Example of Experimental Dermatology format
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Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format
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Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format Example of Experimental Dermatology format
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open access Open Access
recommended Recommended

Experimental Dermatology — Template for authors

Publisher: Wiley
Categories Rank Trend in last 3 yrs
Dermatology #11 of 117 down down by 1 rank
Biochemistry #115 of 415 up up by 3 ranks
Molecular Biology #140 of 382 down down by 6 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 701 Published Papers | 4369 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 14/06/2020
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Related Journals

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Elsevier

Quality:  
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CiteRatio: 9.1
SJR: 1.951
SNIP: 1.537
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CiteRatio: 7.3
SJR: 1.18
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Taylor and Francis

Quality:  
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CiteRatio: 13.9
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De Gruyter

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SJR: 1.246
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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.

3.368

17% from 2018

Impact factor for Experimental Dermatology from 2016 - 2019
Year Value
2019 3.368
2018 2.868
2017 2.608
2016 2.679
graph view Graph view
table view Table view

6.2

15% from 2019

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

insights Insights

  • Impact factor of this journal has increased by 17% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 15% 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.

1.108

9% from 2019

SJR for Experimental Dermatology from 2016 - 2020
Year Value
2020 1.108
2019 1.215
2018 1.153
2017 1.126
2016 1.235
graph view Graph view
table view Table view

1.046

7% from 2019

SNIP for Experimental Dermatology from 2016 - 2020
Year Value
2020 1.046
2019 1.129
2018 0.963
2017 0.835
2016 0.939
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 9% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has decreased by 7% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Experimental Dermatology

Guideline source: View

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Wiley

Experimental Dermatology

Experimental Dermatology provides a vehicle for the rapid publication of innovative and definitive reports, letters to the editor and review articles covering all aspects of experimental dermatology. Preference is given to papers of immediate importance to other investigators,...... Read More

Dermatology

Biochemistry

Molecular Biology

Medicine

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Last updated on
14 Jun 2020
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ISSN
0906-6705
i
Impact Factor
High - 1.198
i
Open Access
Yes
i
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.1600-0625.2008.00786.X
The skin: an indispensable barrier
01 Dec 2008 - Experimental Dermatology

Abstract:

The skin forms an effective barrier between the organism and the environment preventing invasion of pathogens and fending off chemical and physical assaults, as well as the unregulated loss of water and solutes In this review we provide an overview of several components of the physical barrier, explaining how barrier function... The skin forms an effective barrier between the organism and the environment preventing invasion of pathogens and fending off chemical and physical assaults, as well as the unregulated loss of water and solutes In this review we provide an overview of several components of the physical barrier, explaining how barrier function is regulated and altered in dermatoses The physical barrier is mainly localized in the stratum corneum (SC) and consists of protein-enriched cells (corneocytes with cornified envelope and cytoskeletal elements, as well as corneodesmosomes) and lipid-enriched intercellular domains The nucleated epidermis also contributes to the barrier through tight, gap and adherens junctions, as well as through desmosomes and cytoskeletal elements During epidermal differentiation lipids are synthesized in the keratinocytes and extruded into the extracellular domains, where they form extracellular lipid-enriched layers The cornified cell envelope, a tough protein/lipid polymer structure, resides below the cytoplasmic membrane on the exterior of the corneocytes Ceramides A and B are covalently bound to cornified envelope proteins and form the backbone for the subsequent addition of free ceramides, free fatty acids and cholesterol in the SC Filaggrin is cross-linked to the cornified envelope and aggregates keratin filaments into macrofibrils Formation and maintenance of barrier function is influenced by cytokines, 3',5'-cyclic adenosine monophosphate and calcium Changes in epidermal differentiation and lipid composition lead to a disturbed skin barrier, which allows the entry of environmental allergens, immunological reaction and inflammation in atopic dermatitis A disturbed skin barrier is important for the pathogenesis of contact dermatitis, ichthyosis, psoriasis and atopic dermatitis read more read less

Topics:

Cornified envelope (68%)68% related to the paper, Corneocyte (59%)59% related to the paper, Barrier function (57%)57% related to the paper, Stratum corneum (53%)53% related to the paper, Filaggrin (51%)51% related to the paper
View PDF
1,495 Citations
open accessOpen access Journal Article DOI: 10.1034/J.1600-0625.2000.009003165.X
The 500 Dalton rule for the skin penetration of chemical compounds and drugs
Jan D. Bos1, M.M.H.M. Meinardi1
01 Jun 2000 - Experimental Dermatology

