Works matching DE "MICROBIOLOGY periodicals"
Results: 196
High retraction rates raise eyebrows.
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- Nature, 2014, v. 513, n. 7518, p. 283, doi. 10.1038/513283f
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EDITORIAL.
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- Mediterranean Journal of Infection, Microbes & Antimicrobials, 2018, p. 1, doi. 10.4274/mjima.2018.38
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Editorial: Towards a multidisciplinary approach to the study of tick-borne diseases.
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- Frontiers in Cellular & Infection Microbiology, 2014, p. 1, doi. 10.3389/fcimb.2014.00118
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- Article
Announcement / Communiqué.
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- Canadian Journal of Microbiology, 2007, v. 53, n. 4, p. iii, doi. 10.1139/w07-904
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- Article
Editorial Board.
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- Journal of Applied Microbiology, 2017, v. 123, n. 5, p. 1055, doi. 10.1111/jam.13271
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Editorial Board.
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- Journal of Applied Microbiology, 2017, v. 123, n. 4, p. 781, doi. 10.1111/jam.13270
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Editorial Board.
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- Journal of Applied Microbiology, 2016, v. 121, n. 5, p. 1199, doi. 10.1111/jam.13319
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Evaluation of microbial diversity in the pilot-scale beer brewing process by culture-dependent and culture-independent method.
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- Journal of Applied Microbiology, 2015, v. 119, n. 3, p. 904, doi. 10.1111/jam.12900
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Reconsideration of the derivation of Most Probable Numbers, their standard deviations, confidence bounds and rarity values.
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- Journal of Applied Microbiology, 2015, v. 119, n. 3, p. 905, doi. 10.1111/jam.12901
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In vitro fungicidal activity of biocides against pharmaceutical environmental fungal isolates: a response to the Letter of Rout and Humphreys (2015).
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- Journal of Applied Microbiology, 2015, v. 118, n. 3, p. 779, doi. 10.1111/jam.12755
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In vitro fungicidal activity of biocides against pharmaceutical environmental fungal isolates.
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- Journal of Applied Microbiology, 2015, v. 118, n. 3, p. 777, doi. 10.1111/jam.12758
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Issue Information – Cover.
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- Microbiology & Immunology, 2018, v. 62, n. 10, p. i, doi. 10.1111/1348-0421.12526
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Issue Information – Instruction for Authors.
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- Microbiology & Immunology, 2018, v. 62, n. 4, p. 295, doi. 10.1111/1348-0421.12515
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Issue Information - Cover.
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- Microbiology & Immunology, 2017, v. 61, n. 10, p. i, doi. 10.1111/1348-0421.12429
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Issue Information - Instruction for Authors.
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- Microbiology & Immunology, 2017, v. 61, n. 9, p. 403, doi. 10.1111/1348-0421.12428
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Issue Information - Instruction for Authors.
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- Microbiology & Immunology, 2017, v. 61, n. 6, p. 247, doi. 10.1111/1348-0421.12422
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Issue Information - Cover.
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- Microbiology & Immunology, 2017, v. 61, n. 3/4, p. i, doi. 10.1111/1348-0421.12480
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Issue Information - Instruction for Authors.
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- Microbiology & Immunology, 2017, v. 61, n. 3/4, p. 144, doi. 10.1111/1348-0421.12481
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Issue Information - Cover.
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- Microbiology & Immunology, 2017, v. 61, n. 2, p. i, doi. 10.1111/1348-0421.12413
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Issue Information - Cover.
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- Microbiology & Immunology, 2016, v. 60, n. 5, p. i, doi. 10.1111/1348-0421.12300
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Instructions for Authors.
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- Microbiology & Immunology, 2016, v. 60, n. 5, p. 364, doi. 10.1111/1348-0421.12301
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Instructions for Authors.
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- Microbiology & Immunology, 2016, v. 60, n. 2, p. 134, doi. 10.1111/1348-0421.12295
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Corrigendum.
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- Microbiology & Immunology, 2016, v. 60, n. 2, p. 132, doi. 10.1111/1348-0421.12351
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Rubella virus (vaccine strain) foci are visualized after 3-days of post-infection to Vero cells after immunocolorimetric staining.
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- 2014
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- Other
Reviewers.
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- Microbiology & Immunology, 2014, v. 58, n. 12, p. 702, doi. 10.1111/1348-0421.12216
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Corrigendum.
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- Microbiology & Immunology, 2014, v. 58, n. 12, p. 701, doi. 10.1111/1348-0421.12207
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HCMV pp65 antigen slides were used to observe the titer of sera anti-HCMV IgG antibody by indirect fluorescent assay. Apple-green fluorescence was observed on the slides when sera anti-HCMV IgG antibodies existed, and the density of fluorescense paralled the concentration of antibodies. Reddish fluorescence was observed if the cells were uninfected by HCMV, and as the background of images.
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- 2014
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- Publication type:
- Other
Brain sections of hippocampus and fimbria area were obtained from 15-week-old ZrchI Prnp<sup>-/-</sup> mice previously infected with 600 pfu/mouse of EMCV-B on post-infection day (DPI) 7. Sections used in the TUNEL method were counterstained with hematoxylin and eosin. CA1 pyramidal cells in the hippocampus of Rikn Prnp<sup>-/-</sup> mice showed apoptosis. A brain section from Rikn Prnp<sup>-/-</sup> mice shows mild mononuclear round cell infiltration. Modified from Fig. 3 in Nasu-Nishimura et al. (2008) Arch Virol 153: 1007-1012 with permission from Springer.
