BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

260 related articles for article (PubMed ID: 17878646)

  • 1. McCune-Albright syndrome with acromegaly and fibrous dysplasia associated with the GNAS gene mutation identified by sensitive PNA-clamping method.
    Imanaka M; Iida K; Nishizawa H; Fukuoka H; Takeno R; Takahashi K; Kaji H; Takahashi Y; Okimura Y; Kaji H; Imanishi Y; Chihara K
    Intern Med; 2007; 46(18):1577-83. PubMed ID: 17878646
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A highly sensitive polymerase chain reaction method detects activating mutations of the GNAS gene in peripheral blood cells in McCune-Albright syndrome or isolated fibrous dysplasia.
    Lietman SA; Ding C; Levine MA
    J Bone Joint Surg Am; 2005 Nov; 87(11):2489-94. PubMed ID: 16264125
    [TBL] [Abstract][Full Text] [Related]  

  • 3. McCune-Albright syndrome and the extraskeletal manifestations of fibrous dysplasia.
    Collins MT; Singer FR; Eugster E
    Orphanet J Rare Dis; 2012 May; 7 Suppl 1(Suppl 1):S4. PubMed ID: 22640971
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of McCune-Albright syndrome associated with Gs alpha mutation in the bone tissue.
    Sargin H; Gozu H; Bircan R; Sargin M; Avsar M; Ekinci G; Yayla A; Gulec I; Bozbuga M; Cirakoglu B; Tanakol R
    Endocr J; 2006 Feb; 53(1):35-44. PubMed ID: 16543670
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The diagnostic utility of the GNAS mutation in patients with fibrous dysplasia: meta-analysis of 168 sporadic cases.
    Lee SE; Lee EH; Park H; Sung JY; Lee HW; Kang SY; Seo S; Kim BH; Lee H; Seo AN; Ahn G; Choi YL
    Hum Pathol; 2012 Aug; 43(8):1234-42. PubMed ID: 22245114
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Quantitative and sensitive detection of GNAS mutations causing mccune-albright syndrome with next generation sequencing.
    Narumi S; Matsuo K; Ishii T; Tanahashi Y; Hasegawa T
    PLoS One; 2013; 8(3):e60525. PubMed ID: 23536913
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Searching for somatic mutations in McCune-Albright syndrome: a comparative study of the peptidic nucleic acid versus the nested PCR method based on 148 DNA samples.
    Kalfa N; Philibert P; Audran F; Ecochard A; Hannon T; Lumbroso S; Sultan C
    Eur J Endocrinol; 2006 Dec; 155(6):839-43. PubMed ID: 17132753
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of McCune-Albright syndrome with associated multiple endocrinopathies.
    Sung SH; Yoon HD; Shon HS; Kim HT; Choi WY; Seo CJ; Lee JH
    Korean J Intern Med; 2007 Mar; 22(1):45-50. PubMed ID: 17427647
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of Rare Somatic GNAS Mutation in McCune-Albright Syndrome Using a Novel Peptide Nucleic Acid Probe in a Single Tube.
    Lo FS; Chen TL; Chiou CC
    Molecules; 2017 Nov; 22(11):. PubMed ID: 29104223
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic and molecular aspects of McCune-Albright syndrome.
    Lietman SA; Schwindinger WF; Levine MA
    Pediatr Endocrinol Rev; 2007 Aug; 4 Suppl 4():380-5. PubMed ID: 17982384
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Somatic GNAS mutation causes widespread and diffuse pituitary disease in acromegalic patients with McCune-Albright syndrome.
    Vortmeyer AO; Gläsker S; Mehta GU; Abu-Asab MS; Smith JH; Zhuang Z; Collins MT; Oldfield EH
    J Clin Endocrinol Metab; 2012 Jul; 97(7):2404-13. PubMed ID: 22564667
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of GNAS Variants in Circulating Cell-Free DNA from Patients with Fibrous Dysplasia/McCune Albright Syndrome.
    Roszko KL; Guthrie L; Li X; Collins MT; de Castro LF; Boyce AM
    J Bone Miner Res; 2023 Mar; 38(3):443-450. PubMed ID: 36593655
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fibrous Dysplasia of Bone and McCune-Albright Syndrome: A Bench to Bedside Review.
    Hartley I; Zhadina M; Collins MT; Boyce AM
    Calcif Tissue Int; 2019 May; 104(5):517-529. PubMed ID: 31037426
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic diagnosis of multiple affected tissues in a patient with McCune-Albright syndrome.
    Zhou J; Sun LH; Cui B; Song HD; Li XY; Ning G; Liu JM
    Endocrine; 2007 Apr; 31(2):212-7. PubMed ID: 17873334
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fibrous Dysplasia/McCune-Albright Syndrome: Clinical and Translational Perspectives.
    Robinson C; Collins MT; Boyce AM
    Curr Osteoporos Rep; 2016 Oct; 14(5):178-86. PubMed ID: 27492469
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel technique based on a PNA hybridization probe and FRET principle for quantification of mutant genotype in fibrous dysplasia/McCune-Albright syndrome.
    Karadag A; Riminucci M; Bianco P; Cherman N; Kuznetsov SA; Nguyen N; Collins MT; Robey PG; Fisher LW
    Nucleic Acids Res; 2004 Apr; 32(7):e63. PubMed ID: 15096559
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Expression of FGF23 is correlated with serum phosphate level in isolated fibrous dysplasia.
    Kobayashi K; Imanishi Y; Koshiyama H; Miyauchi A; Wakasa K; Kawata T; Goto H; Ohashi H; Koyano HM; Mochizuki R; Miki T; Inaba M; Nishizawa Y
    Life Sci; 2006 Apr; 78(20):2295-301. PubMed ID: 16337659
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lessons from McCune-Albright syndrome-associated intraductal papillary mucinous neoplasms: : GNAS-activating mutations in pancreatic carcinogenesis.
    Parvanescu A; Cros J; Ronot M; Hentic O; Grybek V; Couvelard A; Levy P; Chanson P; Ruszniewski P; Sauvanet A; Gaujoux S
    JAMA Surg; 2014 Aug; 149(8):858-62. PubMed ID: 24898823
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pegvisomant for the treatment of gsp-mediated growth hormone excess in patients with McCune-Albright syndrome.
    Akintoye SO; Kelly MH; Brillante B; Cherman N; Turner S; Butman JA; Robey PG; Collins MT
    J Clin Endocrinol Metab; 2006 Aug; 91(8):2960-6. PubMed ID: 16720661
    [TBL] [Abstract][Full Text] [Related]  

  • 20. GNAS mutation detection is related to disease severity in girls with McCune-Albright syndrome and precocious puberty.
    Wagoner HA; Steinmetz R; Bethin KE; Eugster EA; Pescovitz OH; Hannon TS
    Pediatr Endocrinol Rev; 2007 Aug; 4 Suppl 4():395-400. PubMed ID: 17982386
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.