Example of Pharmacology Biochemistry and Behavior format
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Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format
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Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format Example of Pharmacology Biochemistry and Behavior format
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open access Open Access

Pharmacology Biochemistry and Behavior — Template for authors

Publisher: Elsevier
Categories Rank Trend in last 3 yrs
Behavioral Neuroscience #27 of 78 down down by 21 ranks
Pharmacology #123 of 297 down down by 61 ranks
Toxicology #52 of 122 down down by 36 ranks
Biochemistry #192 of 415 down down by 101 ranks
Clinical Biochemistry #53 of 113 down down by 32 ranks
Biological Psychiatry #24 of 38 down down by 9 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 506 Published Papers | 2388 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 18/06/2020
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Related Journals

open access Open Access

Springer

Quality:  
High
CiteRatio: 4.3
SJR: 0.633
SNIP: 1.433
open access Open Access

Elsevier

Quality:  
Good
CiteRatio: 3.7
SJR: 0.469
SNIP: 0.907
open access Open Access

De Gruyter

Quality:  
High
CiteRatio: 6.5
SJR: 1.246
SNIP: 0.854
open access Open Access

Frontiers Media

Quality:  
High
CiteRatio: 5.1
SJR: 1.128
SNIP: 1.221

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.

2.519

9% from 2018

Impact factor for Pharmacology Biochemistry and Behavior from 2016 - 2019
Year Value
2019 2.519
2018 2.773
2017 2.538
2016 2.748
graph view Graph view
table view Table view

4.7

7% from 2019

CiteRatio for Pharmacology Biochemistry and Behavior from 2016 - 2020
Year Value
2020 4.7
2019 4.4
2018 5.3
2017 6.4
2016 5.7
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 9% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 7% 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.

1.184

45% from 2019

SJR for Pharmacology Biochemistry and Behavior from 2016 - 2020
Year Value
2020 1.184
2019 0.814
2018 0.924
2017 1.15
2016 1.206
graph view Graph view
table view Table view

0.912

20% from 2019

SNIP for Pharmacology Biochemistry and Behavior from 2016 - 2020
Year Value
2020 0.912
2019 0.763
2018 0.816
2017 0.918
2016 0.845
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 45% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 20% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Pharmacology Biochemistry and Behavior

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Elsevier

Pharmacology Biochemistry and Behavior

Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely behavioral, biochemica...... Read More

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Last updated on
18 Jun 2020
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ISSN
0091-3057
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Impact Factor
High - 2.748
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Acceptance Rate
Not provided
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Frequency
Not provided
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Open Access
Yes
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Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Citation Type
Numbered
[25]
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Bibliography Example
G. E. Blonder, M. Tinkham, T. M. Klapwijk, Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion, Phys. Rev. B 25 (7) (1982) 4515–4532. URL 10.1103/PhysRevB.25.4515

Top papers written in this journal

Journal Article DOI: 10.1016/S0091-3057(01)00746-8
Molecular, pharmacological and functional diversity of 5-HT receptors
Daniel Hoyer1, Jason P. Hannon1, Graeme R. Martin1

Abstract:

Serotonin (5-hydroxytryptamine, 5-HT) is probably unique among the monoamines in that its effects are subserved by as many as 13 distinct heptahelical, G-protein-coupled receptors (GPCRs) and one (presumably a family of) ligand-gated ion channel(s). These receptors are divided into seven distinct classes (5-HT(1) to 5-HT(7)) ... Serotonin (5-hydroxytryptamine, 5-HT) is probably unique among the monoamines in that its effects are subserved by as many as 13 distinct heptahelical, G-protein-coupled receptors (GPCRs) and one (presumably a family of) ligand-gated ion channel(s). These receptors are divided into seven distinct classes (5-HT(1) to 5-HT(7)) largely on the basis of their structural and operational characteristics. Whilst this degree of physical diversity clearly underscores the physiological importance of serotonin, evidence for an even greater degree of operational diversity continues to emerge. The challenge for modern 5-HT research has therefore been to define more precisely the properties of the systems that make this incredible diversity possible. Much progress in this regard has been made during the last decade with the realisation that serotonin is possibly the least conservative monoamine transmitter and the cloning of its many receptors. Coupled with the actions of an extremely avid and efficient reuptake system, this array of receptor subtypes provides almost limitless signalling capabilities to the extent that one might even question the need for other transmitter systems. However, the complexity of the system appears endless, since posttranslational modifications, such as alternate splicing and RNA editing, increase the number of proteins, oligomerisation and heteromerisation increase the number of complexes, and multiple G-protein suggest receptor trafficking, allowing phenotypic switching and crosstalk within and possibly between receptor families. Whether all these possibilities are used in vivo under physiological or pathological conditions remains to be firmly established, but in essence, such variety will keep the 5-HT community busy for quite some time. Those who may have predicted that molecular biology would largely simplify the life of pharmacologists have missed the point for 5-HT research in particular and, most probably, for many other transmitters. This chapter is an attempt to summarise very briefly 5-HT receptor diversity. The reward for unravelling this complex array of serotonin receptor--effector systems may be substantial, the ultimate prize being the development of important new drugs in a range of disease areas. read more read less
1,823 Citations
Journal Article DOI: 10.1016/0091-3057(86)90552-6
Anxiolytic and anxiogenic drug effects on exploratory activity in an elevated plus-maze: a novel test of anxiety in the rat
Sharon Pellow1, Sandra E. File1

