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

Cell and Tissue Biology — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Cell Biology #257 of 279 up up by 3 ranks
journal-quality-icon Journal quality:
Low
calendar-icon Last 4 years overview: 231 Published Papers | 257 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 14/06/2020
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Journal Performance & Insights

CiteRatio

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

A measure of average citations received per peer-reviewed paper published in the journal.

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.

1.1

10% from 2019

CiteRatio for Cell and Tissue Biology from 2016 - 2020
Year Value
2020 1.1
2019 1.0
2018 0.8
2017 0.6
2016 0.6
graph view Graph view
table view Table view

0.192

4% from 2019

SJR for Cell and Tissue Biology from 2016 - 2020
Year Value
2020 0.192
2019 0.201
2018 0.191
2017 0.165
2016 0.155
graph view Graph view
table view Table view

0.316

8% from 2019

SNIP for Cell and Tissue Biology from 2016 - 2020
Year Value
2020 0.316
2019 0.292
2018 0.458
2017 0.22
2016 0.21
graph view Graph view
table view Table view

insights Insights

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

insights Insights

  • SJR of this journal has decreased by 4% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 8% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Cell and Tissue Biology

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Springer

Cell and Tissue Biology

The journal publishes papers on vast aspects of cell research, including morphology, biochemistry, biophysics, genetics, molecular biology, immunology. The journal accepts original experimental studies, theoretical articles suggesting novel principles and approaches, presentat...... Read More

Cell Biology

Biochemistry, Genetics and Molecular Biology

i
Last updated on
14 Jun 2020
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ISSN
1990-519X
i
Impact Factor
Low - 0.206
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
Blue 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

Journal Article DOI: 10.1134/S1990519X09010039
Characteristics of human lipoaspirate-isolated mesenchymal stromal cells cultivated under lower oxygen tension
Ludmila Buravkova1, O. S. Grinakovskaya1, Elena R. Andreeva1, A. P. Zhambalova1, M. P. Kozionova1
08 Mar 2009 - Cell and Tissue Biology

Abstract:

In the present study we investigated the effect of low oxygen concentration in the cultivation medium on proliferation, viability and immunophenotype of human mesenchymal stromal cells isolated from lipoaspirate (lMSC). It was shown that proliferation activity of the cells under hypoxic conditions was, on average, 2.9 times h... In the present study we investigated the effect of low oxygen concentration in the cultivation medium on proliferation, viability and immunophenotype of human mesenchymal stromal cells isolated from lipoaspirate (lMSC). It was shown that proliferation activity of the cells under hypoxic conditions was, on average, 2.9 times higher compared to that under commonly accepted normoxic conditions. Redused oxygen level in the culture medium did not cause any change in IMSC viability and immunophenotype. Thus, permanent culture of lMSC in the medium with a lower oxygen tension can prove an efficient approach to obtain a higher mass of cells which maintain their characteristics in a shorter period of time, which can be of demand for regenerative medicine. read more read less

Topics:

Oxygen tension (64%)64% related to the paper
65 Citations
Journal Article DOI: 10.1134/S1990519X12010129
Multipotent mesenchymal stem cells of desquamated endometrium: Isolation, characterization, and application as a feeder layer for maintenance of human embryonic stem cells
17 Feb 2012 - Cell and Tissue Biology

Abstract:

