Example of International Reviews of Immunology format
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Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format
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Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format Example of International Reviews of Immunology format
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open access Open Access

International Reviews of Immunology — Template for authors

Publisher: Taylor and Francis
Categories Rank Trend in last 3 yrs
Immunology and Allergy #32 of 182 up up by 25 ranks
Immunology #38 of 202 up up by 32 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 91 Published Papers | 841 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 20/07/2020
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Top papers
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Related Journals

open access Open Access

Taylor and Francis

Quality:  
High
CiteRatio: 8.4
SJR: 2.078
SNIP: 1.475
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Nature

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CiteRatio: 53.9
SJR: 20.529
SNIP: 8.97
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Frontiers Media

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SJR: 2.646
SNIP: 1.573
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American Association for the Advancement of Science

Quality:  
High
CiteRatio: 17.8
SJR: 8.83
SNIP: 2.831

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.

4.58

32% from 2018

Impact factor for International Reviews of Immunology from 2016 - 2019
Year Value
2019 4.58
2018 3.481
2017 2.933
2016 3.279
graph view Graph view
table view Table view

9.2

31% from 2019

CiteRatio for International Reviews of Immunology from 2016 - 2020
Year Value
2020 9.2
2019 7.0
2018 6.1
2017 6.0
2016 7.1
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 32% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 31% 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.

1.551

37% from 2019

SJR for International Reviews of Immunology from 2016 - 2020
Year Value
2020 1.551
2019 1.132
2018 1.33
2017 1.235
2016 1.531
graph view Graph view
table view Table view

1.599

34% from 2019

SNIP for International Reviews of Immunology from 2016 - 2020
Year Value
2020 1.599
2019 1.19
2018 0.794
2017 0.863
2016 1.027
graph view Graph view
table view Table view

insights Insights

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

insights Insights

  • SNIP of this journal has increased by 34% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

International Reviews of Immunology

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Taylor and Francis

International Reviews of Immunology

This review journal provides the most current information on basic and translational research in immunology and related fields. In addition to invited reviews, the journal accepts for publication articles and editorials on relevant topics proposed by contributors. Each issue o...... Read More

Immunology and Allergy

Medicine

i
Last updated on
20 Jul 2020
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ISSN
0883-0185
i
Impact Factor
High - 1.223
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
Taylor and Francis Custom Citation
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Citation Type
Numbered
[25]
i
Bibliography Example
Blonder GE, Tinkham M, Klapwijk TM. Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion. Phys Rev B. 1982; 25(7):4515–4532. Available from: 10.1103/PhysRevB.25.4515.

Top papers written in this journal

Journal Article DOI: 10.3109/08830185.2010.529976
Pathogen Recognition by the Innate Immune System
Himanshu Kumar, Taro Kawai1, Shizuo Akira1

Abstract:

Microbial infection initiates complex interactions between the pathogen and the host. Pathogens express several signature molecules, known as pathogen-associated molecular patterns (PAMPs), which are essential for survival and pathogenicity. PAMPs are sensed by evolutionarily conserved, germline-encoded host sensors known as ... Microbial infection initiates complex interactions between the pathogen and the host. Pathogens express several signature molecules, known as pathogen-associated molecular patterns (PAMPs), which are essential for survival and pathogenicity. PAMPs are sensed by evolutionarily conserved, germline-encoded host sensors known as pathogen recognition receptors (PRRs). Recognition of PAMPs by PRRs rapidly triggers an array of anti-microbial immune responses through the induction of various inflammatory cytokines, chemokines and type I interferons. These responses also initiate the development of pathogen-specific, long-lasting adaptive immunity through B and T lymphocytes. Several families of PRRs, including Toll-like receptors (TLRs), RIG-I-like receptors (RLRs), NOD-like receptors (NLRs), and DNA receptors (cytosolic sensors for DNA), are known to play a crucial role in host defense. In this review, we comprehensively review the recent progress in the field of PAMP recognition by PRRs and the signaling pathways activated by PRRs. read more read less

Topics:

