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Journal Abstract Search

225 related items for PubMed ID: 24532476

  • 1. p27 variant and corticotropinoma susceptibility: a genetic and in vitro study.
    Sekiya T, Bronstein MD, Benfini K, Longuini VC, Jallad RS, Machado MC, Goncalves TD, Osaki LH, Higashi L, Viana J, Kater C, Lee M, Molatore S, Francisco G, Chammas R, Naslavsky MS, Schlesinger D, Gama P, Duarte YA, Lebrão ML, Zatz M, Meirelles O, Liberman B, Fragoso MC, Toledo SP, Pellegata NS, Toledo RA.
    Endocr Relat Cancer; 2014 Jun; 21(3):395-404. PubMed ID: 24532476
    [Abstract] [Full Text] [Related]

  • 2. The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations.
    Ozawa A, Agarwal SK, Mateo CM, Burns AL, Rice TS, Kennedy PA, Quigley CM, Simonds WF, Weinstein LS, Chandrasekharappa SC, Collins FS, Spiegel AM, Marx SJ.
    J Clin Endocrinol Metab; 2007 May; 92(5):1948-51. PubMed ID: 17299066
    [Abstract] [Full Text] [Related]

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  • 4. Multiple endocrine neoplasia, the old and the new: a mini review.
    Pasquali D, Di Matteo FM, Renzullo A, Accardo G, Esposito D, Barbato F, Colantuoni V, Circelli L, Conzo G.
    G Chir; 2012 May; 33(11-12):370-3. PubMed ID: 23140918
    [Abstract] [Full Text] [Related]

  • 5. The MENX syndrome and p27: relationships with multiple endocrine neoplasia.
    Molatore S, Pellegata NS.
    Prog Brain Res; 2010 May; 182():295-320. PubMed ID: 20541671
    [Abstract] [Full Text] [Related]

  • 6. Characterization of neuroendocrine tumors in heterozygous mutant MENX rats: a novel model of invasive medullary thyroid carcinoma.
    Molatore S, Kügler A, Irmler M, Wiedemann T, Neff F, Feuchtinger A, Beckers J, Robledo M, Roncaroli F, Pellegata NS.
    Endocr Relat Cancer; 2018 Feb; 25(2):145-162. PubMed ID: 29142006
    [Abstract] [Full Text] [Related]

  • 7. MENX and MEN4.
    Pellegata NS.
    Clinics (Sao Paulo); 2012 Feb; 67 Suppl 1(Suppl 1):13-8. PubMed ID: 22584700
    [Abstract] [Full Text] [Related]

  • 8. Multiple endocrine neoplasia type 4.
    Lee M, Pellegata NS.
    Front Horm Res; 2013 Feb; 41():63-78. PubMed ID: 23652671
    [Abstract] [Full Text] [Related]

  • 9. Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans.
    Pellegata NS, Quintanilla-Martinez L, Siggelkow H, Samson E, Bink K, Höfler H, Fend F, Graw J, Atkinson MJ.
    Proc Natl Acad Sci U S A; 2006 Oct 17; 103(42):15558-63. PubMed ID: 17030811
    [Abstract] [Full Text] [Related]

  • 10. MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27(Kip1) and p18(INK4C)) mutations.
    Georgitsi M.
    Best Pract Res Clin Endocrinol Metab; 2010 Jun 17; 24(3):425-37. PubMed ID: 20833334
    [Abstract] [Full Text] [Related]

  • 11. MENX.
    Pellegata NS.
    Ann Endocrinol (Paris); 2012 Apr 17; 73(2):65-70. PubMed ID: 22542001
    [Abstract] [Full Text] [Related]

  • 12. Characterization of MENX-associated pituitary tumours.
    Marinoni I, Lee M, Mountford S, Perren A, Bravi I, Jennen L, Feuchtinger A, Drouin J, Roncaroli F, Pellegata NS.
    Neuropathol Appl Neurobiol; 2013 Apr 17; 39(3):256-69. PubMed ID: 22524684
    [Abstract] [Full Text] [Related]

  • 13. [Multiple endocrine neoplasia type I. Review and presentation of the study group of multiple endocrine neoplasia type I (GENEM I)].
    Saint-André JP, Berger-Dutrieux N, Le Bodic MF, de Micco C, Trouillas J.
    Arch Anat Cytol Pathol; 1994 Apr 17; 42(2):77-82. PubMed ID: 7811118
    [Abstract] [Full Text] [Related]

  • 14. Genetic aberrance of sporadic MEN 2A component tumours: analysis of RET.
    Cho NH, Lee HW, Lim SY, Kang S, Jung WY, Park CS.
    Pathology; 2005 Feb 17; 37(1):10-3. PubMed ID: 15875728
    [Abstract] [Full Text] [Related]

  • 15. Pheochromocytoma in rats with multiple endocrine neoplasia (MENX) shares gene expression patterns with human pheochromocytoma.
    Molatore S, Liyanarachchi S, Irmler M, Perren A, Mannelli M, Ercolino T, Beuschlein F, Jarzab B, Wloch J, Ziaja J, Zoubaa S, Neff F, Beckers J, Höfler H, Atkinson MJ, Pellegata NS.
    Proc Natl Acad Sci U S A; 2010 Oct 26; 107(43):18493-8. PubMed ID: 20937862
    [Abstract] [Full Text] [Related]

  • 16. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations.
    Longuini VC, Lourenço DM, Sekiya T, Meirelles O, Goncalves TD, Coutinho FL, Francisco G, Osaki LH, Chammas R, Alves VA, Siqueira SA, Schlesinger D, Naslavsky MS, Zatz M, Duarte YA, Lebrão ML, Gama P, Lee M, Molatore S, Pereira MA, Jallad RS, Bronstein MD, Cunha-Neto MB, Liberman B, Fragoso MC, Toledo SP, Pellegata NS, Toledo RA.
    Eur J Endocrinol; 2014 Sep 26; 171(3):335-42. PubMed ID: 24920291
    [Abstract] [Full Text] [Related]

  • 17. Characterization of a naturally-occurring p27 mutation predisposing to multiple endocrine tumors.
    Molatore S, Kiermaier E, Jung CB, Lee M, Pulz E, Höfler H, Atkinson MJ, Pellegata NS.
    Mol Cancer; 2010 May 21; 9():116. PubMed ID: 20492666
    [Abstract] [Full Text] [Related]

  • 18. Clinical Features of Multiple Endocrine Neoplasia Type 4: Novel Pathogenic Variant and Review of Published Cases.
    Frederiksen A, Rossing M, Hermann P, Ejersted C, Thakker RV, Frost M.
    J Clin Endocrinol Metab; 2019 Sep 01; 104(9):3637-3646. PubMed ID: 30990521
    [Abstract] [Full Text] [Related]

  • 19. A heterozygous frameshift mutation in exon 1 of CDKN1B gene in a patient affected by MEN4 syndrome.
    Tonelli F, Giudici F, Giusti F, Marini F, Cianferotti L, Nesi G, Brandi ML.
    Eur J Endocrinol; 2014 Aug 01; 171(2):K7-K17. PubMed ID: 24819502
    [Abstract] [Full Text] [Related]

  • 20. Endocrine tumors as part of inherited tumor syndromes.
    Zhang Y, Nosé V.
    Adv Anat Pathol; 2011 May 01; 18(3):206-18. PubMed ID: 21490438
    [Abstract] [Full Text] [Related]

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