Example of Cellular and Molecular Bioengineering format
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open access Open Access

Cellular and Molecular Bioengineering — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Modeling and Simulation #102 of 290 down down by 71 ranks
Biochemistry, Genetics and Molecular Biology (all) #81 of 204 down down by 29 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 168 Published Papers | 565 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 15/06/2020
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Related Journals

open access Open Access
recommended Recommended

Springer

Quality:  
High
CiteRatio: 5.3
SJR: 1.515
SNIP: 0.684
open access Open Access
recommended Recommended

Elsevier

Quality:  
High
CiteRatio: 4.9
SJR: 0.657
SNIP: 0.944
open access Open Access
recommended Recommended

Taylor and Francis

Quality:  
High
CiteRatio: 8.9
SJR: 1.347
SNIP: 3.098

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.

1.72

31% from 2018

Impact factor for Cellular and Molecular Bioengineering from 2016 - 2019
Year Value
2019 1.72
2018 2.477
2017 2.435
2016 2.535
graph view Graph view
table view Table view

3.4

15% from 2019

CiteRatio for Cellular and Molecular Bioengineering from 2016 - 2020
Year Value
2020 3.4
2019 4.0
2018 4.3
2017 4.6
2016 3.5
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 31% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has decreased 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.

0.668

24% from 2019

SJR for Cellular and Molecular Bioengineering from 2016 - 2020
Year Value
2020 0.668
2019 0.876
2018 0.975
2017 1.123
2016 1.182
graph view Graph view
table view Table view

0.6

1% from 2019

SNIP for Cellular and Molecular Bioengineering from 2016 - 2020
Year Value
2020 0.6
2019 0.607
2018 0.553
2017 0.658
2016 0.606
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 24% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

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

Cellular and Molecular Bioengineering

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Springer

Cellular and Molecular Bioengineering

A key challenge in improving human health is to understand how cellular behavior arises from molecular-level interactions. The field of Cellular and Molecular Bioengineering seeks to understand, so that we may ultimately control, the mechanical, chemical, and electrical proces...... Read More

Modelling and Simulation

General Biochemistry, Genetics and Molecular Biology

Mathematics

i
Last updated on
15 Jun 2020
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ISSN
1865-5025
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Impact Factor
Medium - 0.505
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
SPBASIC
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Citation Type
Author Year
(Blonder et al, 1982)
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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

open accessOpen access Journal Article DOI: 10.1007/S12195-016-0458-3
Elucidation of Exosome Migration Across the Blood–Brain Barrier Model In Vitro

Abstract:

The delivery of therapeutics to the central nervous system (CNS) remains a major challenge in part due to the presence of the blood-brain barrier (BBB). Recently, cell-derived vesicles, particularly exosomes, have emerged as an attractive vehicle for targeting drugs to the brain, but whether or how they cross the BBB remains ... The delivery of therapeutics to the central nervous system (CNS) remains a major challenge in part due to the presence of the blood-brain barrier (BBB). Recently, cell-derived vesicles, particularly exosomes, have emerged as an attractive vehicle for targeting drugs to the brain, but whether or how they cross the BBB remains unclear. Here, we investigated the interactions between exosomes and brain microvascular endothelial cells (BMECs) in vitro under conditions that mimic the healthy and inflamed BBB in vivo. Transwell assays revealed that luciferase-carrying exosomes can cross a BMEC monolayer under stroke-like, inflamed conditions (TNF-α activated) but not under normal conditions. Confocal microscopy showed that exosomes are internalized by BMECs through endocytosis, co-localize with endosomes, in effect primarily utilizing the transcellular route of crossing. Together, these results indicate that cell-derived exosomes can cross the BBB model under stroke-like conditions in vitro. This study encourages further development of engineered exosomes as drug delivery vehicles or tracking tools for treating or monitoring neurological diseases. read more read less

Topics:

Exosome (65%)65% related to the paper, Microvesicles (51%)51% related to the paper
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317 Citations
open accessOpen access Journal Article DOI: 10.1007/S12195-010-0102-6
Substrate Stiffness and Cell Area Predict Cellular Traction Stresses in Single Cells and Cells in Contact

