Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 37 Records) |
| Query Trace: Disease and CDKN1B[original query] |
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| 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 |
| CDKN1B V109G polymorphism a new prognostic factor in sporadic medullary thyroid carcinoma. European journal of endocrinology / European Federation of Endocrine Societies 2011 Mar 164 (3): 397-404. Pasquali Daniela, Circelli Luisa, Faggiano Antongiulio, Pancione Massimo, Renzullo Andrea, Elisei Rossella, Romei Cristina, Accardo Giacomo, Coppola Viviana Raffaella, De Palma Maurizio, Ferolla Piero, Grimaldi Franco, Colao Annamaria, Colantuoni Vittor |
| Copy number genome alterations are associated with treatment response and outcome in relapsed childhood ETV6/RUNX1-positive acute lymphoblastic leukemia. Haematologica 2014 Apr 99 (4): 706-14. Bokemeyer Almut, Eckert Cornelia, Meyr Franziska, Koerner Gabriele, von Stackelberg Arend, Ullmann Reinhard, Türkmen Seval, Henze Günter, Seeger Ka |
| Role of DNA repair and cell cycle control genes in ovarian cancer susceptibility. Molecular biology reports 2013 Jan . Mohamed FZ, Hussien YM, Albakry MM, Mohamed RH, Said NM |
Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians.
American journal of human genetics 2013 Jan 92 (1): 41-51. Yang Wanling, Tang Huayang, Zhang Yan, Tang Xianfa, Zhang Jing, Sun Liangdan, Yang Jing, Cui Yong, Zhang Lu, Hirankarn Nattiya, Cheng Hui, Pan Hai-Feng, Gao Jinping, Lee Tsz Leung, Sheng Yujun, Lau Chak Sing, Li Yang, Chan Tak Mao, Yin Xianyong, Ying Dingge, Lu Qianjin, Leung Alexander Moon Ho, Zuo Xianbo, Chen Xiang, Tong Kwok Lung, Zhou Fusheng, Diao Qingchun, Tse Niko Kei Chiu, Xie Hongfu, Mok Chi Chiu, Hao Fei, Wong Sik Nin, Shi Bingjun, Lee Ka Wing, Hui Yan, Ho Marco Hok Kung, Liang Bo, Lee Pamela Pui Wah, Cui Hongzhou, Guo Qing, Chung Brian Hon-Yin, Pu Xiongming, Liu Qiji, Zhang Xiaoguang, Zhang Change, Chong Chun Yin, Fang Hong, Wong Raymond Woon Sing, Sun Yonghu, Mok Mo Yin, Li Xiang-Pei, Avihingsanon Yingyos, Zhai Zhifang, Rianthavorn Pornpimol, Deekajorndej Thavatchai, Suphapeetiporn Kanya, Gao Fei, Shotelersuk Vorasuk, Kang Xiaojing, Ying Shirley King Yee, Zhang Lijuan, Wong Wilfred Hing Sang, Zhu Dingxian, Fung Samuel Ka Shun, Zeng Fanqin, Lai Wai Ming, Wong Chun-Ming, Ng Irene Oi Lin, Garcia-Barceló Maria-Mercè, Cherny Stacey S, Shen Nan, Tam Paul Kwong-Hang, Sham Pak Chung, Ye Dong-Qing, Yang Sen, Zhang Xuejun, Lau Yu Lu |
| Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Feb 17 (2): 131-42. Esteban-Jurado Clara, Vila-Casadesús Maria, Garre Pilar, Lozano Juan José, Pristoupilova Anna, Beltran Sergi, Muñoz Jenifer, Ocaña Teresa, Balaguer Francesc, López-Cerón Maria, Cuatrecasas Miriam, Franch-Expósito Sebastià, Piqué Josep M, Castells Antoni, Carracedo Angel, Ruiz-Ponte Clara, Abulí Anna, Bessa Xavier, Andreu Montserrat, Bujanda Luis, Caldés Trinidad, Castellví-Bel Ser |
| Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations. European journal of endocrinology / European Federation of Endocrine Societies 2014 Sep 171 (3): 335-42. Longuini Viviane C, Lourenço Delmar M, Sekiya Tomoko, Meirelles Osorio, Goncalves Tatiana D, Coutinho Flavia L, Francisco Guilherme, Osaki Luciana H, Chammas Roger, Alves Venancio A F, Siqueira Sheila A C, Schlesinger David, Naslavsky Michel S, Zatz Mayana, Duarte Yeda A O, Lebrão Maria Lucia, Gama Patricia, Lee Misu, Molatore Sara, Pereira Maria Adelaide A, Jallad Raquel S, Bronstein Marcello D, Cunha-Neto Malebranche B, Liberman Bernardo, Fragoso Maria Candida B V, Toledo Sergio P A, Pellegata Natalia S, Toledo Rodrigo |
| Recurrent CDKN1B (p27) mutations in hairy cell leukemia. Blood 2015 Aug 126 (8): 1005-8. Dietrich Sascha, Hüllein Jennifer, Lee Stanley Chun-Wei, Hutter Barbara, Gonzalez David, Jayne Sandrine, Dyer Martin J S, Ole? Ma?gorzata, Else Monica, Liu Xiyang, S?abicki Miko?aj, Wu Bian, Troussard Xavier, Dürig Jan, Andrulis Mindaugas, Dearden Claire, von Kalle Christof, Granzow Martin, Jauch Anna, Fröhling Stefan, Huber Wolfgang, Meggendorfer Manja, Haferlach Torsten, Ho Anthony D, Richter Daniela, Brors Benedikt, Glimm Hanno, Matutes Estella, Abdel Wahab Omar, Zenz Thorst |
| 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 |
| Somatic Mutations and Genetic Heterogeneity at the CDKN1B Locus in Small Intestinal Neuroendocrine Tumors. Annals of surgical oncology 2015 Jan . Crona Joakim, Gustavsson Tobias, Norlén Olov, Edfeldt Katarina, Åkerström Tobias, Westin Gunnar, Hellman Per, Björklund Peyman, Stålberg Pet |
| p27 Is a Candidate Prognostic Biomarker and Metastatic Promoter in Osteosarcoma. Cancer research 2016 Apr . Li Yiting, Nakka Manjula, Kelly Aaron J, Lau Ching C, Krailo Mark, Barkauskas Donald A, Hicks John M, Man Tsz-Kwo |
| Prognostic Importance of Cell Cycle Regulators Cyclin D1 (CCND1) and Cyclin-Dependent Kinase Inhibitor 1B (CDKN1B/p27) in Sporadic Gastric Cancers. Gastroenterology research and practice 2016 2016 9408190. Minarikova Petra, Benesova Lucie, Halkova Tereza, Belsanova Barbora, Tuckova Inna, Belina Frantisek, Dusek Ladislav, Zavoral Miroslav, Minarik Mar |
| 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 large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features. PloS one 2017 10 12 (10): e0186485. Pardi Elena, Borsari Simona, Saponaro Federica, Bogazzi Fausto, Urbani Claudio, Mariotti Stefano, Pigliaru Francesca, Satta Chiara, Pani Fabiana, Materazzi Gabriele, Miccoli Paolo, Grantaliano Lorena, Marcocci Claudio, Cetani Filome |
| 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 |
| 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 |
| Characterization of a novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient. Breast cancer research and treatment 2018 Jul 170 (1): 179-188. Johnson Julie, Bessette Darrell C, Saunus Jodi M, Smart Chanel E, Song Sarah, Johnston Rebecca L, Cocciardi Sibylle, Rozali Esdy N, Johnstone Cameron N, Vargas Ana Christina, Kazakoff Stephen H, BioBank Victorian Cancer, Khanna Kum Kum, Lakhani Sunil R, Chenevix-Trench Georgia, Simpson Peter T, Nones Katia, Waddell Nicola, Al-Ejeh Far |
| A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.
