These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 29461981)

  • 1. CYP3A4 mutation causes vitamin D-dependent rickets type 3.
    Roizen JD; Li D; O'Lear L; Javaid MK; Shaw NJ; Ebeling PR; Nguyen HH; Rodda CP; Thummel KE; Thacher TD; Hakonarson H; Levine MA
    J Clin Invest; 2018 May; 128(5):1913-1918. PubMed ID: 29461981
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Vitamin D-Dependent Rickets Type 3: A Case Report and Systematic Review.
    Mantoanelli L; de Almeida CM; Coelho MCA; Coutinho M; Levine MA; Collett-Solberg PF; Bordallo AP
    Calcif Tissue Int; 2023 Apr; 112(4):512-517. PubMed ID: 36656330
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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.
    Malloy PJ; Wang J; Srivastava T; Feldman D
    Mol Genet Metab; 2010 Jan; 99(1):72-9. PubMed ID: 19815438
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CYP2R1 mutations causing vitamin D-deficiency rickets.
    Thacher TD; Levine MA
    J Steroid Biochem Mol Biol; 2017 Oct; 173():333-336. PubMed ID: 27473561
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary 1,25-dihydroxyvitamin D-resistant rickets due to an opal mutation causing premature termination of the vitamin D receptor.
    Zhu W; Malloy PJ; Delvin E; Chabot G; Feldman D
    J Bone Miner Res; 1998 Feb; 13(2):259-64. PubMed ID: 9495519
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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.
    Forghani N; Lum C; Krishnan S; Wang J; Wilson DM; Blackett PR; Malloy PJ; Feldman D
    J Pediatr Endocrinol Metab; 2010 Aug; 23(8):843-50. PubMed ID: 21073129
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Generation of novel genetically modified rats to reveal the molecular mechanisms of vitamin D actions.
    Nishikawa M; Yasuda K; Takamatsu M; Abe K; Okamoto K; Horibe K; Mano H; Nakagawa K; Tsugawa N; Hirota Y; Horie T; Hinoi E; Okano T; Ikushiro S; Sakaki T
    Sci Rep; 2020 Mar; 10(1):5677. PubMed ID: 32231239
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Vitamin D-Dependent Rickets Type 1B (25-Hydroxylase Deficiency): A Rare Condition or a Misdiagnosed Condition?
    Molin A; Wiedemann A; Demers N; Kaufmann M; Do Cao J; Mainard L; Dousset B; Journeau P; Abeguile G; Coudray N; Mittre H; Richard N; Weryha G; Sorlin A; Jones G; Kottler ML; Feillet F
    J Bone Miner Res; 2017 Sep; 32(9):1893-1899. PubMed ID: 28548312
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Vitamin D-dependent rickets type I and type II.
    Takeda E; Yamamoto H; Taketani Y; Miyamoto K
    Acta Paediatr Jpn; 1997 Aug; 39(4):508-13. PubMed ID: 9316302
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic disorders of Vitamin D biosynthesis and degradation.
    Miller WL
    J Steroid Biochem Mol Biol; 2017 Jan; 165(Pt A):101-108. PubMed ID: 27060335
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Normal 24-hydroxylation of vitamin D metabolites in patients with vitamin D-dependency rickets type I. Structural implications for the vitamin D hydroxylases.
    Mandla S; Jones G; Tenenhouse HS
    J Clin Endocrinol Metab; 1992 Apr; 74(4):814-20. PubMed ID: 1548347
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel mutation in helix 12 of the vitamin D receptor impairs coactivator interaction and causes hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia.
    Malloy PJ; Xu R; Peng L; Clark PA; Feldman D
    Mol Endocrinol; 2002 Nov; 16(11):2538-46. PubMed ID: 12403843
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CYP3A4 Induction by Rifampin: An Alternative Pathway for Vitamin D Inactivation in Patients With CYP24A1 Mutations.
    Hawkes CP; Li D; Hakonarson H; Meyers KE; Thummel KE; Levine MA
    J Clin Endocrinol Metab; 2017 May; 102(5):1440-1446. PubMed ID: 28324001
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Impaired Vitamin D Signaling in T Cells From a Family With Hereditary Vitamin D Resistant Rickets.
    Al-Jaberi FAH; Kongsbak-Wismann M; Aguayo-Orozco A; Krogh N; Buus TB; Lopez DV; Rode AKO; Gravesen E; Olgaard K; Brunak S; Woetmann A; Ødum N; Bonefeld CM; Geisler C
    Front Immunol; 2021; 12():684015. PubMed ID: 34093587
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SIRT1 enzymatically potentiates 1,25-dihydroxyvitamin D
    Sabir MS; Khan Z; Hu C; Galligan MA; Dussik CM; Mallick S; Stone AD; Batie SF; Jacobs ET; Whitfield GK; Haussler MR; Heck MC; Jurutka PW
    J Steroid Biochem Mol Biol; 2017 Sep; 172():117-129. PubMed ID: 28636886
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 2 alpha-(3-hydroxypropyl)- and 2 alpha-(3-hydroxypropoxy)-1 alpha,25-dihydroxyvitamin D3 accessible to vitamin D receptor mutant related to hereditary vitamin D-resistant rickets.
    Kittaka A; Kurihara M; Peleg S; Suhara Y; Takayama H
    Chem Pharm Bull (Tokyo); 2003 Mar; 51(3):357-8. PubMed ID: 12612432
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Vitamin D receptor mutations in patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets.
    Malloy PJ; Tasic V; Taha D; Tütüncüler F; Ying GS; Yin LK; Wang J; Feldman D
    Mol Genet Metab; 2014 Jan; 111(1):33-40. PubMed ID: 24246681
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic disorders and defects in vitamin d action.
    Malloy PJ; Feldman D
    Endocrinol Metab Clin North Am; 2010 Jun; 39(2):333-46, table of contents. PubMed ID: 20511055
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel CYP27B1 mutation causes a feline vitamin D-dependent rickets type IA.
    Grahn RA; Ellis MR; Grahn JC; Lyons LA
    J Feline Med Surg; 2012 Aug; 14(8):587-90. PubMed ID: 22553308
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Constitutively active RAS signaling reduces 1,25 dihydroxyvitamin D-mediated gene transcription in intestinal epithelial cells by reducing vitamin D receptor expression.
    DeSmet ML; Fleet JC
    J Steroid Biochem Mol Biol; 2017 Oct; 173():194-201. PubMed ID: 28104492
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.