Example of PPAR Research format
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Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format
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Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research format Example of PPAR Research 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

PPAR Research — Template for authors

Publisher: Hindawi
Categories Rank Trend in last 3 yrs
Pharmacology (medical) #40 of 246 up up by 23 ranks
Drug Discovery #33 of 145 up up by 11 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 81 Published Papers | 513 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 20/07/2020
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open access Open Access

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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.

2.953

29% from 2018

Impact factor for PPAR Research from 2016 - 2019
Year Value
2019 2.953
2018 4.186
2017 3.386
2016 2.811
graph view Graph view
table view Table view

6.3

11% from 2019

CiteRatio for PPAR Research from 2016 - 2020
Year Value
2020 6.3
2019 7.1
2018 6.7
2017 4.9
2016 4.9
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 29% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has decreased by 11% 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.

1.164

14% from 2019

SJR for PPAR Research from 2016 - 2020
Year Value
2020 1.164
2019 1.025
2018 1.605
2017 1.204
2016 1.079
graph view Graph view
table view Table view

1.413

37% from 2019

SNIP for PPAR Research from 2016 - 2020
Year Value
2020 1.413
2019 1.028
2018 1.206
2017 0.994
2016 0.769
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 14% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 37% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

PPAR Research

Guideline source: View

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Hindawi

PPAR Research

PPAR Research is a multidisciplinary journal devoted to the publication of original high-quality, peer-reviewed research articles on advances in basic research, as well as preclinical and clinical trials, involving Peroxisome Proliferator-Activated Receptors (PPARs). PPAR Rese...... Read More

Pharmacology (medical)

Drug Discovery

Medicine

i
Last updated on
20 Jul 2020
i
ISSN
1687-4757
i
Impact Factor
Low - 0.407
i
Acceptance Rate
55%
i
Frequency
Not provided
i
Open Access
Yes
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
i
Bibliography Name
unsrt
i
Citation Type
Numbered
[25]
i
Bibliography Example
C. W. J. Beenakker. “Specular andreev reflection in graphene”. Phys. Rev. Lett., vol. 97, no. 6, 067007, 2006.

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.1155/2010/612089
Peroxisome Proliferator-Activated Receptor Alpha Target Genes
Maryam Rakhshandehroo1, Bianca Knoch2, Bianca Knoch3, Michael Müller1, Sander Kersten1
26 Sep 2010 - Ppar Research

Abstract:

The peroxisome proliferator-activated receptor alpha (PPARα) is a ligand-activated transcription factor involved in the regulation of a variety of processes, ranging from inflammation and immunity to nutrient metabolism and energy homeostasis. PPARα serves as a molecular target for hypolipidemic fibrates drugs which bind the ... The peroxisome proliferator-activated receptor alpha (PPARα) is a ligand-activated transcription factor involved in the regulation of a variety of processes, ranging from inflammation and immunity to nutrient metabolism and energy homeostasis. PPARα serves as a molecular target for hypolipidemic fibrates drugs which bind the receptor with high affinity. Furthermore, PPARα binds and is activated by numerous fatty acids and fatty acid-derived compounds. PPARα governs biological processes by altering the expression of a large number of target genes. Accordingly, the specific role of PPARα is directly related to the biological function of its target genes. Here, we present an overview of the involvement of PPARα in lipid metabolism and other pathways through a detailed analysis of the different known or putative PPARα target genes. The emphasis is on gene regulation by PPARα in liver although many of the results likely apply to other organs and tissues as well. read more read less

Topics:

Peroxisome proliferator-activated receptor alpha (59%)59% related to the paper
View PDF
1,037 Citations
open accessOpen access Journal Article DOI: 10.1155/2007/95974
PPARs, Obesity, and Inflammation.
Rinke Stienstra1, Caroline Duval, Michael Müller, Sander Kersten
01 Jan 2007 - Ppar Research

Abstract:

