HuGE Literature Finder
Records 1-30
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Lupus susceptibility region containing CDKN1B rs34330 mechanistically influences expression and function of multiple target genes, also linked to proliferation and apoptosis.
Arthritis & rheumatology (Hoboken, N.J.) 2021 May . Singh Bhupinder, Maiti Guru P, Zhou Xujie, Fazel-Najafabadi Mehdi, Bae Sang-Cheol, Sun Celi, Terao Chikashi, Okada Yukinori, Chua Kek Heng, Kochi Yuta, Guthridge Joel M, Zhang Hong, Weirauch Matthew, James Judith A, Harley John B, Varshney Gaurav K, Looger Loren L, Nath Swapan |
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Driver mutations occur frequently in metastases of well-differentiated small intestinal neuroendocrine tumours.
Histopathology 2020 Sep . Samsom Kris G, Levy Sonja, van Veenendaal Linde M, Roepman Paul, Kodach Liudmila L, Steeghs Neeltje, Valk Gerlof D, Dercksen M Wouter, Kuhlmann Koert F D, Verbeek Wieke H M, Meijer Gerrit A, Tesselaar Margot E T, van den Berg José |
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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, Correia Salles Daniela, 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 |
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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 |
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True MEN1 or phenocopy? Evidence for geno-phenotypic correlations in MEN1 syndrome.
Endocrine 2019 May . Kövesdi Annamária, Tóth Miklós, Butz Henriett, Szücs Nikolette, Sármán Beatrix, Pusztai Péter, Toke Judit, Reismann Péter, Fáklya Mónika, Tóth Géza, Somogyi Anikó, Borka Katalin, Erdei Annamária, Nagy Endre V, Deák Veronika, Valkusz Zsuzsanna, Igaz Péter, Patócs Attila, Grolmusz Vince Korn |
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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 |
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
Nature genetics 2018 Jun . Schumacher Fredrick R, Al Olama Ali Amin, Berndt Sonja I, Benlloch Sara, Ahmed Mahbubl, Saunders Edward J, Dadaev Tokhir, Leongamornlert Daniel, Anokian Ezequiel, Cieza-Borrella Clara, Goh Chee, Brook Mark N, Sheng Xin, Fachal Laura, Dennis Joe, Tyrer Jonathan, Muir Kenneth, Lophatananon Artitaya, Stevens Victoria L, Gapstur Susan M, Carter Brian D, Tangen Catherine M, Goodman Phyllis J, Thompson Ian M, Batra Jyotsna, Chambers Suzanne, Moya Leire, Clements Judith, Horvath Lisa, Tilley Wayne, Risbridger Gail P, Gronberg Henrik, Aly Markus, Nordström Tobias, Pharoah Paul, Pashayan Nora, Schleutker Johanna, Tammela Teuvo L J, Sipeky Csilla, Auvinen Anssi, Albanes Demetrius, Weinstein Stephanie, Wolk Alicja, Håkansson Niclas, West Catharine M L, Dunning Alison M, Burnet Neil, Mucci Lorelei A, Giovannucci Edward, Andriole Gerald L, Cussenot Olivier, Cancel-Tassin Géraldine, Koutros Stella, Beane Freeman Laura E, Sorensen Karina Dalsgaard, Orntoft Torben Falck, Borre Michael, Maehle Lovise, Grindedal Eli Marie, Neal David E, Donovan Jenny L, Hamdy Freddie C, Martin Richard M, Travis Ruth C, Key Tim J, Hamilton Robert J, Fleshner Neil E, Finelli Antonio, Ingles Sue Ann, Stern Mariana C, Rosenstein Barry S, Kerns Sarah L, Ostrer Harry, Lu Yong-Jie, Zhang Hong-Wei, Feng Ninghan, Mao Xueying, Guo Xin, Wang Guomin, Sun Zan, Giles Graham G, Southey Melissa C, MacInnis Robert J, FitzGerald Liesel M, Kibel Adam S, Drake Bettina F, Vega Ana, Gómez-Caamaño Antonio, Szulkin Robert, Eklund Martin, Kogevinas Manolis, Llorca Javier, Castaño-Vinyals Gemma, Penney Kathryn L, Stampfer Meir, Park Jong Y, Sellers Thomas A, Lin Hui-Yi, Stanford Janet L, Cybulski Cezary, Wokolorczyk Dominika, Lubinski Jan, Ostrander Elaine A, Geybels Milan S, Nordestgaard Børge G, Nielsen Sune F, Weischer Maren, Bisbjerg Rasmus, Røder Martin Andreas, Iversen Peter, Brenner Hermann, Cuk Katarina, Holleczek