Abstract:

Cells generate traction stresses against their substrate during adhesion and migration, and traction stresses are used in part by the cell to sense the substrate. While it is clear that traction stresses, substrate stiffness, and cell area are related, it is unclear whether or how area and substrate stiffness affect force gen... Cells generate traction stresses against their substrate during adhesion and migration, and traction stresses are used in part by the cell to sense the substrate. While it is clear that traction stresses, substrate stiffness, and cell area are related, it is unclear whether or how area and substrate stiffness affect force generation in cells. Moreover, multiple studies have investigated traction stresses of single cells, but few have focused on forces exerted by cells in contact, which more closely mimics the in vivo environment. Here, cellular traction forces were measured where cell area was modulated by ligand density or substrate stiffness. We coupled these measurements with a multilinear regression model to show that both projected cell area and underlying substrate stiffness are significant predictors of traction forces in endothelial cells, and interestingly, substrate ligand density is not. We further explored the effect of cell–cell contact on the interplay between cell area, substrate stiffness, and force generation and found that again both area and stiffness play a significant role in cell force generation. These data indicate that cellular traction force cannot be determined by cell area alone and that underlying substrate stiffness is a significant contributor to traction force generation. read more read less

Topics:

Tractive force (58%)58% related to the paper, Traction (engineering) (57%)57% related to the paper
309 Citations
open accessOpen access Journal Article DOI: 10.1007/S12195-014-0340-0
Generation of Multi-Scale Vascular Network System within 3D Hydrogel using 3D Bio-Printing Technology.
Vivian K. Lee1, Alison M Lanzi1, Ngo Haygan1, Seung-Schik Yoo2, Peter A. Vincent3, Guohao Dai1

Abstract:

Although 3D bio-printing technology has great potential in creating complex tissues with multiple cell types and matrices, maintaining the viability of thick tissue construct for tissue growth and maturation after the printing is challenging due to lack of vascular perfusion. Perfused capillary network can be a solution for t... Although 3D bio-printing technology has great potential in creating complex tissues with multiple cell types and matrices, maintaining the viability of thick tissue construct for tissue growth and maturation after the printing is challenging due to lack of vascular perfusion. Perfused capillary network can be a solution for this issue; however, construction of a complete capillary network at single cell level using the existing technology is nearly impossible due to limitations in time and spatial resolution of the dispensing technology. To address the vascularization issue, we developed a 3D printing method to construct larger (lumen size of ~1 mm) fluidic vascular channels and to create adjacent capillary network through a natural maturation process, thus providing a feasible solution to connect the capillary network to the large perfused vascular channels. In our model, microvascular bed was formed in between two large fluidic vessels, and then connected to the vessels by angiogenic sprouting from the large channel edge. Our bio-printing technology has a great potential in engineering vascularized thick tissues and vascular niches, as the vascular channels are simultaneously created while cells and matrices are printed around the channels in desired 3D patterns. read more read less
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286 Citations
open accessOpen access Journal Article DOI: 10.1007/S12195-014-0342-Y
Nuclear Deformability Constitutes a Rate-Limiting Step During Cell Migration in 3-D Environments
Patricia M. Davidson1, Celine Denais1, Maya C. Bakshi1, Jan Lammerding1

Abstract:

Cell motility plays a critical role in many physiological and pathological settings, ranging from wound healing to cancer metastasis. While cell migration on 2-dimensional (2-D) substrates has been studied for decades, the physical challenges cells face when moving in 3-D environments are only now emerging. In particular, the... Cell motility plays a critical role in many physiological and pathological settings, ranging from wound healing to cancer metastasis. While cell migration on 2-dimensional (2-D) substrates has been studied for decades, the physical challenges cells face when moving in 3-D environments are only now emerging. In particular, the cell nucleus, which occupies a large fraction of the cell volume and is normally substantially stiffer than the surrounding cytoplasm, may impose a major obstacle when cells encounter narrow constrictions in the interstitial space, the extracellular matrix, or small capillaries. Using novel microfluidic devices that allow observation of cells moving through precisely defined geometries at high spatial and temporal resolution, we determined nuclear deformability as a critical factor in the cells’ ability to pass through constrictions smaller than the size of the nucleus. Furthermore, we found that cells with reduced levels of the nuclear envelope proteins lamins A/C, which are the main determinants of nuclear stiffness, passed significantly faster through narrow constrictions during active migration and passive perfusion. Given recent reports that many human cancers have altered lamin expression, our findings suggest a novel biophysical mechanism by which changes in nuclear structure and composition may promote cancer cell invasion and metastasis. read more read less

