Example of Traffic format
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Example of Traffic format Example of Traffic format Example of Traffic format Example of Traffic format Example of Traffic format Example of Traffic format Example of Traffic format
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Example of Traffic format Example of Traffic format Example of Traffic format Example of Traffic format Example of Traffic format Example of Traffic format Example of Traffic format
Sample paper formatted on SciSpace - SciSpace
This content is only for preview purposes. The original open access content can be found here.
open access Open Access

Traffic — Template for authors

Publisher: Wiley
Categories Rank Trend in last 3 yrs
Genetics #40 of 325 up up by 8 ranks
Biochemistry #53 of 415 up up by 5 ranks
Structural Biology #9 of 48 up up by 2 ranks
Molecular Biology #71 of 382 up up by 8 ranks
Cell Biology #56 of 279 up up by 4 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 247 Published Papers | 2104 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 23/06/2020
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Related Journals

open access Open Access

Elsevier

Quality:  
Good
CiteRatio: 6.2
SJR: 1.173
SNIP: 1.127
open access Open Access
recommended Recommended

American Association for the Advancement of Science

Quality:  
High
CiteRatio: 10.6
SJR: 3.659
SNIP: 1.504
open access Open Access

Springer

Quality:  
High
CiteRatio: 6.8
SJR: 1.329
SNIP: 1.08
open access Open Access

Portland Press

Quality:  
High
CiteRatio: 6.7
SJR: 1.706
SNIP: 1.117

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.

4.038

2% from 2018

Impact factor for Traffic from 2016 - 2019
Year Value
2019 4.038
2018 3.951
2017 4.4
2016 4.133
graph view Graph view
table view Table view

8.5

16% from 2019

CiteRatio for Traffic from 2016 - 2020
Year Value
2020 8.5
2019 7.3
2018 7.9
2017 8.0
2016 7.9
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 2% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 16% in last years.
  • 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.

2.677

15% from 2019

SJR for Traffic from 2016 - 2020
Year Value
2020 2.677
2019 2.319
2018 2.401
2017 2.953
2016 2.871
graph view Graph view
table view Table view

1.204

25% from 2019

SNIP for Traffic from 2016 - 2020
Year Value
2020 1.204
2019 0.963
2018 0.993
2017 1.072
2016 1.039
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 15% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 25% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Traffic

Guideline source: View

All company, product and service names used in this website are for identification purposes only. All product names, trademarks and registered trademarks are property of their respective owners.

Use of these names, trademarks and brands does not imply endorsement or affiliation. Disclaimer Notice

Wiley

Traffic

Traffic covers the cell biology and biochemistry of intracellular transport in health and disease and aims to publish manuscripts at the forefront of this field. Specific topics are outlined in the Aims & Scope.  Traffic encourages and facilitates the publication of papers cov...... Read More

Biochemistry

Structural Biology

Genetics

Molecular Biology

Cell Biology

Biochemistry, Genetics and Molecular Biology

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Last updated on
23 Jun 2020
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ISSN
1398-9219
i
Impact Factor
High - 1.133
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Open Access
Yes
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Sherpa RoMEO Archiving Policy
Yellow faq
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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

Journal Article DOI: 10.1111/J.1600-0854.2011.01225.X
Exosome Secretion: Molecular Mechanisms and Roles in Immune Responses
30 Jun 2011 - Traffic

Abstract:

Exosomes are small membrane vesicles, secreted by most cell types from multivesicular endosomes, and thought to play important roles in intercellular communications. Initially described in 1983, as specifically secreted by reticulocytes, exosomes became of interest for immunologists in 1996, when they were proposed to play a ... Exosomes are small membrane vesicles, secreted by most cell types from multivesicular endosomes, and thought to play important roles in intercellular communications. Initially described in 1983, as specifically secreted by reticulocytes, exosomes became of interest for immunologists in 1996, when they were proposed to play a role in antigen presentation. More recently, the finding that exosomes carry genetic materials, mRNA and miRNA, has been a major breakthrough in the field, unveiling their capacity to vehicle genetic messages. It is now clear that not only immune cells but probably all cell types are able to secrete exosomes: their range of possible functions expands well beyond immunology to neurobiology, stem cell and tumor biology, and their use in clinical applications as biomarkers or as therapeutic tools is an extensive area of research. Despite intensive efforts to understand their functions, two issues remain to be solved in the future: (i) what are the physiological function(s) of exosomes in vivo and (ii) what are the relative contributions of exosomes and of other secreted membrane vesicles in these proposed functions? Here, we will focus on the current ideas on exosomes and immune responses, but also on their mechanisms of secretion and the use of this knowledge to elucidate the latter issue. read more read less

Topics:

Exosome (73%)73% related to the paper, Microvesicles (56%)56% related to the paper
View PDF
940 Citations
open accessOpen access Journal Article DOI: 10.1034/J.1600-0854.2001.21104.X
Total internal reflection fluorescence microscopy in cell biology.
Daniel Axelrod1
01 Nov 2001 - Traffic

