Davis SI - Search Results

1

Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism.

Feng JQ, Ward LM, Liu S, Lu Y, Xie Y, Yuan B, Yu X, Rauch F, Davis SI, Zhang S, Rios H, Drezner MK, Quarles LD, Bonewald LF, White KE. Feng JQ, et al. Among authors: davis si. Nat Genet. 2006 Nov;38(11):1310-5. doi: 10.1038/ng1905. Epub 2006 Oct 8. Nat Genet. 2006. PMID: 17033621 Free PMC article.

2

The role of DMP1 in autosomal recessive hypophosphatemic rickets.

Farrow EG, Davis SI, Ward LM, White KE. Farrow EG, et al. Among authors: davis si. J Musculoskelet Neuronal Interact. 2007 Oct-Dec;7(4):310-2. J Musculoskelet Neuronal Interact. 2007. PMID: 18094488 Free article. No abstract available.

3

Molecular analysis of DMP1 mutants causing autosomal recessive hypophosphatemic rickets.

Farrow EG, Davis SI, Ward LM, Summers LJ, Bubbear JS, Keen R, Stamp TC, Baker LR, Bonewald LF, White KE. Farrow EG, et al. Among authors: davis si. Bone. 2009 Feb;44(2):287-94. doi: 10.1016/j.bone.2008.10.040. Epub 2008 Oct 25. Bone. 2009. PMID: 19007919 Free PMC article.

4

Genetic dissection of phosphate- and vitamin D-mediated regulation of circulating Fgf23 concentrations.

Yu X, Sabbagh Y, Davis SI, Demay MB, White KE. Yu X, et al. Among authors: davis si. Bone. 2005 Jun;36(6):971-7. doi: 10.1016/j.bone.2005.03.002. Bone. 2005. PMID: 15869926

5

A novel recessive mutation in fibroblast growth factor-23 causes familial tumoral calcinosis.

Larsson T, Yu X, Davis SI, Draman MS, Mooney SD, Cullen MJ, White KE. Larsson T, et al. Among authors: davis si. J Clin Endocrinol Metab. 2005 Apr;90(4):2424-7. doi: 10.1210/jc.2004-2238. Epub 2005 Feb 1. J Clin Endocrinol Metab. 2005. PMID: 15687325

6

Two novel GALNT3 mutations in familial tumoral calcinosis.

Garringer HJ, Mortazavi SM, Esteghamat F, Malekpour M, Boztepe H, Tanakol R, Davis SI, White KE. Garringer HJ, et al. Among authors: davis si. Am J Med Genet A. 2007 Oct 15;143A(20):2390-6. doi: 10.1002/ajmg.a.31947. Am J Med Genet A. 2007. PMID: 17853462

7

Initial FGF23-mediated signaling occurs in the distal convoluted tubule.

Farrow EG, Davis SI, Summers LJ, White KE. Farrow EG, et al. Among authors: davis si. J Am Soc Nephrol. 2009 May;20(5):955-60. doi: 10.1681/ASN.2008070783. Epub 2009 Apr 8. J Am Soc Nephrol. 2009. PMID: 19357251 Free PMC article.

8

Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongation.

White KE, Cabral JM, Davis SI, Fishburn T, Evans WE, Ichikawa S, Fields J, Yu X, Shaw NJ, McLellan NJ, McKeown C, Fitzpatrick D, Yu K, Ornitz DM, Econs MJ. White KE, et al. Among authors: davis si. Am J Hum Genet. 2005 Feb;76(2):361-7. doi: 10.1086/427956. Epub 2004 Dec 28. Am J Hum Genet. 2005. PMID: 15625620 Free PMC article.

9

Extended mutational analyses of FGFR1 in osteoglophonic dysplasia.

Farrow EG, Davis SI, Mooney SD, Beighton P, Mascarenhas L, Gutierrez YR, Pitukcheewanont P, White KE. Farrow EG, et al. Among authors: davis si. Am J Med Genet A. 2006 Mar 1;140(5):537-9. doi: 10.1002/ajmg.a.31106. Am J Med Genet A. 2006. PMID: 16470795 No abstract available.

10

The role of mutant UDP-N-acetyl-alpha-D-galactosamine-polypeptide N-acetylgalactosaminyltransferase 3 in regulating serum intact fibroblast growth factor 23 and matrix extracellular phosphoglycoprotein in heritable tumoral calcinosis.

Garringer HJ, Fisher C, Larsson TE, Davis SI, Koller DL, Cullen MJ, Draman MS, Conlon N, Jain A, Fedarko NS, Dasgupta B, White KE. Garringer HJ, et al. Among authors: davis si. J Clin Endocrinol Metab. 2006 Oct;91(10):4037-42. doi: 10.1210/jc.2006-0305. Epub 2006 Jul 25. J Clin Endocrinol Metab. 2006. PMID: 16868048

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