American journal of human genetics 2018 Feb . Sung Yun J, Winkler Thomas W, de Las Fuentes Lisa, Bentley Amy R, Brown Michael R, Kraja Aldi T, Schwander Karen, Ntalla Ioanna, Guo Xiuqing, Franceschini Nora, Lu Yingchang, Cheng Ching-Yu, Sim Xueling, Vojinovic Dina, Marten Jonathan, Musani Solomon K, Li Changwei, Feitosa Mary F, Kilpeläinen Tuomas O, Richard Melissa A, Noordam Raymond, Aslibekyan Stella, Aschard Hugues, Bartz Traci M, Dorajoo Rajkumar, Liu Yongmei, Manning Alisa K, Rankinen Tuomo, Smith Albert Vernon, Tajuddin Salman M, Tayo Bamidele O, Warren Helen R, Zhao Wei, Zhou Yanhua, Matoba Nana, Sofer Tamar, Alver Maris, Amini Marzyeh, Boissel Mathilde, Chai Jin Fang, Chen Xu, Divers Jasmin, Gandin Ilaria, Gao Chuan, Giulianini Franco, Goel Anuj, Harris Sarah E, Hartwig Fernando Pires, Horimoto Andrea R V R, Hsu Fang-Chi, Jackson Anne U, Kähönen Mika, Kasturiratne Anuradhani, Kühnel Brigitte, Leander Karin, Lee Wen-Jane, Lin Keng-Hung, 'an Luan Jian, McKenzie Colin A, Meian He, Nelson Christopher P, Rauramaa Rainer, Schupf Nicole, Scott Robert A, Sheu Wayne H H, Stan?áková Alena, Takeuchi Fumihiko, van der Most Peter J, Varga Tibor V, Wang Heming, Wang Yajuan, Ware Erin B, Weiss Stefan, Wen Wanqing, Yanek Lisa R, Zhang Weihua, Zhao Jing Hua, Afaq Saima, Alfred Tamuno, Amin Najaf, Arking Dan, Aung Tin, Barr R Graham, Bielak Lawrence F, Boerwinkle Eric, Bottinger Erwin P, Braund Peter S, Brody Jennifer A, Broeckel Ulrich, Cabrera Claudia P, Cade Brian, Caizheng Yu, Campbell Archie, Canouil Mickaël, Chakravarti Aravinda, , Chauhan Ganesh, Christensen Kaare, Cocca Massimiliano, , Collins Francis S, Connell John M, de Mutsert Renée, de Silva H Janaka, Debette Stephanie, Dörr Marcus, Duan Qing, Eaton Charles B, Ehret Georg, Evangelou Evangelos, Faul Jessica D, Fisher Virginia A, Forouhi Nita G, Franco Oscar H, Friedlander Yechiel, Gao He, , Gigante Bruna, Graff Misa, Gu C Charles, Gu Dongfeng, Gupta Preeti, Hagenaars Saskia P, Harris Tamara B, He Jiang, Heikkinen Sami, Heng Chew-Kiat, Hirata Makoto, Hofman Albert, Howard Barbara V, Hunt Steven, Irvin Marguerite R, Jia Yucheng, Joehanes Roby, Justice Anne E, Katsuya Tomohiro, Kaufman Joel, Kerrison Nicola D, Khor Chiea Chuen, Koh Woon-Puay, Koistinen Heikki A, Komulainen Pirjo, Kooperberg Charles, Krieger Jose E, Kubo Michiaki, Kuusisto Johanna, Langefeld Carl D, Langenberg Claudia, Launer Lenore J, Lehne Benjamin, Lewis Cora E, Li Yize, , Lim Sing Hui, Lin Shiow, Liu Ching-Ti, Liu Jianjun, Liu Jingmin, Liu Kiang, Liu Yeheng, Loh Marie, Lohman Kurt K, Long Jirong, Louie Tin, Mägi Reedik, Mahajan Anubha, Meitinger Thomas, Metspalu Andres, Milani Lili, Momozawa Yukihide, Morris Andrew P, Mosley Thomas H, Munson Peter, Murray Alison D, Nalls Mike A, Nasri Ubaydah, Norris Jill M, North Kari, Ogunniyi Adesola, Padmanabhan Sandosh, Palmas Walter R, Palmer Nicholette D, Pankow James S, Pedersen Nancy L, Peters