Bernd, Maier Christiane, Luedeke Manuel, Schnoeller Thomas, Kim Jeri, Logothetis Christopher J, John Esther M, Teixeira Manuel R, Paulo Paula, Cardoso Marta, Neuhausen Susan L, Steele Linda, Ding Yuan Chun, De Ruyck Kim, De Meerleer Gert, Ost Piet, Razack Azad, Lim Jasmine, Teo Soo-Hwang, Lin Daniel W, Newcomb Lisa F, Lessel Davor, Gamulin Marija, Kulis Tomislav, Kaneva Radka, Usmani Nawaid, Singhal Sandeep, Slavov Chavdar, Mitev Vanio, Parliament Matthew, Claessens Frank, Joniau Steven, Van den Broeck Thomas, Larkin Samantha, Townsend Paul A, Aukim-Hastie Claire, Dominguez Manuela Gago, Castelao Jose Esteban, Martinez Maria Elena, Roobol Monique J, Jenster Guido, van Schaik Ron H N, Menegaux Florence, Truong Thérèse, Koudou Yves Akoli, , Xu Jianfeng, Khaw Kay-Tee, Cannon-Albright Lisa, Pandha Hardev, Michael Agnieszka, Thibodeau Stephen N, McDonnell Shannon K, Schaid Daniel J, Lindstrom Sara, Turman Constance, Ma Jing, Hunter David J, Riboli Elio, Siddiq Afshan, Canzian Federico, Kolonel Laurence N, Le Marchand Loic, Hoover Robert N, Machiela Mitchell J, Cui Zuxi, Kraft Peter, , , , , , , , , Amos Christopher I, Conti David V, Easton Douglas F, Wiklund Fredrik, Chanock Stephen J, Henderson Brian E, Kote-Jarai Zsofia, Haiman Christopher A, Eeles Rosalind |
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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 |
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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 |
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Elucidating therapeutic molecular targets in premenopausal Asian women with recurrent breast cancers.
NPJ breast cancer 2018 4 19. Yap Yoon-Sim, Singh Angad P, Lim John H C, Ahn Jin-Hee, Jung Kyung-Hae, Kim Jeongeun, Dent Rebecca A, Ng Raymond C H, Kim Sung-Bae, Chiang Derek |
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Cell Cycle Protein Expression in Neuroendocrine Tumors: Association of CDK4/CDK6, CCND1, and Phosphorylated Retinoblastoma Protein With Proliferative Index.
Pancreas 2017 Oct . Shi Yan, Qian Zhi Rong, Zhang Sui, Li Wanwan, Masugi Yohei, Li Tingting, Chan Jennifer A, Yang Juhong, Da Silva Annacarolina, Gu Mancang, Liu Li, Hamada Tsuyoshi, Kosumi Keisuke, Dutton Trevor, Brais Lauren K, Nishihara Reiko, Fuchs Charles S, Ogino Shuji, Kulke Matthew |
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The functional variant rs34330 of CDKN1B is associated with risk of neuroblastoma.
Journal of cellular and molecular medicine 2017 Jun . Capasso Mario, McDaniel Lee D, Cimmino Flora, Cirino Andrea, Formicola Daniela, Russell Mike R, Raman Pichai, Cole Kristina A, Diskin Sharon |
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Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumours.
European journal of endocrinology 2017 Feb . De Sousa Sunita Mc, McCabe Mark J, Wu Kathy, Roscioli Tony, Gayevskiy Velimir, Brook Katelyn, Rawlings Lesley, Scott Hamish S, Thompson Tanya J, Earls Peter, Gill Anthony J, Cowley Mark J, Dinger Marcel E, McCormack Ann |
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Genetic predictors associated with diabetic retinopathy in diabetic foot patients
Polish archives of internal medicine 2017 11 . Mrozikiewicz-Rakowska Beata, ?ukawska Magdalena, Nehring Piotr, Szyma?ski Konrad, Sobczyk-Kopcio? Agnieszka, Krzy?ewska Monika, Maroszek Pawe?, P?oski Rafa?, Czupryniak Lesz |
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P27/CDKN1B Translational Regulators in Pituitary Tumorigenesis.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2016 Dec 48 (12): 840-846. Martins C S, Camargo R C, Saggioro F P, Neder L, Machado H R, Moreira A C, de Castro |
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Polymorphisms in selected DNA repair genes and cell cycle regulating genes involved in the risk of papillary thyroid carcinoma.
