Searching for gene defects that cause high bone mass.

Por Whyte, M P
Publicado em 1997

Alkaline phosphatase (tissue-nonspecific isoenzyme) is a phosphoethanolamine and pyridoxal-5'-phosphate ectophosphatase: normal and hypophosphatasia fibroblast study.

Por Fedde, K N, Whyte, M P
Publicado em 1990

Pseudohypophosphatasia: aberrant localization and substrate specificity of alkaline phosphatase in cultured skin fibroblasts.

Por Fedde, K N, Cole, D E, Whyte, M P
Publicado em 1990

Markedly increased circulating pyridoxal-5'-phosphate levels in hypophosphatasia. Alkaline phosphatase acts in vitamin B6 metabolism.

Por Whyte, M P, Mahuren, J D, Vrabel, L A, Coburn, S P
Publicado em 1985

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

Por Mumm, S, Whyte, M P, Thakker, R V, Buetow, K H, Schlessinger, D
Publicado em 1997

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

Por Henthorn, P S, Raducha, M, Fedde, K N, Lafferty, M A, Whyte, M P
Publicado em 1992

Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.

Por Sly, W S, Hewett-Emmett, D, Whyte, M P, Yu, Y S, Tashian, R E
Publicado em 1983

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

Por Lloyd, S E, Pannett, A A, Dixon, P H, Whyte, M P, Thakker, R V
Publicado em 1999

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

Por Thakker, R V, Davies, K E, Whyte, M P, Wooding, C, O'Riordan, J L
Publicado em 1990

Matrix vesicles in osteomalacic hypophosphatasia bone contain apatite-like mineral crystals.

Por Anderson, H. C., Hsu, H. H., Morris, D. C., Fedde, K. N., Whyte, M. P.
Publicado em 1997

Perinatal hypophosphatasia: tissue levels of vitamin B6 are unremarkable despite markedly increased circulating concentrations of pyridoxal-5'-phosphate. Evidence for an ectoenzyme...

Por Whyte, M P, Mahuren, J D, Fedde, K N, Cole, F S, McCabe, E R, Coburn, S P
Publicado em 1988

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

Por Weiss, M J, Cole, D E, Ray, K, Whyte, M P, Lafferty, M A, Mulivor, R A, Harris, H
Publicado em 1988

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

Por Trump, D, Dixon, P H, Mumm, S, Wooding, C, Davies, K E, Schlessinger, D, Whyte, M P, Thakker, R V
Publicado em 1998

Alkaline phosphatase: placental and tissue-nonspecific isoenzymes hydrolyze phosphoethanolamine, inorganic pyrophosphate, and pyridoxal 5'-phosphate. Substrate accumulation in carr...

Por Whyte, M P, Landt, M, Ryan, L M, Mulivor, R A, Henthorn, P S, Fedde, K N, Mahuren, J D, Coburn, S P
Publicado em 1995

Osteopenia in 37 members of seven families: analysis based on a model of dominant inheritance.

Por Spotila, L. D., Caminis, J., Devoto, M., Shimoya, K., Sereda, L., Ott, J., Whyte, M. P., Tenenhouse, A., Prockop, D. J.
Publicado em 1996

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

Por Weiss, M J, Ray, K, Fallon, M D, Whyte, M P, Fedde, K N, Lafferty, M A, Mulivor, R A, Harris, H
Publicado em 1989

Enzyme Replacement Therapy Prevents Dental Defects in a Model of Hypophosphatasia

Por McKee, M.D., Nakano, Y., Masica, D.L., Gray, J.J., Lemire, I., Heft, R., Whyte, M.P., Crine, P., Millán, J.L.
Publicado em 2011

Bridging markers defining the map position of X linked hypophosphataemic rickets.

Por Thakker, R V, Read, A P, Davies, K E, Whyte, M P, Weksberg, R, Glorieux, F, Davies, M, Mountford, R C, Harris, R, King, A
Publicado em 1987

Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism.

Por Pearce, S H, Trump, D, Wooding, C, Besser, G M, Chew, S L, Grant, D B, Heath, D A, Hughes, I A, Paterson, C R, Whyte, M P
Publicado em 1995

Periodontal Defects in the A116T Knock-in Murine Model of Odontohypophosphatasia

Por Foster, B.L., Sheen, C.R., Hatch, N.E., Liu, J., Cory, E., Narisawa, S., Kiffer-Moreira, T., Sah, R.L., Whyte, M.P., Somerman, M.J., Millán, J.L.
Publicado no J Dent Res (2015)