Annette, Peyser Patricia A, Polasek Ozren, Raitakari Olli T, Renström Frida, Rice Treva K, Ridker Paul M, Robino Antonietta, Robinson Jennifer G, Rose Lynda M, Rudan Igor, Sabanayagam Charumathi, Salako Babatunde L, Sandow Kevin, Schmidt Carsten O, Schreiner Pamela J, Scott William R, Seshadri Sudha, Sever Peter, Sitlani Colleen M, Smith Jennifer A, Snieder Harold, Starr John M, Strauch Konstantin, Tang Hua, Taylor Kent D, Teo Yik Ying, Tham Yih Chung, Uitterlinden André G, Waldenberger Melanie, Wang Lihua, Wang Ya X, Wei Wen Bin, Williams Christine, Wilson Gregory, Wojczynski Mary K, Yao Jie, Yuan Jian-Min, Zonderman Alan B, Becker Diane M, Boehnke Michael, Bowden Donald W, Chambers John C, Chen Yii-Der Ida, de Faire Ulf, Deary Ian J, Esko Tõnu, Farrall Martin, Forrester Terrence, Franks Paul W, Freedman Barry I, Froguel Philippe, Gasparini Paolo, Gieger Christian, Horta Bernardo Lessa, Hung Yi-Jen, Jonas Jost B, Kato Norihiro, Kooner Jaspal S, Laakso Markku, Lehtimäki Terho, Liang Kae-Woei, Magnusson Patrik K E, Newman Anne B, Oldehinkel Albertine J, Pereira Alexandre C, Redline Susan, Rettig Rainer, Samani Nilesh J, Scott James, Shu Xiao-Ou, van der Harst Pim, Wagenknecht Lynne E, Wareham Nicholas J, Watkins Hugh, Weir David R, Wickremasinghe Ananda R, Wu Tangchun, Zheng Wei, Kamatani Yoichiro, Laurie Cathy C, Bouchard Claude, Cooper Richard S, Evans Michele K, Gudnason Vilmundur, Kardia Sharon L R, Kritchevsky Stephen B, Levy Daniel, O'Connell Jeff R, Psaty Bruce M, van Dam Rob M, Sims Mario, Arnett Donna K, Mook-Kanamori Dennis O, Kelly Tanika N, Fox Ervin R, Hayward Caroline, Fornage Myriam, Rotimi Charles N, Province Michael A, van Duijn Cornelia M, Tai E Shyong, Wong Tien Yin, Loos Ruth J F, Reiner Alex P, Rotter Jerome I, Zhu Xiaofeng, Bierut Laura J, Gauderman W James, Caulfield Mark J, Elliott Paul, Rice Kenneth, Munroe Patricia B, Morrison Alanna C, Cupples L Adrienne, Rao Dabeeru C, Chasman Daniel |
| CDKN1B Val 109 Gly variant is not related to risk of prostate cancer. Journal of cellular biochemistry 2019 Jun . Zhu Lijie, Wang Jun, Yue Chuang, Yuan Wei, Zhang Wei, Shi Li, Mi Yuanyuan, Wu Xingyu, Zhang Li-Feng, Zuo |
| Molecular prognostic factors in small-intestinal neuroendocrine tumours. Endocrine connections 2019 6 8 (7): 906-922. Samsom K G, van Veenendaal L M, Valk G D, Vriens M R, Tesselaar M E T, van den Berg J |
| USP8 Mutations and Cell Cycle Regulation in Corticotroph Adenomas. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2020 2 52 (2): 117-123. Martins Clarissa Silva, Camargo Renata Costa, Coeli-Lacchini Fernanda Borchers, Saggioro Fabiano Pinto, Moreira Ayrton Custodio, de Castro Margar |