Cancer biomarkers : section A of Disease markers 2016 Jun . Halkova Tereza, Dvorakova Sarka, Sykorova Vlasta, Vaclavikova Eliska, Vcelak Josef, Vlcek Petr, Sykorova Pavla, Kodetova Daniela, Betka Jan, Lastuvka Petr, Bavor Petr, Hoch Jiri, Katra Rami, Bendlova Be |
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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 |
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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 |
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Genetic Association Between CDKN1B rs2066827 Polymorphism and Susceptibility to Cancer.
Medicine 2015 Nov 94 (46): e1217. Lu Yongchao, Gao Kejian, Zhang Miao, Zhou Aiyan, Zhou Xiaoming, Guan Zhongan, Shi Xuewen, Ge Shuji |
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Somatic alterations of CDKN1B are associated with small bowel neuroendocrine tumors.
Cancer genetics 2015 Sep . Maxwell Jessica E, Sherman Scott K, Li Guiying, Choi Allen B, Bellizzi Andrew M, O'Dorisio Thomas M, Howe James |
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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 |
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Prognostic role of the CDNK1B V109G polymorphism in multiple endocrine neoplasia type 1.
Journal of cellular and molecular medicine 2015 Jul 19 (7): 1735-41. Circelli Luisa, Ramundo Valeria, Marotta Vincenzo, Sciammarella Concetta, Marciello Francesca, Del Prete Michela, Sabatino Lina, Pasquali Daniela, Izzo Francesco, Scala Stefania, Colao Annamaria, Faggiano Antongiulio, Colantuoni Vittorio, |
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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 |
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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 |
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Erratum: 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 2014 Dec 16 (12): 12. Authors are not available |
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Polymorphisms of cell cycle control genes influence the development of sporadic medullary thyroid carcinoma.
European journal of endocrinology / European Federation of Endocrine Societies 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 |
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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 |
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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 |
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Somatic mutation of CDKN1B in small intestine neuroendocrine tumors.
Nature genetics 2013 Dec 45 (12): 1483-6. Francis Joshua M, Kiezun Adam, Ramos Alex H, Serra Stefano, Pedamallu Chandra Sekhar, Qian Zhi Rong, Banck Michaela S, Kanwar Rahul, Kulkarni Amit A, Karpathakis Anna, Manzo Veronica, Contractor Tanupriya, Philips Juliet, Nickerson Elizabeth, Pho Nam, Hooshmand Susanne M, Brais Lauren K, Lawrence Michael S, Pugh Trevor, McKenna Aaron, Sivachenko Andrey, Cibulskis Kristian, Carter Scott L, Ojesina Akinyemi I, Freeman Samuel, Jones Robert T, Voet Douglas, Saksena Gordon, Auclair Daniel, Onofrio Robert, Shefler Erica, Sougnez Carrie, Grimsby Jonna, Green Lisa, Lennon Niall, Meyer Tim, Caplin Martyn, Chung Daniel C, Beutler Andreas S, Ogino Shuji, Thirlwell Christina, Shivdasani Ramesh, Asa Sylvia L, Harris Chris R, Getz Gad, Kulke Matthew, Meyerson Matth |
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Association of CDKN1B gene polymorphisms with susceptibility to breast cancer: a meta-analysis.
Molecular biology reports 2013 Nov 40 (11): 6371-7. Xiang Heping, Li He, Ge Weiwei, Wu Weidong, Gao Ming, Wang Wei, Hong Lei, Jiang Datong, Zhang Chang |
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[Pharmacogenomics of cisplatin-based chemotherapy in ovarian cancer patients from Yakutia].
Molekuliarnaia genetika, mikrobiologiia i virusologiia 2013 (4): 6-9. ?hokhrin D V, Khrunin A V, Ivanova F G, Moiseev A A, Gorbunova V A, Limborskaia S |
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