Example of Journal of Cell Communication and Signaling format
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Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format
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Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format Example of Journal of Cell Communication and Signaling format
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open access Open Access

Journal of Cell Communication and Signaling — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Biochemistry #93 of 415 up up by 124 ranks
Molecular Biology #118 of 382 up up by 113 ranks
Cell Biology #88 of 279 up up by 86 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 199 Published Papers | 1353 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 21/07/2020
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Related Journals

open access Open Access
recommended Recommended

American Association for the Advancement of Science

Quality:  
High
CiteRatio: 10.6
SJR: 3.659
SNIP: 1.504
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Portland Press

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CiteRatio: 6.7
SJR: 1.706
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American Society for Biochemistry and Molecular Biology (ASBMB)

Quality:  
High
CiteRatio: 7.7
SJR: 2.361
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open access Open Access

Elsevier

Quality:  
High
CiteRatio: 5.5
SJR: 0.998
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Journal Performance & Insights

CiteRatio

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

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

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.

6.8

26% from 2019

CiteRatio for Journal of Cell Communication and Signaling from 2016 - 2020
Year Value
2020 6.8
2019 5.4
2018 3.6
2017 3.8
2016 4.3
graph view Graph view
table view Table view

1.329

11% from 2019

SJR for Journal of Cell Communication and Signaling from 2016 - 2020
Year Value
2020 1.329
2019 1.2
2018 0.828
2017 0.836
2016 1.111
graph view Graph view
table view Table view

1.08

0% from 2019

SNIP for Journal of Cell Communication and Signaling from 2016 - 2020
Year Value
2020 1.08
2019 1.076
2018 0.779
2017 0.638
2016 0.737
graph view Graph view
table view Table view

insights Insights

  • CiteRatio of this journal has increased by 26% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

insights Insights

  • SJR of this journal has increased 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 0% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Journal of Cell Communication and Signaling

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Springer

Journal of Cell Communication and Signaling

The Journal of Cell Communication and Signaling (JCCS), the official publication of the International CCN Society (ICCNS), aims to serve as a forum for translational research.  In particular, it wishes to publish papers discussing cell-cell and cell-matrix communication as wel...... Read More

Biochemistry

Molecular Biology

Cell Biology

Biochemistry, Genetics and Molecular Biology

i
Last updated on
20 Jul 2020
i
ISSN
1873-9601
i
Impact Factor
Medium - 0.668
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
i
Bibliography Name
SPBASIC
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Citation Type
Author Year
(Blonder et al., 1982)
i
Bibliography Example
Blonder, G. E., Tinkham, M., and Klapwijk, T. M. (1982). Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and super- current conversion. Phys. Rev. B, 25(7):4515–4532.

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.1007/S12079-009-0068-0
The role of osteopontin in inflammatory processes
Susan Amanda Lund1, Cecilia M. Giachelli1, Marta Scatena1

Abstract:

Osteopontin (OPN) is a matricellular protein that mediates diverse biological functions. OPN is involved in normal physiological processes and is implicated in the pathogenesis of a variety of disease states, including atherosclerosis, glomerulonephritis, cancer, and several chronic inflammatory diseases. Through interactions... Osteopontin (OPN) is a matricellular protein that mediates diverse biological functions. OPN is involved in normal physiological processes and is implicated in the pathogenesis of a variety of disease states, including atherosclerosis, glomerulonephritis, cancer, and several chronic inflammatory diseases. Through interactions with several integrins, OPN mediates cell migration, adhesion, and survival in many cell types. OPN also functions as a Th1 cytokine, promotes cell-mediated immune responses, and plays a role in chronic inflammatory and autoimmune diseases. Besides its function in inflammation, OPN is also a regulator of biomineralization and a potent inhibitor of vascular calcification. read more read less

Topics:

Matricellular protein (55%)55% related to the paper, Osteopontin (53%)53% related to the paper
View PDF
410 Citations
open accessOpen access Journal Article DOI: 10.1007/S12079-009-0075-1
The role of tenascin-C in tissue injury and tumorigenesis.
Kim S. Midwood1, Gertraud Orend2, Gertraud Orend3

