These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 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]
    of 8.