Example of Transgenic Research format
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Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format
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Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format Example of Transgenic Research format
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open access Open Access

Transgenic Research — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Animal Science and Zoology #56 of 416 down down by 34 ranks
Agronomy and Crop Science #67 of 347 down down by 29 ranks
Biotechnology #117 of 282 down down by 47 ranks
Genetics #162 of 325 down down by 30 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 230 Published Papers | 924 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 13/07/2020
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Related Journals

open access Open Access

Springer

Quality:  
High
CiteRatio: 4.1
SJR: 0.833
SNIP: 0.855
open access Open Access
recommended Recommended

IEEE

Quality:  
High
CiteRatio: 6.4
SJR: 0.745
SNIP: 1.278
open access Open Access

Springer

Quality:  
High
CiteRatio: 6.4
SJR: 1.547
SNIP: 1.162
open access Open Access

Springer

Quality:  
High
CiteRatio: 5.8
SJR: 0.875
SNIP: 1.734

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.

1.856

2% from 2018

Impact factor for Transgenic Research from 2016 - 2019
Year Value
2019 1.856
2018 1.817
2017 2.197
2016 2.341
graph view Graph view
table view Table view

4.0

11% from 2019

CiteRatio for Transgenic Research from 2016 - 2020
Year Value
2020 4.0
2019 3.6
2018 4.4
2017 4.6
2016 5.0
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 2% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased 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.

0.724

20% from 2019

SJR for Transgenic Research from 2016 - 2020
Year Value
2020 0.724
2019 0.601
2018 0.826
2017 0.904
2016 1.027
graph view Graph view
table view Table view

0.788

37% from 2019

SNIP for Transgenic Research from 2016 - 2020
Year Value
2020 0.788
2019 0.575
2018 0.714
2017 0.693
2016 0.786
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 20% 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.

Transgenic Research

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Springer

Transgenic Research

Transgenic Research is dedicated to the rapid publication of research in transgenic higher organisms including their production, properties resulting from the transgenic state, use as experimental tools, exploitation and application, and environmental impact. The Journal publi...... Read More

Animal Science and Zoology

Agronomy and Crop Science

Biotechnology

Genetics

Agricultural and Biological Sciences

i
Last updated on
13 Jul 2020
i
ISSN
0962-8819
i
Impact Factor
Medium - 0.866
i
Open Access
Yes
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
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Bibliography Name
SPBASIC
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Citation Type
Author Year
(Blonder et al, 1982)
i
Bibliography Example
Beenakker CWJ (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: 10.1023/A:1008942828960
Conditional gene targeting in macrophages and granulocytes using LysMcre mice.
Björn E. Clausen1, C. Burkhardt1, Walter Reith2, R. Renkawitz3, Irmgard Förster1
01 Aug 1999 - Transgenic Research

Abstract:

Conditional mutagenesis in mice has recently been made possible through the combination of gene targeting techniques and site-directed mutagenesis, using the bacteriophage P1-derived Cre/loxP recombination system. The versatility of this approach depends on the availability of mouse mutants in which the recombinase Cre is exp... Conditional mutagenesis in mice has recently been made possible through the combination of gene targeting techniques and site-directed mutagenesis, using the bacteriophage P1-derived Cre/loxP recombination system. The versatility of this approach depends on the availability of mouse mutants in which the recombinase Cre is expressed in the appropriate cell lineages or tissues. Here we report the generation of mice that express Cre in myeloid cells due to targeted insertion of the cre cDNA into their endogenous M lysozyme locus. In double mutant mice harboring both the LysMcre allele and one of two different loxP-flanked target genes tested, a deletion efficiency of 83-98% was determined in mature macrophages and near 100% in granulocytes. Partial deletion (16%) could be detected in CD11c+ splenic dendritic cells which are closely related to the monocyte/macrophage lineage. In contrast, no significant deletion was observed in tail DNA or purified T and B cells. Taken together, LysMcre mice allow for both specific and highly efficient Cre-mediated deletion of loxP-flanked target genes in myeloid cells. read more read less