Abstract:

Key events in cellular trafficking occur at the cell surface, and it is desirable to visualize these events without interference from other regions deeper within. This review describes a microscopy technique based on total internal reflection fluorescence which is well suited for optical sectioning at cell-substrate regions w... Key events in cellular trafficking occur at the cell surface, and it is desirable to visualize these events without interference from other regions deeper within. This review describes a microscopy technique based on total internal reflection fluorescence which is well suited for optical sectioning at cell-substrate regions with an unusually thin region of fluorescence excitation. The technique has many other applications as well, most notably for studying biochemical kinetics and single biomolecule dynamics at surfaces. A brief summary of these applications is provided, followed by presentations of the physical basis for the technique and the various ways to implement total internal reflection fluorescence in a standard fluorescence microscope. read more read less

Topics:

Total internal reflection fluorescence microscope (66%)66% related to the paper, Fluorescence microscope (58%)58% related to the paper, Optical sectioning (58%)58% related to the paper, Microscopy (56%)56% related to the paper
View PDF
910 Citations
Journal Article DOI: 10.1111/J.1600-0854.2010.01041.X
Cellular Internalization of Exosomes Occurs Through Phagocytosis
Du Feng1, Wen Long Zhao1, Yun Ying Ye1, Xiao Chen Bai1, Rui Qin Liu1, Leifu Chang1, Qiang Zhou1, Sen-Fang Sui1
01 May 2010 - Traffic

Abstract:

Exosomes play important roles in many physiological and pathological processes. However, the exosome-cell interaction mode and the intracellular trafficking pathway of exosomes in their recipient cells remain unclear. Here, we report that exosomes derived from K562 or MT4 cells are internalized more efficiently by phagocytes ... Exosomes play important roles in many physiological and pathological processes. However, the exosome-cell interaction mode and the intracellular trafficking pathway of exosomes in their recipient cells remain unclear. Here, we report that exosomes derived from K562 or MT4 cells are internalized more efficiently by phagocytes than by non-phagocytic cells. Most exosomes were observed attached to the plasma membrane of non-phagocytic cells, while in phagocytic cells these exosomes were found to enter via phagocytosis. Specifically, they moved to phagosomes together with phagocytic polystyrene carboxylate-modified latex beads (biospheres) and were further sorted into phagolysosomes. Moreover, exosome internalization was dependent on the actin cytoskeleton and phosphatidylinositol 3-kinase, and could be inhibited by the knockdown of dynamin2 or overexpression of a dominant-negative form of dynamin2. Further, antibody pretreatment assays demonstrated that tim4 but not tim1 was involved in exosomes uptake. We also found that exosomes did not enter the internalization pathway involving caveolae, macropinocytosis and clathrin-coated vesicles. Our observation that the cellular uptake of exosomes occurs through phagocytosis has important implications for exosome-cell interactions and the exosome intracellular trafficking pathway. read more read less

Topics:

Exosome (71%)71% related to the paper, Internalization (54%)54% related to the paper, Actin cytoskeleton (54%)54% related to the paper, Microvesicles (53%)53% related to the paper, Phagosome (53%)53% related to the paper
View PDF
795 Citations
Journal Article DOI: 10.1111/J.1600-0854.2007.00572.X
A comprehensive model for the cellular uptake of cationic cell-penetrating peptides
Falk Duchardt1, Mariola Fotin-Mleczek1, Heinz Schwarz2, Rainer Fischer1, Roland Brock1, Roland Brock3
01 Jul 2007 - Traffic

Abstract:

The plasma membrane represents an impermeable barrier for most macromolecules. Still some proteins and so-called cell-penetrating peptides enter cells efficiently. It has been shown that endocytosis contributes to the import of these molecules. However, conflicting results have been obtained concerning the nature of the endoc... The plasma membrane represents an impermeable barrier for most macromolecules. Still some proteins and so-called cell-penetrating peptides enter cells efficiently. It has been shown that endocytosis contributes to the import of these molecules. However, conflicting results have been obtained concerning the nature of the endocytic process. In addition, there have been new findings for an endocytosis-independent cellular entry. In this study, we provide evidence that the Antennapedia-homeodomain-derived antennapedia (Antp) peptide, nona-arginine and the HIV-1 Tat-protein-derived Tat peptide simultaneously use three endocytic pathways: macropinocytosis, clathrin-mediated endocytosis and caveolae/lipid-raft-mediated endocytosis. Antennapedia differs from Tat and R9 by the extent by which the different import mechanisms contribute to uptake. Moreover, at higher concentrations, uptake occurs by a mechanism that originates from spatially restricted sites of the plasma membrane and leads to a rapid cytoplasmic distribution of the peptides. Endocytic vesicles could not be detected, suggesting an endocytosis-independent mode of uptake. Heparinase treatment of cells negatively affects this import, as does the protein kinase C inhibitor rottlerin, expression of dominant-negative dynamin and chlorpromazine. This mechanism of uptake was observed for a panel of different cell lines. For Antp, significantly higher peptide concentrations and inhibition of endocytosis were required to induce its uptake. The relevance of these findings for import of biologically active cargos is shown. read more read less

Topics:

Receptor-mediated endocytosis (63%)63% related to the paper, Endocytosis (62%)62% related to the paper, Endocytic cycle (62%)62% related to the paper, Cell-penetrating peptide (61%)61% related to the paper, Endocytic vesicle (60%)60% related to the paper
View PDF
783 Citations
open accessOpen access Journal Article DOI: 10.1034/J.1600-0854.2002.30502.X
The biogenesis and functions of exosomes.
Willem Stoorvogel1, Monique J. Kleijmeer1, Hans J. Geuze1, Graça Raposo2
01 May 2002 - Traffic

Abstract:

Exosomes are membrane vesicles with a diameter of 40-100 nm that are secreted by many cell types into the extracellular milieu. They correspond to the internal vesicles of an endosomal compartment, the multivesicular body and are released upon exocytic fusion of this organelle with the plasma membrane. Intracellularly, they a... Exosomes are membrane vesicles with a diameter of 40-100 nm that are secreted by many cell types into the extracellular milieu. They correspond to the internal vesicles of an endosomal compartment, the multivesicular body and are released upon exocytic fusion of this organelle with the plasma membrane. Intracellularly, they are formed by inward budding of the endosomal membrane in a process that sequesters particular proteins and lipids. The unique composition of exosomes may confer specific functions on them upon secretion. Although their physiological role in vivo is far from being unraveled, it is apparent that they function in a multitude of processes, including intercellular communication during the immune response. Exosomes may have evolved early in the evolution of multicellular organisms and also seem to be important for tissue developmental processes. read more read less

Topics:

Exosome (68%)68% related to the paper, Microvesicles (56%)56% related to the paper, Endosome (54%)54% related to the paper, Multivesicular Body (51%)51% related to the paper, Secretion (51%)51% related to the paper
View PDF
776 Citations
Author Pic

SciSpace is a very innovative solution to the formatting problem and existing providers, such as Mendeley or Word did not really evolve in recent years.

- Andreas Frutiger, Researcher, ETH Zurich, Institute for Biomedical Engineering

Get MS-Word and LaTeX output to any Journal within seconds
1
Choose a template
Select a template from a library of 40,000+ templates
2
Import a MS-Word file or start fresh
It takes only few seconds to import
3
View and edit your final output
SciSpace will automatically format your output to meet journal guidelines
4
Submit directly or Download
Submit to journal directly or Download in PDF, MS Word or LaTeX

(Before submission check for plagiarism via Turnitin)

clock Less than 3 minutes

What to expect from SciSpace?

Speed and accuracy over MS Word

''

With SciSpace, you do not need a word template for Traffic.

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.

Time comparison

Time taken to format a paper and Compliance with guidelines

Plagiarism Reports via Turnitin

SciSpace has partnered with Turnitin, the leading provider of Plagiarism Check software.

Using this service, researchers can compare submissions against more than 170 million scholarly articles, a database of 70+ billion current and archived web pages. How Turnitin Integration works?

Turnitin Stats
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Freedom from formatting guidelines

One editor, 100K journal formats – world's largest collection of journal templates

With such a huge verified library, what you need is already there.

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Easy support from all your favorite tools

Traffic format uses apa citation style.

Automatically format and order your citations and bibliography in a click.

SciSpace allows imports from all reference managers like Mendeley, Zotero, Endnote, Google Scholar etc.

Frequently asked questions

1. Can I write Traffic in LaTeX?

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

2. Do you follow the Traffic guidelines?

Yes, the template is compliant with the Traffic 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 Traffic?

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 Traffic citation style.

4. Can I use the Traffic 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 Traffic.

5. Can I use a manuscript in Traffic 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 Traffic that you can download at the end.

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

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

7. Where can I find the template for the Traffic?

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 Traffic'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 Traffic'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. Traffic an online tool or is there a desktop version?

SciSpace's Traffic 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 Traffic?

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 Traffic?”

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

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

12. Is Traffic'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 Traffic?

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 Traffic. 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 Traffic?

The 5 most common citation types in order of usage for Traffic 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 Traffic?

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 Traffic's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Traffic 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 Traffic Endnote style according to Elsevier guidelines.

Fast and reliable,
built for complaince.

Instant formatting to 100% publisher guidelines on - SciSpace.

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No word template required

Typset automatically formats your research paper to Traffic formatting guidelines and citation style.

Verifed journal formats

One editor, 100K journal formats.
With the largest collection of verified journal formats, what you need is already there.

Trusted by academicians

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.

Andreas Frutiger
Researcher & Ex MS Word user
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