机译:靶向RNA-SEQ成功识别乳腺/卵巢癌敏感性和林奇综合征基因中的正常和致病剪接事件
Maastricht Univ Med Ctr GROW Sch Oncol &
Dev Biol Dept Clin Genet Maastricht Netherlands;
Univ Ghent Dept Data Anal &
Math Modelling Ghent Belgium;
Hosp Clin San Carlos IdISSC Inst Invest Sanitaria Mol Oncol Lab CIBERONC Madrid Spain;
Maastricht Univ Med Ctr GROW Sch Oncol &
Dev Biol Dept Clin Genet Maastricht Netherlands;
Maastricht Univ Med Ctr GROW Sch Oncol &
Dev Biol Dept Clin Genet Maastricht Netherlands;
Univ Otago Dept Pathol &
Biomed Sci Christchurch New Zealand;
Univ Otago Dept Pathol &
Biomed Sci Christchurch New Zealand;
Lund Univ Dept Clin Sci Div Oncol &
Pathol Lund Sweden;
USC Fdn Publ Galega Med Xenom Serv Galgo Saude Grp Med Xenom CIBERER IDIS Santiago De;
VHIO Oncogenet Grp Barcelona Spain;
VHIO Oncogenet Grp Barcelona Spain;
Hosp Clin San Carlos IdISSC Inst Invest Sanitaria Mol Oncol Lab CIBERONC Madrid Spain;
QIMR Berghofer Med Res Inst Dept Genet &
Computat Biol Brisbane Qld Australia;
Univ Ghent Dept Data Anal &
Math Modelling Ghent Belgium;
Maastricht Univ Med Ctr GROW Sch Oncol &
Dev Biol Dept Clin Genet Maastricht Netherlands;
targeted RNA-seq; alternative splicing; inherited breast; ovarian cancer syndrome; lynch syndrome; BRCA1; 2;
机译:靶向RNA-SEQ成功识别乳腺/卵巢癌敏感性和林奇综合征基因中的正常和致病剪接事件
机译:在正常组织以及乳腺癌和卵巢癌中,乳腺癌易感基因BRCA2的启动子中CpG二核苷酸的甲基化缺失
机译:涉嫌遗传性乳腺癌和卵巢癌综合征和林奇综合征妇女遗传咨询和种系突变检测的障碍
机译:生存分析与RNA序列和临床数据的整合,以识别乳腺癌亚型特异性基因。
机译:Lynch综合征患者的修饰基因和对结直肠癌的易感性
机译:靶向RNA-seq成功鉴定了乳腺癌/卵巢癌易感性和Lynch综合征基因中的正常和致病性剪接事件
机译:来自正常和肿瘤组织的Pleiotrope引导的转录组归物鉴定了乳腺癌和卵巢癌的新候选敏感性基因