Topics:

Gene targeting (55%)55% related to the paper, Monocyte (52%)52% related to the paper, Recombinase (52%)52% related to the paper, Mutant (51%)51% related to the paper
1,943 Citations
Journal Article DOI: 10.1007/BF01977351
New Agrobacterium helper plasmids for gene transfer to plants
Elizabeth E. Hood1, Stanton B. Gelvin2, Leo S. Melchers, Andre Hoekema
01 Jul 1993 - Transgenic Research

Abstract:

We describe the construction of new helper Ti plasmids forAgrobacterium-mediated plant transformation. These plasmids are derived from three differentAgrobacterium tumefaciens Ti plasmids, the octopine plasmid pTiB6, the nopaline plasmid pTiC58, and the L,L-succinamopine plasmid pTiBo542. The T-DNA regions of these plasmids w... We describe the construction of new helper Ti plasmids forAgrobacterium-mediated plant transformation. These plasmids are derived from three differentAgrobacterium tumefaciens Ti plasmids, the octopine plasmid pTiB6, the nopaline plasmid pTiC58, and the L,L-succinamopine plasmid pTiBo542. The T-DNA regions of these plasmids were deleted using site-directed mutagenesis to yield replicons carrying thevir genes that will complement binary vectorsin trans. Data are included that demonstrate strain utility. The advantages ofAgrobacterium strains harbouring these ‘disamed’ Ti plasmids for plant transformation viaAgrobacterium are discussed. read more read less

Topics:

T-DNA Binary system (76%)76% related to the paper, Ti plasmid (70%)70% related to the paper, Nopaline (67%)67% related to the paper, Agrobacterium (62%)62% related to the paper, Plasmid (57%)57% related to the paper
1,360 Citations
Journal Article DOI: 10.1007/BF01969712
Ubiquitin promoter-based vectors for high-level expression of selectable and/or screenable marker genes in monocotyledonous plants.
Alan H. Christensen1, Peter H. Quail1, Peter H. Quail2
01 May 1996 - Transgenic Research

Abstract:

A set of plasmids has been constructed utilizing the promoter, 5' untranslated exon, and first intron of the maize ubiquitin (Ubi-1) gene to drive expression of protein coding sequences of choice. Plasmids containing chimaeric genes for ubiquitin-luciferase (Ubi-Luc), ubiquitin-beta-glucuronidase (Ubi-GUS), and ubiquitin-phos... A set of plasmids has been constructed utilizing the promoter, 5' untranslated exon, and first intron of the maize ubiquitin (Ubi-1) gene to drive expression of protein coding sequences of choice. Plasmids containing chimaeric genes for ubiquitin-luciferase (Ubi-Luc), ubiquitin-beta-glucuronidase (Ubi-GUS), and ubiquitin-phosphinothricin acetyl transferase (Ubi-bar) have been generated, as well as a construct containing chimaeric genes for both Ubi-GUS and Ubi-bar in a single plasmid. Another construct was generated to allow cloning of protein coding sequences of choice on Bam HI and Bam HI-compatible restriction fragments downstream of the Ubi-1 gene fragment. Because the Ubi-1 promoter has been shown to be highly active in monocots, these constructs may be useful for generating high-level gene expression of selectable markers to facilitate efficient transformation of monocots, to drive expression of reference reporter genes in studies of gene expression, and to provide expression of biotechnologically important protein products in transgenic plants. read more read less

Topics:

Selectable marker (60%)60% related to the paper, Reporter gene (60%)60% related to the paper, Regulation of gene expression (56%)56% related to the paper, Plasmid (56%)56% related to the paper, Gene (55%)55% related to the paper
1,224 Citations
open accessOpen access Journal Article
Genetic compensation induced by deleterious mutations but not gene knockdowns
Didier Y.R. Stainier1
01 Jan 2016 - Transgenic Research

