85 Publications (Page 2 of 4)
2012
Circulating [alpha]Klotho influences phosphate handling by controlling FGF23 production
Smith, Rosamund C⋅Smith, Rosamund⋅O'Bryan, Linda⋅O'Bryan, Linda M⋅Farrow, Emily G⋅Farrow, Emily⋅Summers, Lelia⋅Summers, Lelia J⋅Clinkenbeard, Erica L⋅Clinkenbeard, Erica⋅Roberts, Jessica⋅Roberts, Jessica L⋅Cass, Taryn A⋅Cass, Taryn⋅Saha, Joy⋅Saha, Joy⋅Broderick, Carol⋅Broderick, Carol⋅Ma, Y.⋅Ma, Y. L⋅Zeng, Qing⋅Zeng, Qing Q⋅Kharitonenkov, Alexei⋅Kharitonenkov, Alexei⋅Wilson, Jonathan M⋅Wilson, Jonathan⋅Guo, Qianxu⋅Guo, Qianxu⋅Sun, Haijun⋅Sun, Haijun⋅Allen, Matthew R⋅Allen, Matthew⋅Burr, David⋅Burr, David B⋅Breyer, Matthew⋅Breyer, Matthew D⋅White, Kenneth and White, Kenneth E
Journal of Clinical Investigation, vol. 122, (no. 12), pp. 4710-4715, Dec 2012. | Journal Article
 
Circulating αKlotho influences phosphate handling by controlling FGF23 production.
Smith, Rosamund C⋅Smith, Rosamund C⋅O'Bryan, Linda M⋅O'Bryan, Linda M⋅Farrow, Emily G⋅Farrow, Emily G⋅Summers, Lelia J⋅Summers, Lelia J⋅Clinkenbeard, Erica L⋅Clinkenbeard, Erica L⋅Roberts, Jessica L⋅Roberts, Jessica L⋅Cass, Taryn A⋅Cass, Taryn A⋅Saha, Joy⋅Saha, Joy⋅Broderick, Carol⋅Broderick, Carol⋅Ma, Y Linda⋅Ma, Y L⋅Zeng, Qing Qiang⋅Zeng, Qing Q⋅Kharitonenkov, Alexei⋅Kharitonenkov, Alexei⋅Wilson, Jonathan M⋅Wilson, Jonathan M⋅Guo, Qianxu⋅Guo, Qianxu⋅Sun, Haijun⋅Sun, Haijun⋅Allen, Matthew R⋅Allen, Matthew R⋅Burr, David B⋅Burr, David B⋅Breyer, Matthew D⋅Breyer, Matthew D⋅White, Kenneth E and White, Kenneth E
The Journal of clinical investigation, vol. 122, (no. 12), pp. 4710-5, 2012/Dec/3. | Journal Article
2011
Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice
Farrow, Emily G⋅Farrow, Emily⋅Yu, Xijie⋅Yu, Xijie⋅Summers, Lelia⋅Summers, Lelia J⋅Davis, Siobhan⋅Davis, Siobhan I⋅Fleet, James⋅Fleet, James C⋅Allen, Matthew R⋅Allen, Matthew⋅Robling, Alexander⋅Robling, Alexander⋅Stayrook, Keith R⋅Stayrook, Keith⋅Jideonwo, Victoria⋅Jideonwo, Victoria⋅Magers, Martin⋅Magers, Martin J⋅Garringer, Holly⋅Garringer, Holly J⋅Vidal, Ruben⋅Vidal, Ruben⋅Chan, Rebecca J⋅Chan, Rebecca⋅Goodwin, Charles⋅Goodwin, Charles B⋅Hui, Siu L⋅Hui, Siu⋅Peacock, Munro⋅Peacock, Munro⋅White, Kenneth and White, Kenneth E
Proceedings of the National Academy of Sciences of the United States of America, vol. 108, (no. 46), Nov 15, 2011. | Journal Article
 
Miscellaneous non-inflammatory musculoskeletal conditions. Hyperphosphatemic familial tumoral calcinosis (FGF23, GALNT3 and αKlotho).
Farrow, Emily G⋅Imel, Erik A and White, Kenneth E
Best practice & research. Clinical rheumatology, vol. 25, (no. 5), pp. 735-47, 2011/Oct. | Journal Article
 
Parathyroid hormone receptor signaling in osteocytes increases the expression of fibroblast growth factor-23 in vitro and in vivo.
Rhee, Yumie⋅Rhee, Yumie⋅Bivi, Nicoletta⋅Bivi, Nicoletta⋅Farrow, Emily⋅Farrow*, Emily⋅Farrow, Emily⋅Lezcano, Virginia⋅Lezcano, Virginia⋅Lezcano*, Virginia⋅Plotkin, Lilian I⋅Plotkin, Lilian I⋅White*, Kenneth E⋅White, Kenneth E⋅White, Kenneth E⋅Bellido, Teresita and Bellido, Teresita
Bone, vol. 49, (no. 4), pp. 636-643, October 2011. | Journal Article
 
