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6 in total

1. Removal of the 26-methyl group from 19-nor-1α,25-dihydroxyvitamin D₃ markedly reduces in vivo calcemic activity without altering in vitro VDR binding, HL-60 cell differentiation, and transcription.

Authors: Pawel Grzywacz; Grazia Chiellini; Lori A Plum; Margaret Clagett-Dame; Hector F DeLuca
Journal: J Med Chem Date: 2010-11-24 Impact factor: 7.446

2. 26- and 27-Methyl groups of 2-substituted, 19-nor-1α,25-dihydroxylated vitamin D compounds are essential for calcium mobilization in vivo.

Authors: Pawel Grzywacz; Lori A Plum; Margaret Clagett-Dame; Hector F DeLuca
Journal: Bioorg Chem Date: 2013-02-09 Impact factor: 5.275

3. Removal of the 20-methyl group from 2-methylene-19-nor-(20S)-1alpha,25-dihydroxyvitamin D(3) (2MD) selectively eliminates bone calcium mobilization activity.

Authors: Rafal Barycki; Rafal R Sicinski; Lori A Plum; Pawel Grzywacz; Margaret Clagett-Dame; Hector F Deluca
Journal: Bioorg Med Chem Date: 2009-09-29 Impact factor: 3.641

4. 26-Desmethyl-2-methylene-22-ene-19-nor-1α,25-dihydroxyvitamin D3 compounds selectively active on intestine.

Authors: Grazia Chiellini; Pawel Grzywacz; Lori A Plum; Margaret Clagett-Dame; Hector F DeLuca
Journal: Steroids Date: 2014-02-07 Impact factor: 2.668

Review 5. Genomic mechanisms involved in the pleiotropic actions of 1,25-dihydroxyvitamin D3.

Authors: S Christakos; M Raval-Pandya; R P Wernyj; W Yang
Journal: Biochem J Date: 1996-06-01 Impact factor: 3.857

6. The effects of 1 alpha,25-dihydroxyvitamin D(3) on matrix metalloproteinase and prostaglandin E(2) production by cells of the rheumatoid lesion.

Authors: L C Tetlow; D E Woolley
Journal: Arthritis Res Date: 1999-10-14

6 in total