Abstract:

Cells sense their environment and adapt to it by fine-tuning their transcriptome. Wired into this network of gene expression control are mechanisms to compensate for gene dosage. The increasing use of reverse genetics in zebrafish, and other model systems, has revealed profound differences between the phenotypes caused by gen... Cells sense their environment and adapt to it by fine-tuning their transcriptome. Wired into this network of gene expression control are mechanisms to compensate for gene dosage. The increasing use of reverse genetics in zebrafish, and other model systems, has revealed profound differences between the phenotypes caused by genetic mutations and those caused by gene knockdowns at many loci, an observation previously reported in mouse and Arabidopsis. To identify the reasons underlying the phenotypic differences between mutants and knockdowns, we generated mutations in zebrafish egfl7, an endothelial extracellular matrix gene of therapeutic interest, as well as in vegfaa. Here we show that egfl7 mutants do not show any obvious phenotypes while animals injected with egfl7 morpholino (morphants) exhibit severe vascular defects. We further observe that egfl7 mutants are less sensitive than their wild-type siblings to Egfl7 knockdown, arguing against residual protein function in the mutants or significant off-target effects of the morpholinos when used at a moderate dose. Comparing egfl7 mutant and morphant proteomes and transcriptomes, we identify a set of proteins and genes that are upregulated in mutants but not in morphants. Among them are extracellular matrix genes that can rescue egfl7 morphants, indicating that they could be compensating for the loss of Egfl7 function in the phenotypically wild-type egfl7 mutants. Moreover, egfl7 CRISPR interference, which obstructs transcript elongation and causes severe vascular defects, does not cause the upregulation of these genes. Similarly, vegfaa mutants but not morphants show an upregulation of vegfab. Taken together, these data reveal the activation of a compensatory network to buffer against deleterious mutations, which was not observed after translational or transcriptional knockdown. read more read less

Topics:

Mutation (genetic algorithm) (63%)63% related to the paper
774 Citations
Journal Article DOI: 10.1007/BF01969123
pBINPLUS: an improved plant transformation vector based on pBIN19.
01 Jul 1995 - Transgenic Research

Abstract:

We describe the construction of a new plant transformation vector, pBINPLUS, based on the popular pBIN19 vector. Improvements over pBIN19 include location of the selectable marker gene at the left T-DNA border, a higher copy number in E. coli, and two rare restriction sites around the multiple cloning site for easier cloning ... We describe the construction of a new plant transformation vector, pBINPLUS, based on the popular pBIN19 vector. Improvements over pBIN19 include location of the selectable marker gene at the left T-DNA border, a higher copy number in E. coli, and two rare restriction sites around the multiple cloning site for easier cloning and analysis of T-DNA insertions in plant genomes. read more read less

Topics:

Plant transformation vector (57%)57% related to the paper, Multiple cloning site (56%)56% related to the paper, Selectable marker (51%)51% related to the paper
584 Citations
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Transgenic Research format uses SPBASIC citation style.

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Frequently asked questions

1. Can I write Transgenic 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 Transgenic Research guidelines and auto format it.

2. Do you follow the Transgenic Research guidelines?

Yes, the template is compliant with the Transgenic 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 Transgenic 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 Transgenic Research citation style.

4. Can I use the Transgenic 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 Transgenic Research.

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

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

7. Where can I find the template for the Transgenic 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 Transgenic 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 Transgenic 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. Transgenic Research an online tool or is there a desktop version?

SciSpace's Transgenic 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 Transgenic 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 Transgenic Research?”

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

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

12. Is Transgenic 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 Transgenic 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 Transgenic 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 Transgenic Research?

The 5 most common citation types in order of usage for Transgenic 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 Transgenic 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 Transgenic Research's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Transgenic 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 Transgenic 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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