The Pathophysiology of Early-Stage Chronic Kidney Disease-Mineral Bone Disorder (CKD-MBD) and Response to Phosphate Binders in the Rat
Moe, Sharon M⋅Radcliffe, John S⋅White, Ke⋅Gattone, Vincent H⋅Seifert, Mark F⋅Chen, Xuening⋅Aldridge, B. and Chen, Neal X
Journal of Bone and Mineral Research, vol. 26, (no. 11), pp. 2672-2681, 2011. | Journal Article
2010
Altered renal FGF23-mediated activity involving MAPK and Wnt: effects of the Hyp mutation.
Farrow, Emily G⋅Summers, Lelia J⋅Schiavi, Susan C⋅McCormick, James A⋅Ellison, David H and White, Kenneth E
The Journal of endocrinology, vol. 207, (no. 1), pp. 67-75, 2010/Oct. | Journal Article
 
Recent advances in renal phosphate handling.
Farrow, Emily G⋅Farrow, Emily G⋅White, Kenneth E and White, Kenneth E
Nature reviews. Nephrology, vol. 6, (no. 4), pp. 207-17, 2010/Apr. | Journal Article
2009
A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features.
Dumitrescu, C E⋅Kelly, M H⋅Khosravi, A⋅Hart, Thomas C⋅Brahim, J⋅White, Kenneth E⋅Farrow, E G⋅Nathan, Muriel⋅Murphey, M D and Collins, Michael T
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, vol. 20, (no. 7), pp. 1273-8, 2009/Jul. | Journal Article
 
A rat model of chronic kidney disease-mineral bone disorder
Moe, Sharon M⋅Chen, Xuening⋅Seifert, Mark F⋅Sinders, Rachel M⋅Duan, Dana⋅Chen, Xianming⋅Liang, Yun⋅Radcliff, J. S⋅White, Kenneth E and Gattone, Vincent H
Kidney International, vol. 75, (no. 2), pp. 176-184, 2009. | Journal Article
 
Hypophosphatemia with elevations in serum fibroblast growth factor 23 in a child with Jansen's metaphyseal chondrodysplasia.
Brown, Whitney W⋅Jüppner, Harald⋅Langman, Craig B⋅Price, Heather⋅Farrow, Emily G⋅White, Kenneth E and McCormick, Kenneth L
The Journal of clinical endocrinology and metabolism, vol. 94, (no. 1), pp. 17-20, 2009/Jan. | Journal Article
 
Initial FGF23-mediated signaling occurs in the distal convoluted tubule.
Farrow, Emily G⋅Davis, Siobhan I⋅Summers, Lelia J and White, Kenneth E
Journal of the American Society of Nephrology : JASN, vol. 20, (no. 5), pp. 955-60, 2009/May. | Journal Article
 
Molecular analysis of DMP1 mutants causing autosomal recessive hypophosphatemic rickets
Farrow, EG⋅Davis, SI⋅Ward, LM⋅Summers, LJ⋅Bubbear, JS⋅Keen, R.⋅Stamp, TCB⋅Baker, LRI⋅Bonewald, Lynda and White, Kenneth E
Bone, vol. 44, (no. 2), pp. 287-294, 2009. | Journal Article
 
Tumor-induced osteomalacia
Farrow, Emily G and White, Kenneth E
Expert Review of Endocrinology & Metabolism, vol. 4, (no. 5), pp. 435-442, 2009. | Journal Article
 
Tumor-induced osteomalacia.
Farrow, Emily G and White, Kenneth E
Expert review of endocrinology & metabolism, vol. 4, (no. 5), pp. 435-442, September 1, 2009. | Journal Article
2008
Molecular genetic and biochemical analyses of FGF23 mutations in familial tumoral calcinosis
Garringer, Holly⋅Garringer, Holly⋅Malekpour, Mahdi⋅Malekpour, Mahdi⋅Esteghamat, Fatemehsadat⋅Esteghamat, Fatemehsadat⋅Mortazavi, Seyed⋅Mortazavi, Seyed M⋅Davis, Siobhan I⋅Davis, Siobhan⋅Farrow, Emily⋅Farrow, Emily G⋅Yu, Xijie⋅Yu, Xijie⋅Arking, Dan E⋅Arking, Dan⋅Dietz, Harry⋅Dietz, Harry C⋅White, Kenneth E and White, Kenneth
American Journal of Physiology, vol. 295, (no. 4), Oct 2008. | Journal Article
2007
A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis
Ichikawa, Shoji⋅Imel, Erik A⋅Kreiter, Mary L⋅Yu, X.⋅Mac Kenzie, Duncan S⋅Sorenson, AH⋅Goetz, R.⋅Mohammadi, Moosa⋅White, Kenneth E and Econs, Michael
Journal of Musculoskeletal & Neuronal Interactions, vol. 7, (no. 4), pp. 318-319, 2007. | Journal Article
 
