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201 related items for PubMed ID: 8803711
1. A possible tumor suppressor gene for parathyroid adenomas. Iwasaki H. Int Surg; 1996; 81(1):71-6. PubMed ID: 8803711 [Abstract] [Full Text] [Related]
2. Loss of heterozygosity in 11q13-14 regions in gastric neuroendocrine tumors not associated with multiple endocrine neoplasia type 1 syndrome. D'Adda T, Keller G, Bordi C, Höfler H. Lab Invest; 1999 Jun; 79(6):671-7. PubMed ID: 10378509 [Abstract] [Full Text] [Related]
3. 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 01; 56(3):599-605. PubMed ID: 8564978 [Abstract] [Full Text] [Related]
4. Allelic loss from chromosome 11 in parathyroid tumors. Friedman E, De Marco L, Gejman PV, Norton JA, Bale AE, Aurbach GD, Spiegel AM, Marx SJ. Cancer Res; 1992 Dec 15; 52(24):6804-9. PubMed ID: 1360870 [Abstract] [Full Text] [Related]
5. Cytogenetic and molecular analyses of multiple endocrine neoplasias of the MEN1 syndrome. Pourani J, Kaserer K, Pfragner R. Int J Oncol; 2002 May 15; 20(5):971-6. PubMed ID: 11956591 [Abstract] [Full Text] [Related]
6. 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 [Abstract] [Full Text] [Related]
7. Somatic mutations of multiple endocrine neoplasia type 1 gene in the sporadic endocrine tumors. Shan L, Nakamura Y, Nakamura M, Yokoi T, Tsujimoto M, Arima R, Kameya T, Kakudo K. Lab Invest; 1998 Apr 01; 78(4):471-5. PubMed ID: 9564891 [Abstract] [Full Text] [Related]
9. 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 Apr 01; 18(4A):2685-9. PubMed ID: 9703929 [Abstract] [Full Text] [Related]
10. Clonal analysis by chromosome 11 microsatellite-PCR of microdissected parathyroid tumors from MEN 1 patients. Morelli A, Falchetti A, Amorosi A, Tonelli F, Bearzi I, Ranaldi R, Tomassetti P, Brandi ML. Biochem Biophys Res Commun; 1996 Oct 23; 227(3):736-42. PubMed ID: 8886003 [Abstract] [Full Text] [Related]
11. 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 23; 83(8):1003-8. PubMed ID: 10993646 [Abstract] [Full Text] [Related]
12. Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1. Friedman E, Sakaguchi K, Bale AE, Falchetti A, Streeten E, Zimering MB, Weinstein LS, McBride WO, Nakamura Y, Brandi ML. N Engl J Med; 1989 Jul 27; 321(4):213-8. PubMed ID: 2568586 [Abstract] [Full Text] [Related]
13. Allelic loss on chromosome 11 in hereditary and sporadic tumors related to familial multiple endocrine neoplasia type 1. Bale AE, Norton JA, Wong EL, Fryburg JS, Maton PN, Oldfield EH, Streeten E, Aurbach GD, Brandi ML, Friedman E. Cancer Res; 1991 Feb 15; 51(4):1154-7. PubMed ID: 1671755 [Abstract] [Full Text] [Related]
14. 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 [Abstract] [Full Text] [Related]
15. Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11. Thakker RV, Bouloux P, Wooding C, Chotai K, Broad PM, Spurr NK, Besser GM, O'Riordan JL. N Engl J Med; 1989 Jul 27; 321(4):218-24. PubMed ID: 2568587 [Abstract] [Full Text] [Related]
16. 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 27; 21(4):727-35. PubMed ID: 12239610 [Abstract] [Full Text] [Related]
17. Parathyroid tumor suppressor on 1p: analysis of the p18 cyclin-dependent kinase inhibitor gene as a candidate. Tahara H, Smith AP, Gaz RD, Zariwala M, Xiong Y, Arnold A. J Bone Miner Res; 1997 Sep 27; 12(9):1330-4. PubMed ID: 9286748 [Abstract] [Full Text] [Related]
18. Putative tumor-suppressor gene on chromosome 11 is important in sporadic endocrine tumor formation. Eubanks PJ, Sawicki MP, Samara GJ, Gatti R, Nakamura Y, Tsao D, Johnson C, Hurwitz M, Wan YJ, Passaro E. Am J Surg; 1994 Jan 27; 167(1):180-5. PubMed ID: 7906100 [Abstract] [Full Text] [Related]
19. Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes. Moley JF, Brother MB, Fong CT, White PS, Baylin SB, Nelkin B, Wells SA, Brodeur GM. Cancer Res; 1992 Feb 15; 52(4):770-4. PubMed ID: 1346584 [Abstract] [Full Text] [Related]
20. Six novel MEN1 gene mutations in sporadic parathyroid tumors. Cetani F, Pardi E, Giovannetti A, Cerrai P, Borsari S, Vignali E, Picone A, Cianferotti L, Miccoli P, Pinchera A, Marcocci C. Hum Mutat; 2000 Nov 15; 16(5):445. PubMed ID: 11058905 [Abstract] [Full Text] [Related] Page: [Next] [New Search]