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浏览/检索结果: 共7条，第1-7条 帮助 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 A de novo mutation in DHD domain of SKI causing spina bifida with no craniofacial malformation or intellectual disability 期刊论文 AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2019, 卷号: 179, 期号: 6 作者:  Zhang, Ling;  Xu, Ximing;  Sun, Kaiqiang;  Sun, Jingchuan;  Wang, Yuan 收藏  |  浏览/下载：26/0  |  提交时间：2019/12/05 DHD domain  lipomeningomyelocele  Shprintzen-Goldberg syndrome  SKI gene  tethered cord   Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk 期刊论文 Genetic Epidemiology, 2015, 卷号: 39, 期号: 8 作者:  Amankwah, Ernest K./55638506400[0];  Lin, Huiyi/57043709500[1];  Tyrer, Jonathan P./15045992700[2];  Lawrenson, Kate/26040889200[3];  Dennis, Joe G./56956361900[4] 收藏  |  浏览/下载：30/0  |  提交时间：2019/12/19 Epithelial-mesenchymal transition  Ovarian cancer  Single-nucleotide polymorphisms   De novo GLI3 mutation in esophageal atresia: Reproducing the phenotypic spectrum of Gli3 defects in murine models 期刊论文 BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2014, 卷号: 1842, 期号: 9, 页码: 1755-1761 Yang, L; Shen, C; Mei, M; Zhan, GD; Zhao, YK; Wang, HJ; Huang, GY; Qiu, ZL; Lu, WN; Zhou, WH 收藏  |  浏览/下载：39/0  |  提交时间：2014/12/15 PALLISTER-HALL-SYNDROME  TRACHEOESOPHAGEAL FISTULA  MENTAL-RETARDATION  COPY NUMBER  GENE  FEATURES  CANCER  MICRODELETION  ASSOCIATION  ANOMALIES   576 kb deletion in 1p36.33-p36.32 containing SKI is associated with limb malformation, congenital heart disease and epilepsy. 期刊论文 Gene, 2013, 卷号: 528, 期号: 2, 页码: 352-355 作者:  Zhu, Xin;  Zhang, Yi;  Wang, Jian;  Yang, Jin-Fu;  Yang, Yi-Feng 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/03 1p36 deletion  ASD  CHD  CNV  CT  Congenital heart defect  Copy number variation  DGV  Database of Genomic Variants  Epilepsy  Hg19  OMIM  Online Mendelian Inheritance in Man  PCR  SGS  SNP  SNP array  Shprintzen-Goldberg syndrome  atrial septal defect  computed tomography  congenital heart defects  copy number variation  human genome 19  polymerase chain reaction  single nucleotide polymorphism   Expression Profiles of SnoN in Normal and Cancerous Human Tissues Support Its Tumor Suppressor Role in Human Cancer 期刊论文 http://dx.doi.org/10.1371/journal.pone.0055794, 2013 Jahchan, Nadine S.; Ouyang, Gaoliang; Luo, Kunxin; 欧阳高亮 收藏  |  浏览/下载：7/0  |  提交时间：2015/07/22 TGF-BETA  CDNA-CLONES  SKI  OVEREXPRESSION  TUMORIGENESIS  GROWTH  MICROENVIRONMENT  ADENOCARCINOMA  AMPLIFICATION  CARCINOMAS   Mechanism of Cellular Uptake of Graphene Oxide Studied by Surface-Enhanced Raman Spectroscopy 期刊论文 Small, 2012, 卷号: 8, 期号: 16, 页码: 2577-2584 作者:  Zhijun Zhang(张智军);  Jie Huang(黄洁);  Zhijun Zhang(张智军);  Jie Huang(黄洁);  Zhijun Zhang(张智军) 收藏  |  浏览/下载：30/0  |  提交时间：2013/01/22 cellular uptake  gold  graphene oxide  nanoparticles  Raman spectroscopy   Mechanism of Cellular Uptake of Graphene Oxide Studied by Surface-Enhanced Raman Spectroscopy 期刊论文 2012 Huang, Jie; Zong, Cheng; Shen, He; Liu, Min; Chen, Biao; Ren, Bin; 任斌; Zhang, Zhijun 收藏  |  浏览/下载：5/0  |  提交时间：2013/02/26 GOLD NANOPARTICLES  ENDOCYTOSIS  DELIVERY  SCATTERING  GRAPHITE  BIOLOGY  DRUGS  CELLS  DYES