Example of Molecular Microbiology format
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Example of Molecular Microbiology format Example of Molecular Microbiology format Example of Molecular Microbiology format Example of Molecular Microbiology format Example of Molecular Microbiology format Example of Molecular Microbiology format Example of Molecular Microbiology format
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Example of Molecular Microbiology format Example of Molecular Microbiology format Example of Molecular Microbiology format Example of Molecular Microbiology format Example of Molecular Microbiology format Example of Molecular Microbiology format Example of Molecular Microbiology format
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This content is only for preview purposes. The original open access content can be found here.
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Molecular Microbiology — Template for authors

Publisher: Wiley
Categories Rank Trend in last 3 yrs
Microbiology #34 of 150 down down by 14 ranks
Molecular Biology #111 of 382 down down by 20 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 854 Published Papers | 5954 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 04/06/2020
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Related Journals

open access Open Access
recommended Recommended

PLOS

Quality:  
High
CiteRatio: 11.0
SJR: 3.719
SNIP: 1.882
open access Open Access
recommended Recommended

American Society for Microbiology

Quality:  
High
CiteRatio: 21.2
SJR: 6.358
SNIP: 3.807
open access Open Access

Elsevier

Quality:  
High
CiteRatio: 8.0
SJR: 1.329
SNIP: 1.224
open access Open Access

Elsevier

Quality:  
High
CiteRatio: 5.2
SJR: 1.085
SNIP: 1.175

Journal Performance & Insights

Impact Factor

CiteRatio

Determines the importance of a journal by taking a measure of frequency with which the average article in a journal has been cited in a particular year.

A measure of average citations received per peer-reviewed paper published in the journal.

3.418

6% from 2018

Impact factor for Molecular Microbiology from 2016 - 2019
Year Value
2019 3.418
2018 3.649
2017 3.816
2016 3.898
graph view Graph view
table view Table view

7.0

CiteRatio for Molecular Microbiology from 2016 - 2020
Year Value
2020 7.0
2019 7.0
2018 7.4
2017 7.4
2016 7.5
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 6% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

1.857

11% from 2019

SJR for Molecular Microbiology from 2016 - 2020
Year Value
2020 1.857
2019 2.089
2018 2.249
2017 2.384
2016 2.631
graph view Graph view
table view Table view

1.027

2% from 2019

SNIP for Molecular Microbiology from 2016 - 2020
Year Value
2020 1.027
2019 1.002
2018 0.99
2017 1.044
2016 1.002
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 11% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 2% in last years.
  • This journal’s SNIP is in the top 10 percentile category.
Molecular Microbiology

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Wiley

Molecular Microbiology

Molecular Microbiology publishes research articles reporting the results of molecular studies of eukaryotic microorganisms and of prokaryotes and their viruses. Studies that include genetic, biochemical, biophysical, bioinformatic and structural analyses leading to a deeper un...... Read More

Microbiology

Molecular Biology

Immunology and Microbiology

i
Last updated on
04 Jun 2020
i
ISSN
0950-382X
i
Impact Factor
High - 1.295
i
Open Access
Yes
i
Sherpa RoMEO Archiving Policy
Yellow faq
i
Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
apa
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Citation Type
Numbered
[25]
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Bibliography Example
Beenakker, C.W.J. (2006) Specular andreev reflection in graphene.Phys. Rev. Lett., 97 (6), 067 007. URL 10.1103/PhysRevLett.97.067007.

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.1046/J.1365-2958.1998.01062.X
Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development
George A. O'Toole1, Roberto Kolter1
01 Oct 1998 - Molecular Microbiology

Abstract:

