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The Journal of Biological Chemistry|February 5, 1992
Calcium ionophore treatment impairs the sterol-mediated suppression of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, 3-hydroxy-3-methylglutaryl-coenzyme A synthase, and farnesyl diphosphate synthetaseD J Wilkin, P A Edwards
Current Opinion in Genetics & Development|June 1, 1996
Bone dysplasias in man: molecular insightsC A Francomano, I McIntosh, D J Wilkin
Endocrine Reviews|March 4, 2000
The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricansZ Vajo, C A Francomano, D J Wilkin
The Journal of Biological Chemistry|March 15, 1990
Isolation and sequence of the human farnesyl pyrophosphate synthetase cDNA. Coordinate regulation of the mRNAs for farnesyl pyrophosphate synthetase, 3-hydroxy-3-methylglutaryl coenzyme A reductase, and 3-hydroxy-3-methylglutaryl coenzyme A synthase by phorbol esterD J Wilkin, S Y Kutsunai, P A Edwards
Genomics|February 1, 1993
Heteroduplex analysis can increase the informativeness of PCR-amplified VNTR markers: application using a marker tightly linked to the COL2A1 geneD J Wilkin, K E Koprivnikar, D H Cohn
Development (Cambridge, England)|May 1, 1990
The Xenopus XIHbox 6 homeo protein, a marker of posterior neural induction, is expressed in proliferating neuronsC V Wright, E A Morita, D J Wilkin, et al.
Human Molecular Genetics|November 1, 1994
A single amino acid substitution (G103D) in the type II collagen triple helix produces Kniest dysplasiaD J Wilkin, R Bogaert, R S Lachman, et al.
American Journal of Medical Genetics|September 13, 2000
Rapid determination of COL2A1 mutations in individuals with Stickler syndrome: analysis of potential premature termination codonsD J Wilkin, R Liberfarb, J Davis, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 1999
Conservation of the Caenorhabditis elegans timing gene clk-1 from yeast to human: a gene required for ubiquinone biosynthesis with potential implications for agingZ Vajo, L M King, T Jonassen, et al.
Human Molecular Genetics|February 1, 1995
A radiographic, morphologic, biochemical and molecular analysis of a case of achondrogenesis type II resulting from substitution for a glycine residue (Gly691-->Arg) in the type II collagen trimerG R Mortier, D J Wilkin, W R Wilcox, et al.
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