Human Genome Epidemiology Literature Finder
|
Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and CDKN2C[original query] |
|---|
| Tagging single nucleotide polymorphisms in cell cycle control genes and susceptibility to invasive epithelial ovarian cancer. Cancer research 2007 Apr 67 (7): 3027-35. Gayther Simon A, Song Honglin, Ramus Susan J, Kjaer Susan Krüger, Whittemore Alice S, Quaye Lydia, Tyrer Jonathan, Shadforth Danielle, Hogdall Estrid, Hogdall Claus, Blaeker Jan, DiCioccio Richard, McGuire Valerie, Webb Penelope M, Beesley Jonathan, Green Adele C, Whiteman David C, , Goodman Marc T, Lurie Galina, Carney Michael E, Modugno Francesmary, Ness Roberta B, Edwards Robert P, Moysich Kirsten B, Goode Ellen L, Couch Fergus J, Cunningham Julie M, Sellers Thomas A, Wu Anna H, Pike Malcolm C, Iversen Edwin S, Marks Jeffrey R, Garcia-Closas Montserrat, Brinton Louise, Lissowska Jolanta, Peplonska Beata, Easton Douglas F, Jacobs Ian, Ponder Bruce A J, Schildkraut Joellen, Pearce C Leigh, Chenevix-Trench Georgia, Berchuck Andrew, Pharoah Paul D P, |
| 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 |
| Polymorphisms of cell cycle control genes influence the development of sporadic medullary thyroid carcinoma. European journal of endocrinology 2014 Dec 171 (6): 761-7. Barbieri R B, Bufalo N E, Secolin R, Assumpção L V M, Maciel R M B, Cerutti J M, Ward L |
| Role of CDKN2C Copy Number in Sporadic Medullary Thyroid Carcinoma. Thyroid : official journal of the American Thyroid Association 2016 Sep . Grubbs Elizabeth G, Williams Michelle D, Scheet Paul, Vattathil Selina, Perrier Nancy, Lee Jeffrey E, Gagel Robert F, Hai Tao, Feng Lei, Cabanillas Maria, Cote Gilbert |
| Primary hyperparathyroidism in young patients in Russia: high frequency of hyperparathyroidism-jaw tumor syndrome. Endocrine connections 2017 9 6 (8): 557-565. Mamedova Elizaveta, Mokrysheva Natalya, Vasilyev Evgeny, Petrov Vasily, Pigarova Ekaterina, Kuznetsov Sergey, Kuznetsov Nikolay, Rozhinskaya Liudmila, Melnichenko Galina, Dedov Ivan, Tiulpakov Anato |
| Mutational and copy number asset of primary sporadic neuroendocrine tumors of the small intestine. Virchows Archiv : an international journal of pathology 2018 Sep . Simbolo Michele, Vicentini Caterina, Mafficini Andrea, Fassan Matteo, Pedron Serena, Corbo Vincenzo, Mastracci Luca, Rusev Borislav, Pedrazzani Corrado, Landoni Luca, Grillo Federica, Cingarlini Sara, Rindi Guido, Luchini Claudio, Scarpa Aldo, Lawlor Rita |
| Novel use of a Clinical Laboratory Improvements Amendments (CLIA)-certified Cyclin-Dependent Kinase N2C (CDKN2C) loss assay in sporadic medullary thyroid carcinoma. Surgery 2019 Oct . Maxwell Jessica E, Gule-Monroe Maria K, Subbiah Vivek, Hu Mimi, Perrier Nancy D, Cabanillas Maria E, Lee Jeffery E, Graham Paul H, Cote Gilbert J, Busaidy Naifa L, Grubbs Elizabeth |
| CDKN2C-Null Leiomyosarcoma: A Novel, Genomically Distinct Class of TP53/RB1-Wild-Type Tumor With Frequent CIC Genomic Alterations and 1p/19q-Codeletion. JCO precision oncology 2020 10 4 . Williams Erik A, Sharaf Radwa, Decker Brennan, Werth Adrienne J, Toma Helen, Montesion Meagan, Sokol Ethan S, Pavlick Dean C, Shah Nikunj, Williams Kevin Jon, Venstrom Jeffrey M, Alexander Brian M, Ross Jeffrey S, Albacker Lee A, Lin Douglas I, Ramkissoon Shakti H, Elvin Julia |
| Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort. Frontiers in endocrinology 2023 10 14 1244361. Isabel Mazarico-Altisent, Ismael Capel, Neus Baena, Maria Rosa Bella-Cueto, Santi Barcons, Xavier Guirao, Rocío Pareja, Andreea Muntean, Valeria Arsentales, Assumpta Caixàs, Mercedes Rig |
- Page last reviewed:Feb 1, 2024
- Content source: