M. C. Dormanen

Comparison of 6-s-cis- and 6-s-trans-locked analogs of 1alpha,25-dihydroxyvitamin D3 indicates that the 6-s-cis conformation is preferred for rapid nongenomic biological responses and that neither 6-s-cis- nor 6-s-trans-locked analogs are preferred for genomic biological responses.

R. Bouillon, A. Norman, M. Farach-Carson, 1997, Molecular endocrinology.

Differing shapes of 1α,25-dihydroxyvitamin D3 function as ligands for the D-binding protein, nuclear receptor and membrane receptor: A status report

S. Zanello, R. Bouillon, A. Norman, 1996, The Journal of Steroid Biochemistry and Molecular Biology.

Nonnuclear effects of the steroid hormone 1 alpha,25(OH)2-vitamin D3: analogs are able to functionally differentiate between nuclear and membrane receptors.

A. Norman, I. Nemere, W. Okamura, 1994, Biochemical and biophysical research communications.

Identification of a specific binding protein for 1 alpha,25-dihydroxyvitamin D3 in basal-lateral membranes of chick intestinal epithelium and relationship to transcaltachia.

A. Norman, I. Nemere, W. Okamura, 1994, The Journal of biological chemistry.

Biochemical Significance of the 6‐s‐cis Conformation of the Steroid Hormone lα,25‐Dihydroxyvitamin D3 Based on the Provitamin D Skeleton a

A. Norman, I. Nemere, W. Okamura, 1995, Annals of the New York Academy of Sciences.

Chemistry and conformation of vitamin D molecules

A. Norman, I. Nemere, W. Okamura, 1995, The Journal of Steroid Biochemistry and Molecular Biology.