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2. Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders. Giraud S; Zhang CX; Serova-Sinilnikova O; Wautot V; Salandre J; Buisson N; Waterlot C; Bauters C; Porchet N; Aubert JP; Emy P; Cadiot G; Delemer B; Chabre O; Niccoli P; Leprat F; Duron F; Emperauger B; Cougard P; Goudet P; Sarfati E; Riou JP; Guichard S; Rodier M; Meyrier A; Caron P; Vantyghem MC; Assayag M; Peix JL; Pugeat M; Rohmer V; Vallotton M; Lenoir G; Gaudray P; Proye C; Conte-Devolx B; Chanson P; Shugart YY; Goldgar D; Murat A; Calender A Am J Hum Genet; 1998 Aug; 63(2):455-67. PubMed ID: 9683585 [TBL] [Abstract][Full Text] [Related]
3. 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; 18(4A):2685-9. PubMed ID: 9703929 [TBL] [Abstract][Full Text] [Related]
4. A novel germline mutation in exon 5 of the multiple endocrine neoplasia type 1 gene. Chico A; Gallart L; Mato E; Mayoral C; Martin-Campos JM; Catasús L; Rodriguez-Espinosa J; Matías-Guiu X; Blanco-Vaca F; de Leiva A J Mol Med (Berl); 1998; 76(12):837-9. PubMed ID: 9846954 [TBL] [Abstract][Full Text] [Related]
5. Menin mutations in the diagnosis and prediction of multiple endocrine neoplasia type 1. Karges W; Ludwig L; Kessler H; Wissmann A; Wagner PK; Boehm BO Langenbecks Arch Surg; 1998 Apr; 383(2):183-6. PubMed ID: 9641896 [TBL] [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; 58(19):4417-20. PubMed ID: 9766672 [TBL] [Abstract][Full Text] [Related]
7. Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases. Poncin J; Abs R; Velkeniers B; Bonduelle M; Abramowicz M; Legros JJ; Verloes A; Meurisse M; Van Gaal L; Verellen C; Koulischer L; Beckers A Hum Mutat; 1999; 13(1):54-60. PubMed ID: 9888389 [TBL] [Abstract][Full Text] [Related]
8. Allelic loss of 11q13 as detected by MEN1-FISH is not associated with mutation of the MEN1 gene in lymphoid neoplasms. Thieblemont C; Pack S; Sakai A; Beaty M; Pak E; Vortmeyer AO; Wellmann A; Zhuang Z; Jaffe ES; Raffeld M Leukemia; 1999 Jan; 13(1):85-91. PubMed ID: 10049065 [TBL] [Abstract][Full Text] [Related]
9. Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated hyperparathyroidism. Cetani F; Pardi E; Giovannetti A; Vignali E; Borsari S; Golia F; Cianferotti L; Viacava P; Miccoli P; Gasperi M; Pinchera A; Marcocci C Clin Endocrinol (Oxf); 2002 Apr; 56(4):457-64. PubMed ID: 11966738 [TBL] [Abstract][Full Text] [Related]
10. Molecular pathology of multiple endocrine neoplasia type I: two novel germline mutations and updated classification of mutations affecting MEN1 gene. Martín-Campos JM; Catasús L; Chico A; Mayoral C; Lagarda E; Gallart L; Mato E; Rodríguez-Espinosa J; Matías-Guiu X; De Leiva A; Blanco-Vaca F Diagn Mol Pathol; 1999 Dec; 8(4):195-204. PubMed ID: 10617276 [TBL] [Abstract][Full Text] [Related]
12. Multiple endocrine neoplasia type 1 (MEN1): clinical heterogeneity in a large family with a nonsense mutation in the MEN1 gene (Trp471Stop). Valdés N; Pérez de Nanclares G; Alvarez V; Castaño L; Díaz-Cadórniga F; Aller J; Coto E Clin Endocrinol (Oxf); 1999 Mar; 50(3):309-13. PubMed ID: 10435055 [TBL] [Abstract][Full Text] [Related]
14. Type 1 multiple endocrine neoplasia (MEN1): contribution of genetic analysis to the screening and follow-up of a large French kindred. Waterlot C; Porchet N; Bauters C; Decoulx M; Wémeau JL; Proye C; Degand PM; Aubert JP; Cortet C; Dewailly D Clin Endocrinol (Oxf); 1999 Jul; 51(1):101-7. PubMed ID: 10468972 [TBL] [Abstract][Full Text] [Related]
15. Lack of MEN1 gene mutations in 27 sporadic insulinomas. Cupisti K; Höppner W; Dotzenrath C; Simon D; Berndt I; Röher HD; Goretzki PE Eur J Clin Invest; 2000 Apr; 30(4):325-9. PubMed ID: 10759881 [TBL] [Abstract][Full Text] [Related]
16. Deletion of exons 1-3 of the MEN1 gene in a large Italian family causes the loss of menin expression. Zatelli MC; Tagliati F; Di Ruvo M; Castermans E; Cavazzini L; Daly AF; Ambrosio MR; Beckers A; degli Uberti E Fam Cancer; 2014 Jun; 13(2):273-80. PubMed ID: 24522746 [TBL] [Abstract][Full Text] [Related]