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浏览/检索结果: 共22条，第1-10条 帮助 限定条件 专题：中国医学科学院 北京协和医学院    第一署名单位    第一作者单位    通讯作者单位     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择发表日期升序发表日期降序提交时间升序提交时间降序题名升序题名降序作者升序作者降序 Genome-wide CRISPR-Cas9 screen reveals selective vulnerability of ATRX-mutant cancers to WEE1 inhibition 期刊论文 2019 作者:  Liang Junbo;  Zhao Hong;  Diplas Bill H;  Liu Song;  Liu Jianmei 收藏  |  浏览/下载：13/0  |  提交时间：2020/01/03 Multilevel defects in the hematopoietic niche in essential thrombocythemia 期刊论文 2019 作者:  Sun Ting;  Ju Mankai;  Dai Xinyue;  Dong Huan;  Gu Wenjing 收藏  |  浏览/下载：46/0  |  提交时间：2020/01/03 Bone Marrow Microenvironment  Chronic Myeloproliferative Disorders  Hematopoiesis   Exome sequencing reveals a novel variant in NFX1 causing intracranial aneurysm in a Chinese family 期刊论文 2019 作者:   收藏  |  浏览/下载：7/0  |  提交时间：2020/01/03 Aneurysm  Genetic  Hemorrhage   Sensitive and rapid detection of TERT promoter and IDH mutations in diffuse gliomas 期刊论文 2019, 卷号: 21, 期号: 4, 页码: 440-450 作者:  Diplas, Bill H.;  Liu, Heng;  Yang, Rui;  Hansen, Landon J.;  Zachem, Alexis L. 收藏  |  浏览/下载：15/0  |  提交时间：2020/01/03 glioma classification  IDH mutation  qPCR  sequencing  TERT promoter mutation   Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population 期刊论文 2019, 卷号: 688, 页码: 215-220 作者:  Liu, Gang;  Liu, Sen;  Li, Xiaoxin;  Chen, Jia;  Chen, Weisheng 收藏  |  浏览/下载：4/0  |  提交时间：2020/01/03 Adolescent idiopathic scoliosis (AIS)  PAX1  Northern Han Chinese  Single nucleotide polymorphism (SNP)  PUMC classification system   Genome-wide DNA methylation profile of thymomas and potential epigenetic regulation of thymoma subtypes 期刊论文 2019, 卷号: 41, 期号: 5, 页码: 2762-2774 作者:  Bi, Yalan;  Meng, Yunxiao;  Niu, Yuchen;  Li, Shanqing;  Liu, Hongsheng 收藏  |  浏览/下载：25/0  |  提交时间：2020/01/03 thymomas  differential methylation  integrative analysis  molecular subtypes  tumorigenesis mechanism   TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model 期刊论文 2019, 卷号: 21, 期号: 7, 页码: 1548-1558 作者:  Liu, Jiaqi;  Wu, Nan;  Yang, Nan;  Takeda, Kazuki;  Chen, Weisheng 收藏  |  浏览/下载：33/0  |  提交时间：2020/01/03 congenital scoliosis (CS)  16p11.2/TBX6  compound inheritance model  genotype-phenotype correlation  gene dosage   Gender differences in the relationship between alcohol consumption and insomnia in the northern Chinese population 期刊论文 2018, 卷号: 13, 期号: 12, 页码: e0207392 作者:  Guo, Yuchen;  Hu, Hongpu;  Liu, Yingping;  Leng, Yue;  Gao, Xing 收藏  |  浏览/下载：7/0  |  提交时间：2020/01/03 Perturbations of BMP/TGF-beta and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM) 期刊论文 2018, 卷号: 55, 期号: 10, 页码: 675-684 作者:  Wang, Kun;  Zhao, Sen;  Liu, Bowen;  Zhang, Qianqian;  Li, Yaqi 收藏  |  浏览/下载：6/0  |  提交时间：2020/01/03 brain arteriovenous malformation (bavm)  whole exome sequencing  genetics heterogeneity  vasculogenesis   The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease 期刊论文 2018, 卷号: 137, 期号: 6-7, 页码: 553-567 作者:  Liu, Jiaqi;  Zhou, Yangzhong;  Liu, Sen;  Song, Xiaofei;  Yang, Xin-Zhuang 收藏  |  浏览/下载：9/0  |  提交时间：2020/01/03