机译:遗传和功能分析暗示NUDT11,HNF1B和SLC22A3基因与前列腺癌的发病机理有关
Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115;
Department of Biostatistics and Computational Biology,Dana-Farber Cancer Institute, Boston, MA 02115;
Department of Medical Oncology,Dana-Farber Cancer Institute, Boston, MA 02115 Cancer Program Broad Institute of Harvard and MIT, Cambridge, MA 02142;
Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115;
Department of Medical Oncology,Dana-Farber Cancer Institute, Boston, MA 02115 Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115;
Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115 Department of Urology, Jikei University School of Medicine, Minato-ku, Tokyo 105-8461, Japan;
Department of Urology, Lefrak Center of Robotic Surgery and Prostate Cancer Institute, Weill Cornell Medical College, New York, NY 10065;
Department of Urology, Lefrak Center of Robotic Surgery and Prostate Cancer Institute, Weill Cornell Medical College, New York, NY 10065;
Department of Urology, Lefrak Center of Robotic Surgery and Prostate Cancer Institute, Weill Cornell Medical College, New York, NY 10065;
Center for Cancer Genome Discovery, Dana-Farber Cancer Institute, Boston, MA 02115;
Centre for Molecular Medicine Norway (NCMM), University of Oslo, N-0349 Oslo,Norway Departments of Urology Oslo University Hospitals, N-0370 Oslo, Norway Departments of Cancer Prevention, Oslo University Hospitals, N-0370 Oslo, Norway;
Uro-Oncology Research Group, Cancer Research United Kingdom, Cambridge Research Institute, Cambridge CB2 ORE, United Kingdom;
Uro-Oncology Research Group, Cancer Research United Kingdom, Cambridge Research Institute, Cambridge CB2 ORE, United Kingdom;
Department of Urology, Jikei University School of Medicine, Minato-ku, Tokyo 105-8461, Japan;
Department of Urology, Jikei University School of Medicine, Minato-ku, Tokyo 105-8461, Japan;
Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115;
Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115;
Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115 Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115;
Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115;
Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115 Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115 Center for Cancer Genome Discovery, Dana-Farber Cancer Institute, Boston, MA 02115 Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115;
Department of Medicine and Urology, Tulane Cancer Center,Tulane University School of Medicine, New Orleans, LA 70112;
Department of Urology, Jikei University School of Medicine, Minato-ku, Tokyo 105-8461, Japan;
Department of Urology, Lefrak Center of Robotic Surgery and Prostate Cancer Institute, Weill Cornell Medical College, New York, NY 10065;
Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115 Cancer Program Broad Institute of Harvard and MIT, Cambridge, MA 02142 Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115 Center for Cancer Genome Discovery, Dana-Farber Cancer Institute, Boston, MA 02115;
Department of Medicine Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115 Center for Cancer Genome Discovery, Dana-Farber Cancer Institute, Boston, MA 02115 Medical and Population Genetics Program, Broad Institute of Harvard and MIT, Cambridge, MA 02142;
expression quantitative trait loci; prostate cancer risk snps; multi-ethnic;
机译:遗传关联分析暗示系统性红斑狼疮发病中先天和适应性免疫基因的异常调节
机译:鉴定功能性SNPs可能是角化细胞终末分化中涉及的编码人脱氧核糖核酸酶I样2(DNase 1L2)的基因中角化不全发病机理的遗传危险因素。
机译:使用新型sumLINK和sumLOD分析,对国际前列腺癌遗传学联盟的1,233个前列腺癌谱系进行全基因组连锁分析。
机译:解开癌症发病机制:从遗传修饰的小鼠到干细胞病理学
机译:遗传变异对特殊马铃薯功能成分的影响及其对前列腺癌细胞系的影响。
机译:遗传和功能分析暗示NUDT11HNF1B和SLC22A3基因与前列腺癌的发病机理有关
机译:遗传和功能分析暗示了NUDT11,HNF1B和SLC22A3基因与前列腺癌的发病机理有关。