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机译:使用BCR-ABL1基因组断点的童年监测识别具有CML样生物学的子组
Charles Univ Prague Fac Med 2 CLIP Prague Czech Republic;
Charles Univ Prague Fac Med 2 CLIP Prague Czech Republic;
Univ New South Wales Lowy Canc Res Ctr Childrens Canc Inst Sydney NSW Australia;
Univ Med Ctr Schleswig Holstein Dept Pediat Campus Kiel Kiel Germany;
Gennet Ctr Fetal Med &
Reprod Genet Prague Czech Republic;
Charles Univ Prague Fac Med 2 CLIP Prague Czech Republic;
Charles Univ Prague Fac Med 2 CLIP Prague Czech Republic;
Inst Hematol &
Blood Transfus Prague Czech Republic;
Inst Hematol &
Blood Transfus Prague Czech Republic;
Charles Univ Prague Fac Med 2 CLIP Prague Czech Republic;
Univ New South Wales Lowy Canc Res Ctr Childrens Canc Inst Sydney NSW Australia;
Univ New South Wales Lowy Canc Res Ctr Childrens Canc Inst Sydney NSW Australia;
Childrens Hosp Westmead Blood &
Marrow Transplant Serv Sydney NSW Australia;
Univ Med Ctr Schleswig Holstein Dept Pediat Campus Kiel Kiel Germany;
Univ New South Wales Lowy Canc Res Ctr Childrens Canc Inst Sydney NSW Australia;
Charles Univ Prague Fac Med 2 Dept Pediat Hematol &
Oncol Prague Czech Republic;
Charles Univ Prague Fac Med 2 CLIP Prague Czech Republic;
Charles Univ Prague Fac Med 2 CLIP Prague Czech Republic;
机译:使用BCR-ABL1基因组断点的童年监测识别具有CML样生物学的子组
机译:在儿童急性淋巴细胞白血病中使用次要BCR-ABL1基因组断点的最小残留疾病监测确定了生物学和预后很差的亚组
机译:没有已知畸变的儿童ALL的基因组和基因表达数据的整合确定了具有特定遗传特征的亚组。
机译:通过基因组学确定的CD33-re re re resed siglec子组的新I型章程
机译:整合基因组学和分子生物学:鉴定前列腺癌致癌基因SOX4的转录靶标并评估Aurora激酶抑制作用对化疗耐药的卵巢癌的疗效
机译:通过多策略方法对慢性髓样白血病患者的残留疾病进行个性化监测的基因组BCR-ABL1断点鉴定
机译:没有已知畸变的儿童ALL基因组和基因表达数据的整合识别具有特定遗传标志的亚组