Abstract:

The current studies further investigated the effects, in animal models of anxiety, of novel putative anxiolytic and anxiogenic compounds believed to induce their effects by actions at the GABA-benzodiazepine receptor complex. It was expected that the results would also provide further validation for a novel test of anxiety ba... The current studies further investigated the effects, in animal models of anxiety, of novel putative anxiolytic and anxiogenic compounds believed to induce their effects by actions at the GABA-benzodiazepine receptor complex. It was expected that the results would also provide further validation for a novel test of anxiety based on the ratio of open to closed arm entries in an elevated plus maze in the rat. The novel putative anxiolytics CL 218,872 (10–20 mg/kg) and tracazolate (5 mg/kg) significantly elevated the percentage of time spent on the open arms of an elevated plus-maze, consistent with their anxiolytic activity in several other animal tests. Also consistent with results from other animal tests, no anxiolytic activity was observed for the phenylquinoline PK 8165 (10–25 mg/kg), the 3,4-benzodiazepine tofisopam (25–50 mg/kg), or buspirone (0.5–20 mg/kg). The benzodiazepine receptor inverse agonists FG 7142 (1–5 mg/kg) and CGS 8216 (3–10 mg/kg) had anxiogenic activity in this test, as did the atypical benzodiazepine Ro 5-4864 (1–5 mg/kg). Interestingly, however, the benzodiazepine receptor antagonists Ro 15-1788 (10–20 mg/kg) and ZK 93426 (5–10 mg/kg) had no anxiogenic activity in this test. read more read less

Topics:

Elevated plus maze (63%)63% related to the paper, Anxiogenic (62%)62% related to the paper, Anxiolytic (61%)61% related to the paper, ZK-93426 (58%)58% related to the paper, CGS-8216 (57%)57% related to the paper
1,467 Citations
Journal Article DOI: 10.1016/0091-3057(80)90067-2
Preliminary report of a simple animal behavior model for the anxiolytic effects of benzodiazepines

Abstract:

A simple system is described to analyze the possibility that increased exploratory behavior is an index for the anxiolytic effects of benzodiazepines in laboratory rodents. Mice were allowed free run in a two-chambered arena, where two-thirds of the area was illuminated and one-third was darkened. The two chambers were separa... A simple system is described to analyze the possibility that increased exploratory behavior is an index for the anxiolytic effects of benzodiazepines in laboratory rodents. Mice were allowed free run in a two-chambered arena, where two-thirds of the area was illuminated and one-third was darkened. The two chambers were separated by a black partition equipped with photocells across the opening, and the entire cage rested on an Animex activity monitor. Transitions across the partition between the light and dark chambers, and total Animex locomotor activity, were increased by clonazepam and chlordiazepoxide, in dose-dependent ranges consistent with previously reported behavior models. The increased exploratory activity with benzodiazepines does not appear to be a non-specific increase in general motor activity, as locomotion in clonazepam and chlordiazepoxide treated mice placed in a bare, undifferentiated cage was not significantly different from vehicle treated mice. read more read less

Topics:

Chlordiazepoxide (51%)51% related to the paper
1,290 Citations
Journal Article DOI: 10.1016/0091-3057(95)02126-4
A review of the validity and variability of the elevated plus-maze as an animal model of anxiety.
Sandy Hogg1

Abstract:

