×
验证码:
换一张
忘记密码?
记住我
CORC
首页
科研机构
检索
知识图谱
申请加入
托管服务
登录
注册
在结果中检索
科研机构
山东大学 [18]
复旦大学上海医学院 [15]
中国医学科学院 北... [12]
北京大学 [11]
西北高原生物研究所 [9]
厦门大学 [8]
更多...
内容类型
期刊论文 [136]
会议论文 [4]
发表日期
2021 [2]
2019 [19]
2018 [16]
2017 [19]
2016 [12]
2015 [20]
更多...
学科主题
Cell Biolo... [4]
Biochemist... [2]
Science & ... [2]
Biochemist... [1]
Biophysics [1]
Endocrinol... [1]
更多...
×
知识图谱
CORC
开始提交
已提交作品
待认领作品
已认领作品
未提交全文
收藏管理
QQ客服
官方微博
反馈留言
浏览/检索结果:
共140条,第1-10条
帮助
已选(
0
)
清除
条数/页:
5
10
15
20
25
30
35
40
45
50
55
60
65
70
75
80
85
90
95
100
排序方式:
请选择
作者升序
作者降序
题名升序
题名降序
发表日期升序
发表日期降序
提交时间升序
提交时间降序
A Semi-Dominant Mutation in OsCESA9 Improves Salt Tolerance and Favors Field Straw Decay Traits by Altering Cell Wall Properties in Rice
期刊论文
RICE, 2021, 卷号: 14
作者:
Ye, Yafeng
;
Wang, Shuoxun
;
Wu, Kun
;
Ren, Yan
;
Jiang, Hongrui
收藏
  |  
浏览/下载:321/0
  |  
提交时间:2021/04/26
Secondary cell wall (SCW)
Rice
Cellulose synthesis
Salt tolerance
Straw process
Oridonin inhibits DNMT3A R882 mutation-driven clonal hematopoiesis and leukemia by inducing apoptosis and necroptosis
期刊论文
CELL DEATH DISCOVERY, 2021, 卷号: 7, 期号: 1, 页码: 12
作者:
Liao, Min
;
Dong, Qiongye
;
Chen, Ruiqing
;
Xu, Liqian
;
Jiang, Yuxuan
收藏
  |  
浏览/下载:33/0
  |  
提交时间:2021/12/01
Whole-Exome Sequencing Identified a Novel Compound Heterozygous Genotype in ASL in a Chinese Han Patient with Argininosuccinate Lyase Deficiency
期刊论文
BIOMED RESEARCH INTERNATIONAL, 2019, 页码: 7
作者:
Zhao, Mei
;
Hou, Lingling
;
Teng, Huajing
;
Li, Jinchen
;
Wang, Jiesi
收藏
  |  
浏览/下载:59/0
  |  
提交时间:2019/06/12
A novel heterozygous large deletion of MSH6 gene in a Chinese family with Lynch syndrome
期刊论文
GENE, 2019, 卷号: 704
作者:
Liu, Yuanyuan
;
Wang, Mingwei
;
Chen, Qiongrong
;
Zheng, Qiaosong
;
Li, Guangyu
收藏
  |  
浏览/下载:12/0
  |  
提交时间:2019/12/05
Novel gene deletion mutation
Targeted next-generation sequencing
Multiplex ligation-dependent probe amplification
Colorectal cancer
A Nonsense Mutation in COL4A4 Gene Causing Isolated Hematuria in Either Heterozygous or Homozygous State
期刊论文
FRONTIERS IN GENETICS, 2019, 卷号: 10
作者:
Yang, Cheng
;
Song, Yuan
;
Chen, Zhaowei
;
Yuan, Xiaohan
;
Chen, Xinhua
收藏
  |  
浏览/下载:24/0
  |  
提交时间:2019/12/05
human genetics
collagen type IV
Alport syndrome
COL4A4
genomic variant
hereditary nephropathy
A, p.R322H; c.334 G > C, p.G112R) identified in a Chinese patient with leukodystrophy involved in brain and spinal cord">A novel compound heterozygous mutation in AARS2 gene (c.965 G > A, p.R322H; c.334 G > C, p.G112R) identified in a Chinese patient with leukodystrophy involved in brain and spinal cord
期刊论文
JOURNAL OF HUMAN GENETICS, 2019, 卷号: 64, 期号: 10, 页码: 979-983
作者:
Song, Chengyuan
;
Peng, Linliu
;
Wang, Shengjun
;
Liu, Yiming
收藏
  |  
浏览/下载:15/0
  |  
提交时间:2019/12/11
Establishment of a human iPSC line (SDQLCHi010-A) from a patient with optic nerve malformation carrying a heterozygous mutation in PAX6 gene
期刊论文
Stem Cell Research, 2019, 卷号: 41
作者:
Zhang H.
;
Ma Y.
;
Yu S.
;
Yang X.
;
Li Y.
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/11
Establishment of a human induced pluripotent stem cell line (SDQLCHi005-A) from a patient with mastocytosis carrying heterozygous mutation in KIT gene
期刊论文
STEM CELL RESEARCH, 2019, 卷号: 40
作者:
Zhang, Haiyan
;
Ma, Yanyan
;
Yan, Beibei
;
Yang, Xiaomeng
;
Li, Yue
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/11
Establishment of a human induced pluripotent stem cell line (SDQLCHi004-A) from a patient with nemaline myopathy-4 disease carrying heterozygous mutation in TPM2 gene
期刊论文
STEM CELL RESEARCH, 2019, 卷号: 40
作者:
Ma, Yanyan
;
Zhang, Haiyan
;
Yang, Xiaomeng
;
Li, Yue
;
Guan, Jingyun
收藏
  |  
浏览/下载:14/0
  |  
提交时间:2019/12/11
Two Novel CCM2 Heterozygous Mutations Associated with Cerebral Cavernous Malformation in a Chinese Family.
期刊论文
Journal of molecular neuroscience, 2019
作者:
Qin Du
;
Ziyan Shi
;
Hongxi Chen
;
Ying Zhang
;
Jiancheng Wang
收藏
  |  
浏览/下载:11/0
  |  
提交时间:2019/12/17
CCM2
mutation
Familial
cerebral
cavernous
malformation
Novel
mutations
Susceptibility-weighted
imaging
©版权所有 ©2017 CSpace - Powered by
CSpace