Abstract:

Human skin has unique properties of which functioning as a physicochemical barrier is one of the most apparent. The human integument is able to resist the penetration of many molecules. However, especially smaller molecules can surpass transcutaneously. They are able to go by the corneal layer, which is thought to form the ma... Human skin has unique properties of which functioning as a physicochemical barrier is one of the most apparent. The human integument is able to resist the penetration of many molecules. However, especially smaller molecules can surpass transcutaneously. They are able to go by the corneal layer, which is thought to form the main deterrent. We argue that the molecular weight (MW) of a compound must be under 500 Dalton to allow skin absorption. Larger molecules cannot pass the corneal layer. Arguments for this "500 Dalton rule" are; 1) virtually all common contact allergens are under 500 Dalton, larger molecules are not known as contact sensitizers. They cannot penetrate and thus cannot act as allergens in man; 2) the most commonly used pharmacological agents applied in topical dermatotherapy are all under 500 Dalton; 3) all known topical drugs used in transdermal drug-delivery systems are under 500 Dalton. In addition, clinical experience with topical agents such as cyclosporine, tacrolimus and ascomycins gives further arguments for the reality of the 500 Dalton rule. For pharmaceutical development purposes, it seems logical to restrict the development of new innovative compounds to a MW of under 500 Dalton, when topical dermatological therapy or percutaneous systemic therapy or vaccination is the objective. read more read less
View PDF
1,132 Citations
Journal Article DOI: 10.1034/J.1600-0625.2001.100102.X
The eczema area and severity index (EASI): assessment of reliability in atopic dermatitis
Jon M. Hanifin1, Thurston M2, Thurston M1, Omoto M1, Omoto M2, R. Cherill1, R. Cherill2, Susan J. Tofte1, Graeber M2, Graeber M1
01 Feb 2001 - Experimental Dermatology

Abstract:

:Objective– To test the reliability of the eczema area and severity index (EASI) scoring system by assessing inter- and intra-observer consistency. Design: Training of evaluators, application, and assessment over 2 consecutive days. Setting– An academic center. Patients– Twenty adults and children with atopic dermatitis (AD);... :Objective– To test the reliability of the eczema area and severity index (EASI) scoring system by assessing inter- and intra-observer consistency. Design: Training of evaluators, application, and assessment over 2 consecutive days. Setting– An academic center. Patients– Twenty adults and children with atopic dermatitis (AD); cohort 1 (10 patients ≥8 years) and cohort 2 (10 patients <8 years). Interventions– None. Main outcome measure– The EASI was used by 15 dermatologist evaluators to assess atopic dermatitis in cohort 1 and cohort 2 on 2 consecutive days. Inter- and intraobserver reliability were analyzed. Results– Overall intra-evaluator reliability of the EASI was in the fair-to-good range. Inter-evaluator reliability analyses indicated that the evaluators assessed the patients consistently across both study days. Conclusions– This study demonstrated that the EASI can be learned quickly and utilized reliably in the assessment of severity and extent of AD. There was consistency among the evaluators between consecutive days of evaluation. These results support the use of the EASI in clinical trials of therapeutic agents for AD. read more read less

Topics:

Eczema Area and Severity Index (60%)60% related to the paper, Cohort (51%)51% related to the paper, Atopic dermatitis (50%)50% related to the paper, Cohort study (50%)50% related to the paper
View PDF
846 Citations
open accessOpen access Journal Article DOI: 10.1111/J.1600-0625.1997.TB00164.X
Matrix metalloproteinases in skin
Veli-Matti Kähäri1, Ulpu Saarialho-Kere2
01 Oct 1997 - Experimental Dermatology

Abstract:

Matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases collectively capable of degrading essentially all extracellular matrix components. These enzymes can be produced by several different types of cells in skin such as fibroblasts, keratinocytes, macrophages, endothelial cells, mast cells, and eosinop... Matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases collectively capable of degrading essentially all extracellular matrix components. These enzymes can be produced by several different types of cells in skin such as fibroblasts, keratinocytes, macrophages, endothelial cells, mast cells, and eosinophils and their activity can be specifically inhibited by TIMPs (tissue inhibitors of metalloproteinases), which bind to active MMPs with 1:1 stoichiometry. In general, MMPs are not constitutively expressed in skin but are induced temporarily in response to exogenous signals such as various cytokines, growth factors, cell matrix interactions and altered cell-cell contacts. At present, more evidence is accumulating that MMPs play an important role in proteolytic remodeling of extracellular matrix in various physiologic situations, including developmental tissue morphogenesis, tissue repair, and angiogenesis. On the other hand, MMPs play an important pathogenetic role in excessive breakdown of connective tissue components, e.g. in rheumatoid arthritis, osteoarthritis, chronic ulcers, dermal photoageing, and periodontitis, as well as in tumor cell invasion and metastasis. In this review we discuss the role of MMPs and TIMPs in human skin based on new observations on the regulation of the expression of MMPs, on their substrate specificity, and MMP expression in physiologic and pathologic conditions of skin involving matrix remodeling. Furthermore, therapeutic modalities based on regulating MMP activity will be reviewed. read more read less

Topics:

Matrix metalloproteinase (60%)60% related to the paper, Wound healing (55%)55% related to the paper, Extracellular matrix (54%)54% related to the paper, Angiogenesis (53%)53% related to the paper, Connective tissue (52%)52% related to the paper
View PDF
598 Citations
open accessOpen access Journal Article DOI: 10.1111/J.1600-0625.2007.00629.X
Immunopathogenesis of psoriasis
01 Oct 2007 - Experimental Dermatology

Abstract:

Psoriasis is a chronic skin disease that affects about 1.5% of the Caucasian population and is characterized by typical macroscopic and microscopic skin alterations. Psoriatic lesions are sharply demarcated, red and slightly raised lesions with silver-whitish scales. The microscopic alterations of psoriatic plaques include an... Psoriasis is a chronic skin disease that affects about 1.5% of the Caucasian population and is characterized by typical macroscopic and microscopic skin alterations. Psoriatic lesions are sharply demarcated, red and slightly raised lesions with silver-whitish scales. The microscopic alterations of psoriatic plaques include an infiltration of immune cells in the dermis and epidermis, a dilatation and an increase in the number of blood vessels in the upper dermis, and a massively thickened epidermis with atypical keratinocyte differentiation. It is considered a fact that the immune system plays an important role in the pathogenesis of psoriasis. Since the early 1990s, it has been assumed that T1 cells play the dominant role in the initiation and maintenance of psoriasis. However, the profound success of anti-tumor necrosis factor-alpha therapy, when compared with T-cell depletion therapies, should provoke us to critically re-evaluate the current hypothesis for psoriasis pathogenesis. Recently made discoveries regarding other T-cell populations such as Th17 and regulatory T cells, dendritic cells, macrophages, the keratinocyte signal transduction and novel cytokines including interleukin (IL)-22, IL-23 and IL-20, let us postulate that the pathogenesis of psoriasis consists of distinct subsequent stages, in each of them different cell types playing a dominant role. Our model helps to explain the varied effectiveness of the currently tested immune modulating therapies and may enable the prediction of the success of future therapies. read more read less

Topics:

Psoriasis (60%)60% related to the paper, Dermis (51%)51% related to the paper, Immune system (50%)50% related to the paper
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530 Citations
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Experimental Dermatology format uses apa citation style.

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Frequently asked questions

1. Can I write Experimental Dermatology in LaTeX?

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

2. Do you follow the Experimental Dermatology guidelines?

Yes, the template is compliant with the Experimental Dermatology 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 Experimental Dermatology?

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 Experimental Dermatology citation style.

4. Can I use the Experimental Dermatology 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 Experimental Dermatology.

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

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

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

7. Where can I find the template for the Experimental Dermatology?

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

SciSpace's Experimental Dermatology 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 Experimental Dermatology?

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 Experimental Dermatology?”

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

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

12. Is Experimental Dermatology'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 Experimental Dermatology?

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 Experimental Dermatology. 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 Experimental Dermatology?

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

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

16. Can I download Experimental Dermatology 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 Experimental Dermatology 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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