Whyte MP - Search Results

1

AP2σ Mutations Impair Calcium-Sensing Receptor Trafficking and Signaling, and Show an Endosomal Pathway to Spatially Direct G-Protein Selectivity.

Gorvin CM, Rogers A, Hastoy B, Tarasov AI, Frost M, Sposini S, Inoue A, Whyte MP, Rorsman P, Hanyaloglu AC, Breitwieser GE, Thakker RV. Gorvin CM, et al. Among authors: whyte mp. Cell Rep. 2018 Jan 23;22(4):1054-1066. doi: 10.1016/j.celrep.2017.12.089. Epub 2018 Jan 28. Cell Rep. 2018. PMID: 29420171 Free PMC article.

2

Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies.

Thakker RV, Davies KE, Whyte MP, Wooding C, O'Riordan JL. Thakker RV, et al. Among authors: whyte mp. J Clin Invest. 1990 Jul;86(1):40-5. doi: 10.1172/JCI114712. J Clin Invest. 1990. PMID: 1973175 Free PMC article.

3

Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH.

Trump D, Whyte MP, Wooding C, Pang JT, Pearce SH, Kocher DB, Thakker RV. Trump D, et al. Among authors: whyte mp. Hum Genet. 1995 Aug;96(2):183-7. doi: 10.1007/BF00207376. Hum Genet. 1995. PMID: 7635467

4

mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation.

Mumm S, Whyte MP, Thakker RV, Buetow KH, Schlessinger D. Mumm S, et al. Among authors: whyte mp. Am J Hum Genet. 1997 Jan;60(1):153-9. Am J Hum Genet. 1997. PMID: 8981958 Free PMC article.

5

Calcium-sensing receptor mutations in familial hypocalciuric hypercalcaemia with recurrent pancreatitis.

Pearce SH, Wooding C, Davies M, Tollefsen SE, Whyte MP, Thakker RV. Pearce SH, et al. Among authors: whyte mp. Clin Endocrinol (Oxf). 1996 Dec;45(6):675-80. doi: 10.1046/j.1365-2265.1996.750891.x. Clin Endocrinol (Oxf). 1996. PMID: 9039332

6

Expression and cloning of the human X-linked hypophosphatemia gene cDNA.

Grieff M, Mumm S, Waeltz P, Mazzarella R, Whyte MP, Thakker RV, Schlessinger D. Grieff M, et al. Among authors: whyte mp. Biochem Biophys Res Commun. 1997 Feb 24;231(3):635-9. doi: 10.1006/bbrc.1997.6153. Biochem Biophys Res Commun. 1997. PMID: 9070861

7

Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneity.

Gertner JM, Whyte MP, Dixon PH, Pang JT, Trump D, Pearce SH, Wooding C, Thakker RV. Gertner JM, et al. Among authors: whyte mp. J Bone Miner Res. 1997 Aug;12(8):1204-9. doi: 10.1359/jbmr.1997.12.8.1204. J Bone Miner Res. 1997. PMID: 9258750 Free article.

8

Sequence analysis of 139 kb in Xp22.1 containing spermine synthase and the 5' region of PEX.

Grieff M, Whyte MP, Thakker RV, Mazzarella R. Grieff M, et al. Among authors: whyte mp. Genomics. 1997 Sep 1;44(2):227-31. doi: 10.1006/geno.1997.4876. Genomics. 1997. PMID: 9299240

9

Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.

Trump D, Dixon PH, Mumm S, Wooding C, Davies KE, Schlessinger D, Whyte MP, Thakker RV. Trump D, et al. Among authors: whyte mp. J Med Genet. 1998 Nov;35(11):905-9. doi: 10.1136/jmg.35.11.905. J Med Genet. 1998. PMID: 9832036 Free PMC article.

10

Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13.

Lloyd SE, Pannett AA, Dixon PH, Whyte MP, Thakker RV. Lloyd SE, et al. Among authors: whyte mp. Am J Hum Genet. 1999 Jan;64(1):189-95. doi: 10.1086/302202. Am J Hum Genet. 1999. PMID: 9915958 Free PMC article.

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