Works about MICROBIOLOGY periodicals

Results: 196

Issue Information.

Published in:: Cellular Microbiology, 2018, v. 20, n. 10, p. 1, doi. 10.1111/cmi.12782
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Published in:: Cellular Microbiology, 2018, v. 20, n. 8, p. 1, doi. 10.1111/cmi.12780
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Published in:: Cellular Microbiology, 2018, v. 20, n. 3, p. 1, doi. 10.1111/cmi.12775
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Published in:: Cellular Microbiology, 2018, v. 20, n. 2, p. 1, doi. 10.1111/cmi.12774
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Published in:: Cellular Microbiology, 2017, v. 19, n. 10, p. n/a, doi. 10.1111/cmi.12705
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Published in:: Cellular Microbiology, 2017, v. 19, n. 3, p. n/a, doi. 10.1111/cmi.12698
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Published in:: Cellular Microbiology, 2016, v. 18, n. 5, p. 615, doi. 10.1111/cmi.12507
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Published in:: Cellular Microbiology, 2015, v. 17, n. 6, p. i, doi. 10.1111/cmi.12348
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Published in:: Cellular Microbiology, 2015, v. 17, n. 5, p. i, doi. 10.1111/cmi.12347
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Published in:: Cellular Microbiology, 2015, v. 17, n. 2, p. i, doi. 10.1111/cmi.12345
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Thank you to our Reviewers.

Published in:: Cellular Microbiology, 2015, v. 17, n. 1, p. 146, doi. 10.1111/cmi.12395
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Published in:: Cellular Microbiology, 2015, v. 17, n. 1, p. i, doi. 10.1111/cmi.12344
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cellular microbiology.

Published in:: Cellular Microbiology, 2014, v. 16, n. 6, p. i, doi. 10.1111/cmi.12198
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Published in:: Cellular Microbiology, 2014, v. 16, n. 4, p. i, doi. 10.1111/cmi.12194
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Published in:: Cellular Microbiology, 2014, v. 16, n. 3, p. i, doi. 10.1111/cmi.12192
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Published in:: Cellular Microbiology, 2014, v. 16, n. 2, p. i, doi. 10.1111/cmi.12190
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Published in:: Cellular Microbiology, 2013, v. 15, n. 11, p. i, doi. 10.1111/cmi.12019
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Published in:: Cellular Microbiology, 2013, v. 15, n. 8, p. i, doi. 10.1111/cmi.12016
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Published in:: Cellular Microbiology, 2013, v. 15, n. 7, p. i, doi. 10.1111/cmi.12015
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Published in:: Cellular Microbiology, 2013, v. 15, n. 5, p. i, doi. 10.1111/cmi.12013
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Published in:: Cellular Microbiology, 2013, v. 15, n. 4, p. i, doi. 10.1111/cmi.12012
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Published in:: Cellular Microbiology, 2013, v. 15, n. 3, p. i, doi. 10.1111/cmi.12011
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Published in:: Cellular Microbiology, 2013, v. 15, n. 2, p. i, doi. 10.1111/cmi.12010
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Published in:: Cellular Microbiology, 2012, v. 14, n. 11, p. i, doi. 10.1111/cmi.12023
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Published in:: Cellular Microbiology, 2012, v. 14, n. 10, p. 1, doi. 10.1111/j.1462-5822.2012.01839.x
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Published in:: Cellular Microbiology, 2012, v. 14, n. 8, p. i, doi. 10.1111/j.1462-5822.2012.01821.x
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Published in:: Cellular Microbiology, 2012, v. 14, n. 7, p. i, doi. 10.1111/j.1462-5822.2010.01810.x
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Published in:: Cellular Microbiology, 2012, v. 14, n. 6, p. i, doi. 10.1111/j.1462-5822.2012.01797.x
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Published in:: Cellular Microbiology, 2012, v. 14, n. 5, p. i, doi. 10.1111/j.1462-5822.2012.01808.x
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Published in:: Cellular Microbiology, 2012, v. 14, n. 2, p. i, doi. 10.1111/j.1462-5822.2011.01732.x
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Published in:: Cellular Microbiology, 2011, v. 13, n. 12, p. i, doi. 10.1111/j.1462-5822.2010.01723.x
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Published in:: 2011
Publication type:: Other

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Published in:: 2011
Publication type:: Other

Issue Information.

Published in:: Microbial Biotechnology, 2015, v. 8, n. 1, p. i, doi. 10.1111/1751-7915.12169
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A microbial decade.

Published in:: Nature Reviews Microbiology, 2013, v. 11, n. 10, p. 657, doi. 10.1038/nrmicro3128
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Looking inwards.

Published in:: Nature Reviews Microbiology, 2013, v. 11, n. 3, p. 143, doi. 10.1038/nrmicro2987
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EDITORIAL.

Published in:

Mediterranean Journal of Infection, Microbes & Antimicrobials, 2018, p. 1, doi. 10.4274/mjima.2018.38

By:

SİPAHİ, Oğuz Reşat

Publication type:

Article

Issue Information.

Published in:: IUBMB Life, 2019, v. 71, n. 2, p. 143, doi. 10.1002/iub.1898
Publication type:: Article

Evaluation of microbial diversity in the pilot-scale beer brewing process by culture-dependent and culture-independent method.