Despite or possibly by virtue of the fact that it is one of the most commonly used animal models of anxiety the Elevated Plus-Maze (EPM) results in a wide range of, often contradictory, results following pharmacological experiments. The responses from a questionnaire distributed to 65 groups that have published studies using ... Despite or possibly by virtue of the fact that it is one of the most commonly used animal models of anxiety the Elevated Plus-Maze (EPM) results in a wide range of, often contradictory, results following pharmacological experiments. The responses from a questionnaire distributed to 65 groups that have published studies using the EPM in the past 3 years has, along with reference to published reports, enabled some conclusions regarding the influencing factors to be drawn. Some evidence for differential sensitivities between strains exists, with albino rats being more sensitive to the anxiolytic effects of 5-HT3 receptor antagonists and 5-HT1A receptor agonists than pigmented animals. Most important, however, is the manipulation of the animals prior to testing and the aversiveness of the test conditions themselves. Stressing animals before testing (e.g., by moving from holding to test room) or using more aversive test conditions (e.g., elevated light levels) increases sensitivity to potential anxiolytics. Animals that are habituated to gentle handling or tested in less aversive conditions (e.g., EPM with ledges) show reduced likelihood of anxiolytic responses with administration of 5-HT3 antagonists, 5-HT1A agonists, and benzodiazepines. read more read less

Topics:

Elevated plus maze (62%)62% related to the paper, Anxiolytic (54%)54% related to the paper
1,122 Citations
Journal Article DOI: 10.1016/J.PBB.2006.12.001
Adolescent cortical development : A critical period of vulnerability for addiction
Fulton T. Crews1, Jun He1, Clyde W. Hodge1

Abstract:

Cortical growth and remodeling continues from birth through youth and adolescence to stable adult levels changing slowly into senescence. There are critical periods of cortical development when specific experiences drive major synaptic rearrangements and learning that only occur during the critical period. For example, visual... Cortical growth and remodeling continues from birth through youth and adolescence to stable adult levels changing slowly into senescence. There are critical periods of cortical development when specific experiences drive major synaptic rearrangements and learning that only occur during the critical period. For example, visual cortex is characterized by a critical period of plasticity involved in establishing visual acuity. Adolescence is defined by characteristic behaviors that include high levels of risk taking, exploration, novelty and sensation seeking, social interaction and play behaviors. In addition, adolescence is the final period of development of the adult during which talents, reasoning and complex adult behaviors mature. This maturation of behaviors corresponds with periods of marked changes in neurogenesis, cortical synaptic remodeling, neurotransmitter receptors and transporters, as well as major changes in hormones. Frontal cortical development is later in adolescence and likely contributes to refinement of reasoning, goal and priority setting, impulse control and evaluating long and short term rewards. Adolescent humans have high levels of binge drinking and experimentation with other drugs. This review presents findings supporting adolescence as a critical period of cortical development important for establishing life long adult characteristics that are disrupted by alcohol and drug use. read more read less
974 Citations
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Frequently asked questions

1. Can I write Pharmacology Biochemistry and Behavior in LaTeX?

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

2. Do you follow the Pharmacology Biochemistry and Behavior guidelines?

Yes, the template is compliant with the Pharmacology Biochemistry and Behavior 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 Pharmacology Biochemistry and Behavior?

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 Pharmacology Biochemistry and Behavior citation style.

4. Can I use the Pharmacology Biochemistry and Behavior 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 Pharmacology Biochemistry and Behavior.

5. Can I use a manuscript in Pharmacology Biochemistry and Behavior 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 Pharmacology Biochemistry and Behavior that you can download at the end.

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

7. Where can I find the template for the Pharmacology Biochemistry and Behavior?

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 Pharmacology Biochemistry and Behavior'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 Pharmacology Biochemistry and Behavior'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.

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SciSpace's Pharmacology Biochemistry and Behavior 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 Pharmacology Biochemistry and Behavior?

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 Pharmacology Biochemistry and Behavior?”

11. What is the output that I would get after using Pharmacology Biochemistry and Behavior?

After writing your paper autoformatting in Pharmacology Biochemistry and Behavior, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Pharmacology Biochemistry and Behavior'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 Pharmacology Biochemistry and Behavior?

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 Pharmacology Biochemistry and Behavior. 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 Pharmacology Biochemistry and Behavior?

The 5 most common citation types in order of usage for Pharmacology Biochemistry and Behavior 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 Pharmacology Biochemistry and Behavior?

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

16. Can I download Pharmacology Biochemistry and Behavior 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 Pharmacology Biochemistry and Behavior Endnote style according to Elsevier guidelines.

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