| Comprehensive Genomic Profile of Heterogeneous Long Follow-Up Triple-Negative Breast Cancer and Its Clinical Characteristics Shows DNA Repair Deficiency Has Better Prognostic. Genes 2020 11 11 (11): . Rojas-Jiménez Ernesto, Mejía-Gómez Javier César, Díaz-Velásquez Clara, Quezada-Urban Rosalía, Martínez Gregorio Héctor, Vallejo-Lecuona Fernando, de la Cruz-Montoya Aldo, Porras Reyes Fany Iris, Pérez-Sánchez Víctor Manuel, Maldonado-Martínez Héctor Aquiles, Robles-Estrada Maybelline, Bargalló-Rocha Enrique, Cabrera-Galeana Paula, Ramos-Ramírez Maritza, Chirino Yolanda Irasema, Alonso Herrera Luis, Terrazas Luis Ignacio, Oliver Javier, Frecha Cecilia, Perdomo Sandra, Vaca-Paniagua Feli |
| Genomic characterization reveals potential biomarkers in nasopharyngeal carcinoma patients with relapse. Expert review of molecular diagnostics 2020 10 20 (11): 1149-1159. Cho William C S, Tse Ka-Po, Ngan Roger K C, Cheuk Wah, Ma Victor W S, Yang Yi-Ting, Yip Timothy T C, Tan Kien Thiam, Chen Shu-J |
| CDKN1B Deletions are Associated with Metastasis in African American Men with Clinically Localized, Surgically Treated Prostate Cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 2020 Jan . Faisal Farzana A, Murali Sanjana, Kaur Harsimar, Vidotto Thiago, Guedes Liana B, Salles Daniela Correia, Kothari Vishal, Tosoian Jeffrey J, Han Sumin, Hovelson Daniel H, Hu Kevin, Spratt Daniel E, Baras Alexander S, Tomlins Scott A, Schaeffer Edward M, Lotan Tamara |
| The genomic characteristics of different progression patterns in advanced non-small cell lung cancer patients treated with immune checkpoint inhibitors. Annals of translational medicine 2021 7 9 (9): 779. Li Jingwen, Xiang Chan, Wang Yue, Zhou Yan, Cao Shuhui, Ling Xuxinyi, Ye Junyi, Zheng Jingjing, Shao Lin, Zhong Hua, Han Yuch |
| Analysis of the genomic landscape of yolk sac tumors reveals mechanisms of evolution and chemoresistance. Nature communications 2021 6 12 (1): 3579. Zong Xuan, Zhang Ying, Peng Xinxin, Cao Dongyan, Yu Mei, Wang Jinhui, Li Hongyue, Guo Xuejiao, Liang Han, Yang Jiax |
| Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders. European journal of endocrinology 2022 1 186 (3): 351-366. Canaff Lucie, Guarnieri Vito, Kim Yoojung, Wong Betty Y L, Nolin-Lapalme Alexis, Cole David E C, Minisola Salvatore, Eller-Vainicher Cristina, Cetani Filomena, Repaci Andrea, Turchetti Daniela, Corbetta Sabrina, Scillitani Alfredo, Goltzman Dav |
| Genetic and clinical screening for hereditary primary hyperparathyroidism in a large Chinese cohort: a single-center study. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2023 7 . An Song, Yi Yang, Yue Jiang, Min Nie, Yan Jiang, Mei Li, Weibo Xia, Xiaoping Xing, Ou Wa |
| Molecular characterization of large cell calcifying sertoli cell tumors: A multi-institutional study of 6 benign and 2 malignant tumors. Human pathology 2023 12 . Eman Abdulfatah, Khaleel I Al-Obaidy, Dan Robinson, Yi-Mi Wu, Amer Heider, Muhammad T Idrees, Thomas M Ulbright, Lakshmi Pryia Kunju, Angela |
| 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 |
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