Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: Adenoma and AIP[original query] |
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Pituitary adenoma predisposition caused by germline mutations in the AIP gene. Science (New York, N.Y.) 2006 May 312 (5777): 1228-30. Vierimaa Outi, Georgitsi Marianthi, Lehtonen Rainer, Vahteristo Pia, Kokko Antti, Raitila Anniina, Tuppurainen Karoliina, Ebeling Tapani M L, Salmela Pasi I, Paschke Ralf, Gündogdu Sadi, De Menis Ernesto, Mäkinen Markus J, Launonen Virpi, Karhu Auli, Aaltonen Lauri |
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 |
Mutation analysis of aryl hydrocarbon receptor interacting protein (AIP) gene in colorectal, breast, and prostate cancers. British journal of cancer 2007 Jan 96 (2): 352-6. Georgitsi M, Karhu A, Winqvist R, Visakorpi T, Waltering K, Vahteristo P, Launonen V, Aaltonen L |
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 |
Aryl hydrocarbon receptor interacting protein gene (AIP) mutations are rare in patients with hormone secreting or non-secreting pituitary adenomas. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2008 Nov 116 (10): 625-8. Buchbinder S, Bierhaus A, Zorn M, Nawroth P P, Humpert P, Schilling |
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 |
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer. Journal of endocrinological investigation 2009 May 32 (5): 426-9. Raitila A, Georgitsi M, Bonora E, Vargiolu M, Tuppurainen K, Mäkinen M J, Vierimaa O, Salmela P I, Launonen V, Vahteristo P, Aaltonen L A, Romeo G, Karhu |
Clinical characteristics and therapeutic responses in patients with germ-line AIP mutations and pituitary adenomas: an international collaborative study. The Journal of clinical endocrinology and metabolism 2010 Nov 95 (11): E373-83. Daly Adrian F, Tichomirowa Maria A, Petrossians Patrick, Heliövaara Elina, Jaffrain-Rea Marie-Lise, Barlier Anne, Naves Luciana A, Ebeling Tapani, Karhu Auli, Raappana Antti, Cazabat Laure, De Menis Ernesto, Montañana Carmen Fajardo, Raverot Gerald, Weil Robert J, Sane Timo, Maiter Dominique, Neggers Sebastian, Yaneva Maria, Tabarin Antoine, Verrua Elisa, Eloranta Eija, Murat Arnaud, Vierimaa Outi, Salmela Pasi I, Emy Philippe, Toledo Rodrigo A, Sabaté Maria Isabel, Villa Chiara, Popelier Marc, Salvatori Roberto, Jennings Juliet, Longás Angel Ferrandez, Labarta Aizpún José Ignacio, Georgitsi Marianthi, Paschke Ralf, Ronchi Cristina, Valimaki Matti, Saloranta Carola, De Herder Wouter, Cozzi Renato, Guitelman Mirtha, Magri Flavia, Lagonigro Maria Stefania, Halaby Georges, Corman Vinciane, Hagelstein Marie-Thérèse, Vanbellinghen Jean-François, Barra Gustavo Barcelos, Gimenez-Roqueplo Anne-Paule, Cameron Fergus J, Borson-Chazot Françoise, Holdaway Ian, Toledo Sergio P A, Stalla Günter K, Spada Anna, Zacharieva Sabina, Bertherat Jerome, Brue Thierry, Bours Vincent, Chanson Philippe, Aaltonen Lauri A, Beckers Albe |
Prevalence of AIP mutations in a large series of sporadic Italian acromegalic patients and evaluation of CDKN1B status in acromegalic patients with multiple endocrine neoplasia. European journal of endocrinology / European Federation of Endocrine Societies 2010 Sep 163 (3): 369-76. Occhi G, Trivellin G, Ceccato F, De Lazzari P, Giorgi G, Demattè S, Grimaldi F, Castello R, Davì M V, Arnaldi G, Salviati L, Opocher G, Mantero F, Scaroni |
High prevalence of AIP gene mutations following focused screening in young patients with sporadic pituitary macroadenomas. European journal of endocrinology / European Federation of Endocrine Societies 2011 Oct 165 (4): 509-15. Tichomirowa Maria A, Barlier Anne, Daly Adrian F, Jaffrain-Rea Marie-Lise, Ronchi Cristina, Yaneva Maria, Urban Jonathan D, Petrossians Patrick, Elenkova Atanaska, Tabarin Antoine, Desailloud Rachel, Maiter Dominique, Schürmeyer Thomas, Cozzi Renato, Theodoropoulou Marily, Sievers Caroline, Bernabeu Ignacio, Naves Luciana A, Chabre Olivier, Montañana Carmen Fajardo, Hana Vaclav, Halaby Georges, Delemer Brigitte, Aizpún José Ignacio Labarta, Sonnet Emmanuel, Longás Angel Ferrandez, Hagelstein Marie-Thérèse, Caron Philippe, Stalla Günter K, Bours Vincent, Zacharieva Sabina, Spada Anna, Brue Thierry, Beckers Albe |
Anterior pituitary adenomas: inherited syndromes, novel genes and molecular pathways. Expert review of endocrinology & metabolism 2011 1 5 (5): 697-709. Xekouki Paraskevi, Azevedo Monalisa, Stratakis Constantine |
Aryl hydrocarbon receptor interacting protein (AIP) mutations occur rarely in sporadic parathyroid adenomas. The Journal of clinical endocrinology and metabolism 2013 Jul 98 (7): 2800-10. Pardi Elena, Marcocci Claudio, Borsari Simona, Saponaro Federica, Torregrossa Liborio, Tancredi Mariella, Raspini Benedetta, Basolo Fulvio, Cetani Filome |
