BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

83 related articles for article (PubMed ID: 7593455)

  • 1. Genetic abnormalities in sporadic parathyroid adenomas: loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus.
    Thompson DB; Samowitz WS; Odelberg S; Davis RK; Szabo J; Heath H
    J Clin Endocrinol Metab; 1995 Nov; 80(11):3377-80. PubMed ID: 7593455
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism.
    Farnebo F; Teh BT; Dotzenrath C; Wassif WS; Svensson A; White I; Betz R; Goretzki P; Sandelin K; Farnebo LO; Larsson C
    Hum Genet; 1997 Mar; 99(3):342-9. PubMed ID: 9050920
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tumor-specific decreased expression of calcium sensing receptor messenger ribonucleic acid in sporadic primary hyperparathyroidism.
    Farnebo F; Enberg U; Grimelius L; Bäckdahl M; Schalling M; Larsson C; Farnebo LO
    J Clin Endocrinol Metab; 1997 Oct; 82(10):3481-6. PubMed ID: 9329389
    [TBL] [Abstract][Full Text] [Related]  

  • 4. No evidence for mutations in the calcium-sensing receptor gene in sporadic parathyroid adenomas.
    Cetani F; Pinchera A; Pardi E; Cianferotti L; Vignali E; Picone A; Miccoli P; Viacava P; Marcocci C
    J Bone Miner Res; 1999 Jun; 14(6):878-82. PubMed ID: 10352095
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor.
    Carling T; Szabo E; Bai M; Ridefelt P; Westin G; Gustavsson P; Trivedi S; Hellman P; Brown EM; Dahl N; Rastad J
    J Clin Endocrinol Metab; 2000 May; 85(5):2042-7. PubMed ID: 10843194
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of heterozygosity in parathyroid glands of familial hypercalcemia with hypercalciuria and point mutation in calcium receptor.
    Szabo E; Carling T; Hessman O; Rastad J
    J Clin Endocrinol Metab; 2002 Aug; 87(8):3961-5. PubMed ID: 12161540
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A possible tumor suppressor gene for parathyroid adenomas.
    Iwasaki H
    Int Surg; 1996; 81(1):71-6. PubMed ID: 8803711
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Aryl hydrocarbon receptor interacting protein (AIP) mutations occur rarely in sporadic parathyroid adenomas.
    Pardi E; Marcocci C; Borsari S; Saponaro F; Torregrossa L; Tancredi M; Raspini B; Basolo F; Cetani F
    J Clin Endocrinol Metab; 2013 Jul; 98(7):2800-10. PubMed ID: 23633209
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains.
    Heath H; Odelberg S; Jackson CE; Teh BT; Hayward N; Larsson C; Buist NR; Krapcho KJ; Hung BC; Capuano IV; Garrett JE; Leppert MF
    J Clin Endocrinol Metab; 1996 Apr; 81(4):1312-7. PubMed ID: 8636323
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A reappraisal of the Rb1 gene abnormalities in the diagnosis of parathyroid cancer.
    Cetani F; Pardi E; Viacava P; Pollina GD; Fanelli G; Picone A; Borsari S; Gazzerro E; Miccoli P; Berti P; Pinchera A; Marcocci C
    Clin Endocrinol (Oxf); 2004 Jan; 60(1):99-106. PubMed ID: 14678295
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas.
    Tahara H; Smith AP; Gas RD; Cryns VL; Arnold A
    Cancer Res; 1996 Feb; 56(3):599-605. PubMed ID: 8564978
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutational analysis of the extracellular Ca(2+)-sensing receptor gene in human parathyroid tumors.
    Hosokawa Y; Pollak MR; Brown EM; Arnold A
    J Clin Endocrinol Metab; 1995 Nov; 80(11):3107-10. PubMed ID: 7593409
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutational analysis of the vitamin D receptor does not support its candidacy as a tumor suppressor gene in parathyroid adenomas.
    Samander EH; Arnold A
    J Clin Endocrinol Metab; 2006 Dec; 91(12):5019-21. PubMed ID: 17003089
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Distinct target regions for chromosome 1p deletions in parathyroid adenomas and carcinomas.
    Välimäki S; Forsberg L; Farnebo LO; Larsson C
    Int J Oncol; 2002 Oct; 21(4):727-35. PubMed ID: 12239610
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clonal loss of one chromosome 11 in a parathyroid adenoma.
    Arnold A; Kim HG
    J Clin Endocrinol Metab; 1989 Sep; 69(3):496-9. PubMed ID: 2569472
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of somatic mutations of the MEN1 gene in sporadic endocrine tumours.
    Bergman L; Boothroyd C; Palmer J; Grimmond S; Walters M; Teh B; Shepherd J; Hartley L; Hayward N
    Br J Cancer; 2000 Oct; 83(8):1003-8. PubMed ID: 10993646
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Progression of uremic hyperparathyroidism involves allelic loss on chromosome 11.
    Falchetti A; Bale AE; Amorosi A; Bordi C; Cicchi P; Bandini S; Marx SJ; Brandi ML
    J Clin Endocrinol Metab; 1993 Jan; 76(1):139-44. PubMed ID: 8421078
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic and clinical characterization of sporadic cystic parathyroid tumours.
    Villablanca A; Farnebo F; Teh BT; Farnebo LO; Höög A; Larsson C
    Clin Endocrinol (Oxf); 2002 Feb; 56(2):261-9. PubMed ID: 11874419
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism.
    Carling T; Correa P; Hessman O; Hedberg J; Skogseid B; Lindberg D; Rastad J; Westin G; Akerström G
    J Clin Endocrinol Metab; 1998 Aug; 83(8):2960-3. PubMed ID: 9709976
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Somatic mutation of the MEN1 gene in parathyroid tumours.
    Heppner C; Kester MB; Agarwal SK; Debelenko LV; Emmert-Buck MR; Guru SC; Manickam P; Olufemi SE; Skarulis MC; Doppman JL; Alexander RH; Kim YS; Saggar SK; Lubensky IA; Zhuang Z; Liotta LA; Chandrasekharappa SC; Collins FS; Spiegel AM; Burns AL; Marx SJ
    Nat Genet; 1997 Aug; 16(4):375-8. PubMed ID: 9241276
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.