Complete genome sequence of a dahlia common mosaic virus isolate from New Zealand-Reference-Cited by-同舟云学术

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Complete genome sequence of a dahlia common mosaic virus isolate from New Zealand

Published:2011-09-30 Issue:12 Volume:156 Page:2297-2301
ISSN:0304-8608
Container-title:Archives of Virology
language:en
Short-container-title:Arch Virol

Author:

Hadfield James,Linderme Daphné,Shepherd Dionne N.,Bezuidenhout Marion,Lefeuvre Pierre,Martin Darren P.,Varsani Arvind

Publisher

Springer Science and Business Media LLC

Subject

Virology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00705-011-1112-y.pdf

Reference23 articles.

1. Anisimova M, Gascuel O (2006) Approximate likelihood-ratio test for branches: a fast, accurate, and powerful alternative. Syst Biol 55:539

2. Bhattacharyya S, Dey N, Maiti IB (2002) Analysis of cis-sequence of subgenomic transcript promoter from the Figwort mosaic virus and comparison of promoter activity with the cauliflower mosaic virus promoters in monocot and dicot cells. Virus Res 90:47–62

3. Brunt A (1971) Some hosts and properties of dahlia mosaic virus. Ann Appl Biol 67:357–368

4. Cooke R, Penon P (1990) In vitro transcription from cauliflower mosaic virus promoters by a cell-free extract from tobacco cells. Plant Mol Biol 14:391–405

5. De Tapia M, Himmelbach A, Hohn T (1993) Molecular dissection of the cauliflower mosaic virus translation transactivator. EMBO J 12:3305

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1. Identification and Molecular Characterization of Dahlia Common Mosaic Virus from Silphium spp., a New Natural Host of the Virus;PhytoFrontiers™;2024-05-31

2. Identification and Genome Characterization of a Dahlia Common Mosaic Virus Isolate from China;Genes;2023-09-22

3. Untangling the taxonomy of dahlia mosaic virus;Archives of Virology;2022-08-15

4. Molecular and biological characterizations of dahlia-infecting caulimoviruses in Iraq;Tropical Plant Pathology;2022-06-09

5. Comparison of two highly sensitive methods to detect potato spindle tuber viroid in Dahlia using quantitative-reverse transcription-polymerase chain reaction assays;Journal of Virological Methods;2022-02

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