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 *

261 related articles for article (PubMed ID: 16636593)

  • 1. Two novel PHEX mutations in Taiwanese patients with X-linked hypophosphatemic rickets.
    Lo FS; Kuo MT; Wang CJ; Chang CH; Lee ZL; Van YH
    Nephron Physiol; 2006; 103(4):p157-63. PubMed ID: 16636593
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Three novel PHEX gene mutations in Japanese patients with X-linked hypophosphatemic rickets.
    Sato K; Tajima T; Nakae J; Adachi M; Asakura Y; Tachibana K; Suwa S; Katsumata N; Tanaka T; Hayashi Y; Abe S; Murashita M; Okuhara K; Shinohara N; Fujieda K
    Pediatr Res; 2000 Oct; 48(4):536-40. PubMed ID: 11004247
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Somatic and germline mosaicism for a mutation of the PHEX gene can lead to genetic transmission of X-linked hypophosphatemic rickets that mimics an autosomal dominant trait.
    Goji K; Ozaki K; Sadewa AH; Nishio H; Matsuo M
    J Clin Endocrinol Metab; 2006 Feb; 91(2):365-70. PubMed ID: 16303832
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel PHEX gene mutations in two Taiwanese patients with hypophosphatemic rickets.
    Chou YY; Chao SC; Tsai SC; Lin SJ
    J Formos Med Assoc; 2005 Mar; 104(3):198-202. PubMed ID: 15818436
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets.
    Li SS; Gu JM; Yu WJ; He JW; Fu WZ; Zhang ZL
    Int J Mol Med; 2016 Dec; 38(6):1703-1714. PubMed ID: 27840894
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis for a novel splice mutation of PHEX gene in a large Han Chinese family affected with X-linked hypophosphatemic rickets.
    Qiu G; Liu C; Zhou J; Liu P; Wang J; Jiang H; Hou Z; Zhao Y; Sun K; Li-Ling J
    Genet Test Mol Biomarkers; 2010 Jun; 14(3):385-91. PubMed ID: 20578943
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Three novel mutations of the PHEX gene in three Chinese families with X-linked dominant hypophosphatemic rickets.
    Xia W; Meng X; Jiang Y; Li M; Xing X; Pang L; Wang O; Pei Y; Yu LY; Sun Y; Hu Y; Zhou X
    Calcif Tissue Int; 2007 Dec; 81(6):415-20. PubMed ID: 18046499
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets.
    Ma SL; Vega-Warner V; Gillies C; Sampson MG; Kher V; Sethi SK; Otto EA
    PLoS One; 2015; 10(6):e0130729. PubMed ID: 26107949
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Three novel PHEX gene mutations in four Chinese families with X-linked dominant hypophosphatemic rickets.
    Kang QL; Xu J; Zhang Z; He JW; Lu LS; Fu WZ; Zhang ZL
    Biochem Biophys Res Commun; 2012 Jul; 423(4):793-8. PubMed ID: 22713460
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of fifteen novel PHEX gene mutations in Finnish patients with hypophosphatemic rickets.
    Tyynismaa H; Kaitila I; Näntö-Salonen K; Ala-Houhala M; Alitalo T
    Hum Mutat; 2000 Apr; 15(4):383-4. PubMed ID: 10737991
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic advances, biochemical and clinical features and critical approach to treatment of patients with X-linked hypophosphatemic rickets.
    Baroncelli GI; Bertelloni S; Sodini F; Galli L; Vanacore T; Fiore L; Saggese G
    Pediatr Endocrinol Rev; 2004 Jun; 1(4):361-79. PubMed ID: 16437029
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel PHEX mutation associated with hypophosphatemic rickets.
    Roetzer KM; Varga F; Zwettler E; Nawrot-Wawrzyniak K; Haller J; Forster E; Klaushofer K
    Nephron Physiol; 2007; 106(1):p8-12. PubMed ID: 17406123
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel Phex mutation in a new mouse model of hypophosphatemic rickets.
    Owen C; Chen F; Flenniken AM; Osborne LR; Ichikawa S; Adamson SL; Rossant J; Aubin JE
    J Cell Biochem; 2012 Jul; 113(7):2432-41. PubMed ID: 22573557
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets.
    Econs MJ; Friedman NE; Rowe PS; Speer MC; Francis F; Strom TM; Oudet C; Smith JA; Ninomiya JT; Lee BE; Bergen H
    J Clin Endocrinol Metab; 1998 Oct; 83(10):3459-62. PubMed ID: 9768646
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutational survey of the PHEX gene in patients with X-linked hypophosphatemic rickets.
    Ichikawa S; Traxler EA; Estwick SA; Curry LR; Johnson ML; Sorenson AH; Imel EA; Econs MJ
    Bone; 2008 Oct; 43(4):663-6. PubMed ID: 18625346
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutational analysis and genotype-phenotype correlation of the PHEX gene in X-linked hypophosphatemic rickets.
    Holm IA; Nelson AE; Robinson BG; Mason RS; Marsh DJ; Cowell CT; Carpenter TO
    J Clin Endocrinol Metab; 2001 Aug; 86(8):3889-99. PubMed ID: 11502829
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A clinical and molecular genetic study of hypophosphatemic rickets in children.
    Cho HY; Lee BH; Kang JH; Ha IS; Cheong HI; Choi Y
    Pediatr Res; 2005 Aug; 58(2):329-33. PubMed ID: 16055933
    [TBL] [Abstract][Full Text] [Related]  

  • 18. PHEX 3'-UTR c.*231A>G near the polyadenylation signal is a relatively common, mild, American mutation that masquerades as sporadic or X-linked recessive hypophosphatemic rickets.
    Mumm S; Huskey M; Cajic A; Wollberg V; Zhang F; Madson KL; Wenkert D; McAlister WH; Gottesman GS; Whyte MP
    J Bone Miner Res; 2015 Jan; 30(1):137-43. PubMed ID: 25042154
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of two novel mutations in the PHEX gene in Chinese patients with hypophosphatemic rickets/osteomalacia.
    Yue H; Yu JB; He JW; Zhang Z; Fu WZ; Zhang H; Wang C; Hu WW; Gu JM; Hu YQ; Li M; Liu YJ; Zhang ZL
    PLoS One; 2014; 9(5):e97830. PubMed ID: 24836714
    [TBL] [Abstract][Full Text] [Related]  

  • 20. FGF23, PHEX, and MEPE regulation of phosphate homeostasis and skeletal mineralization.
    Quarles LD
    Am J Physiol Endocrinol Metab; 2003 Jul; 285(1):E1-9. PubMed ID: 12791601
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.