In this study, we characterize new multipotent human mesenchymal stem cell lines (MSCs) derived from desquamated (shedding) endometrium of menstrual blood. The isolated endometrial MSC (eMSC) is an adhesive to plastic heterogeneous population composed mainly of endometrial glandular and stromal cells. The established cell lin... In this study, we characterize new multipotent human mesenchymal stem cell lines (MSCs) derived from desquamated (shedding) endometrium of menstrual blood. The isolated endometrial MSC (eMSC) is an adhesive to plastic heterogeneous population composed mainly of endometrial glandular and stromal cells. The established cell lines meet the criteria of the International Society for Cellular Therapy for defining multipotent human MSCs of any origin. The eMSCs have positive expression of CD13, CD29, CD44, CD73, CD90, and CD105 markers and lack hematopoietic cell surface antigens CD19, CD34, CD45, CD117, CD130, and HLA-DR (class II). Multipotency of the established eMSCs is confirmed by their ability to differentiate into other mesodermal lineages, such as osteocytes and adipocytes. In addition, the isolated eMSCs partially (over 50%) express the pluripotency marker SSEA-4. However, they do not express Oct-4. Immunofluorescent analysis of the derived cells revealed the expression of the neural precursor markers nestin and β-III-tubulin. This suggests a neural predisposition of the established eMSCs. These cells are characterized by a high proliferation rate (doubling time 22–23 h) and a high colony-forming efficiency (about 60%). In vitro, the eMSCs undergo more than 45 population doublings without karyotypic abnormalities. We demonstrate that mitotically inactivated eMSCs are perfect feeder cells for maintenance of human embryonic stem cell lines (hESCs) C612 and C910. The eMSCs, being a feeder culture, sustain the hESC pluripotent status that verified by expression of Oct-4, alkaline phosphatase and SSEA-4 markers. The hESCs cocultured with the eMSCs retain their morphology and proliferative rate for more than 40 passages and exhibit the capability for spontaneous differentiation into embryoid bodies comprising three embryonic germ layers. Thus, an easy and noninvasive isolation of the eMSCs from menstrual blood, their multipotency and high proliferative activity in vitro without karyotypic abnormalities demonstrate the potential of use of these stem cells in regenerative medicine. Using the derived eMSCs as the feeder culture eliminates the risks associated with animal cells while transferring hESCs to clinical setting. read more read less

Topics:

Embryoid body (56%)56% related to the paper, Stem cell (55%)55% related to the paper, Mesenchymal stem cell (55%)55% related to the paper, Embryonic stem cell (55%)55% related to the paper, Population (51%)51% related to the paper
62 Citations
Journal Article DOI: 10.1134/S1990519X09030122
Chloroplast structure of diatoms of different classes
Ye. D. Bedoshvili1, T. P. Popkova1, Ye. V. Likhoshway1
25 Jul 2009 - Cell and Tissue Biology

Abstract:

The diversity of chloroplast forms, and their number and cellular location, as well as pyrenoid structure, distinguishes diatoms from other groups of heterokont algae. The fine chloroplast structure is considered to be informative for taxonomic and phylogenetic studies of diatoms. Six species of diatoms belonging to different... The diversity of chloroplast forms, and their number and cellular location, as well as pyrenoid structure, distinguishes diatoms from other groups of heterokont algae. The fine chloroplast structure is considered to be informative for taxonomic and phylogenetic studies of diatoms. Six species of diatoms belonging to different classes have been examined with transmission electron microscopy. New data on the chloroplast structure have been obtained. Characteristics of the pyrenoid ultrastructure of diatoms belonging to various phylogenetic clades have been defined more precisely. The results specify the ultrastructure of pyrenoids for different phylogenetic clades of diatoms and contribute to the previously obtained data. read more read less

Topics:

Pyrenoid (59%)59% related to the paper, Heterokont (58%)58% related to the paper
61 Citations
Journal Article DOI: 10.1134/S1990519X13030140
Neurogenic potential of human mesenchymal stem cells isolated from bone marrow, adipose tissue and endometrium: a Comparative study
08 Jun 2013 - Cell and Tissue Biology

Abstract:

