151 related articles for article (PubMed ID: 9554741)
1. Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland.
Olufemi SE; Green JS; Manickam P; Guru SC; Agarwal SK; Kester MB; Dong Q; Burns AL; Spiegel AM; Marx SJ; Collins FS; Chandrasekharappa SC
Hum Mutat; 1998; 11(4):264-9. PubMed ID: 9554741
[TBL] [Abstract][Full Text] [Related]
2. 11q13 allelotype analysis in 27 northern American MEN1 kindreds identifies two distinct founder chromosomes.
Emmert-Buck MR; Debelenko LV; Agarwal S; Kester MB; Manickam P; Zhuang Z; Guru SC; Olufemi SE; Burns AL; Chandrasekharappa SC; Lubensky IA; Liotta LA; Skarulis MC; Spiegel AM; Marx SJ; Collins FS
Mol Genet Metab; 1998 Feb; 63(2):151-5. PubMed ID: 9562970
[TBL] [Abstract][Full Text] [Related]
3. Haplotype analysis defines a minimal interval for the multiple endocrine neoplasia type 1 (MEN1) gene.
Debelenko LV; Emmert-Buck MR; Manickam P; Kester M; Guru SC; DiFranco EM; Olufemi SE; Agarwal S; Lubensky IA; Zhuang Z; Burns AL; Spiegel AM; Liotta LA; Collins FS; Marx SJ; Chandrasekharappa SC
Cancer Res; 1997 Mar; 57(6):1039-42. PubMed ID: 9067266
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families.
Agarwal SK; Debelenko LV; Kester MB; Guru SC; Manickam P; Olufemi SE; Skarulis MC; Heppner C; Crabtree JS; Lubensky IA; Zhuang Z; Kim YS; Chandrasekharappa SC; Collins FS; Liotta LA; Spiegel AM; Burns AL; Emmert-Buck MR; Marx SJ
Hum Mutat; 1998; 12(2):75-82. PubMed ID: 9671267
[TBL] [Abstract][Full Text] [Related]
6. Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland.
Petty EM; Green JS; Marx SJ; Taggart RT; Farid N; Bale AE
Am J Hum Genet; 1994 Jun; 54(6):1060-6. PubMed ID: 7911003
[TBL] [Abstract][Full Text] [Related]
7. Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1).
Courseaux A; Grosgeorge J; Gaudray P; Pannett AA; Forbes SA; Williamson C; Bassett D; Thakker RV; Teh BT; Farnebo F; Shepherd J; Skogseid B; Larsson C; Giraud S; Zhang CX; Salandre J; Calender A
Genomics; 1996 Nov; 37(3):354-65. PubMed ID: 8938448
[TBL] [Abstract][Full Text] [Related]
8. Isolated familial somatotropinomas: clinical and genetic considerations.
Frohman LA
Trans Am Clin Climatol Assoc; 2003; 114():165-77. PubMed ID: 12813918
[TBL] [Abstract][Full Text] [Related]
9. Multiple endocrine neoplasia type 1 variant with frequent prolactinoma and rare gastrinoma.
Hao W; Skarulis MC; Simonds WF; Weinstein LS; Agarwal SK; Mateo C; James-Newton L; Hobbs GR; Gibril F; Jensen RT; Marx SJ
J Clin Endocrinol Metab; 2004 Aug; 89(8):3776-84. PubMed ID: 15292304
[TBL] [Abstract][Full Text] [Related]
10. 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; 54():397-438; discussion 438-9. PubMed ID: 10548885
[TBL] [Abstract][Full Text] [Related]
11. 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
[TBL] [Abstract][Full Text] [Related]
12. 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
[TBL] [Abstract][Full Text] [Related]
13. MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1.
Balogh K; Hunyady L; Patocs A; Gergics P; Valkusz Z; Toth M; Racz K
Clin Endocrinol (Oxf); 2007 Nov; 67(5):727-34. PubMed ID: 17953629
[TBL] [Abstract][Full Text] [Related]
14. Novel mutations in the MEN1 gene in subjects with multiple endocrine neoplasia-1.
Jap TS; Chiu CY; Won JG; Wu YC; Chen HS
Clin Endocrinol (Oxf); 2005 Mar; 62(3):336-42. PubMed ID: 15730416
[TBL] [Abstract][Full Text] [Related]
15. Multiple endocrine neoplasia type 1: from bedside to benchside.
Yoshimoto K
J Med Invest; 2000 Aug; 47(3-4):108-17. PubMed ID: 11019489
[TBL] [Abstract][Full Text] [Related]
16. Characteristics of the Danish families with multiple endocrine neoplasia type 1.
Jäger AC; Friis-Hansen L; Hansen TV; Eskildsen PC; Sølling K; Knigge U; Hansen CP; Andersen PH; Brixen K; Feldt-Rasmussen U; Kroustrup JP; Mollerup CL; Rehfeld JF; Blichert-Toft M; Nielsen FC
Mol Cell Endocrinol; 2006 Apr; 249(1-2):123-32. PubMed ID: 16563611
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [Identification of the gene associated with type 1 multiple endocrine neoplasia (NEM 1) susceptibility: a new pathway in the pathogenesis of neuro-endocrine tumors].
Calender A
Bull Cancer; 1997 Oct; 84(10):993-5. PubMed ID: 9435804
[TBL] [Abstract][Full Text] [Related]
19. A kindred with a variant of multiple endocrine neoplasia type 1 demonstrating frequent expression of pituitary tumors but not linked to the multiple endocrine neoplasia type 1 locus at chromosome region 11q13.
Stock JL; Warth MR; Teh BT; Coderre JA; Overdorf JH; Baumann G; Hintz RL; Hartman ML; Seizinger BR; Larsson C; Aronin N
J Clin Endocrinol Metab; 1997 Feb; 82(2):486-92. PubMed ID: 9024241
[TBL] [Abstract][Full Text] [Related]
20. Definition of the Minimal MEN1 Candidate Area Based on a 5-Mb Integrated Map of Proximal 11q13.
Courseaux A; Grosgeorge J; Gaudray P; Pannett AAJ; Forbes SA; Williamson C; Bassett D; Thakker RV; Teh BT; Farnebo F; Shepherd J; Skogseid B; Larsson C; Giraud S; Zhang CX; Salandre J; Calender A
Genomics; 1996 Nov; 37(3):345-53. PubMed ID: 8977082
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
