×
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
中国医学科学院 北... [26]
复旦大学上海医学院 [24]
山东大学 [10]
西安交通大学 [8]
华南理工大学 [4]
吉林大学白求恩第一医... [3]
更多...
内容类型
期刊论文 [98]
会议论文 [1]
发表日期
2023 [1]
2021 [1]
2019 [18]
2018 [17]
2017 [13]
2016 [16]
更多...
学科主题
Environmen... [1]
Pharmacolo... [1]
agricultur... [1]
×
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99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
High-precision early warning system for rice cadmium accumulation risk assessment
期刊论文
SCIENCE OF THE TOTAL ENVIRONMENT, 2023, 卷号: 859
作者:
Yan, Huili
;
Guo, Hanyao
;
Li, Ting
;
Zhang, Hezifan
;
Xu, Wenxiu
收藏
  |  
浏览/下载:1/0
  |  
提交时间:2024/03/07
Genotype-to-phenotype prediction
Rice
Cd risk early warning
Phenotypic and genomic adaptations to the extremely high elevation in plateau zokor (Myospalax baileyi)
期刊论文
MOLECULAR ECOLOGY, 2021
作者:
Zhang, Tao
;
Chen, Jie
;
Zhang, Jia
;
Guo, Yuan-Ting
;
Zhou, Xin
收藏
  |  
浏览/下载:17/0
  |  
提交时间:2021/11/18
heterogeneous stresses
high elevation adaptation
phenotype and genotype
plateau zokor
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
GENETICS IN MEDICINE, 2019, 卷号: 21, 期号: 7
作者:
Liu, Jiaqi
;
Wu, Nan
;
Yang, Nan
;
Takeda, Kazuki
;
Chen, Weisheng
收藏
  |  
浏览/下载:63/0
  |  
提交时间:2019/12/05
congenital scoliosis (CS)
16p11.2/TBX6
compound inheritance model
genotype-phenotype correlation
gene dosage
NOVEL BEST1 MUTATIONS DETECTED BY NEXT-GENERATION SEQUENCING IN A CHINESE POPULATION WITH VITELLIFORM MACULAR DYSTROPHY
期刊论文
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2019, 卷号: 39, 期号: 8
作者:
Guo, Jingli
;
Gao, Fengjuan
;
Tang, Wenyi
;
Qi, Yuhe
;
Xuan, Yi
收藏
  |  
浏览/下载:36/0
  |  
提交时间:2019/12/05
adult-onset foveomacular vitelliform dystrophy
BEST1
genotype-phenotype
next-generation sequencing
optical coherence tomography angiography
Genotype-phenotype correlation study and mutational and hormonal analysis in a Chinese cohort with 21-hydroxylase deficiency
期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 6
作者:
Xu, Chao
;
Jia, Wenyu
;
Cheng, Xiangdeng
;
Ying, Hui
;
Chen, Jing
收藏
  |  
浏览/下载:29/0
  |  
提交时间:2019/12/11
congenital adrenal hyperplasia (CAH)
CYP21A2
genotype-phenotype
associations
mutation
steroid 21-hydroxylase deficiency (21OHD)
Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta
期刊论文
HUMAN MUTATION, 2019, 卷号: 40, 期号: 5, 页码: 588-600
作者:
Li, Lulu
;
Mao, Bin
;
Li, Shan
;
Xiao, Jifang
;
Wang, Han
收藏
  |  
浏览/下载:141/0
  |  
提交时间:2019/12/11
Chinese cohort
genomic rearrangements
genotype-phenotype correlations
mutation spectrum
osteogenesis imperfecta
Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome
期刊论文
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2019, 卷号: 42, 期号: 6, 页码: 653-665
作者:
Zhong, F.
;
Ying, H.
;
Jia, W.
;
Zhou, X.
;
Zhang, H.
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/11
Gitelman syndrome
Pedigree
Solute carrier family 12
member 3
(SLC12A3)
Genotype
Phenotype
Follow-up
Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta.
期刊论文
Human mutation, 2019
作者:
Lulu Li
;
Bin Mao
;
Shan Li
;
Jifang Xiao
;
Han Wang
收藏
  |  
浏览/下载:32/0
  |  
提交时间:2019/12/17
Chinese
cohort
Osteogenesis
imperfecta
genomic
rearrangements
genotype-phenotype
correlations
mutation
spectrum
TBX6-associated congenital scoliosis as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model.
期刊论文
Genetics in medicine : official journal of the American College of Medical Genetics, 2019
作者:
Jiaqi Liu
;
Nan Wu
;
Nan Yang
;
Kazuki Takeda
;
Weisheng Chen
收藏
  |  
浏览/下载:48/0
  |  
提交时间:2019/12/13
16p11.2/TBX6
compound
inheritance
model
congenital
scoliosis
(CS)
gene
dosage
genotype-phenotype
correlation
Steroid metabolism gene variants and their genotype-phenotype correlations in Chinese early-onset hypertension patients
期刊论文
2019, 卷号: 42, 期号: 10, 页码: 1536-1543
作者:
Qin Fang
;
Liu Kai
;
Zhang Ce
;
Sun Xiaolu
;
Zhang Yang
收藏
  |  
浏览/下载:52/0
  |  
提交时间:2020/01/03
congenital adrenal hyperplasia
genotype–phenotype correlation
hypertension
rare variant
steroid metabolism
©版权所有 ©2017 CSpace - Powered by
CSpace