The formation of complex bacterial communities known as biofilms begins with the interaction of planktonic cells with a surface in response to appropriate environmental signals. We report the isolation and characterization of mutants of Pseudomonas aeruginosa PA14 defective in the initiation of biofilm formation on an abiotic... The formation of complex bacterial communities known as biofilms begins with the interaction of planktonic cells with a surface in response to appropriate environmental signals. We report the isolation and characterization of mutants of Pseudomonas aeruginosa PA14 defective in the initiation of biofilm formation on an abiotic surface, polyvinylchloride (PVC) plastic. These mutants are designated surface attachment defective (sad ). Two classes of sad mutants were analysed: (i) mutants defective in flagellar-mediated motility and (ii) mutants defective in biogenesis of the polar-localized type IV pili. We followed the development of the biofilm formed by the wild type over 8 h using phase-contrast microscopy. The wild-type strain first formed a monolayer of cells on the abiotic surface, followed by the appearance of microcolonies that were dispersed throughout the monolayer of cells. Using time-lapse microscopy, we present evidence that microcolonies form by aggregation of cells present in the monolayer. As observed with the wild type, strains with mutations in genes required for the synthesis of type IV pili formed a monolayer of cells on the PVC plastic. However, in contrast to the wild-type strain, the type IV pili mutants did not develop microcolonies over the course of the experiments, suggesting that these structures play an important role in microcolony formation. Very few cells of a non-motile strain (carrying a mutation in flgK) attached to PVC even after 8 h of incubation, suggesting a role for flagella and/or motility in the initial cell-to-surface interactions. The phenotype of these mutants thus allows us to initiate the dissection of the developmental pathway leading to biofilm formation. read more read less

Topics:

Type IV pilus biogenesis (58%)58% related to the paper, Biofilm (56%)56% related to the paper, Wild type (50%)50% related to the paper
2,712 Citations
open accessOpen access Journal Article DOI: 10.1046/J.1365-2958.1998.00797.X
Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways: a genetic analysis
George A. O'Toole1, Roberto Kolter1
01 Apr 1998 - Molecular Microbiology

Abstract:

Populations of surface-attached microorganisms comprising either single or multiple species are commonly referred to as biofilms. Using a simple assay for the initiation of biofilm formation (e.g. attachment to an abiotic surface) by Pseudomonas fluorescens strain WCS365, we have shown that: (i) P. fluorescens can form biofil... Populations of surface-attached microorganisms comprising either single or multiple species are commonly referred to as biofilms. Using a simple assay for the initiation of biofilm formation (e.g. attachment to an abiotic surface) by Pseudomonas fluorescens strain WCS365, we have shown that: (i) P. fluorescens can form biofilms on an abiotic surface when grown on a range of nutrients; (ii) protein synthesis is required for the early events of biofilm formation; (iii) one (or more) extracytoplasmic protein plays a role in interactions with an abiotic surface; (iv) the osmolarity of the medium affects the ability of the cell to form biofilms. We have isolated transposon mutants defective for the initiation of biofilm formation, which we term surface attachment defective (sad). Molecular analysis of the sad mutants revealed that the ClpP protein (a component of the cytoplasmic Clp protease) participates in biofilm formation in this organism. Our genetic analyses suggest that biofilm formation can proceed via multiple, convergent signalling pathways, which are regulated by various environmental signals. Finally, of the 24 sad mutants analysed in this study, only three had defects in genes of known function. This result suggests that our screen is uncovering novel aspects of bacterial physiology. read more read less

Topics:

Biofilm (58%)58% related to the paper, Pseudomonas fluorescens (54%)54% related to the paper
2,439 Citations
open accessOpen access Journal Article DOI: 10.1046/J.1365-2958.2003.03425.X
Genes required for mycobacterial growth defined by high density mutagenesis
Christopher M. Sassetti1, Dana Boyd1, Eric J. Rubin1
01 Apr 2003 - Molecular Microbiology

Abstract:

Despite over a century of research, tuberculosis remains a leading cause of infectious death worldwide. Faced with increasing rates of drug resistance, the identification of genes that are required for the growth of this organism should provide new targets for the design of antimycobacterial agents. Here, we describe the use ... Despite over a century of research, tuberculosis remains a leading cause of infectious death worldwide. Faced with increasing rates of drug resistance, the identification of genes that are required for the growth of this organism should provide new targets for the design of antimycobacterial agents. Here, we describe the use of transposon site hybridization (TraSH) to comprehensively identify the genes required by the causative agent, Mycobacterium tuberculosis, for optimal growth. These genes include those that can be assigned to essential pathways as well as many of unknown function. The genes important for the growth of M. tuberculosis are largely conserved in the degenerate genome of the leprosy bacillus, Mycobacterium leprae, indicating that non-essential functions have been selectively lost since this bacterium diverged from other mycobacteria. In contrast, a surprisingly high proportion of these genes lack identifiable orthologues in other bacteria, suggesting that the minimal gene set required for survival varies greatly between organisms with different evolutionary histories. read more read less

