Example of DNA and Cell Biology format
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Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format
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Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format Example of DNA and Cell Biology format
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open access Open Access

DNA and Cell Biology — Template for authors

Categories Rank Trend in last 3 yrs
Genetics #134 of 325 up up by 31 ranks
Cell Biology #146 of 279 up up by 29 ranks
Molecular Biology #203 of 382 up up by 31 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 637 Published Papers | 3100 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 07/07/2020
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Related Journals

open access Open Access

Wiley

Quality:  
High
CiteRatio: 8.5
SJR: 2.677
SNIP: 1.204
open access Open Access

The Scientific and Technological Research Council of Turkey (TUBITAK)

Quality:  
Good
CiteRatio: 2.0
SJR: 0.323
SNIP: 0.468
open access Open Access

Elsevier

Quality:  
Good
CiteRatio: 6.2
SJR: 1.173
SNIP: 1.127
open access Open Access

Springer

Quality:  
Medium
CiteRatio: 3.8
SJR: 0.865
SNIP: 0.461

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.

3.191

9% from 2018

Impact factor for DNA and Cell Biology from 2016 - 2019
Year Value
2019 3.191
2018 2.918
2017 2.634
2016 2.236
graph view Graph view
table view Table view

4.9

9% from 2019

CiteRatio for DNA and Cell Biology from 2016 - 2020
Year Value
2020 4.9
2019 4.5
2018 4.2
2017 3.7
2016 4.2
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased 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 9% 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.

0.895

5% from 2019

SJR for DNA and Cell Biology from 2016 - 2020
Year Value
2020 0.895
2019 0.854
2018 0.862
2017 0.872
2016 0.96
graph view Graph view
table view Table view

0.745

1% from 2019

SNIP for DNA and Cell Biology from 2016 - 2020
Year Value
2020 0.745
2019 0.736
2018 0.644
2017 0.7
2016 0.632
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 5% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 1% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

DNA and Cell Biology

Guideline source: View

All company, product and service names used in this website are for identification purposes only. All product names, trademarks and registered trademarks are property of their respective owners.

Use of these names, trademarks and brands does not imply endorsement or affiliation. Disclaimer Notice

Mary Ann Liebert, Inc.

DNA and Cell Biology

DNA and Cell Biology covers the latest research in the field of DNA and cell biology. This peer-reviewed journal includes original reports and cutting-edge reviews on: Gene Structure, Function, and Regulation, including topics on genomic organization; the role of histones in g...... Read More

Medicine

i
Last updated on
07 Jul 2020
i
ISSN
1044-5498
i
Impact Factor
Medium - 0.636
i
Acceptance Rate
Not provided
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
Citation Type
Author Year
(Blonder et al., 1982)
i
Bibliography Example
Blonder, G. E., Tinkham, M., and Klapwijk, T. M. 1982. Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and super- current conversion. Phys Rev B, 25(7), 4515– 4532.

Top papers written in this journal

Journal Article DOI: 10.1089/DNA.1993.12.1
The P450 superfamily: update on new sequences, gene mapping, accession numbers, early trivial names of enzymes, and nomenclature.
01 Jan 1993 - DNA and Cell Biology

Abstract:

We provide here a list of 221 P450 genes and 12 putative pseudogenes that have been characterized as of December 14, 1992. These genes have been described in 31 eukaryotes (including 11 mammalian and 3 plant species) and 11 prokaryotes. Of 36 gene families so far described, 12 families exist in all mammals examined to date. T... We provide here a list of 221 P450 genes and 12 putative pseudogenes that have been characterized as of December 14, 1992. These genes have been described in 31 eukaryotes (including 11 mammalian and 3 plant species) and 11 prokaryotes. Of 36 gene families so far described, 12 families exist in all mammals examined to date. These 12 families comprise 22 mammalian subfamilies, of which 17 and 15 have been mapped in the human and mouse genome, respectively. To date, each subfamily appears to represent a cluster of tightly linked genes. This revision supersedes the previous updates [Nebert et al., DNA 6, 1–11, 1987; Nebert et al., DNA 8, 1–13, 1989; Nebert et al., DNA Cell Biol. 10, 1–14 (1991)] in which a nomenclature system, based on divergent evolution of the superfamily, has been described. For the gene and cDNA, we recommend that the italicized root symbol "CYP" for human ("Cyp" for mouse), representing "cytochrome P450," be followed by an Arabic number denoting the family, a letter designating... read more read less