The worldwide prevalence of obesity and related metabolic disorders is rising rapidly, increasing the burden on our healthcare system. Obesity is often accompanied by excess fat storage in tissues other than adipose tissue, including liver and skeletal muscle, which may lead to local insulin resistance and may stimulate infla... The worldwide prevalence of obesity and related metabolic disorders is rising rapidly, increasing the burden on our healthcare system. Obesity is often accompanied by excess fat storage in tissues other than adipose tissue, including liver and skeletal muscle, which may lead to local insulin resistance and may stimulate inflammation, as in steatohepatitis. In addition, obesity changes the morphology and composition of adipose tissue, leading to changes in protein production and secretion. Some of these secreted proteins, including several proinflammatory mediators, may be produced by macrophages resident in the adipose tissue. The changes in inflammatory status of adipose tissue and liver with obesity feed a growing recognition that obesity represents a state of chronic low-level inflammation. Various molecular mechanisms have been implicated in obesity-induced inflammation, some of which are modulated by the peroxisome proliferator-activated receptors (PPARs). PPARs are ligand-activated transcription factors involved in the regulation of numerous biological processes, including lipid and glucose metabolism, and overall energy homeostasis. Importantly, PPARs also modulate the inflammatory response, which makes them an interesting therapeutic target to mitigate obesity-induced inflammation and its consequences. This review will address the role of PPARs in obesity-induced inflammation specifically in adipose tissue, liver, and the vascular wall. read more read less

Topics:

Adipose tissue (62%)62% related to the paper, Steatohepatitis (55%)55% related to the paper, Proinflammatory cytokine (54%)54% related to the paper, Inflammation (52%)52% related to the paper
View PDF
274 Citations
open accessOpen access Journal Article DOI: 10.1155/2008/102737
The Role of PPARs in Cancer.
Keisuke Tachibana1, Daisuke Yamasaki1, Kenji Ishimoto1, Takefumi Doi1
18 Jun 2008 - Ppar Research

Abstract:

Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors that belong to the nuclear hormone receptor superfamily. PPAR 𝛼 is mainly expressed in the liver, where it activates fatty acid catabolism. PPAR 𝛼 activators have been used to treat dyslipidemia, causing a reduction in plasma trigly... Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors that belong to the nuclear hormone receptor superfamily. PPAR 𝛼 is mainly expressed in the liver, where it activates fatty acid catabolism. PPAR 𝛼 activators have been used to treat dyslipidemia, causing a reduction in plasma triglyceride and elevation of high-density lipoprotein cholesterol. PPAR 𝛿 is expressed ubiquitously and is implicated in fatty acid oxidation and keratinocyte differentiation. PPAR 𝛿 activators have been proposed for the treatment of metabolic disease. PPAR 𝛾 2 is expressed exclusively in adipose tissue and plays a pivotal role in adipocyte differentiation. PPAR 𝛾 is involved in glucose metabolism through the improvement of insulin sensitivity and represents a potential therapeutic target of type 2 diabetes. Thus PPARs are molecular targets for the development of drugs treating metabolic syndrome. However, PPARs also play a role in the regulation of cancer cell growth. Here, we review the function of PPARs in tumor growth. read more read less

Topics:

Peroxisome proliferator-activated receptor (57%)57% related to the paper, Nuclear receptor (51%)51% related to the paper
View PDF
218 Citations
open accessOpen access Journal Article DOI: 10.1155/2007/89369
Mechanism of the Anti-inflammatory Effect of Curcumin: PPAR-γ Activation
Asha Jacob1, Rongqian Wu2, Mian Zhou2, Ping Wang
01 Jan 2007 - Ppar Research

Abstract:

Curcumin, the phytochemical component in turmeric, is used as a dietary spice and a topical ointment for the treatment of inflammation in India for centuries. Curcumin (diferuloylmethane) is relatively insoluble in water, but dissolves in acetone, dimethylsulphoxide, and ethanol. Commercial grade curcumin contains 10–20% curc... Curcumin, the phytochemical component in turmeric, is used as a dietary spice and a topical ointment for the treatment of inflammation in India for centuries. Curcumin (diferuloylmethane) is relatively insoluble in water, but dissolves in acetone, dimethylsulphoxide, and ethanol. Commercial grade curcumin contains 10–20% curcuminoids, desmethoxycurcumin, and bisdesmethoxycurcumin and they are as effective as pure curcumin. Based on a number of clinical studies in carcinogenesis, a daily oral dose of 3.6 g curcumin has been efficacious for colorectal cancer and advocates its advancement into Phase II clinical studies. In addition to the anticancer effects, curcumin has been effective against a variety of disease conditions in both in vitro and in vivo preclinical studies. The present review highlights the importance of curcumin as an anti-inflammatory agent and suggests that the beneficial effect of curcumin is mediated by the upregulation of peroxisome proliferator-activated receptor-γ (PPAR-γ) activation. read more read less