Mesenchymal stem cells (MSCs) can be isolated from many adult tissue sources. These cells are a valuable substrate in cell therapy for a substantial number of diseases and injuries. Different types of MSCs vary in plasticity. We performed a comparative study of the neurogenic potential of three types of human MSCs derived fro... Mesenchymal stem cells (MSCs) can be isolated from many adult tissue sources. These cells are a valuable substrate in cell therapy for a substantial number of diseases and injuries. Different types of MSCs vary in plasticity. We performed a comparative study of the neurogenic potential of three types of human MSCs derived from bone marrow (BMSCs), subcutaneous adipose tissue (ADSCs) and endometrium (isolated from the menstrual blood) (eMSCs). It was shown that all three types of MSC cultures demonstrate multipotent plasticity and predisposition to neurogenesis, based on the expression of pluripotency marker SSEA-4 and neuronal precursors markers nestin and beta-III-tubulin. Further analysis revealed a transcription of the neuronal marker MAP2 and neurotrophin-3 in the undifferentiated BMSCs and ADSCs. Additionally, a significant basal level of synthesis of brain-derived neurotrophic factor (BDNF) in the eMSC culture was also observed. Stimulation of neural induction with agents such as 5-azacytidine, recombinant human basic fibroblast growth factor (bFGF), recombinant human epidermal growth factor (EGF), a recombinant human fibroblast growth factor 8 (FGF8), morphogen SHH (sonic hedgehog), retinoic acid (RA) and isobutyl-methyl-xanthine (IBMX), showed further differences in the neurogenic potential of the MSCs. The components of the extracellular matrix, such as Matrigel and laminin, were also the important inducers of differentiation. The most effective neural induction in the BMSCs proceeded without the RA participation while pretreated with 5-azacytidine. In contrary, in case of eMSCs RA was a necessary agent of neural differentiation as it stimulated the transcription of neurotrophin-4 and the elevation of secretion level of BDNF. The use of laminin as the substrate in the derived eMSCs appeared to be critical, though an incubation of the cells with 5-azacytidine was optional. As far as the derived ADSCs, RA in combination with 5-azacytidine caused the elevation of expression of MAP2, but reduced the secretion of BDNF. Thus, the effect of RA on neural differentiation of ADSCs is ambiguous and, together with the study of its signaling pathways in the MSCs, requires further research. The therapeutic effect of transplanted MSCs is commonly explained by their paracrine activity. The high basal level of BDNF synthesis in the eMSCs, along with their high proliferative rate, non-invasive extraction and neural predisposition, is a powerful argument for the use of the intact eMSCs as a substrate in cell therapy to repair a nerve tissue. read more read less

Topics:

Mesenchymal stem cell (55%)55% related to the paper, Fibroblast growth factor (53%)53% related to the paper, Matrigel (52%)52% related to the paper, Neurotrophic factors (52%)52% related to the paper, Cell therapy (52%)52% related to the paper
42 Citations
Journal Article DOI: 10.1134/S1990519X07060144
Peculiarities of cytomixis in pollen mother cells of transgenic tobacco plants (Nicotiana tabacum L.) with mutant phenotype
Yu. V. Sidorchuk1, Elena V. Deineko1, V. K. Shumny1
01 Dec 2007 - Cell and Tissue Biology

Abstract:

The frequency characteristics and cytological picture of cytomixis in the course of male meiosis are described in transgenic tobacco plants (Nicotiana tabacum L.) with altered flower morphology and male sterility. Effects of cytomixis on qualitative composition of meiotic products are studied (formation of cytoplasts and poly... The frequency characteristics and cytological picture of cytomixis in the course of male meiosis are described in transgenic tobacco plants (Nicotiana tabacum L.) with altered flower morphology and male sterility. Effects of cytomixis on qualitative composition of meiotic products are studied (formation of cytoplasts and polyads). Doubling of the chromosome number was established to increase frequency of cytomixis in the studied plants. read more read less

Topics:

Cytomixis (71%)71% related to the paper, Nicotiana tabacum (56%)56% related to the paper
33 Citations
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Cell and Tissue Biology format uses SPBASIC citation style.

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Frequently asked questions

1. Can I write Cell and Tissue 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 Cell and Tissue Biology guidelines and auto format it.

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

Yes, the template is compliant with the Cell and Tissue 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 Cell and Tissue 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 Cell and Tissue Biology citation style.

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

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

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

7. Where can I find the template for the Cell and Tissue 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 Cell and Tissue 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 Cell and Tissue 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. Cell and Tissue Biology an online tool or is there a desktop version?

SciSpace's Cell and Tissue 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 Cell and Tissue 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 Cell and Tissue Biology?”

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

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

12. Is Cell and Tissue 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 Cell and Tissue 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 Cell and Tissue 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 Cell and Tissue Biology?

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

16. Can I download Cell and Tissue 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 Cell and Tissue Biology Endnote style according to Elsevier guidelines.

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