Topics:

Subfamily (56%)56% related to the paper, Pseudogene (54%)54% related to the paper, Gene family (53%)53% related to the paper, Genome (51%)51% related to the paper, Gene (51%)51% related to the paper
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1,660 Citations
Journal Article DOI: 10.1089/DNA.1991.10.1
The P450 superfamily: update on new sequences, gene mapping, and recommended nomenclature.
01 Jan 1991 - DNA and Cell Biology

Abstract:

We provide here a list of 154 P450 genes and seven putative pseudogenes that have been characterized as of October 20, 1990. These genes have been described in a total of 23 eukaryotes (including nine mammalian and one plant species) and six prokaryotes. Of 27 gene families so far described, 10 exist in all mammals. These 10 ... We provide here a list of 154 P450 genes and seven putative pseudogenes that have been characterized as of October 20, 1990. These genes have been described in a total of 23 eukaryotes (including nine mammalian and one plant species) and six prokaryotes. Of 27 gene families so far described, 10 exist in all mammals. These 10 families comprise 18 subfamilies, of which 16 and 14 have been mapped in the human and mouse genomes, respectively; to date, each subfamily appears to represent a cluster of tightly linked genes. We propose here a modest revision of the initially proposed (Nebert et al., DNA 6, 1–11,1987) and updated (Nebert et al., DNA 8, 1–13, 1989) nomenclature system based on evolution of the superfamily. For the gene we recommend that the italicized root symbol CYP for human (Cyp for mouse), representing cytochrome P450, be followed by an Arabic number denoting the family, a letter designating the subfamily (when two or more exist), and an Arabic numeral representing the individual gene ... read more read less

Topics:

Gene family (56%)56% related to the paper, Subfamily (55%)55% related to the paper, Pseudogene (55%)55% related to the paper, Genome (51%)51% related to the paper, Gene (50%)50% related to the paper
996 Citations
Journal Article DOI: 10.1089/DNA.1992.11.1
Sequence alignment of the G-protein coupled receptor superfamily.
W.C. Probst1, Lenore A. Snyder, David I. Schuster, Jürgen Brosius, Stuart C. Sealfon
01 Jan 1992 - DNA and Cell Biology

Abstract:

The multitude of G-protein coupled receptor (GPR) superfamily cDNAs recently isolated has exceeded the number of receptor subtypes anticipated by pharmacological studies. Analysis of the sequence similarities and unique features of the members of this family is valuable for designing strategies to isolate related cDNAs, for d... The multitude of G-protein coupled receptor (GPR) superfamily cDNAs recently isolated has exceeded the number of receptor subtypes anticipated by pharmacological studies. Analysis of the sequence similarities and unique features of the members of this family is valuable for designing strategies to isolate related cDNAs, for developing hypotheses concerning substrate-ligand and receptor-effector interactions, and for understanding the evolution of these genes. We have compiled and aligned the 74 unique amino acid sequences published to date and review the present understanding of the structural motifs contributing to ligand binding and G-protein coupling. read more read less

Topics:

Sequence alignment (54%)54% related to the paper, Peptide sequence (52%)52% related to the paper
906 Citations
Journal Article DOI: 10.1089/DNA.1997.16.871
Cloning and Characterization of Two Human Polyspecific Organic Cation Transporters
01 Jul 1997 - DNA and Cell Biology

Abstract:

Previously we cloned a polyspecific transporter from rat (rOCT1) that is expressed in renal proximal tubules and hepatocytes and mediates electrogenic uptake of organic cations with different molecular structures. Recently a homologous transporter from rat kidney (rOCT2) was cloned but not characterized in detail. We report c... Previously we cloned a polyspecific transporter from rat (rOCT1) that is expressed in renal proximal tubules and hepatocytes and mediates electrogenic uptake of organic cations with different molecular structures. Recently a homologous transporter from rat kidney (rOCT2) was cloned but not characterized in detail. We report cloning and characterization of two homologous transporters from man (hOCT1 and hOCT2) displaying approximately 80% amino acid identity to rOCT1 and rOCT2, respectively. Northern blots showed that hOCT1 is mainly transcribed in liver, while hOCT2 is found in kidney. Using in situ hybridization and immunohistochemistry, expression of hOCT2 was mainly detected in the distal tubule where the transporter is localized at the luminal membrane. After expression in Xenopus laevis oocytes, hOCT1 and hOCT2 mediate tracer influx of N-1-methylnicotinamide (NMN), tetraethylammonium (TEA), and 1-methyl-4-phenylpyridinium (MPP). For cation transport by hOCT2 apparent κm and κi values were determined ... read more read less

Topics:

Organic cation transport (61%)61% related to the paper, Cation transport (59%)59% related to the paper, Organic cation transport proteins (54%)54% related to the paper, SLC22A3 (54%)54% related to the paper, Plasma membrane monoamine transporter (52%)52% related to the paper
629 Citations
Journal Article DOI: 10.1089/DNA.1992.11.511
cDNA cloning and sequence analysis of βig-h3, a novel gene induced in a human adenocarcinoma cell line after treatment with transforming growth factor-β
01 Sep 1992 - DNA and Cell Biology

Abstract:

Transforming growth factor-β (TGF-β) is capable of affecting the proliferation of many cell types. To identify novel genes whose protein products may mediate cellular responses to this factor, a cDNA library was made from mRNA isolated from a human lung adenocarcinoma cell line (A549) that had been treated for 3 days with TGF... Transforming growth factor-β (TGF-β) is capable of affecting the proliferation of many cell types. To identify novel genes whose protein products may mediate cellular responses to this factor, a cDNA library was made from mRNA isolated from a human lung adenocarcinoma cell line (A549) that had been treated for 3 days with TGF-β. The library was screened by differential hybridization and a cDNA clone, βig-h3, was isolated. This gene was induced up to 20-fold in A549 cells after 2 days of treatment with TGF-β1. It was also induced in several other cell lines, including PC-3 and H2981. DNA sequence analysis of βig-h3 indicated that it encoded a novel protein, βIG-H3, of 683 amino acids, which contained an amino-terminal secretory sequence and a carboxy-terminal Arg-Gly-Asp (RGD) sequence that can serve as a ligand recognition site for several integrins. βIG-H3 also contained short amino acid regions homologous to similar regions in Drosophila fasciclin-I and four homologous internal domains, which c... read more read less

Topics:

cDNA library (61%)61% related to the paper, Peptide sequence (59%)59% related to the paper, Sequence analysis (58%)58% related to the paper, Nucleic acid sequence (56%)56% related to the paper, Gene (54%)54% related to the paper
510 Citations
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You can download a submission ready research paper in pdf, LaTeX and docx formats.

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Frequently asked questions

1. Can I write DNA and Cell Biology in LaTeX?

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

2. Do you follow the DNA and Cell Biology guidelines?

Yes, the template is compliant with the DNA and Cell Biology 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 DNA and Cell Biology?

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 DNA and Cell Biology citation style.

4. Can I use the DNA and Cell Biology 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 DNA and Cell Biology.

5. Can I use a manuscript in DNA and Cell Biology 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 DNA and Cell Biology that you can download at the end.

6. How long does it usually take you to format my papers in DNA and Cell Biology?

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

7. Where can I find the template for the DNA and Cell Biology?

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 DNA and Cell Biology'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 DNA and Cell Biology'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. DNA and Cell Biology an online tool or is there a desktop version?

SciSpace's DNA and Cell Biology 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 DNA and Cell Biology?

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 DNA and Cell Biology?”

11. What is the output that I would get after using DNA and Cell Biology?

After writing your paper autoformatting in DNA and Cell Biology, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is DNA and Cell Biology'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 DNA and Cell Biology?

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 DNA and Cell Biology. 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 DNA and Cell Biology?

The 5 most common citation types in order of usage for DNA and Cell Biology 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 DNA and Cell Biology?

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

16. Can I download DNA and Cell Biology 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 DNA and Cell Biology 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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