Please use this identifier to cite or link to this item:
https://hdl.handle.net/20.500.12540/111
DC Field | Value | Language |
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dc.contributor.author | Khosravi, Yalda | en_US |
dc.contributor.author | Rehvathy, Vellaya | en_US |
dc.contributor.author | Wee, Wei Y. | en_US |
dc.contributor.author | Wang, Susana | en_US |
dc.contributor.author | Baybayan, Primo | en_US |
dc.contributor.author | Singh, Siddarth | en_US |
dc.contributor.author | Ashby, Meredith | en_US |
dc.contributor.author | Ong, Junxian | en_US |
dc.contributor.author | Amoyo, Arlaine A. | en_US |
dc.contributor.author | Seow, Shih W. | en_US |
dc.contributor.author | Choo, Siew W. | en_US |
dc.contributor.author | Perkins, Tim | en_US |
dc.contributor.author | Chua, Eng G. | en_US |
dc.contributor.author | Tay, Alfred | en_US |
dc.contributor.author | Marshall, Barry J. | en_US |
dc.contributor.author | Loke, Mun F. | en_US |
dc.contributor.author | Goh, Khean L. | en_US |
dc.contributor.author | Pettersson, Sven | en_US |
dc.contributor.author | Vadivelu, Jamuna | en_US |
dc.date.accessioned | 2020-07-21T06:09:14Z | - |
dc.date.available | 2020-07-21T06:09:14Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | Khosravi, Y., Rehvathy, V., Wee, W. Y., Wang, S., Baybayan, P., Singh, S., ... & Choo, S. W. (2013). Comparing the genomes of Helicobacter pylori clinical strain UM032 and Mice-adapted derivatives. Gut Pathogens, 5(1), 25. | en_US |
dc.identifier.uri | https://hdl.handle.net/20.500.12540/111 | - |
dc.description.abstract | Background: Helicobacter pylori is a Gram-negative bacterium that persistently infects the human stomach inducing chronic inflammation. The exact mechanisms of pathogenesis are still not completely understood. Although not a natural host for H. pylori, mouse infection models play an important role in establishing the immunology and pathogenicity of H. pylori. In this study, for the first time, the genome sequences of clinical H. pylori strain UM032 and mice-adapted derivatives, 298 and 299, were sequenced using the PacBio Single Molecule, Real-Time (SMRT) technology. | en_US |
dc.format.extent | 6 pages | en_US |
dc.format.mimetype | application/pdf | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Springer Nature | en_US |
dc.relation.ispartof | Gut Pathogens | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by-nc/4.0/ | - |
dc.subject.lcsh | Helicobacter Pylori | en_US |
dc.title | Comparing the genomes of Helicobacter pylori clinical strain UM032 and Mice-adapted derivatives | en_US |
dc.type | Article | en_US |
dc.rights.license | Attribution-NonCommercial 4.0 International (CC BY-NC 4.0) | en_US |
dc.identifier.doi | 10.1186/1757-4749-5-25 | - |
dc.subject.keywords | PacBio Single Molecule | en_US |
dc.subject.keywords | Real-Time (SMRT) Technology | en_US |
dc.subject.keywords | Clinical H. Pylori | en_US |
dc.subject.keywords | Mice-adapted | en_US |
Appears in Collections: | Scholarly Publications |
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File | Description | Size | Format | |
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wku_schlrs_publcn_000084.pdf | 1.6 MB | Adobe PDF | View/Open |
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