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期刊论文 [15]
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学科主题:Genetics & Heredity
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Haplotype-resolved genome assembly provides insights into evolutionary history of the tea plant Camellia sinensis
期刊论文
NATURE GENETICS, 2021, 卷号: 53, 期号: 8, 页码: 1250-+
作者:
Zhang, Xingtan
;
Chen, Shuai
;
Shi, Longqing
;
Gong, Daping
;
Zhang, Shengcheng
收藏
  |  
浏览/下载:51/0
  |  
提交时间:2021/09/08
Identification and genetic analysis of EMS-mutagenized wheat mutants conferring lesion-mimic premature aging
期刊论文
BMC GENETICS, 2020, 卷号: 21, 期号: 1
作者:
Kong, Weiwei
;
Wang, Liming
;
Cao, Pei
;
Li, Xingfeng
;
Ji, Jingjing
收藏
  |  
浏览/下载:21/0
  |  
提交时间:2022/03/01
Wheat
lmpa1
Mutant
Chromosomal location
RNA methylomes reveal the m(6)A-mediated regulation of DNA demethylase gene SlDML2 in tomato fruit ripening
期刊论文
GENOME BIOLOGY, 2019, 卷号: 20, 期号: 1
作者:
Zhou, Leilei
;
Tian, Shiping
;
Qin, Guozheng
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  |  
浏览/下载:9/0
  |  
提交时间:2022/01/06
Fruit ripening
DNA methylation
mRNA m(6)A methylation
m(6)A RNA methylome
RNA demethylase SlALKBH2
DNA demethylase SlDML2
Colorless non-ripening
Tomato
Evolution of plastid genomes of Holcoglossum (Orchidaceae) with recent radiation
期刊论文
BMC EVOLUTIONARY BIOLOGY, 2019, 卷号: 19
作者:
Li, Zhang-Hai
;
Ma, Xiao
;
Wang, De-Yi
;
Li, Yun-Xia
;
Wang, Cheng-Wang
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2022/01/06
Holcoglossum
Plastid genome
NDH complex
Divergence hotspot
Intraspecific variation
Tandem repeat
Hairpin inversion
Evolution of Darwin's Peloric Gloxinia (Sinningia speciosa) Is Caused by a Null Mutation in a Pleiotropic TCP Gene
期刊论文
MOLECULAR BIOLOGY AND EVOLUTION, 2018, 卷号: 35, 期号: 8, 页码: 1901-1915
作者:
Dong, Yang
;
Liu, Jing
;
Li, Peng-Wei
;
Li, Chao-Qun
;
Lu, Tian-Feng
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  |  
浏览/下载:8/0
  |  
提交时间:2022/02/25
peloric gloxinia
Sinningia speciosa
domestication
molecular mechanism
floral horizontal orientation
pleiotropic gene
The impact and origin of copy number variations in the Oryza species
期刊论文
BMC GENOMICS, 2016, 卷号: 17
作者:
Bai, Zetao
;
Chen, Jinfeng
;
Liao, Yi
;
Wang, Meijiao
;
Liu, Rong
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  |  
浏览/下载:0/0
  |  
提交时间:2022/07/05
Oryza species
Copy number variation (CNV)
NGS-based survey
CNV genes
Mutation mechanisms
The impact and origin of copy number variations in the Oryza species
期刊论文
BMC GENOMICS, 2016, 卷号: 17
作者:
Bai, Zetao
;
Chen, Jinfeng
;
Liao, Yi
;
Wang, Meijiao
;
Liu, Rong
收藏
  |  
浏览/下载:0/0
  |  
提交时间:2022/07/08
Oryza species
Copy number variation (CNV)
NGS-based survey
CNV genes
Mutation mechanisms
Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population
期刊论文
JOURNAL OF HUMAN GENETICS, 2015, 卷号: 60, 期号: 10, 页码: 625-630
作者:
Zhou, Yu
;
Saikia, Bibhuti B.
;
Jiang, Zhilin
;
Zhu, Xiong
;
Liu, Yuqing
收藏
  |  
浏览/下载:34/0
  |  
提交时间:2016/12/22
CILIARY PROTEIN
The Coevolution of Phycobilisomes: Molecular Structure Adapting to Functional Evolution
期刊论文
COMPARATIVE AND FUNCTIONAL GENOMICS, 2011, 页码: 230236
作者:
Shi, Fei
;
Qin, Song
;
Wang, Yin-Chu
收藏
  |  
浏览/下载:12/0
  |  
提交时间:2012/03/06
Multiple Sequence Alignment
Crystal-structure Analysis
2.2 Angstrom Resolution
C-phycocyanin
Spirulina-platensis
Statistical-methods
Lacks Thylakoids
Protein Residues
Cyanobacterium
Phycobiliproteins
Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome
期刊论文
CLINICAL GENETICS, 2010, 卷号: 77, 期号: 2, 页码: 155-162
Yu, Y.
;
Xu, C.
;
Pan, X.
;
Ren, H.
;
Wang, W.
;
Meng, X.
;
Huang, F.
;
Chen, N.
收藏
  |  
浏览/下载:26/0
  |  
提交时间:2012/07/13
Bartter syndrome
ClC-Kb
CLCNKB
mutation
CHLORIDE CHANNEL GENE
CALCIUM-SENSING RECEPTOR
SYNDROME TYPE-III
CL TRANSPORT
HENLE LOOP
INNER-EAR
KB GENE
GITELMAN
KIDNEY
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