Example of Purinergic Signalling format
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Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format Example of Purinergic Signalling format
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This content is only for preview purposes. The original open access content can be found here.
open access Open Access

Purinergic Signalling — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Molecular Biology #174 of 382 down down by 24 ranks
Cell Biology #135 of 279 down down by 9 ranks
Cellular and Molecular Neuroscience #46 of 88 down down by 2 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 183 Published Papers | 983 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 16/06/2020
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Related Journals

open access Open Access
recommended Recommended

Springer

Quality:  
High
CiteRatio: 12.8
SJR: 2.928
SNIP: 1.815
open access Open Access
recommended Recommended

Taylor and Francis

Quality:  
High
CiteRatio: 15.1
SJR: 3.934
SNIP: 2.351
open access Open Access
recommended Recommended

PLOS

Quality:  
High
CiteRatio: 7.3
SJR: 2.628
SNIP: 1.713
open access Open Access

Nature

Quality:  
High
CiteRatio: 6.7
SJR: 1.542
SNIP: 1.216

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.

3.065

1% from 2018

Impact factor for Purinergic Signalling from 2016 - 2019
Year Value
2019 3.065
2018 3.038
2017 3.19
2016 3.022
graph view Graph view
table view Table view

5.4

13% from 2019

CiteRatio for Purinergic Signalling from 2016 - 2020
Year Value
2020 5.4
2019 6.2
2018 5.5
2017 5.3
2016 5.7
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 1% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has decreased by 13% 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.

1.064

2% from 2019

SJR for Purinergic Signalling from 2016 - 2020
Year Value
2020 1.064
2019 1.086
2018 1.01
2017 1.104
2016 1.358
graph view Graph view
table view Table view

0.754

18% from 2019

SNIP for Purinergic Signalling from 2016 - 2020
Year Value
2020 0.754
2019 0.921
2018 0.851
2017 0.834
2016 0.854
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 2% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has decreased by 18% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Purinergic Signalling

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Springer

Purinergic Signalling

Nucleotides and nucleosides are primitive biological molecules that were utilized early in evolution both as intracellular energy sources and as extracellular signalling molecules. ATP was first identified as a neurotransmitter and later as a co-transmitter with all the establ...... Read More

Molecular Biology

Cell Biology

Cellular and Molecular Neuroscience

Biochemistry, Genetics and Molecular Biology

i
Last updated on
16 Jun 2020
i
ISSN
1573-9538
i
Impact Factor
Medium - 0.895
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
i
Citation Type
Author Year
(Blonder et al, 1982)
i
Bibliography Example
Beenakker CWJ (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: 10.1007/S11302-006-9003-5
The E-NTPDase family of ectonucleotidases: Structure function relationships and pathophysiological significance
Simon C. Robson1, Jean Sévigny2, Herbert Zimmermann3
30 May 2006 - Purinergic Signalling

Abstract:

Ectonucleotidases are ectoenzymes that hydrolyze extracellular nucleotides to the respective nucleosides. Within the past decade, ectonucleotidases belonging to several enzyme families have been discovered, cloned and characterized. In this article, we specifically address the cell surface-located members of the ecto-nucleosi... Ectonucleotidases are ectoenzymes that hydrolyze extracellular nucleotides to the respective nucleosides. Within the past decade, ectonucleotidases belonging to several enzyme families have been discovered, cloned and characterized. In this article, we specifically address the cell surface-located members of the ecto-nucleoside triphosphate diphosphohydrolase (E-NTPDase/CD39) family (NTPDase1,2,3, and 8). The molecular identification of individual NTPDase subtypes, genetic engineering, mutational analyses, and the generation of subtype-specific antibodies have resulted in considerable insights into enzyme structure and function. These advances also allow definition of physiological and patho-physiological implications of NTPDases in a considerable variety of tissues. Biological actions of NTPDases are a consequence (at least in part) of the regulated phosphohydrolytic activity on extracellular nucleotides and consequent effects on P2-receptor signaling. It further appears that the spatial and temporal expression of NTPDases by various cell types within the vasculature, the nervous tissues and other tissues impacts on several patho-physiological processes. Examples include acute effects on cellular metabolism, adhesion, activation and migration with other protracted impacts upon developmental responses, inclusive of cellular proliferation, differentiation and apoptosis, as seen with atherosclerosis, degenerative neurological diseases and immune rejection of transplanted organs and cells. Future clinical applications are expected to involve the development of new therapeutic strategies for transplantation and various inflammatory cardiovascular, gastrointestinal and neurological diseases. read more read less

