Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
3R01DK042482-05A1S1
Application #
2436683
Study Section
Orthopedics and Musculoskeletal Study Section (ORTH)
Program Officer
Margolis, Ronald N
Project Start
1991-06-01
Project End
2001-04-30
Budget Start
1997-01-29
Budget End
1997-04-30
Support Year
5
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Stanford University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Malloy, Peter J; Tasic, Velibor; Taha, Doris et al. (2014) Vitamin D receptor mutations in patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets. Mol Genet Metab 111:33-40
Huang, Karen; Malloy, Peter; Feldman, David et al. (2013) Enteral calcium infusion used successfully as treatment for a patient with hereditary vitamin D resistant rickets (HVDRR) without alopecia: a novel mutation. Gene 512:554-9
Sequeira, Vanessa B; Rybchyn, Mark S; Tongkao-On, Wannit et al. (2012) The role of the vitamin D receptor and ERp57 in photoprotection by 1?,25-dihydroxyvitamin D3. Mol Endocrinol 26:574-82
Malloy, Peter J; Zhou, Yulin; Wang, Jining et al. (2011) Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor. J Bone Miner Res 26:2710-8
Malloy, Peter J; Feldman, David (2011) The role of vitamin D receptor mutations in the development of alopecia. Mol Cell Endocrinol 347:90-6
Aljubeh, Jamal M; Wang, Jining; Al-Remeithi, Sareea S et al. (2011) Report of two unrelated patients with hereditary vitamin D resistant rickets due to the same novel mutation in the vitamin D receptor. J Pediatr Endocrinol Metab 24:793-9
Krishnan, Aruna V; Feldman, David (2010) Molecular pathways mediating the anti-inflammatory effects of calcitriol: implications for prostate cancer chemoprevention and treatment. Endocr Relat Cancer 17:R19-38
Malloy, Peter J; Feldman, David (2010) Genetic disorders and defects in vitamin d action. Endocrinol Metab Clin North Am 39:333-46, table of contents
Forghani, Nikta; Lum, Catherine; Krishnan, Sowmya et al. (2010) Two new unrelated cases of hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from the same novel nonsense mutation in the vitamin D receptor gene. J Pediatr Endocrinol Metab 23:843-50
Malloy, Peter J; Wang, Jining; Srivastava, Tarak et al. (2010) Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor. Mol Genet Metab 99:72-9

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