Frequency of AIP gene mutations in young patients with acromegaly: a registry-based study. The Journal of clinical endocrinology and metabolism 2014 Dec 99 (12): E2789-93. Schöfl Christof, Honegger Jürgen, Droste Michael, Grussendorf Martin, Finke Reinhard, Plöckinger Ursula, Berg Christian, Willenberg Holger S, Lammert Alexander, Klingmüller Dietrich, Jaursch-Hancke Cornelia, Tönjes Anke, Schneidewind Sabine, Flitsch Jörg, Bullmann Catharina, Dimopoulou Christina, Stalla Günter, Mayr Bernhard, Hoeppner Wolfgang, Schopohl Joch |
AHR over-expression in papillary thyroid carcinoma: clinical and molecular assessments in a series of Italian acromegalic patients with a long-term follow-up. PloS one 2014 9 (7): e101560. Mian Caterina, Ceccato Filippo, Barollo Susi, Watutantrige-Fernando Sara, Albiger Nora, Regazzo Daniela, de Lazzari Paola, Pennelli Gianmaria, Rotondi Sandra, Nacamulli Davide, Pelizzo Maria Rosa, Jaffrain-Rea Marie-Lise, Grimaldi Franco, Occhi Gianluca, Scaroni Car |
Do the aryl hydrocarbon receptor interacting protein variants (Q228K and Q307R) play a role in patients with familial and sporadic hormone-secreting pituitary adenomas? Genetic testing and molecular biomarkers 2015 Jul 19 (7): 394-8. Yarman Sema, Ogret Yeliz Duvarci, Oguz Fatma Savr |
Polymorphisms in MEN1 and DRD2 genes are associated with the occurrence and characteristics of pituitary adenomas. European journal of endocrinology / European Federation of Endocrine Societies 2016 May . Peculis Raitis, Balcere Inga, Rovite Vita, Megnis Kaspars, Valtere Andra, Stukens Janis, Arnicane Ligita, Nikitina-Zake Liene, Lejnieks Aivars, Pirags Valdis, Klovins Jan |
Very low frequency of germline GPR101 genetic variation and no biallelic defects with AIP in a large cohort of patients with sporadic pituitary adenomas. European journal of endocrinology / European Federation of Endocrine Societies 2016 Jan . Lecoq Anne-Lise, Bouligand Jérôme, Hage Mirella, Cazabat Laure, Salenave Sylvie, Linglart Agnès, Young Jacques, Guiochon-Mantel Anne, Chanson Philippe, Kamenicky Pet |
Risk category system to identify pituitary adenoma patients with AIP mutations. Journal of medical genetics 2018 Feb . Caimari Francisca, Hernández-Ramírez Laura Cristina, Dang Mary N, Gabrovska Plamena, Iacovazzo Donato, Stals Karen, Ellard Sian, Korbonits Márta, |
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 |
SNPs of miR-23b, miR-107 and HMGA2 and their Relations with the Response to Medical Treatment in Acromegaly Patients. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2020 Aug . Armagan Derya Metin, Akdemir Ayse Seda, Ozkaya Hande Mefkure, Korkmaz Ozge Polat, Gazioglu Nurperi, Kadioglu Pinar, Tanriover Necmettin, Dagistanli Kaya-Fatma, Dirican Ahmet, Ozturk Mel |
Differentiated thyroid carcinoma in sporadic and familial presentations of acromegaly: A case series. Annales d'endocrinologie 2020 8 81 (5): 482-486. Rogozinski Amelia, Daly Adrian F, Reyes Adriana, Furioso Alejandra, Beckers Albert, Lowenstein Alic |
The role of AIP variants in pituitary adenomas and concomitant thyroid carcinomas in the Netherlands: a nationwide pathology registry (PALGA) study. Endocrine 2020 4 68 (3): 640-649. Coopmans E C, Muhammad A, Daly A F, de Herder W W, van Kemenade F J, Beckers A, de Haan M, van der Lely A J, Korpershoek E, Neggers S J C M |
Phenotypic and genotypic features of a large kindred with a germline AIP variant. Clinical endocrinology 2020 4 93 (2): 146-153. Dal Jakob, Nielsen Eigil H, Klose Marianne, Feldt-Rasmussen Ulla, Andersen Marianne, Vang Søren, Korbonits Márta, Jørgensen Jens Otto |
Achalasia and acromegaly: Co-incidence of these diseases or a new syndrome? Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia 2021 7 166 (2): 228-235. Dolina Jiri, Kunovsky Lumir, Kroupa Radek, Stary Karel, Jabandziev Petr, Nesporova Tereza, Maca Karel, Andrasina Tomas, Marek Filip, Kala Zdenek, Vaculova Jitka, Said David, Zapletalova Martina, Lochman Jan, Palova Noskova Hana, Slaby Ondrej, Izakovicova Holla Lydie, Borilova Linhartova Pet |
Apoplexy in sporadic pituitary adenomas: a single referral center experience and AIP mutation analysis. Archives of endocrinology and metabolism 2021 4 65 (3): 295-304. Fialho Christhiane, Barbosa Monique Álvares, Lima Carlos Henrique Azeredo, Wildemberg Luiz Eduardo Armondi, Gadelha Mônica R, Kasuki Leand |
The clinical and therapeutic profiles of prolactinomas associated with germline pathogenic variants in the aryl hydrocarbon receptor interacting protein (AIP) gene. Frontiers in endocrinology 2023 9 14 1242588. Laurent Vroonen, Albert Beckers, Severine Camby, Thomas Cuny, Pablo Beckers, Marie-Lise Jaffrain-Rea, Muriel Cogne, Luciana Naves, Amandine Ferriere, Pauline Romanet, Atanaska Elenkova, Auli Karhu, Thierry Brue, Anne Barlier, Patrick Pétrossians, Adrian F Da |
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