A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis.
Ichikawa, Shoji⋅Imel, Erik A⋅Kreiter, Mary L⋅Yu, Xijie⋅Mackenzie, Donald S⋅Sorenson, Andrea H⋅Goetz, Regina⋅Mohammadi, Moosa⋅White, Kenneth E and Econs, Michael J
The Journal of clinical investigation, vol. 117, (no. 9), pp. 2684-91, 2007/Sep. | Journal Article
 
Hypophosphatemic rickets in opsismodysplasia.
Zeger, Martha D⋅Adkins, Deanna⋅Fordham, Lynn A⋅White, Kenneth E⋅Schoenau, Eckhard⋅Rauch, Frank and Loechner, Karen J
Journal of pediatric endocrinology & metabolism : JPEM, vol. 20, (no. 1), pp. 79-86, 2007/Jan. | Journal Article
 
Hypophosphatemic Rickets in Opsismodysplasia
Zeger, Martha Dechert⋅Adkins, Deanna⋅Fordham, Lynn A⋅White, Kenneth E⋅Schoenau, Eckhard⋅Rauch, Frank and Loechner, Karen J
Journal of pediatric endocrinology & metabolism : JPEM, vol. 20, (no. 1), pp. 79, 2007-Jan. | Journal Article
 
Molecular insights into the klotho-dependent, endocrine mode of action of fibroblast growth factor 19 subfamily members.
Goetz, Regina⋅Beenken, Andrew⋅Ibrahimi, Omar A⋅Kalinina, Juliya⋅Olsen, Shaun K⋅Eliseenkova, Anna V⋅Xu, Chongfeng⋅Neubert, Thomas A⋅Zhang, Fuming⋅Linhardt, Robert J⋅Yu, Xijie⋅White, Kenneth E⋅Inagaki, Takeshi⋅Kliewer, Steven A⋅Yamamoto, Masaya⋅Kurosu, Hiroshi⋅Ogawa, Yasushi⋅Kuro-O, Makoto⋅Kuro-o, Makoto⋅Lanske, Beate⋅Razzaque, Mohammed S and Mohammadi, Moosa
Molecular and cellular biology, vol. 27, (no. 9), pp. 3417-28, 2007/May. | Journal Article
 
Two novel GALNT3 mutations in familial tumoral calcinosis.
Garringer, Holly⋅Garringer, Holly J⋅Mortazavi, Seyed Mohammad Javad⋅Mortazavi, Seyed M⋅Esteghamat, Fatemehsadat⋅Esteghamat, Fatemehsadat⋅Malekpour, Mahdi⋅Malekpour, Mahdi⋅Boztepe, Harika⋅Boztepe, Harika⋅Tanakol, Refik⋅Tanakol, Refik⋅Davis, Siobhan I⋅Davis, Siobhan I⋅White, Kenneth E and White, Kenneth E
American journal of medical genetics. Part A, vol. 143A, (no. 20), pp. 2390-6, 2007/Oct/15. | Journal Article
2006
Extended mutational analyses of FGFR1 in osteoglophonic dysplasia
Farrow, Emily G⋅Davis, Siobhan I⋅Mooney, Sean D⋅Beighton, Peter⋅Mascarenhas, Leo⋅Gutierrez, Yvonne R⋅Pitukcheewanont, Pisit and White, Kenneth E
American Journal of Medical Genetics Part A, vol. 140A, (no. 5), pp. 537-539, 2006. | Journal Article
 
Extended mutational analyses of FGFR1 in osteoglophonic dysplasia.
Farrow, Emily G⋅Davis, Siobhan I⋅Mooney, Sean D⋅Beighton, Peter⋅Mascarenhas, Leo⋅Gutierrez, Yvonne R⋅Pitukcheewanont, Pisit and White, Kenneth E
American journal of medical genetics. Part A, vol. 140, (no. 5), pp. 537-9, 2006/Mar/1. | Journal Article
 
Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism
Feng, Jian Q⋅Ward, Leanne⋅Liu, Shiguang⋅Lu, Yongbo B⋅Xie, Yixia⋅Yuan, Baozhi⋅Yu, Xijie⋅Rauch, Frank⋅Davis, Siobhan I⋅Zhang, Shubin⋅Rios, Hector⋅Drezner, Marc K⋅Quarles, L. D⋅Bonewald, Lynda and White, Kenneth E
Nature Genetics, vol. 38, (no. 11), pp. 1310-1315, 2006. | Journal Article