@article {Wang:2007p7984,
	title = {[Analysis on genetic diversity of different Salvia miltiorrhiza geographical populations in China]},
	journal = {Zhongguo Zhong Yao Za Zhi},
	volume = {32},
	number = {19},
	year = {2007},
	month = {Oct},
	pages = {1988{\textendash}91},
	abstract = {OBJECTIVE: To research on genetic diversity of different Salvia miltiorrhiza geographical populations in China. METHOD: The genetic diversity of 27 S. miltiorrhiza geographical populations from ten provinces in China was estimated using amplified fragment length polymorphism (AFLP) markers. The data of amplified bands were analyzed by the software POPGENE and SPSS. RESULT: The ten primers employed produced a total of 528 discernable and reproduceable amplified fragments. There were 476 polymorphic brands. The percentage of polymorphic bands with in different populations was 90.15\%. Genetic diversity analysis showed that Neis gene diversity (He) was 0.261 2 and Shannon{\textquoteright}s genetic diversity index (1) was 0.403 3. The coefficient of gene similarity was 0.504 0-0.789 0 between populations. The cluster map including all samples were obtained by UPGMA. In the map, there were seven cluster groups and one individual outside the groups. CONCLUSION: The genetic diversity with in different geographical population of S. miltiorrhiza in China is plentiful.},
	keywords = {Amplified Fragment Length Polymorphism Analysis, China, Cluster Analysis, DNA Primers, DNA: Plant, Genetic Variation, Genetics: Population, Phylogeny, Plants: Medicinal, Salvia miltiorrhiza},
	author = {Bing Wang and Yong Zhang and Cheng-Bin Chen and Xiu-Lan Li and Rui-Yang Chen and Li Chen}
}
@article {Zhang:2007p7990,
	title = {[Correlation between ITS genotype and geographical distribution of Pogostemon cablin]},
	journal = {Yao Xue Xue Bao},
	volume = {42},
	number = {1},
	year = {2007},
	month = {Jan},
	pages = {93{\textendash}7},
	abstract = {To investigate the correlation between genotype and distribution of Pogostemon cablin by sequencing ITS1 and ITS2 genes, and provide molecular information for its germplasm evaluation, ITS1 and ITS2 genes of Pogostemon cablin from different localities were identified by PCR direct sequencing. The sequences of ITS1 and ITS2 genes were 424 bp and 380 bp in length, respectively. And nineteen base substitutions were observed in ITS1 gene, and five in ITS2 gene. The results showed a good correlation between genotype and distribution of Pogostemon cablin, and ITS gene sequencing could provide useful molecular information for germplasm evaluation of the plant species verification.},
	keywords = {Base Sequence, Biodiversity, China, Cluster Analysis, DNA: Plant, DNA: Ribosomal, DNA: Ribosomal Spacer, Genotype, Geography, Lamiaceae, Molecular Sequence Data, Phylogeny, Plant Leaves, Plants: Medicinal, Sequence Analysis: DNA},
	author = {Ying Zhang and Yao Chen and Jin-Chao Zhang and Meng-Su Yang and Hui Cao and Pei-Gen Xiao}
}
@article {Pan:2006p8001,
	title = {[Study on intraspecific genetic diversity in different plant populations of Pogostemon cabli]},
	journal = {Zhongguo Zhong Yao Za Zhi},
	volume = {31},
	number = {9},
	year = {2006},
	month = {May},
	pages = {723{\textendash}6},
	abstract = {OBJECTIVE: To study the genetic polymorphism and intraspecific genetic differentiation of different populations of Pogostemon cablin, and find out the effective method to distinguish DNA fingerprint of different populations of P. cablin. METHOD: Five plant populations of P. cablin were analyzed by RAPD markers. PopGen 32 software for clustering analysis and calculating. Fourteen of the 80 random primers were tested to possess the stronger detecting effect of polymorphous character. RESULT: A total of 84 bands was amplified by the 10 primers, among them 17 bands were monomorphic. 67 of them were polymorphic. The results indicated that the genetic variations existed within the different plant populations of the same species. CONCLUSION: It is feasible by RAPD technique with specifically primer to analyze the genetic diversity and identify 5 plant populations of P. cablin. RAPD technique has provided a new path for identification and classification of P. cablin genetic germplasm.},
	keywords = {China, Cluster Analysis, Dna Fingerprinting, DNA: Plant, Ecosystem, Lamiaceae, Phylogeny, Plants: Medicinal, Polymorphism: Genetic, Random Amplified Polymorphic DNA Technique},
	author = {Chao-mei Pan and Wei Li and Hong He and Wang-qiu Deng and Tai-hui Li and Hong-hua Xu}
}
@article {Liu:2006p8004,
	title = {Genetic diversity and population structure of Lamiophlomis rotata (Lamiaceae), an endemic species of Qinghai-Tibet Plateau},
	journal = {Genetica},
	volume = {128},
	number = {1-3},
	year = {2006},
	month = {Jan},
	pages = {385{\textendash}94},
	abstract = {{Lamiophlomis rotata (Lamiaceae), a perennial medicinal herb, is endemic to the Qinghai-Tibet Plateau. A total of 188 individuals from eight natural populations of L. rotata in Qinghai-Tibet Plateau (four from Tibet, two from Yunnan, and two from Qinghai) were analyzed using intersimple sequence repeats (ISSR) and randomly amplified polymorphic DNA (RAPD) techniques. Our results revealed that the level of genetic variation in L. rotata was relatively high (P = 94.85\%},
	keywords = {China, Conservation of Natural Resources, DNA: Plant, Genetic Variation, Lamiaceae, Minisatellite Repeats, Phylogeny, Random Amplified Polymorphic DNA Technique, Tibet},
	doi = {10.1007/s10709-006-7517-y},
	author = {Jimei Liu and Li Wang and Yupeng Geng and Qingbiao Wang and Lijun Luo and Yang Zhong}
}
@article {Xiong:2005p8007,
	title = {Stachytarpheta leaf curl virus is a novel monopartite begomovirus species},
	journal = {Arch Virol},
	volume = {150},
	number = {11},
	year = {2005},
	month = {Nov},
	pages = {2257{\textendash}70},
	abstract = {Begomovirus isolates were obtained from Stachytarpheta jamaicensis plants showing leaf curl and chlorosis symptoms collected in the Hainan province of China. The complete sequences of isolates Hn5-4, Hn6-1, Hn30 and Hn34 were determined to be 2748, 2751, 2748 and 2748 nucleotides long, respectively. The complete sequences of the four isolates share more than 94.9\% nucleotide sequence identity, but all of them have less than 86\% nucleotide sequence identity with other reported begomoviruses. The molecular data show that Hn5-4, Hn6-1, Hn30 and Hn34 are isolates of a distinct begomovirus species, for which the name Stachytarpheta leaf curl virus (StaLCV) is proposed. PCR and Southern blot analyses demonstrate that all the collected field samples are not associated with DNAbeta or DNA-B components. An infectious clone of StaLCV isolate Hn5-4 was constructed, and could efficiently infect Nicotiana benthamiana, N. tabacum Samsun, N. glutinosa, Lycopersicon esculentum and Petunia hybrida plants, inducing upward leaf roll and vein swelling symptoms. In addition, we illustrate that StaLCV can functionally interact with distinct DNAbeta molecules in plants.},
	keywords = {China, DNA: Viral, Geminiviridae, Lamiaceae, Molecular Sequence Data, Phylogeny, Plant Diseases, Plant Leaves, Polymerase Chain Reaction},
	doi = {10.1007/s00705-005-0568-z},
	author = {Q Xiong and S Fan and X Guo and X Zhou}
}