Abstract:

The extracellular matrix molecule tenascin-C is highly expressed during embryonic development, tissue repair and in pathological situations such as chronic inflammation and cancer. Tenascin-C interacts with several other extracellular matrix molecules and cell-surface receptors, thus affecting tissue architecture, tissue resi... The extracellular matrix molecule tenascin-C is highly expressed during embryonic development, tissue repair and in pathological situations such as chronic inflammation and cancer. Tenascin-C interacts with several other extracellular matrix molecules and cell-surface receptors, thus affecting tissue architecture, tissue resilience and cell responses. Tenascin-C modulates cell migration, proliferation and cellular signaling through induction of pro-inflammatory cytokines and oncogenic signaling molecules amongst other mechanisms. Given the causal role of inflammation in cancer progression, common mechanisms might be controlled by tenascin-C during both events. Drugs targeting the expression or function of tenascin-C or the tenascin-C protein itself are currently being developed and some drugs have already reached advanced clinical trials. This generates hope that increased knowledge about tenascin-C will further improve management of diseases with high tenascin-C expression such as chronic inflammation, heart failure, artheriosclerosis and cancer. read more read less

Topics:

Cell signaling (55%)55% related to the paper, Tenascin C (55%)55% related to the paper, Extracellular matrix (53%)53% related to the paper, Fibronectin (53%)53% related to the paper, Carcinogenesis (51%)51% related to the paper
View PDF
378 Citations
open accessOpen access Journal Article DOI: 10.1007/S12079-011-0132-4
3D tumour models: novel in vitro approaches to cancer studies
Agata Nyga1, Umber Cheema1, Marilena Loizidou2, Marilena Loizidou1

Abstract:

3D in vitro models have been used in cancer research as a compromise between 2-dimensional cultures of isolated cancer cells and the manufactured complexity of xenografts of human cancers in immunocompromised animal hosts. 3D models can be tailored to be biomimetic and accurately recapitulate the native in vivo scenario in wh... 3D in vitro models have been used in cancer research as a compromise between 2-dimensional cultures of isolated cancer cells and the manufactured complexity of xenografts of human cancers in immunocompromised animal hosts. 3D models can be tailored to be biomimetic and accurately recapitulate the native in vivo scenario in which they are found. These 3D in vitro models provide an important alternative to both complex in vivo whole organism approaches, and 2D culture with its spatial limitations. Approaches to create more biomimetic 3D models of cancer include, but are not limited to, (i) providing the appropriate matrix components in a 3D configuration found in vivo, (ii) co-culturing cancer cells, endothelial cells and other associated cells in a spatially relevant manner, (iii) monitoring and controlling hypoxia- to mimic levels found in native tumours and (iv) monitoring the release of angiogenic factors by cancer cells in response to hypoxia. This article aims to overview current 3D in vitro models of cancer and review strategies employed by researchers to tackle these aspects with special reference to recent promising developments, as well as the current limitations of 2D cultures and in vivo models. 3D in vitro models provide an important alternative to both complex in vivo whole organism approaches, and 2D culture with its spatial limitations. Here we review current strategies in the field of modelling cancer, with special reference to advances in complex 3D in vitro models. read more read less
373 Citations
open accessOpen access Journal Article DOI: 10.1007/S12079-016-0352-8
VEGF-A/VEGFR2 signaling network in endothelial cells relevant to angiogenesis
Chandran S Abhinand1, Rajesh Raju2, Sasikumar J. Soumya1, Prabha S. Arya1, Perumana R. Sudhakaran1

Abstract:

