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西北高原生物研究所 [10]
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期刊论文 [47]
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浏览/检索结果:
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Genetic Evaluation of Growth and Survival-Related Traits in Yesso Scallop Patinopecten yessoensis in Sea-Based Culture System
期刊论文
FRONTIERS IN MARINE SCIENCE, 2022, 卷号: 9, 页码: 9
作者:
Wu, Fucun
;
Liu, Chao
;
Zhang, Jibiao
;
Zhang, Guofan
收藏
  |  
浏览/下载:18/0
  |  
提交时间:2022/07/18
yesso scallop Patinopecten yessoensis
heritability
genetic correlation
shell growth
sea-based culture
Characteristic analysis of simple sequence repeats in the ridgetail white prawn Exopalaemon carinicauda genome and its application in parentage assignment
期刊论文
JOURNAL OF THE WORLD AQUACULTURE SOCIETY, 2019, 页码: 12
作者:
Zhang, Qian
;
Zhang, Chengsong
;
Yu, Yang
;
Wang, Quanchao
;
Li, Fuhua
收藏
  |  
浏览/下载:59/0
  |  
提交时间:2020/01/03
Exopalaemon carinicauda
genome-wide
parentage assignment
SSR
SCN4A p.R675Q Mutation Leading to Normokalemic Periodic Paralysis: A Family Report and Literature Review
期刊论文
FRONTIERS IN NEUROLOGY, 2019, 卷号: 10
作者:
Shi, Jiejing
;
Qu, Qianqian
;
Liu, Haiyan
;
Cui, Wenhao
;
Zhang, Yan
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2019/12/05
normokalemic periodic paralysis
SCN4A mutation
muscle imaging
muscle biopsy
pedigree
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
A family pedigree of malignancies associated with BRCA1 pathogenic variants: a reflection of the state of art in China
期刊论文
2019, 卷号: 17, 页码: 26
作者:
Li Wenhui
;
Li Lei
;
Wu Ming
收藏
  |  
浏览/下载:11/0
  |  
提交时间:2020/01/03
BRCA mutations
Genetic counseling
Ovarian cancer
Risk-reducing salpingo-oophorectomy
First Case Report of Maturity-Onset Diabetes of the Young Type 4 Pedigree in a Chinese Family
期刊论文
2019, 卷号: 10, 页码: 406
作者:
Deng, Mingqun
;
Xiao, Xinhua
;
Zhou, Liyuan
;
Wang, Tong
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2020/01/03
MODY4
PDX1
pancreatic exocrine dysfunction
obese
Chinese
Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome
期刊论文
2019, 卷号: 18, 期号: 2, 页码: 261-265
作者:
Baig, Shahid Mahmood
;
Fatima, Ambrin
;
Tariq, Muhammad
;
Khan, Tahir Naeem
;
Ali, Zafar
收藏
  |  
浏览/下载:30/0
  |  
提交时间:2020/01/03
Constitutional mismatch repair deficiency (CMMRD) syndrome
Hereditary brain tumor
Prenatal diagnosis
Genetic counseling
PMS2
Novel mutation in FTHL17 gene in pedigree with 46,XY pure gonadal dysgenesis
期刊论文
2019, 卷号: 111, 期号: 6, 页码: 1226-+
作者:
Tang, Ruiyi
;
Liu, Xiao
;
Pan, Lingya
;
Chen, Rong
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2020/01/03
46
XY pure gonadal dysgenesis
family pedigree
ferritin heavy chain-like 17
gonadal tumor
whole-genome sequencing
Clinical and Physiological Characterization of Elevated Plasma Glucagon-Like Peptide-1 Levels (Hyperglipemia) in a Dipeptidyl Peptidase IV Mutation Carrier
期刊论文
FRONTIERS IN ENDOCRINOLOGY, 2018, 卷号: 9
作者:
Zhao, Dandan
;
Zhao, Shaoqian
;
Wang, Xiao
;
Su, Mingbo
;
Liu, Wen
收藏
  |  
浏览/下载:59/0
  |  
提交时间:2019/01/08
dipeptidyl peptidase IV
glucagon-like peptide-1
beta-cell function
type 2 diabetes
incretin effect
Deep pedigree analysis reveals family specific "fingerprint" pattern of DNA methylation for men
期刊论文
SCIENCE BULLETIN, 2018, 卷号: 63, 期号: 1
作者:
Li, Guochao
;
Zhang, Minjie
;
Chen, Hua
;
An, Ke
;
Liu, Zongzhi
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/05
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