Topics:

Ectonucleotidase (57%)57% related to the paper, Enzyme structure (55%)55% related to the paper, Transplantation (51%)51% related to the paper
View PDF
866 Citations
open accessOpen access Journal Article DOI: 10.1007/S11302-012-9309-4
Cellular function and molecular structure of ecto-nucleotidases
H. Zimmermann1, Matthias Zebisch2, Norbert Sträter3
04 May 2012 - Purinergic Signalling

Abstract:

Ecto-nucleotidases play a pivotal role in purinergic signal transmission. They hydrolyze extracellular nucleotides and thus can control their availability at purinergic P2 receptors. They generate extracellular nucleosides for cellular reuptake and salvage via nucleoside transporters of the plasma membrane. The extracellular ... Ecto-nucleotidases play a pivotal role in purinergic signal transmission. They hydrolyze extracellular nucleotides and thus can control their availability at purinergic P2 receptors. They generate extracellular nucleosides for cellular reuptake and salvage via nucleoside transporters of the plasma membrane. The extracellular adenosine formed acts as an agonist of purinergic P1 receptors. They also can produce and hydrolyze extracellular inorganic pyrophosphate that is of major relevance in the control of bone mineralization. This review discusses and compares four major groups of ecto-nucleotidases: the ecto-nucleoside triphosphate diphosphohydrolases, ecto-5′-nucleotidase, ecto-nucleotide pyrophosphatase/phosphodiesterases, and alkaline phosphatases. Only recently and based on crystal structures, detailed information regarding the spatial structures and catalytic mechanisms has become available for members of these four ecto-nucleotidase families. This permits detailed predictions of their catalytic mechanisms and a comparison between the individual enzyme groups. The review focuses on the principal biochemical, cell biological, catalytic, and structural properties of the enzymes and provides brief reference to tissue distribution, and physiological and pathophysiological functions. read more read less

Topics:

Purinergic receptor (58%)58% related to the paper, Extracellular (53%)53% related to the paper, Nucleotidases (52%)52% related to the paper, Signal transduction (51%)51% related to the paper
View PDF
817 Citations
open accessOpen access Journal Article DOI: 10.1007/S11302-005-0649-1
Neuroprotection by adenosine in the brain: From A1 receptor activation to A2A receptor blockade
Rodrigo A. Cunha1
17 Mar 2005 - Purinergic Signalling

Abstract:

Adenosine is a neuromodulator that operates via the most abundant inhibitory adenosine A1 receptors (A1Rs) and the less abundant, but widespread, facilitatory A2ARs. It is commonly assumed that A1Rs play a key role in neuroprotection since they decrease glutamate release and hyperpolarize neurons. In fact, A1R activation at t... Adenosine is a neuromodulator that operates via the most abundant inhibitory adenosine A1 receptors (A1Rs) and the less abundant, but widespread, facilitatory A2ARs. It is commonly assumed that A1Rs play a key role in neuroprotection since they decrease glutamate release and hyperpolarize neurons. In fact, A1R activation at the onset of neuronal injury attenuates brain damage, whereas its blockade exacerbates damage in adult animals. However, there is a down-regulation of central A1Rs in chronic noxious situations. In contrast, A2ARs are up-regulated in noxious brain conditions and their blockade confers robust brain neuroprotection in adult animals. The brain neuroprotective effect of A2AR antagonists is maintained in chronic noxious brain conditions without observable peripheral effects, thus justifying the interest of A2AR antagonists as novel protective agents in neurodegenerative diseases such as Parkinson’s and Alzheimer’s disease, ischemic brain damage and epilepsy. The greater interest of A2AR blockade compared to A1R activation does not mean that A1R activation is irrelevant for a neuroprotective strategy. In fact, it is proposed that coupling A2AR antagonists with strategies aimed at bursting the levels of extracellular adenosine (by inhibiting adenosine kinase) to activate A1Rs might constitute the more robust brain neuroprotective strategy based on the adenosine neuromodulatory system. This strategy should be useful in adult animals and especially in the elderly (where brain pathologies are prevalent) but is not valid for fetus or newborns where the impact of adenosine receptors on brain damage is different. read more read less

