenhouse HS. Abnormal renal mitochondrial 25-hydroxyvitamin D3-1-hydroxylase activity in the vitamin D and calcium deficient X-linked Hyp mouse. Endocrinology. 113: 816-8. PMID 6683624 DOI: 10.1210/Endo-113-2-816 |
0.442 |
|
| 1981 |
Tenenhouse HS, Scriver CR, Vizel EJ. Alkaline phosphatase activity does not mediate phosphate transport in the renal-cortical brush-border membrane. The Biochemical Journal. 190: 473-6. PMID 7470062 DOI: 10.1042/bj1900473 |
0.303 |
|
| 1981 |
Tenenhouse HS, Fast DK, Scriver CR, Koltay M. Intestinal transport of phosphate anion is not impaired in the Hyp (hypophosphatemic) mouse Biochemical and Biophysical Research Communications. 100: 537-543. PMID 7271771 DOI: 10.1016/S0006-291X(81)80210-0 |
0.33 |
|
| 1981 |
Tenenhouse HS, Scriver CR. Effect of 1,25-dihydroxyvitamin D3 on phosphate homeostasis in the X-linked hypophosphatemic (Hyp) mouse. Endocrinology. 109: 658-60. PMID 6894727 DOI: 10.1210/Endo-109-2-658 |
0.417 |
|
| 1981 |
Tenenhouse HS, Koltay M, Scriver CR. 1184 PERSISTANCE OF THE DEFECT IN RENAL BRUSH-BORDER MEMBRANE PHOSPHATE TRANSPORT IN 1α,25-(OH)2 VITAMIN D3 (l,25-(OH)2D3)-TREATED X-LINKED HYPOPHOSPHATEMIA Pediatric Research. 15: 640-640. DOI: 10.1203/00006450-198104001-01210 |
0.325 |
|
| 1979 |
Tenenhouse HS, Scriver CR. Renal brush border membrane adaptation to phosphorus deprivation in the Hyp/Y mouse. Nature. 281: 225-7. PMID 481591 DOI: 10.1038/281225A0 |
0.394 |
|
| 1978 |
Tenenhouse HS, Scriver CR. The defect in transcellular transport of phosphate in the nephron is located in brush-border membranes in X-linked hypophosphatemia (Hyp mouse model). Canadian Journal of Biochemistry. 56: 640-6. PMID 566613 DOI: 10.1139/o78-096 |
0.361 |
|
| 1978 |
Tenenhouse HS, Scriver CR, McInnes RR, Glorieux FH. Renal handling of phosphate in vivo and in vitro by the X-linked hypophosphatemic male mouse: evidence for a defect in the brush border membrane Kidney International. 14: 236-244. PMID 214620 DOI: 10.1038/Ki.1978.115 |
0.438 |
|
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