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Journal Abstract Search

360 related items for PubMed ID: 10931084

  • 1. Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13.
    Dwight T, Twigg S, Delbridge L, Wong FK, Farnebo F, Richardson AL, Nelson A, Zedenius J, Philips J, Larsson C, Teh BT, Robinson B.
    Clin Endocrinol (Oxf); 2000 Jul; 53(1):85-92. PubMed ID: 10931084
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  • 5. 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
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  • 6. Genetic analysis of lithium-associated parathyroid tumors.
    Dwight T, Kytölä S, Teh BT, Theodosopoulos G, Richardson AL, Philips J, Twigg S, Delbridge L, Marsh DJ, Nelson AE, Larsson C, Robinson BG.
    Eur J Endocrinol; 2002 May; 146(5):619-27. PubMed ID: 11980616
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  • 8. Alterations of the MEN1 gene in sporadic parathyroid tumors.
    Farnebo F, Teh BT, Kytölä S, Svensson A, Phelan C, Sandelin K, Thompson NW, Höög A, Weber G, Farnebo LO, Larsson C.
    J Clin Endocrinol Metab; 1998 Aug; 83(8):2627-30. PubMed ID: 9709922
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  • 9. 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
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  • 10. Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndrome.
    Wassif WS, Farnebo F, Teh BT, Moniz CF, Li FY, Harrison JD, Peters TJ, Larsson C, Harris P.
    Clin Endocrinol (Oxf); 1999 Feb; 50(2):191-6. PubMed ID: 10396361
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  • 11. 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
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  • 12. Cytogenetic and molecular analyses of multiple endocrine neoplasias of the MEN1 syndrome.
    Pourani J, Kaserer K, Pfragner R.
    Int J Oncol; 2002 May; 20(5):971-6. PubMed ID: 11956591
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  • 14. Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families.
    Teh BT, Farnebo F, Twigg S, Höög A, Kytölä S, Korpi-Hyövälti E, Wong FK, Nordenström J, Grimelius L, Sandelin K, Robinson B, Farnebo LO, Larsson C.
    J Clin Endocrinol Metab; 1998 Jun; 83(6):2114-20. PubMed ID: 9626148
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  • 15. Putative parathyroid tumor suppressor on 1p: independent molecular mechanisms of tumorigenesis from 11q allelic loss.
    Imanishi Y, Tahara H.
    Am J Kidney Dis; 2001 Oct; 38(4 Suppl 1):S165-7. PubMed ID: 11576946
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  • 16. Sequence analysis and transcript expression of the MEN1 gene in sporadic pituitary tumours.
    Farrell WE, Simpson DJ, Bicknell J, Magnay JL, Kyrodimou E, Thakker RV, Clayton RN.
    Br J Cancer; 1999 Apr; 80(1-2):44-50. PubMed ID: 10389976
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  • 18. 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
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  • 19. Loss of wild-type MEN1 gene expression in multiple endocrine neoplasia type 1-associated parathyroid adenoma.
    Ludwig L, Schleithoff L, Kessler H, Wagner PK, Boehm BO, Karges W.
    Endocr J; 1999 Aug; 46(4):539-44. PubMed ID: 10580746
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  • 20. Mutation of the MENIN gene in sporadic pancreatic endocrine tumors.
    Wang EH, Ebrahimi SA, Wu AY, Kashefi C, Passaro E, Sawicki MP.
    Cancer Res; 1998 Oct 01; 58(19):4417-20. PubMed ID: 9766672
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