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- 2014
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- Other
Issue Information.
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- APMIS, 2014, v. 122, n. 11, p. i, doi. 10.1111/apm.12179
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Author Index.
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- APMIS, 2014, v. 122, p. 40, doi. 10.1111/apm.12265
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Issue Information.
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- Molecular Microbiology, 2019, v. 111, n. 2, p. N.PAG, doi. 10.1111/mmi.14013
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Issue Information.
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- Molecular Microbiology, 2019, v. 111, n. 1, p. N.PAG, doi. 10.1111/mmi.14011
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Front Cover.
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- Molecular Microbiology, 2019, v. 111, n. 1, p. N.PAG, doi. 10.1111/mmi.14010
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Issue Information.
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- Molecular Microbiology, 2018, v. 109, n. 4, p. 1, doi. 10.1111/mmi.13809
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The targets of small regulatory RNAs can be mapped using High-throughput Global sRNA target Identifi cation by Ligation and Sequencing (Hi-GRIL-seq). The position on the x and y axes identifies the genome coordinates of the interacting RNAs. Highlighted chimeras include those containing either the prrF1/2 sRNAs (blue) or the oprD (red) or pagL (green) mRNAs. For details, see the article by Zhang et al. on pp. 919-937 of this issue.
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- Molecular Microbiology, 2017, v. 106, n. 6, p. i, doi. 10.1111/mmi.13523
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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.
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- 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.
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- 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.
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- 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.
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- Molecular Microbiology, 2015, v. 96, n. 3, p. i, doi. 10.1111/mmi.13025
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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.
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- Molecular Microbiology, 2015, v. 95, n. 6, p. i, doi. 10.1111/mmi.12980
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A volume rendered visualization of a Yersinia enterocolitica bacterium containing clusters of type III secretion systems (injectisomes) as imaged by cryo-electron tomography (injectisomes in red, cell envelope in blue). Clustering of type III secretion systems may facilitiate fast and efficient protein injection into host cells during infection. For details, see the article by Kudryashev et al. on pp. 875-884 of this issue.
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- Molecular Microbiology, 2015, v. 95, n. 5, p. i, doi. 10.1111/mmi.12968
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The image 'Staring Down the Barrel of a Gun,' created by Dr. Martin Cheung (University of Bristol), who used electron microscopy to reconstruct the tip of a molecular syringe that many pathogenic bacteria use to cause disease. This image shared 1st Prize at University of Bristol's annual 2013 Art of Science Competition and has been deposited with Wellcome Images (
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- Molecular Microbiology, 2015, v. 95, n. 1, p. i, doi. 10.1111/mmi.12903
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False-colored scanning electron microscopy images of Trypanosoma brucei gambiense (length: 15 micrometers) laying on the peritoneal epithelium and awaiting entrance into the bloodstream of an infected mouse. The parasite is responsible for human sleeping sickness in Western and Central Africa. Image is from the Laboratory of Molecular Parasitology and Center for Microscopy and Molecular Imaging, Université Libre de Bruxelles, Gosselies, Belgium (David Pé rez-Morga, Daniel Monteyne, Gilles Vanwalleghem and Etienne Pays). For further details readers are referred to the article by Lecordier et al. on pp. 625-636 of this issue
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- Molecular Microbiology, 2014, v. 94, n. 3, p. i, doi. 10.1111/mmi.12827
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Ribbon representation of the structure of the Mycobacterium tuberculosis type VII secretion system chaperone (EspG5) in complex with the heterodimeric substrate, PE25-PPE41. EspG5 interacts with the PE25-PPE41 dimer on the opposite side from the conserved YxxxD/E and WxG motifs. For further details readers are referred to the article by Korotkova et al. on pp. 367-382 of this issue
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- Molecular Microbiology, 2014, v. 94, n. 2, p. i, doi. 10.1111/mmi.12803
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The DprA (DNA-protecting protein A) homolog from Rhodobacter capsulatus (RcDprA) is required in recipients of the gene transfer agent (RcGTA). A model of the RcDprA structure reveals a C-terminal DNA-binding domain (purple) (Top panel). Expression analysis reveals that RcDprA is expressed in the majority of cells throughout a population (Bottom panel). For further details readers are referred to the article by Brimacombe et al. on pp. 1260-1278 of this issue.
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- Molecular Microbiology, 2014, v. 92, n. 6, p. i, doi. 10.1111/mmi.12652
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A Winogradsky-based culture system shows an association between microbial fermentation and cystic fibrosis exacerbation.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2015, v. 9, n. 4, p. 1052, doi. 10.1038/ismej.2014.266
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The host metabolite D-serine contributes to bacterial niche specificity through gene selection.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2015, v. 9, n. 4, p. 1052, doi. 10.1038/ismej.2015.17
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Open access to oral microbiology.
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- Journal of Oral Microbiology, 2009, v. 1, p. 1, doi. 10.3402/jom.v1i0.1941
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Referees 2010.
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- Innate Immunity, 2011, v. 17, n. 1, p. 120, doi. 10.1177/1753425910399829
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Message from Editor in Chief ( Indian Journal of Microbiology).
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- Indian Journal of Microbiology, 2013, v. 53, n. 1, p. 116, doi. 10.1007/s12088-013-0349-4
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- Article