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Journal Abstract Search


524 related items for PubMed ID: 9241276

  • 1. 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
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  • 2. 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
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  • 4. Screening of the Men1 gene and discovery of germ-line and somatic mutations in apparently sporadic parathyroid tumors.
    Uchino S, Noguchi S, Sato M, Yamashita H, Yamashita H, Watanabe S, Murakami T, Toda M, Ohshima A, Futata T, Mizukoshi T, Koike E, Takatsu K, Terao K, Wakiya S, Nagatomo M, Adachi M.
    Cancer Res; 2000 Oct 01; 60(19):5553-7. PubMed ID: 11034102
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  • 5. Somatic mutations of the multiple endocrine neoplasia type 1 (MEN1) gene in patients with sporadic, nonfamilial primary hyperparathyroidism.
    Sato K, Yamazaki K, Zhu H, Kanbe M, Iihara M, Wada Y, Tanaka R, Okamoto T, Ito Y, Obara T.
    Surgery; 2000 Mar 01; 127(3):337-41. PubMed ID: 10715991
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  • 6. Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias.
    Marx SJ, Agarwal SK, Kester MB, Heppner C, Kim YS, Skarulis MC, James LA, Goldsmith PK, Saggar SK, Park SY, Spiegel AM, Burns AL, Debelenko LV, Zhuang Z, Lubensky IA, Liotta LA, Emmert-Buck MR, Guru SC, Manickam P, Crabtree J, Erdos MR, Collins FS, Chandrasekharappa SC.
    Recent Prog Horm Res; 1999 Mar 01; 54():397-438; discussion 438-9. PubMed ID: 10548885
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  • 8. Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas.
    Haven CJ, van Puijenbroek M, Tan MH, Teh BT, Fleuren GJ, van Wezel T, Morreau H.
    Clin Endocrinol (Oxf); 2007 Sep 01; 67(3):370-6. PubMed ID: 17555500
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  • 9. 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 01; 53(1):85-92. PubMed ID: 10931084
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  • 11. Multiple endocrine neoplasia type 1 (MEN1): LOH studies in a affected family and in sporadic cases.
    Valdes N, Alvarez V, Diaz-Cadorniga F, Aller J, Villazon F, Garcia I, Herrero A, Coto E.
    Anticancer Res; 1998 Jul 01; 18(4A):2685-9. PubMed ID: 9703929
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  • 12. Allelic deletions on chromosome 11q13 in multiple tumors from individual MEN1 patients.
    Lubensky IA, Debelenko LV, Zhuang Z, Emmert-Buck MR, Dong Q, Chandrasekharappa S, Guru SC, Manickam P, Olufemi SE, Marx SJ, Spiegel AM, Collins FS, Liotta LA.
    Cancer Res; 1996 Nov 15; 56(22):5272-8. PubMed ID: 8912868
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  • 18. Mutation of the multiple endocrine neoplasia type 1 gene in nonfamilial, malignant tumors of the endocrine pancreas.
    Hessman O, Lindberg D, Skogseid B, Carling T, Hellman P, Rastad J, Akerström G, Westin G.
    Cancer Res; 1998 Feb 01; 58(3):377-9. PubMed ID: 9458074
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  • 19. Cytogenetic and molecular analyses of multiple endocrine neoplasias of the MEN1 syndrome.
    Pourani J, Kaserer K, Pfragner R.
    Int J Oncol; 2002 May 01; 20(5):971-6. PubMed ID: 11956591
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