Topics:

Lamin (56%)56% related to the paper, Cell migration (53%)53% related to the paper, Cancer cell (50%)50% related to the paper
253 Citations
open accessOpen access Journal Article DOI: 10.1007/S12195-016-0457-4
Oncogene Knockdown via Active Loading of Small RNAs into Extracellular Vesicles by Sonication

Abstract:

Extracellular vesicles (EVs), including exosomes and microvesicles, have emerged as promising drug delivery vehicles for small RNAs (siRNA and miRNA) due to their natural role in intercellular RNA transport. However, the application of EVs for therapeutic RNA delivery may be limited by loading approaches that can induce cargo... Extracellular vesicles (EVs), including exosomes and microvesicles, have emerged as promising drug delivery vehicles for small RNAs (siRNA and miRNA) due to their natural role in intercellular RNA transport. However, the application of EVs for therapeutic RNA delivery may be limited by loading approaches that can induce cargo aggregation or degradation. Here, we report the use of sonication as a means to actively load functional small RNAs into EVs. Conditions under which EVs could be loaded with small RNAs with minimal detectable aggregation were identified, and EVs loaded with therapeutic siRNA via sonication were observed to be taken up by recipient cells and capable of target mRNA knockdown leading to reduced protein expression. This system was ultimately applied to reduce expression of HER2, an oncogenic receptor tyrosine kinase that critically mediates breast cancer development and progression, and could be extended to other therapeutic targets. These results define important parameters informing the application of sonication as a small RNA loading method for EVs and demonstrate the potential utility of this approach for versatile cancer therapy. read more read less

Topics:

RNA (54%)54% related to the paper, Microvesicles (53%)53% related to the paper, Small RNA (52%)52% related to the paper, Gene knockdown (51%)51% related to the paper, microRNA (51%)51% related to the paper
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213 Citations
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Cellular and Molecular Bioengineering format uses SPBASIC citation style.

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Frequently asked questions

1. Can I write Cellular and Molecular Bioengineering in LaTeX?

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

2. Do you follow the Cellular and Molecular Bioengineering guidelines?

Yes, the template is compliant with the Cellular and Molecular Bioengineering 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 Cellular and Molecular Bioengineering?

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 Cellular and Molecular Bioengineering citation style.

4. Can I use the Cellular and Molecular Bioengineering 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 Cellular and Molecular Bioengineering.

5. Can I use a manuscript in Cellular and Molecular Bioengineering 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 Cellular and Molecular Bioengineering that you can download at the end.

6. How long does it usually take you to format my papers in Cellular and Molecular Bioengineering?

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

7. Where can I find the template for the Cellular and Molecular Bioengineering?

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 Cellular and Molecular Bioengineering'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 Cellular and Molecular Bioengineering'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. Cellular and Molecular Bioengineering an online tool or is there a desktop version?

SciSpace's Cellular and Molecular Bioengineering 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 Cellular and Molecular Bioengineering?

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 Cellular and Molecular Bioengineering?”

11. What is the output that I would get after using Cellular and Molecular Bioengineering?

After writing your paper autoformatting in Cellular and Molecular Bioengineering, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Cellular and Molecular Bioengineering'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 Cellular and Molecular Bioengineering?

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 Cellular and Molecular Bioengineering. 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 Cellular and Molecular Bioengineering?

The 5 most common citation types in order of usage for Cellular and Molecular Bioengineering 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 Cellular and Molecular Bioengineering?

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

16. Can I download Cellular and Molecular Bioengineering 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 Cellular and Molecular Bioengineering 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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