Vascular endothelial growth factor-A (VEGF-A) is essential for endothelial cell functions associated with angiogenesis. Signal transduction networks initiated by VEGFA/VEGFR2, the most prominent ligand-receptor complex in the VEGF system, leads to endothelial cell proliferation, migration, survival and new vessel formation in... Vascular endothelial growth factor-A (VEGF-A) is essential for endothelial cell functions associated with angiogenesis. Signal transduction networks initiated by VEGFA/VEGFR2, the most prominent ligand-receptor complex in the VEGF system, leads to endothelial cell proliferation, migration, survival and new vessel formation involved in angiogenesis. Considering its biomedical importance, we have developed the first comprehensive map of endothelial cell-specific signaling events of VEGFA/VEGFR2 system pertaining to angiogenesis. Screening over 20,000 published research articles and following the post-translational modification (PTM) and site specificity of VEGFR2, we have documented 240 proteins and their diverse PTM-dependent reactions involved in VEGFA/VEGFR2 signal transduction. From the ligand-receptor complex, this map has been extended to the level of major transcriptionally regulated genes for which the signaling cascades leading to their transcription factors are reported. We believe that this map would serve as a novel platform for reference, integration, and representation and more significantly, the progressive analysis of dynamic features of VEGF signaling in endothelial cells including their cross-talks with other ligand-receptor systems involved in angiogenesis. read more read less

Topics:

Angiogenesis (66%)66% related to the paper, Vascular endothelial growth factor A (64%)64% related to the paper, Vascular endothelial growth factor B (58%)58% related to the paper, Vascular endothelial growth factor (58%)58% related to the paper, Vascular endothelial growth factor C (57%)57% related to the paper
274 Citations
open accessOpen access Journal Article DOI: 10.1007/S12079-011-0121-7
Proteasome inhibitors in cancer therapy
Lisa J. Crawford1, Brian Walker1, Alexandra E. Irvine1

Abstract:

The ubiquitin proteasome pathway plays a critical role in regulating many processes in the cell which are important for tumour cell growth and survival. Inhibition of proteasome function has emerged as a powerful strategy for anti-cancer therapy. Clinical validation of the proteasome as a therapeutic target was achieved with ... The ubiquitin proteasome pathway plays a critical role in regulating many processes in the cell which are important for tumour cell growth and survival. Inhibition of proteasome function has emerged as a powerful strategy for anti-cancer therapy. Clinical validation of the proteasome as a therapeutic target was achieved with bortezomib and has prompted the development of a second generation of proteasome inhibitors with improved pharmacological properties. This review summarises the main mechanisms of action of proteasome inhibitors in cancer, the development of proteasome inhibitors as therapeutic agents and the properties and progress of next generation proteasome inhibitors in the clinic. read more read less

Topics:

Proteasome inhibitor (75%)75% related to the paper, Bortezomib (59%)59% related to the paper, Proteasome (54%)54% related to the paper
View PDF
257 Citations
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Journal of Cell Communication and Signaling format uses SPBASIC citation style.

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Frequently asked questions

1. Can I write Journal of Cell Communication and Signaling in LaTeX?

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

2. Do you follow the Journal of Cell Communication and Signaling guidelines?

Yes, the template is compliant with the Journal of Cell Communication and Signaling 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 Journal of Cell Communication and Signaling?

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 Journal of Cell Communication and Signaling citation style.

4. Can I use the Journal of Cell Communication and Signaling 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 Journal of Cell Communication and Signaling.

5. Can I use a manuscript in Journal of Cell Communication and Signaling 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 Journal of Cell Communication and Signaling that you can download at the end.

6. How long does it usually take you to format my papers in Journal of Cell Communication and Signaling?

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

7. Where can I find the template for the Journal of Cell Communication and Signaling?

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 Journal of Cell Communication and Signaling'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 Journal of Cell Communication and Signaling'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. Journal of Cell Communication and Signaling an online tool or is there a desktop version?

SciSpace's Journal of Cell Communication and Signaling 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 Journal of Cell Communication and Signaling?

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 Journal of Cell Communication and Signaling?”

11. What is the output that I would get after using Journal of Cell Communication and Signaling?

After writing your paper autoformatting in Journal of Cell Communication and Signaling, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Journal of Cell Communication and Signaling'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 Journal of Cell Communication and Signaling?

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 Journal of Cell Communication and Signaling. 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 Journal of Cell Communication and Signaling?

The 5 most common citation types in order of usage for Journal of Cell Communication and Signaling 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 Journal of Cell Communication and Signaling?

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 Journal of Cell Communication and Signaling's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Journal of Cell Communication and Signaling 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 Journal of Cell Communication and Signaling 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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