Pathogen-associated molecular pattern (62%)62% related to the paper, Pattern recognition receptor (60%)60% related to the paper, Immune receptor (58%)58% related to the paper, Innate immune system (56%)56% related to the paper, Acquired immune system (54%)54% related to the paper
1,896 Citations
Journal Article DOI: 10.3109/08830189809043005
Interleukin-1, interleukin-1 receptors and interleukin-1 receptor antagonist.
Charles A. Dinarello1

Abstract:

IL-1 (IL-1 alpha or IL-1 beta) is the prototypic "multifunctional" cytokine. Unlike the lymphocyte and colony stimulating growth factors, IL-1 affects nearly every cell type, and often in concert with other cytokines or small mediator molecules. Although some lymphocyte and colony stimulating growth factors may be therapeutic... IL-1 (IL-1 alpha or IL-1 beta) is the prototypic "multifunctional" cytokine. Unlike the lymphocyte and colony stimulating growth factors, IL-1 affects nearly every cell type, and often in concert with other cytokines or small mediator molecules. Although some lymphocyte and colony stimulating growth factors may be therapeutically useful, IL-1 is a highly inflammatory cytokine and the margin between clinical benefit and unacceptable toxicity in humans is exceedingly narrow. In contrast, agents that reduce the production and/or activity of IL-1 are likely to have an impact on clinical medicine. In support of this concept, there is growing evidence that the production and activity of IL-1, particularly IL-1 beta, are tightly regulated events as if nature has placed specific "road blocks" to reduce the response to IL-1 during disease. In addition to controlling gene expression, synthesis and secretion, this regulation extends to surface receptors, soluble receptors and a receptor antagonist. Investigators have studied how production of the different members of the IL-1 family is controlled, the various biological activities of IL-1, the distinct and various functions of the IL-1 receptor (IL-1R) family and the complexity of intracellular signaling. Mice deficient in IL-1 beta, IL-1 beta converting enzyme (ICE) and IL-1R type I have also been studied. Humans have been injected with IL-1 (either IL-1 alpha or IL-1 beta) for enhancing bone marrow recovery and for cancer treatment. The IL-1 specific receptor antagonist (IL-1Ra) has also been tested in clinical trials. read more read less

Topics:

Interleukin 1 receptor antagonist (65%)65% related to the paper, Common gamma chain (63%)63% related to the paper, Receptor antagonist (60%)60% related to the paper, Interleukin (58%)58% related to the paper, Receptor (57%)57% related to the paper
788 Citations
Journal Article DOI: 10.3109/08830189809042997
Interleukin 6 and its receptor: ten years later.
Toshio Hirano1

Abstract:

Ten years have passed since the molecular cloning of interleukin 6 (IL-6) in 1986. IL-6 is a typical cytokine, exhibiting functional pleiotropy and redundancy. IL-6 is involved in the immune response, inflammation, and hematopoiesis. The IL-6 receptor consists of an IL-6 binding alpha chain and a signal transducer, gp130, whi... Ten years have passed since the molecular cloning of interleukin 6 (IL-6) in 1986. IL-6 is a typical cytokine, exhibiting functional pleiotropy and redundancy. IL-6 is involved in the immune response, inflammation, and hematopoiesis. The IL-6 receptor consists of an IL-6 binding alpha chain and a signal transducer, gp130, which is shared among the receptors for the IL-6 related cytokine subfamily. The sharing of a receptor subunit is a general feature of cytokine receptors and provides the molecular basis for the functional redundancy of cytokines. JAK tyrosine kinase is a key molecule that can initiate multiple signal-transduction pathways by inducing the tyrosine-phosphorylation of the cytokine receptor, gp130 in the case of IL-6, on which several signaling molecules are recruited, including STAT, a signal transducer and activator of transcription, and SHP-2, which links to the Ras-MAP kinase pathway. JAK can also directly activate signaling molecules such as STAT and Tec. These multiple signal-transduction pathways intimately regulate the expression of several genes including c-myc, c-myb, junB, IRF1, egr-1, and bcl-2, leading to the induction of cell growth, differentiation, and survival. The deregulated expression of IL-6 and its receptor is involved in a variety of diseases. read more read less

Topics:

Cytokine receptor (69%)69% related to the paper, Interleukin-21 receptor (66%)66% related to the paper, Common gamma chain (65%)65% related to the paper, Janus kinase 1 (65%)65% related to the paper, Glycoprotein 130 (65%)65% related to the paper
731 Citations
Journal Article DOI: 10.3109/08830189509061738
Human Antibodies from Transgenic Mice
Nils Lonberg, Dennis Huszar1

Abstract:

We have used homologous recombination in ES cells to engineer B cell-deficient mice that are incapable of expressing endogenous immunoglobulin heavy and kappa light chain genes. We find that B cell development in these mutant mice can be rescued by the introduction of human germline-configuration heavy- and kappa light-chain ... We have used homologous recombination in ES cells to engineer B cell-deficient mice that are incapable of expressing endogenous immunoglobulin heavy and kappa light chain genes. We find that B cell development in these mutant mice can be rescued by the introduction of human germline-configuration heavy- and kappa light-chain minilocus transgenes. The transgenes rearrange during B cell differentiation, and subsequently undergo class switching and somatic mutation in response to antigen stimulation; thus recapitulating both stages of the humoral immune response using human, rather than mouse, sequences. The mice can be immunized; and human sequence, antigen specific, monoclonal antibodies can be obtained using conventional rodent hybridoma technology. These animals are also of interest for studying the normal processes of immunoglobulin gene expression. We discuss the example of heavy chain class switching, which has not been previously observed within an autonomous transgene. read more read less

Topics:

Immunoglobulin gene (64%)64% related to the paper, Immunoglobulin class switching (61%)61% related to the paper, B cell (58%)58% related to the paper, Hybridoma technology (57%)57% related to the paper, Antibody (56%)56% related to the paper
558 Citations
Journal Article DOI: 10.3109/08830185.2012.755176
Reactive oxygen species in the immune system.
Yuhui Yang1, Alexandr V. Bazhin1, Jens Werner1, Svetlana Karakhanova1

Abstract:

Reactive oxygen species (ROS) are a group of highly reactive chemicals containing oxygen produced either exogenously or endogenously. ROS are related to a wide variety of human disorders, such as chronic inflammation, age-related diseases and cancers. Besides, ROS are also essential for various biological functions, including... Reactive oxygen species (ROS) are a group of highly reactive chemicals containing oxygen produced either exogenously or endogenously. ROS are related to a wide variety of human disorders, such as chronic inflammation, age-related diseases and cancers. Besides, ROS are also essential for various biological functions, including cell survival, cell growth, proliferation and differentiation, and immune response. At present there are a number of excellent publications including some reviews about functions of these molecules either in normal cell biology or in pathophysiology. In this work, we reviewed available information and recent advances about ROS in the main immune cell types and gave summary about functions of these highly reactive molecules both in innate immunity as conservative defense mechanisms and in essential immune cells involved in adaptive immunity, and particularly in immune suppression. read more read less

Topics:

Acquired immune system (59%)59% related to the paper, Innate immune system (58%)58% related to the paper, Innate lymphoid cell (57%)57% related to the paper, Immune system (56%)56% related to the paper, Immunity (51%)51% related to the paper
372 Citations
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Frequently asked questions

1. Can I write International Reviews of Immunology in LaTeX?

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

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Yes, the template is compliant with the International Reviews of Immunology 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 International Reviews of Immunology?

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 International Reviews of Immunology citation style.

4. Can I use the International Reviews of Immunology 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 International Reviews of Immunology.

5. Can I use a manuscript in International Reviews of Immunology 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 International Reviews of Immunology that you can download at the end.

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7. Where can I find the template for the International Reviews of Immunology?

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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.

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SciSpace's International Reviews of Immunology 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.

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After writing your paper autoformatting in International Reviews of Immunology, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is International Reviews of Immunology'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 International Reviews of Immunology?

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 International Reviews of Immunology. 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 International Reviews of Immunology?

The 5 most common citation types in order of usage for International Reviews of Immunology 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 International Reviews of Immunology?

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16. Can I download International Reviews of Immunology 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 International Reviews of Immunology Endnote style according to Elsevier guidelines.

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