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科研机构
山东大学 [16]
内容类型
期刊论文 [13]
会议论文 [3]
发表日期
2019 [1]
2018 [2]
2017 [3]
2015 [1]
2014 [1]
2012 [5]
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专题:山东大学
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Clinical and genetic analysis of 7 Chinese patients with beta-ureidopropionase deficiency
期刊论文
MEDICINE, 2019, 卷号: 98, 期号: 1
作者:
Fang, Yulian
;
Cai, Chunquan
;
Wang, Chao
;
Sun, Bei
;
Zhang, Xinjie
收藏
  |  
浏览/下载:11/0
  |  
提交时间:2019/12/11
beta-ureidopropionase deficiency
genetic analysis
mutation
UPB1
The finding of a new heterozygous mutation site of the SCN2A gene in a monozygotic twin family carrying and exhibiting genetic epilepsy with febrile seizures plus (GEFS plus ) using targeted next-generation sequencing
期刊论文
CLINICAL NEUROLOGY AND NEUROSURGERY, 2018, 卷号: 169, 页码: 86-91
作者:
Liu, Xue-wu
;
Li, Wenna
;
Han, Tao
;
Wei, Kunkun
;
Qiao, Shan
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/11
Genetic epilepsy with febrile seizures plus
SCN2A
Epilepsy
Mutation
Competitive Interactions Between Incompatible Mutants of the Social Bacterium Myxococcus xanthus DK1622
期刊论文
FRONTIERS IN MICROBIOLOGY, 2018, 卷号: 9
作者:
Gong, Ya
;
Zhang, Zheng
;
Zhou, Xiu-wen
;
Anwar, Mian N.
;
Hu, Xiao-zhuang
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/11
Myxococcus xanthus
transposon-mutation
multiple genetic loci
self-identification
competitive interaction
colony-merger
incompatibility
Familial progressive hyper- and hypopigmentation: a report on a Chinese family and evidence for genetic heterogeneity
期刊论文
ANAIS BRASILEIROS DE DERMATOLOGIA, 2017, 卷号: 92, 期号: 3, 页码: 329-333
作者:
Xiao-Kai, Fang
;
Yan-Jia, Li
;
He-Peng, Wang
;
Yue-Xi, He
;
Li-Rong, Chen
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/12
Genetic heterogeneity
Hyperpigmentation
Hypopigmentation
Immunohistochemistry
Mutation
A new heterozygous mutation site of SCN2A gene in a monozygotic twin family with genetic epilepsy with febrile seizures plus(GEFS+) using targeted nextgeneration sequencing
会议论文
第七届CAAE国际癫痫论坛
作者:
Li WN(李文娜)
;
Liu XW(刘学伍)
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/31
SCN
A new heterozygous mutation site of SCN2A gene in a monozygotic twin family with genetic epilepsy with febrile seizures plus
using targeted nextgeneration sequencing
Study on A Class of Genetic Variation Algorithm in Gene Expression
会议论文
Chinese Automation Congress (CAC), OCT 20-22, 2017
作者:
Zhao, Yuqing
;
Gao, Rui
;
Dong, Guiying
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/31
gene mutation
DNA sequence alignment
genetic variation algorithm
Novel missensemutation in WNT6 in 100 couples with unexplained recurrent miscarriage
期刊论文
Human Reproduction, 2015, 卷号: 30, 期号: 4, 页码: 994-999
作者:
Zhang, Yimei
;
Li, Guangyu
;
Fan, Yuanyuan
;
Cui, Yuqian
;
Huang, Sexin
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/17
genetic association
miscarriage
point mutation
missense
WNT6 gene
3D resistivity inversion using improved parallel genetic algorithm
期刊论文
Yantu Gongcheng Xuebao/Chinese Journal of Geotechnical Engineering, 2014, 卷号: 36, 期号: 7, 页码: 1252-1261
作者:
Liu, Bin
;
Wang, Chuan-Wu
;
Yang, Wei-Min
;
Li, Shu-Cai
;
Nie, Li-Chao
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/17
3D resistivity inversion imaging
Improved parallel genetic algorithm
Joint mutation algorithm
Multi-level master-slave parallel computing strategy
Random ratio arithmetical crossover algorithm
3D resistivity inversion using an improved Genetic Algorithm based on control method of mutation direction
期刊论文
Journal of Applied Geophysics, 2012, 页码: 1-8
作者:
Liu, B.
;
Li, S.C.
;
Nie, L.C.
;
Wang, J.
;
L, X.
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/23
3D resistivity inversion
Control method of mutation direction
Improved Genetic Algorithm
Joint algorithm
Colored petri nets to model gene mutation classification
期刊论文
Proceedings of the World Congress on Intelligent Control and Automation (WCICA), 2012, 页码: 5077-5082
作者:
Yang, Jinliang
;
Gao, Rui
;
Meng, Max Q.-H.
;
Tarn, Tzyh-Jong
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/23
Amino acid codon
Gene mutation
Genetic information transmission
Molecular biology
Type classification
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