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科研机构
北京大学 [9]
内容类型
期刊论文 [9]
发表日期
2017 [1]
2016 [1]
2014 [2]
2013 [3]
2011 [1]
1998 [1]
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专题:北京大学
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Genome-wide study of an elite rice pedigree reveals a complex history of genetic architecture for breeding improvement
期刊论文
SCIENTIFIC REPORTS, 2017
Chen, Shaoxia
;
Lin, Zechuan
;
Zhou, Degui
;
Wang, Chongrong
;
Li, Hong
;
Yu, Renbo
;
Deng, Hanchao
;
Tang, Xiaoyan
;
Zhou, Shaochuan
;
Deng, Xing Wang
;
He, Hang
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2017/12/03
ORYZA-SATIVA L.
ARTIFICIAL SELECTION
MOLECULAR-GENETICS
RESISTANCE GENES
GRAIN WIDTH
ASSOCIATION
POLYMORPHISM
STARCH
OVEREXPRESSION
SIMULATION
Germline mutations in the VHL gene associated with 3 different renal lesions in a Chinese von Hippel-Lindau disease family
期刊论文
CANCER BIOLOGY & THERAPY, 2016
Yuan, Ping
;
Sun, Qipeng
;
Liang, Hao
;
Wang, Wenjun
;
Li, Ling
;
Wang, Ye
;
Deng, Huan
;
Lai, Luhua
;
Chen, Xiaoli
;
Zhou, Xiangfu
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2017/12/03
Clear cell renal cell carcinoma
multilocular cystic renal cell carcinoma
mutation
von Hippel-Lindau disease
VHL
CELL CARCINOMA
PHEOCHROMOCYTOMA
EXPERIENCE
DIAGNOSIS
PATHOLOGY
NEOPLASIA
VARIANTS
COMPLEX
Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients
期刊论文
bmc medical genetics, 2014
Zhao, Ying
;
Zhang, Xiaoying
;
Bao, Xinhua
;
Zhang, Qingping
;
Zhang, Jingjing
;
Cao, Guangna
;
Zhang, Jie
;
Li, Jiarui
;
Wei, Liping
;
Pan, Hong
;
Wu, Xiru
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2015/11/10
CDKL5 mutations
Early-onset epileptic encephalopathy
X chromosome inactivation
ONSET INTRACTABLE EPILEPSY
X-CHROMOSOME INACTIVATION
CDKL5 MUTATIONS
RETT-SYNDROME
INFANTILE SPASMS
MENTAL-RETARDATION
SEVERE ENCEPHALOPATHY
FEMALE-PATIENTS
BOYS
SEIZURES
ATP1A3 Mutations and Genotype-Phenotype Correlation of Alternating Hemiplegia of Childhood in Chinese Patients
期刊论文
plos one, 2014
Yang, Xiaoling
;
Gao, Hua
;
Zhang, Jie
;
Xu, Xiaojing
;
Liu, Xiaoyan
;
Wu, Xiru
;
Wei, Liping
;
Zhang, Yuehua
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2015/11/10
ONSET DYSTONIA-PARKINSONISM
DE-NOVO MUTATIONS
CRYSTAL-STRUCTURE
SEQUENCING DATA
GENE MUTATION
SWISS-MODEL
WEB SERVER
MIGRAINE
IDENTIFICATION
ENVIRONMENT
Involvement of and Interaction between WNT10A and EDA Mutations in Tooth Agenesis Cases in the Chinese Population
期刊论文
plos one, 2013
He, Huiying
;
Han, Dong
;
Feng, Hailan
;
Qu, Hong
;
Song, Shujuan
;
Bai, Baojing
;
Zhang, Zhenting
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2015/11/11
HYPOHIDROTIC ECTODERMAL DYSPLASIA
NON-SYNDROMIC HYPODONTIA
ECTODYSPLASIN-A
GENETIC-BASIS
INHERITED ANOMALIES
HAIR-FOLLICLES
KAPPA-B
IDENTIFICATION
MORPHOGENESIS
EXPRESSION
Interactions between Social/behavioral factors and ADRB2 genotypes may be associated with health at advanced ages in China
期刊论文
bmc geriatrics, 2013
Zeng, Yi
;
Cheng, Lingguo
;
Zhao, Ling
;
Tan, Qihua
;
Feng, Qiushi
;
Chen, Huashuai
;
Shen, Ke
;
Li, Jianxin
;
Zhang, Fengyu
;
Cao, Huiqing
;
Gregory, Simon G.
;
Yang, Ze
;
Gu, Jun
;
Tao, Wei
;
Tian, Xiao-Li
;
Hauser, Elizabeth R.
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2015/11/11
Health aging
Oldest-old
Social/behavioral factors
ADRB2 genotypes
GxE Interactions
Cognitive function
Self-reported health
Regular exercise
Social-leisure activities
Negative emotion
BETA-ADRENERGIC-RECEPTORS
SELF-RATED HEALTH
BETA(2)-ADRENERGIC RECEPTOR
REPORTED HEALTH
MORTALITY
SURVIVAL
POLYMORPHISMS
STRESS
RISK
ADRENOCEPTORS
Causal Models of Clinically Significant Behaviors in Angelman, Cornelia de Lange, Prader-Willi and Smith-Magenis Syndromes
期刊论文
2013
Oliver, Chris
;
Adams, Dawn
;
Allen, Debbie
;
Bull, Leah
;
Heald, Mary
;
Moss, Jo
;
Wilde, Lucy
;
Woodcock, Kate
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2015/11/16
SELF-INJURIOUS-BEHAVIOR
BRACHMANN-DELANGE SYNDROME
SYNDROME DEL 17P11.2
DU-CHAT-SYNDROMES
GENOTYPE-PHENOTYPE CORRELATIONS
AUTISM SPECTRUM DISORDERS
FRAGILE-X-SYNDROME
COMPULSIVE BEHAVIOR
ENVIRONMENTAL EVENTS
GENETIC SUBTYPES
The study on venom proteins of Lapemis hardwickii by cDNA phage display
期刊论文
毒理学快报, 2011
Tan, Taochao
;
Xiang, Xi
;
Qu, Hong
;
Zhu, Shenggeng
;
Bi, Qun
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2015/11/10
Venom protein
Sea snake
cDNA phage display
T7 display vector
Neurotoxin
ACETYLCHOLINE-RECEPTOR
ALPHA-NEUROTOXINS
POSTSYNAPTIC NEUROTOXINS
SWISS-MODEL
SNAKE
BINDING
CLONING
IDENTIFICATION
PURIFICATION
INHIBITION
PPF-1, a post-floral-specific gene expressed in short-day-grown G2 pea, may be important for its never-senescing phenotype
期刊论文
gene, 1998
Zhu, YX
;
Zhang, YF
;
Luo, JC
;
Davies, PJ
;
Ho, DTH
收藏
  |  
浏览/下载:1/0
  |  
提交时间:2015/11/11
cloning
G2 pea
gibberellins
senescence
PPF-1 gene
SENESCENCE
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