Whyte MP - Search Results

1

Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia.

Shore EM, Ahn J, Jan de Beur S, Li M, Xu M, Gardner RJ, Zasloff MA, Whyte MP, Levine MA, Kaplan FS. Shore EM, et al. Among authors: whyte mp. N Engl J Med. 2002 Jan 10;346(2):99-106. doi: 10.1056/NEJMoa011262. N Engl J Med. 2002. PMID: 11784876 Free article.

2

Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossification.

Eddy MC, Jan De Beur SM, Yandow SM, McAlister WH, Shore EM, Kaplan FS, Whyte MP, Levine MA. Eddy MC, et al. Among authors: whyte mp. J Bone Miner Res. 2000 Nov;15(11):2074-83. doi: 10.1359/jbmr.2000.15.11.2074. J Bone Miner Res. 2000. PMID: 11092390 Free article.

3

Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasia.

Henthorn PS, Raducha M, Fedde KN, Lafferty MA, Whyte MP. Henthorn PS, et al. Among authors: whyte mp. Proc Natl Acad Sci U S A. 1992 Oct 15;89(20):9924-8. doi: 10.1073/pnas.89.20.9924. Proc Natl Acad Sci U S A. 1992. PMID: 1409720 Free PMC article.

4

Infantile hypophosphatasia: successful prenatal assessment by testing for tissue-non-specific alkaline phosphatase isoenzyme gene mutations.

Henthorn PS, Whyte MP. Henthorn PS, et al. Among authors: whyte mp. Prenat Diagn. 1995 Nov;15(11):1001-6. doi: 10.1002/pd.1970151104. Prenat Diagn. 1995. PMID: 8606878

5

Missense mutations of the tissue-nonspecific alkaline phosphatase gene in hypophosphatasia.

Henthorn PS, Whyte MP. Henthorn PS, et al. Among authors: whyte mp. Clin Chem. 1992 Dec;38(12):2501-5. Clin Chem. 1992. PMID: 1360878 Review.

6

Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutation.

Rickels MR, Zhang X, Mumm S, Whyte MP. Rickels MR, et al. Among authors: whyte mp. J Bone Miner Res. 2005 May;20(5):878-85. doi: 10.1359/JBMR.041223. Epub 2004 Dec 20. J Bone Miner Res. 2005. PMID: 15824861 Free article.

7

Osteoprotegerin deficiency and juvenile Paget's disease.

Whyte MP, Obrecht SE, Finnegan PM, Jones JL, Podgornik MN, McAlister WH, Mumm S. Whyte MP, et al. N Engl J Med. 2002 Jul 18;347(3):175-84. doi: 10.1056/NEJMoa013096. N Engl J Med. 2002. PMID: 12124406 Free article.

8

A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasia.

Weiss MJ, Cole DE, Ray K, Whyte MP, Lafferty MA, Mulivor RA, Harris H. Weiss MJ, et al. Among authors: whyte mp. Proc Natl Acad Sci U S A. 1988 Oct;85(20):7666-9. doi: 10.1073/pnas.85.20.7666. Proc Natl Acad Sci U S A. 1988. PMID: 3174660 Free PMC article.

9

Analysis of liver/bone/kidney alkaline phosphatase mRNA, DNA, and enzymatic activity in cultured skin fibroblasts from 14 unrelated patients with severe hypophosphatasia.

Weiss MJ, Ray K, Fallon MD, Whyte MP, Fedde KN, Lafferty MA, Mulivor RA, Harris H. Weiss MJ, et al. Among authors: whyte mp. Am J Hum Genet. 1989 May;44(5):686-94. Am J Hum Genet. 1989. PMID: 2705456 Free PMC article.

10

First identification of a gene defect for hypophosphatasia: evidence that alkaline phosphatase acts in skeletal mineralization.

Weiss MJ, Cole DE, Ray K, Whyte MP, Lafferty MA, Mulivor R, Harris H. Weiss MJ, et al. Among authors: whyte mp. Connect Tissue Res. 1989;21(1-4):99-104; discussion 104-6. doi: 10.3109/03008208909050000. Connect Tissue Res. 1989. PMID: 2605956

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