Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Public Health Genomics and Precision Health Knowledge Base (v6.3)

Note: Javascript is disabled or is not supported by your browser. For this reason, some items on this page will be unavailable. For more information about this message, please visit this page: About CDC.gov.

HuGE Navigator|HuGE Literature Finder|PHGKB

HuGE Literature Finder

Records 1-7

Query Trace: Multiple Endocrine Neoplasia Type 1 and AIP[orginal query]

Three Novel MEN1 Variants in AIP-Negative Familial Isolated Pituitary Adenoma Patients. Pathobiology : journal of immunopathology, molecular and cellular biology 2019 Jan 1-7. Yarman Sema, Tuncer Feyza Nur, Serbest Es Similar articles in PubMed
Co-occurrence of MEN1 p.Gly111fs and AIP p.Arg16His Variants in Familial MEN1 Phenotype. Anticancer research 2018 Jun 38 (6): 3683-3687. DE Melo Flavia Marques, Bastos-Rodrigues Luciana, Sarquis Maria Marta, Friedman Eitan, DE Marco Lu Similar articles in PubMed
Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis. European journal of endocrinology / European Federation of Endocrine Societies 2013 Apr 168 (4): 533-41. Cuny Thomas, Pertuit Morgane, Sahnoun-Fathallah Mona, Daly Adrian, Occhi Gianluca, Odou Marie Françoise, Tabarin Antoine, Nunes Marie Laure, Delemer Brigitte, Rohmer Vincent, Desailloud Rachel, Kerlan Véronique, Chabre Olivier, Sadoul Jean-Louis, Cogne Muriel, Caron Philippe, Cortet-Rudelli Christine, Lienhardt Anne, Raingeard Isabelle, Guedj Anne-Marie, Brue Thierry, Beckers Albert, Weryha Georges, Enjalbert Alain, Barlier An Similar articles in PubMed
The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes. Clinical genetics 2010 Nov 78 (5): 457-63. Stratakis C A, Tichomirowa M A, Boikos S, Azevedo M F, Lodish M, Martari M, Verma S, Daly A F, Raygada M, Keil M F, Papademetriou J, Drori-Herishanu L, Horvath A, Tsang K M, Nesterova M, Franklin S, Vanbellinghen J-F, Bours V, Salvatori R, Beckers Similar articles in PubMed
Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition. Journal of endocrinological investigation 2009 Jun 32 (6): 512-8. Vierimaa O, Villablanca A, Alimov A, Georgitsi M, Raitila A, Vahteristo P, Larsson C, Ruokonen A, Eloranta E, Ebeling T M L, Ignatius J, Aaltonen L A, Leisti J, Salmela P Similar articles in PubMed
Assessment of p27 (cyclin-dependent kinase inhibitor 1B) and aryl hydrocarbon receptor-interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations. Clinical endocrinology 2009 Feb 70 (2): 259-64. Igreja Susana, Chahal Harvinder S, Akker Scott A, Gueorguiev Maria, Popovic Vera, Damjanovic Svetozar, Burman Pia, Wass John A, Quinton Richard, Grossman Ashley B, Korbonits Már Similar articles in PubMed
Mutations in the aryl hydrocarbon receptor interacting protein gene are not highly prevalent among subjects with sporadic pituitary adenomas. The Journal of clinical endocrinology and metabolism 2007 May 92 (5): 1952-5. Barlier Anne, Vanbellinghen Jean-François, Daly Adrian F, Silvy Monique, Jaffrain-Rea Marie-Lise, Trouillas Jacqueline, Tamagno Gianluca, Cazabat Laure, Bours Vincent, Brue Thierry, Enjalbert Alain, Beckers Albe Similar articles in PubMed

File Formats Help:

How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?

Page last reviewed:Mar 16, 2019
Page last updated:Aug 05, 2020
Content source:

TOP