Published in:

Journal of Applied Microbiology, 2015, v. 119, n. 3, p. 904, doi. 10.1111/jam.12900

By:

Takahashi, M.;
Kita, Y.;
Kusaka, K.;
Mizuno, A.;
Goto‐Yamamoto, N.

Publication type:

Article

Reconsideration of the derivation of Most Probable Numbers, their standard deviations, confidence bounds and rarity values.

Published in:

Journal of Applied Microbiology, 2015, v. 119, n. 3, p. 905, doi. 10.1111/jam.12901

By:

Jarvis, B.;
Wilrich, C.;
Wilrich, P.‐T.

Publication type:

Article

In vitro fungicidal activity of biocides against pharmaceutical environmental fungal isolates: a response to the Letter of Rout and Humphreys (2015).

Published in:

Journal of Applied Microbiology, 2015, v. 118, n. 3, p. 779, doi. 10.1111/jam.12755

By:

Sandle, T.;
Vijayakumar, R.;
Saleh Al Aboody, M.;
Saravanakumar, S.

Publication type:

Article

In vitro fungicidal activity of biocides against pharmaceutical environmental fungal isolates.

Published in:

Journal of Applied Microbiology, 2015, v. 118, n. 3, p. 777, doi. 10.1111/jam.12758

By:

Rout, S.;
Humphreys, P.

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Article

Annual Review of Microbiology, 2015.

Published in:

2017

By:

Joshi, Mohan C.

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Book Review

OBJECTIVE LENS.

Published in:

2016

By:

MCKILLIP, JOHN L.

Publication type:

Opinion

Editorial: Anthropogenic Impacts on the Microbial Ecology and Function of Aquatic Environments.

Published in:

2016

By:

Labbate, Maurizio;
Seymour, Justin R.;
Lauro, Federico;
Brown, Mark V.;
Church, Matthew

Publication type:

Editorial

Spatially directed secretion in higher filamentous fungi supports the development of a structure called the Spitzenkörper, through which membrane flows to the hyphal apex. Two flippases, DnfA and DnfB, function in polar growth of hyphae of Aspergillus nidulans, and possibly localize to distinct secretory vesicles, as demonstrated by spatial separation in growing cells. Fully developed A. nidulans conidiophores were here imaged using bright field (top left), with DnfA::GFP (top right), DnfB::mCherry (bottom left panel), and with both channels merged (bottom right). For details, see the article by Schultzhaus et al. on pp. 18-32 and the related MicroCommentary by Penalva on pp. 1-6 of this issue.

Published in:: Molecular Microbiology, 2015, v. 97, n. 1, p. i, doi. 10.1111/mmi.13092
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DdrO regulates the radiation desiccation response and apoptotic-like cell death in the Deinococcus radiodurans. Light microscopy was used to visualize the effects of depleting the DdrO repressor on D. radiodurans morphology (left to right): Nomarski interference contrast (DIC), membrane staining (FM4-64), DNA staining (DAPI), and merged images. The cells were depleted of DrdO from 8h (top), 16 h (middle), or 24 h (bottom). DdrO-depleted cells display morphological changes evocative of an apoptotic-like response including DNA condensation and vesicle formation. For details, see the article by Devigne et al. on pp. 1069-1084 of this issue.

Published in:: Molecular Microbiology, 2015, v. 96, n. 5, p. i, doi. 10.1111/mmi.13057
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Molecular modeling of the Trypanosoma brucei aminopurine transporter P2/TbAT1, implicated in resistance to both diamidine and melaminophenyl arsenical classes of drugs, predicts that residues F19 (left), D140 (top) and F316 (right) interact with substrates. The binding site of adenosine (green carbon atoms) and diminazene (yellow carbon atoms) is shown with hydrogen bonds between Asp140 and bound adenosine in dashed blue lines. For details, see the article by Munday et al. on pp. 887-900 of this issue.

Published in:: Molecular Microbiology, 2015, v. 96, n. 4, p. i, doi. 10.1111/mmi.13043
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In the cyanobacterium Synechocystis sp PCC6803 the repair protease FtsH2 is located in the thylakoid membranes, but has a different distribution from the photosynthetic reaction centers suggesting the existence of dedicated repair zones. False-color 3D surface plots from fluorescence micrographs show the distribution of fluorescence from chlorophyll (left) and GFP-tagged FtsH2 (right) in cells grown under low light (top) or high light (bottom). For details, see the article by Sacharz et al. on pp. 448-462 of this issue.

Published in:: Molecular Microbiology, 2015, v. 96, n. 3, p. i, doi. 10.1111/mmi.13025
Publication type:: Article

The DsbA2 disulfide-bond oxidase/isomerase system from Legionella pneumophila is coupled to two membrane spanning DsbD proteins and two DsbB oxidases. Homodimeric DsbA2 is partially reduced (thereby providing both DsbA oxidase and DsbC-like protein disulfide isomerase functions) and is required to manage disulfide bonding in DotG, a core component of the Dot/Icm secretion system. For details, see the article by Kpadeh et al. on pp. 1054-1069 of this issue.

Published in:: Molecular Microbiology, 2015, v. 95, n. 6, p. i, doi. 10.1111/mmi.12980
Publication type:: Article