Topics:

Minimal genome (62%)62% related to the paper, Mycobacterium leprae (53%)53% related to the paper, Mycobacterium tuberculosis (52%)52% related to the paper, Genome (51%)51% related to the paper, Gene (50%)50% related to the paper
View PDF
2,362 Citations
open accessOpen access Journal Article DOI: 10.1111/J.1365-2958.2006.05172.X
Sex and virulence in Escherichia coli: an evolutionary perspective
01 Jun 2006 - Molecular Microbiology

Abstract:

Summary Pathogenic Escherichia coli cause over 160 million cases of dysentery and one million deaths per year, whereas non-pathogenic E. coli constitute part of the normal intestinal flora of healthy mammals and birds. The evolutionary pathways underlying this dichotomy in bacterial lifestyle were investigated by multilocus s... Summary Pathogenic Escherichia coli cause over 160 million cases of dysentery and one million deaths per year, whereas non-pathogenic E. coli constitute part of the normal intestinal flora of healthy mammals and birds. The evolutionary pathways underlying this dichotomy in bacterial lifestyle were investigated by multilocus sequence typing of a global collection of isolates. Specific pathogen types (enterohaemorrhagic E. coli , enteropathogenic E. coli , enteroinvasive E. coli , K1 and Shigella ) have arisen independently and repeat- edly in several lineages, whereas other lineages con- tain only few pathogens. Rates of evolution have accelerated in pathogenic lineages, culminating in highly virulent organisms whose genomic contents are altered frequently by increased rates of homolo- gous recombination; thus, the evolution of virulence is linked to bacterial sex. This long-term pattern of evolution was observed in genes distributed through- out the genome, and thereby is the likely result of episodic selection for strains that can escape the host immune response. read more read less

Topics:

Extraintestinal Pathogenic Escherichia coli (60%)60% related to the paper, Virulence (56%)56% related to the paper, Pathogenic Escherichia coli (55%)55% related to the paper, Escherichia coli (54%)54% related to the paper, Multilocus sequence typing (51%)51% related to the paper
View PDF
1,773 Citations
Journal Article DOI: 10.1046/J.1365-2958.2002.02839.X
Identification of genes that are associated with DNA repeats in prokaryotes.
Ruud Jansen1, Jan D. A. van Embden, Wim Gaastra1, Leo M. Schouls
01 Mar 2002 - Molecular Microbiology

Abstract:

Using in silico analysis we studied a novel family of repetitive DNA sequences that is present among both domains of the prokaryotes (Archaea and Bacteria), but absent from eukaryotes or viruses. This family is characterized by direct repeats, varying in size from 21 to 37 bp, interspaced by similarly sized non-repetitive seq... Using in silico analysis we studied a novel family of repetitive DNA sequences that is present among both domains of the prokaryotes (Archaea and Bacteria), but absent from eukaryotes or viruses. This family is characterized by direct repeats, varying in size from 21 to 37 bp, interspaced by similarly sized non-repetitive sequences. To appreciate their characteri-stic structure, we will refer to this family as the clustered regularly interspaced short palindromic repeats (CRISPR). In most species with two or more CRISPR loci, these loci were flanked on one side by a common leader sequence of 300-500 b. The direct repeats and the leader sequences were conserved within a species, but dissimilar between species. The presence of multiple chromosomal CRISPR loci suggests that CRISPRs are mobile elements. Four CRISPR-associated (cas) genes were identified in CRISPR-containing prokaryotes that were absent from CRISPR-negative prokaryotes. The cas genes were invariably located adjacent to a CRISPR locus, indicating that the cas genes and CRISPR loci have a functional relationship. The cas3 gene showed motifs characteristic for helicases of the superfamily 2, and the cas4 gene showed motifs of the RecB family of exonucleases, suggesting that these genes are involved in DNA metabolism or gene expression. The spatial coherence of CRISPR and cas genes may stimulate new research on the genesis and biological role of these repeats and genes. read more read less

Topics:

CRISPR Loci (73%)73% related to the paper, CRISPR Spacers (67%)67% related to the paper, CRISPR interference (62%)62% related to the paper, CRISPR (61%)61% related to the paper, Trans-activating crRNA (60%)60% related to the paper
View PDF
1,639 Citations
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With SciSpace, you do not need a word template for Molecular Microbiology.