Topics:

Adenosine kinase (61%)61% related to the paper, Adenosine A3 receptor (61%)61% related to the paper, Brain damage (60%)60% related to the paper, Adenosine receptor (60%)60% related to the paper, Neuroprotection (60%)60% related to the paper
View PDF
518 Citations
open accessOpen access Journal Article DOI: 10.1007/S11302-005-5302-5
Physiological roles for ecto-5'-nucleotidase (CD73).
01 Jun 2006 - Purinergic Signalling

Abstract:

Nucleotides and nucleosides influence nearly every aspect of physiology and pathophysiology. Extracellular nucleotides are metabolized through regulated phosphohydrolysis by a series of ecto-nucleotidases. The formation of extracellular adenosine from adenosine 5’-monophosphate is accomplished primarily through ecto-5’-nucleo... Nucleotides and nucleosides influence nearly every aspect of physiology and pathophysiology. Extracellular nucleotides are metabolized through regulated phosphohydrolysis by a series of ecto-nucleotidases. The formation of extracellular adenosine from adenosine 5’-monophosphate is accomplished primarily through ecto-5’-nucleotidase (CD73), a glycosyl phosphatidylinositol-linked membrane protein found on the surface of a variety of cell types. Recent in vivo studies implicating CD73 in a number of tissue protective mechanisms have provided new insight into its regulation and function and have generated considerable interest. Here, we review contributions of CD73 to cell and tissue stress responses, with a particular emphasis on physiologic responses to regulated CD73 expression and function, as well as new findings utilizing Cd73-deficient animals. read more read less

Topics:

Nucleotidase (52%)52% related to the paper, Adenosine (52%)52% related to the paper, Extracellular (51%)51% related to the paper
View PDF
474 Citations
open accessOpen access Journal Article DOI: 10.1007/S11302-005-5435-6
Alkaline Phosphatases : Structure, substrate specificity and functional relatedness to other members of a large superfamily of enzymes
José Luis Millán1
17 Jun 2006 - Purinergic Signalling

Abstract:

Our knowledge of the structure and function of alkaline phosphatases has increased greatly in recent years. The crystal structure of the human placental isozyme has enabled us to probe salient features of the mammalian enzymes that differ from those of the bacterial enzymes. The availability of knockout mice deficient in each... Our knowledge of the structure and function of alkaline phosphatases has increased greatly in recent years. The crystal structure of the human placental isozyme has enabled us to probe salient features of the mammalian enzymes that differ from those of the bacterial enzymes. The availability of knockout mice deficient in each of the murine alkaline phosphatase isozymes has also given deep insights into their in vivo role. This has been particularly true for probing the biological role of bone alkaline phosphatase during skeletal mineralization. Due to space constraints this mini-review focuses exclusively on structural and functional features of mammalian alkaline phosphatases as identified by crystallography and probed by site-directed mutagenesis and kinetic analysis. An emphasis is also placed on the substrate specificity of alkaline phosphatases, their catalytic properties as phosphohydrolases as well as phosphodiesterases and their structural and functional relatedness to a large superfamily of enzymes that includes nucleotide pyrophosphatase/phosphodiesterase. read more read less

Topics:

Alkaline phosphatase (57%)57% related to the paper, Phosphatase (53%)53% related to the paper, Isozyme (52%)52% related to the paper
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439 Citations
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Frequently asked questions

1. Can I write Purinergic Signalling in LaTeX?

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

2. Do you follow the Purinergic Signalling guidelines?

Yes, the template is compliant with the Purinergic Signalling 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 Purinergic Signalling?

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 Purinergic Signalling citation style.

4. Can I use the Purinergic Signalling 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 Purinergic Signalling.

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

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

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

7. Where can I find the template for the Purinergic Signalling?

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

SciSpace's Purinergic Signalling 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 Purinergic Signalling?

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 Purinergic Signalling?”

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

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

12. Is Purinergic Signalling'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 Purinergic Signalling?

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 Purinergic Signalling. 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 Purinergic Signalling?

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

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

16. Can I download Purinergic Signalling 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 Purinergic Signalling Endnote style according to Elsevier guidelines.

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