White KE - Search Results

1

Measurement of tartrate-resistant acid phosphatase and the brain isoenzyme of creatine kinase accurately diagnoses type II autosomal dominant osteopetrosis but does not identify gene carriers.

Waguespack SG, Hui SL, White KE, Buckwalter KA, Econs MJ. Waguespack SG, et al. Among authors: white ke. J Clin Endocrinol Metab. 2002 May;87(5):2212-7. doi: 10.1210/jcem.87.5.8497. J Clin Endocrinol Metab. 2002. PMID: 11994366

2

Localization of PiUS, a stimulator of cellular phosphate uptake to human chromosome 3p21.3.

White KE, Econs MJ. White KE, et al. Somat Cell Mol Genet. 1998 Jan;24(1):71-4. doi: 10.1007/BF02677496. Somat Cell Mol Genet. 1998. PMID: 9776982

3

A PDZ domain-containing protein with homology to Diphor-1 maps to human chromosome 1q21.

White KE, Biber J, Murer H, Econs MJ. White KE, et al. Ann Hum Genet. 1998 Jul;62(Pt 4):287-90. doi: 10.1046/j.1469-1809.1998.6240287.x. Ann Hum Genet. 1998. PMID: 9924606

4

Locus heterogeneity of autosomal dominant osteopetrosis (ADO).

White KE, Koller DL, Takacs I, Buckwalter KA, Foroud T, Econs MJ. White KE, et al. J Clin Endocrinol Metab. 1999 Mar;84(3):1047-51. doi: 10.1210/jcem.84.3.5578. J Clin Endocrinol Metab. 1999. PMID: 10084593

5

Chromosomal localization of two human genes involved in phosphate homeostasis: the type IIb sodium-phosphate cotransporter and stanniocalcin-2.

White KE, Biber J, Murer H, Econs MJ. White KE, et al. Somat Cell Mol Genet. 1998 Nov;24(6):357-62. doi: 10.1023/a:1024442524808. Somat Cell Mol Genet. 1998. PMID: 10763414

6

Molecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) gene.

White KE, Lorenz B, Evans WE, Meitinger T, Strom TM, Econs MJ. White KE, et al. Gene. 2000 Apr 4;246(1-2):347-56. doi: 10.1016/s0378-1119(00)00050-0. Gene. 2000. PMID: 10767557

7

MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia.

Rowe PS, de Zoysa PA, Dong R, Wang HR, White KE, Econs MJ, Oudet CL. Rowe PS, et al. Among authors: white ke. Genomics. 2000 Jul 1;67(1):54-68. doi: 10.1006/geno.2000.6235. Genomics. 2000. PMID: 10945470

8

Disorders of phosphate metabolism.

DiMeglio LA, White KE, Econs MJ. DiMeglio LA, et al. Among authors: white ke. Endocrinol Metab Clin North Am. 2000 Sep;29(3):591-609. doi: 10.1016/s0889-8529(05)70152-3. Endocrinol Metab Clin North Am. 2000. PMID: 11033762 Review.

9

The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting.

White KE, Jonsson KB, Carn G, Hampson G, Spector TD, Mannstadt M, Lorenz-Depiereux B, Miyauchi A, Yang IM, Ljunggren O, Meitinger T, Strom TM, Jüppner H, Econs MJ. White KE, et al. J Clin Endocrinol Metab. 2001 Feb;86(2):497-500. doi: 10.1210/jcem.86.2.7408. J Clin Endocrinol Metab. 2001. PMID: 11157998

10

Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23.

White KE, Carn G, Lorenz-Depiereux B, Benet-Pages A, Strom TM, Econs MJ. White KE, et al. Kidney Int. 2001 Dec;60(6):2079-86. doi: 10.1046/j.1523-1755.2001.00064.x. Kidney Int. 2001. PMID: 11737582 Free article.

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