It automatically formats your research paper to Wiley formatting guidelines and citation style.

You can download a submission ready research paper in pdf, LaTeX and docx formats.

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Molecular Microbiology format uses apa citation style.

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Frequently asked questions

1. Can I write Molecular Microbiology in LaTeX?

Absolutely not! Our tool has been designed to help you focus on writing. You can write your entire paper as per the Molecular Microbiology guidelines and auto format it.

2. Do you follow the Molecular Microbiology guidelines?

Yes, the template is compliant with the Molecular Microbiology guidelines. Our experts at SciSpace ensure that. If there are any changes to the journal's guidelines, we'll change our algorithm accordingly.

3. Can I cite my article in multiple styles in Molecular Microbiology?

Of course! We support all the top citation styles, such as APA style, MLA style, Vancouver style, Harvard style, and Chicago style. For example, when you write your paper and hit autoformat, our system will automatically update your article as per the Molecular Microbiology citation style.

4. Can I use the Molecular Microbiology templates for free?

Sign up for our free trial, and you'll be able to use all our features for seven days. You'll see how helpful they are and how inexpensive they are compared to other options, Especially for Molecular Microbiology.

5. Can I use a manuscript in Molecular Microbiology that I have written in MS Word?

Yes. You can choose the right template, copy-paste the contents from the word document, and click on auto-format. Once you're done, you'll have a publish-ready paper Molecular Microbiology that you can download at the end.

6. How long does it usually take you to format my papers in Molecular Microbiology?

It only takes a matter of seconds to edit your manuscript. Besides that, our intuitive editor saves you from writing and formatting it in Molecular Microbiology.

7. Where can I find the template for the Molecular Microbiology?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Molecular Microbiology's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

8. Can I reformat my paper to fit the Molecular Microbiology's guidelines?

Of course! You can do this using our intuitive editor. It's very easy. If you need help, our support team is always ready to assist you.

9. Molecular Microbiology an online tool or is there a desktop version?

SciSpace's Molecular Microbiology is currently available as an online tool. We're developing a desktop version, too. You can request (or upvote) any features that you think would be helpful for you and other researchers in the "feature request" section of your account once you've signed up with us.

10. I cannot find my template in your gallery. Can you create it for me like Molecular Microbiology?

Sure. You can request any template and we'll have it setup within a few days. You can find the request box in Journal Gallery on the right side bar under the heading, "Couldn't find the format you were looking for like Molecular Microbiology?”

11. What is the output that I would get after using Molecular Microbiology?

After writing your paper autoformatting in Molecular Microbiology, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Molecular Microbiology's impact factor high enough that I should try publishing my article there?

To be honest, the answer is no. The impact factor is one of the many elements that determine the quality of a journal. Few of these factors include review board, rejection rates, frequency of inclusion in indexes, and Eigenfactor. You need to assess all these factors before you make your final call.

13. What is Sherpa RoMEO Archiving Policy for Molecular Microbiology?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Molecular Microbiology. The table below indicates the level of access a journal has as per Sherpa Romeo's archiving policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

14. What are the most common citation types In Molecular Microbiology?

The 5 most common citation types in order of usage for Molecular Microbiology are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

15. How do I submit my article to the Molecular Microbiology?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Molecular Microbiology's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Molecular Microbiology in Endnote format?

Yes, SciSpace provides this functionality. After signing up, you would need to import your existing references from Word or Bib file to SciSpace. Then SciSpace would allow you to download your references in Molecular Microbiology Endnote style according to Elsevier guidelines.

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I spent hours with MS word for reformatting. It was frustrating - plain and simple. With SciSpace, I can draft my manuscripts and once it is finished I can just submit. In case, I have to submit to another journal it is really just a button click instead of an afternoon of reformatting.

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