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Miller, Walter L (2002) Androgen biosynthesis from cholesterol to DHEA. Mol Cell Endocrinol 198:7-14
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Wang, Xuemei; Zhang, Martin Y H; Miller, Walter L et al. (2002) Novel gene mutations in patients with 1alpha-hydroxylase deficiency that confer partial enzyme activity in vitro. J Clin Endocrinol Metab 87:2424-30
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Zhang, Martin Y H; Wang, Xuemei; Wang, Jonathan T et al. (2002) Dietary phosphorus transcriptionally regulates 25-hydroxyvitamin D-1alpha-hydroxylase gene expression in the proximal renal tubule. Endocrinology 143:587-95
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Schalkwijk, J; Zweers, M C; Steijlen, P M et al. (2001) A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency. N Engl J Med 345:1167-75
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Huang, M C; Miller, W L (2001) Creation and activity of COS-1 cells stably expressing the F2 fusion of the human cholesterol side-chain cleavage enzyme system. Endocrinology 142:2569-76
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Song, M; Shao, H; Mujeeb, A et al. (2001) Molten-globule structure and membrane binding of the N-terminal protease-resistant domain (63-193) of the steroidogenic acute regulatory protein (StAR). Biochem J 356:151-8
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Lin, C J; Martens, J W; Miller, W L (2001) NF-1C, Sp1, and Sp3 are essential for transcription of the human gene for P450c17 (steroid 17alpha-hydroxylase/17,20 lyase) in human adrenal NCI-H295A cells. Mol Endocrinol 15:1277-93
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Miller, W L; Portale, A A (2001) Genetics of vitamin D biosynthesis and its disorders. Best Pract Res Clin Endocrinol Metab 15:95-109
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Bose, H S; Sato, S; Aisenberg, J et al. (2000) Mutations in the steroidogenic acute regulatory protein (StAR) in six patients with congenital lipoid adrenal hyperplasia. J Clin Endocrinol Metab 85:3636-9
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Miller, W L; Portale, A A (2000) Vitamin D 1 alpha-hydroxylase. Trends Endocrinol Metab 11:315-9
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Showing the most recent 10 out of 70 publications