Topics:

Curcumin (62%)62% related to the paper
View PDF
210 Citations
open accessOpen access Journal Article DOI: 10.1155/2007/26839
Comprehensive analysis of PPARalpha-dependent regulation of hepatic lipid metabolism by expression profiling.
10 Sep 2007 - Ppar Research

Abstract:

PPARα is a ligand-activated transcription factor involved in the regulation of nutrient metabolism and inflammation. Although much is already known about the function of PPARα in hepatic lipid metabolism, many PPARα-dependent pathways and genes have yet to be discovered. In order to obtain an overview of PPARα-regulated genes... PPARα is a ligand-activated transcription factor involved in the regulation of nutrient metabolism and inflammation. Although much is already known about the function of PPARα in hepatic lipid metabolism, many PPARα-dependent pathways and genes have yet to be discovered. In order to obtain an overview of PPARα-regulated genes relevant to lipid metabolism, and to probe for novel candidate PPARα target genes, livers from several animal studies in which PPARα was activated and/or disabled were analyzed by Affymetrix GeneChips. Numerous novel PPARα-regulated genes relevant to lipid metabolism were identified. Out of this set of genes, eight genes were singled out for study of PPARα-dependent regulation in mouse liver and in mouse, rat, and human primary hepatocytes, including thioredoxin interacting protein (Txnip), electron-transferring-flavoprotein β polypeptide (Etfb), electron-transferring-flavoprotein dehydrogenase (Etfdh), phosphatidylcholine transfer protein (Pctp), endothelial lipase (EL, Lipg), adipose triglyceride lipase (Pnpla2), hormone-sensitive lipase (HSL, Lipe), and monoglyceride lipase (Mgll). Using an in silico screening approach, one or more PPAR response elements (PPREs) were identified in each of these genes. Regulation of Pnpla2, Lipe, and Mgll, which are involved in triglyceride hydrolysis, was studied under conditions of elevated hepatic lipids. In wild-type mice fed a high fat diet, the decrease in hepatic lipids following treatment with the PPARα agonist Wy14643 was paralleled by significant up-regulation of Pnpla2, Lipe, and Mgll, suggesting that induction of triglyceride hydrolysis may contribute to the anti-steatotic role of PPARα. Our study illustrates the power of transcriptional profiling to uncover novel PPARα-regulated genes and pathways in liver. read more read less

Topics:

Adipose triglyceride lipase (59%)59% related to the paper, Lipid metabolism (59%)59% related to the paper, Monoacylglycerol lipase (57%)57% related to the paper, Endothelial lipase (55%)55% related to the paper, Peroxisome proliferator-activated receptor (52%)52% related to the paper
View PDF
210 Citations
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It automatically formats your research paper to Hindawi formatting guidelines and citation style.

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

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Time taken to format a paper and Compliance with guidelines

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PPAR Research format uses unsrt 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 PPAR Research in LaTeX?

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

2. Do you follow the PPAR Research guidelines?

Yes, the template is compliant with the PPAR Research 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 PPAR Research?

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 PPAR Research citation style.

4. Can I use the PPAR Research 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 PPAR Research.

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

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

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

7. Where can I find the template for the PPAR Research?

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

SciSpace's PPAR Research 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 PPAR Research?

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 PPAR Research?”

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

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

12. Is PPAR Research'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 PPAR Research?

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 PPAR Research. 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 PPAR Research?

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

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

16. Can I download PPAR Research 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 PPAR Research 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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