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 *

180 related articles for article (PubMed ID: 37293695)

  • 21. Vitamin D-dependent rickets (VDDR) type 1: case series of two siblings with a CYP27B1 mutation and review of the literature.
    Dhull RS; Jain R; Deepthi B; Cheong HI; Saha A; Mehndiratta M; Basu S
    J Bras Nefrol; 2020; 42(4):494-497. PubMed ID: 32926064
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The molecular basis of vitamin D-dependent rickets type I.
    Kitanaka S; Takeyama K; Murayama A; Kato S
    Endocr J; 2001 Aug; 48(4):427-32. PubMed ID: 11603564
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Inactivating mutations in the 25-hydroxyvitamin D3 1alpha-hydroxylase gene in patients with pseudovitamin D-deficiency rickets.
    Kitanaka S; Takeyama K; Murayama A; Sato T; Okumura K; Nogami M; Hasegawa Y; Niimi H; Yanagisawa J; Tanaka T; Kato S
    N Engl J Med; 1998 Mar; 338(10):653-61. PubMed ID: 9486994
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Conventional and tissue-specific inactivation of the 25-hydroxyvitamin D-1alpha-hydroxylase (CYP27B1).
    St-Arnaud R; Dardenne O; Prud'homme J; Hacking SA; Glorieux FH
    J Cell Biochem; 2003 Feb; 88(2):245-51. PubMed ID: 12520522
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of vitamin D-dependent rickets type IA caused by a mutation of the CYP27B1 using whole exome sequencing.
    Wang SF; Zhou T; Du MR; Sheng J
    Asian J Surg; 2022 May; 45(5):1160-1161. PubMed ID: 35279323
    [No Abstract]   [Full Text] [Related]  

  • 26. Identification of the amino acid residue of CYP27B1 responsible for binding of 25-hydroxyvitamin D3 whose mutation causes vitamin D-dependent rickets type 1.
    Yamamoto K; Uchida E; Urushino N; Sakaki T; Kagawa N; Sawada N; Kamakura M; Kato S; Inouye K; Yamada S
    J Biol Chem; 2005 Aug; 280(34):30511-6. PubMed ID: 15972816
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel compound mutation of CYP27B1 in a Chinese family with vitamin D-dependent rickets type 1A.
    Hu WW; Ke YH; He JW; Fu WZ; Wang C; Zhang H; Yue H; Gu JM; Zhang ZL
    J Pediatr Endocrinol Metab; 2014 Mar; 27(3-4):335-41. PubMed ID: 24197768
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Vitamin D dependent rickets, diagnostic and therapeutic difficulties: two case reports.
    Donghi V; Di Frenna M; di Lascio A; Chiumello G; Weber G
    J Pediatr Endocrinol Metab; 2011; 24(9-10):801-5. PubMed ID: 22145480
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Long-term clinical outcome and the identification of homozygous
    Cho JH; Kang E; Kim GH; Lee BH; Choi JH; Yoo HW
    Ann Pediatr Endocrinol Metab; 2016 Sep; 21(3):169-173. PubMed ID: 27777911
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Two novel 1alpha-hydroxylase mutations in French-Canadians with vitamin D dependency rickets type I1.
    Yoshida T; Monkawa T; Tenenhouse HS; Goodyer P; Shinki T; Suda T; Wakino S; Hayashi M; Saruta T
    Kidney Int; 1998 Nov; 54(5):1437-43. PubMed ID: 9844119
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Rescue of the pseudo-vitamin D deficiency rickets phenotype of CYP27B1-deficient mice by treatment with 1,25-dihydroxyvitamin D3: biochemical, histomorphometric, and biomechanical analyses.
    Dardenne O; Prudhomme J; Hacking SA; Glorieux FH; St-Arnaud R
    J Bone Miner Res; 2003 Apr; 18(4):637-43. PubMed ID: 12674324
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A.
    Demir K; Kattan WE; Zou M; Durmaz E; BinEssa H; Nalbantoğlu Ö; Al-Rijjal RA; Meyer B; Özkan B; Shi Y
    PLoS One; 2015; 10(7):e0131376. PubMed ID: 26132292
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Vitamin D-dependent rickets type 1: a rare, but treatable, cause of severe hypotonia in infancy.
    Yan Y; Calikoglu AS; Jain N
    J Child Neurol; 2011 Dec; 26(12):1571-5. PubMed ID: 21700898
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Targeted inactivation of the 25-hydroxyvitamin D(3)-1(alpha)-hydroxylase gene (CYP27B1) creates an animal model of pseudovitamin D-deficiency rickets.
    Dardenne O; Prud'homme J; Arabian A; Glorieux FH; St-Arnaud R
    Endocrinology; 2001 Jul; 142(7):3135-41. PubMed ID: 11416036
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Vitamin D-dependent hereditary rickets type I in a cat.
    Geisen V; Weber K; Hartmann K
    J Vet Intern Med; 2009; 23(1):196-9. PubMed ID: 19138382
    [No Abstract]   [Full Text] [Related]  

  • 38. Metabolism of vitamin D3 by cytochromes P450.
    Sakaki T; Kagawa N; Yamamoto K; Inouye K
    Front Biosci; 2005 Jan; 10():119-34. PubMed ID: 15574355
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetics of vitamin D 1alpha-hydroxylase deficiency in 17 families.
    Wang JT; Lin CJ; Burridge SM; Fu GK; Labuda M; Portale AA; Miller WL
    Am J Hum Genet; 1998 Dec; 63(6):1694-702. PubMed ID: 9837822
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Novel Compound Heterozygous Mutations in the CYP27B1 Gene Lead to Pseudovitamin D-Deficient Rickets.
    Koek WN; Zillikens MC; van der Eerden BC; van Leeuwen JP
    Calcif Tissue Int; 2016 Sep; 99(3):326-31. PubMed ID: 27364341
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.