Example of Histochemistry and Cell Biology format
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Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format
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Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format Example of Histochemistry and Cell Biology format
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open access Open Access
recommended Recommended

Histochemistry and Cell Biology — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Medical Laboratory Technology #3 of 27 up up by 2 ranks
Histology #10 of 60 up up by 5 ranks
Cell Biology #84 of 279 up up by 48 ranks
Molecular Biology #116 of 382 up up by 56 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 371 Published Papers | 2555 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 08/06/2020
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Quality:  
High
CiteRatio: 7.5
SJR: 1.64
SNIP: 1.281

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.

3.418

29% from 2018

Impact factor for Histochemistry and Cell Biology from 2016 - 2019
Year Value
2019 3.418
2018 2.64
2017 2.164
2016 2.553
graph view Graph view
table view Table view

6.9

19% from 2019

CiteRatio for Histochemistry and Cell Biology from 2016 - 2020
Year Value
2020 6.9
2019 5.8
2018 4.5
2017 5.0
2016 5.2
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 29% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 19% 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.

1.107

15% from 2019

SJR for Histochemistry and Cell Biology from 2016 - 2020
Year Value
2020 1.107
2019 1.308
2018 0.919
2017 1.044
2016 1.163
graph view Graph view
table view Table view

0.923

2% from 2019

SNIP for Histochemistry and Cell Biology from 2016 - 2020
Year Value
2020 0.923
2019 0.904
2018 0.679
2017 0.622
2016 0.657
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 15% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 2% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Histochemistry and Cell Biology

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Springer

Histochemistry and Cell Biology

Histochemistry and Cell Biology is a journal devoted specifically to the field of molecular histology and cell biology. Only original articles dealing with the localization and identification of molecular components, metabolic activities and cell biological aspects of cells an...... Read More

Medical Laboratory Technology

Histology

Molecular Biology

Cell Biology

Health Professions

i
Last updated on
07 Jun 2020
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ISSN
0948-6143
i
Impact Factor
Medium - 0.864
i
Open Access
Yes
i
Sherpa RoMEO Archiving Policy
Green faq
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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

open accessOpen access Journal Article DOI: 10.1007/S00418-008-0435-6
The human keratins: biology and pathology
Roland Moll1, Markus Divo1, Lutz Langbein2

Abstract:

The keratins are the typical intermediate filament proteins of epithelia, showing an outstanding degree of molecular diversity. Heteropolymeric filaments are formed by pairing of type I and type II molecules. In humans 54 functional keratin genes exist. They are expressed in highly specific patterns related to the epithelial ... The keratins are the typical intermediate filament proteins of epithelia, showing an outstanding degree of molecular diversity. Heteropolymeric filaments are formed by pairing of type I and type II molecules. In humans 54 functional keratin genes exist. They are expressed in highly specific patterns related to the epithelial type and stage of cellular differentiation. About half of all keratins—including numerous keratins characterized only recently—are restricted to the various compartments of hair follicles. As part of the epithelial cytoskeleton, keratins are important for the mechanical stability and integrity of epithelial cells and tissues. Moreover, some keratins also have regulatory functions and are involved in intracellular signaling pathways, e.g. protection from stress, wound healing, and apoptosis. Applying the new consensus nomenclature, this article summarizes, for all human keratins, their cell type and tissue distribution and their functional significance in relation to transgenic mouse models and human hereditary keratin diseases. Furthermore, since keratins also exhibit characteristic expression patterns in human tumors, several of them (notably K5, K7, K8/K18, K19, and K20) have great importance in immunohistochemical tumor diagnosis of carcinomas, in particular of unclear metastases and in precise classification and subtyping. Future research might open further fields of clinical application for this remarkable protein family. read more read less

Topics:

Keratin (53%)53% related to the paper, Intermediate filament (51%)51% related to the paper
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1,186 Citations
Journal Article DOI: 10.1007/BF00267823
A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes.

Abstract:

We have developed a simple non-radioactive in situ hybridization procedure for tissue sections and cultured cells using digoxigenin-labelled cRNA probes. This protocol can be applied for the detection of various transcripts present at a wide range of expression levels in the central nervous system. Cerebellar hybridization si... We have developed a simple non-radioactive in situ hybridization procedure for tissue sections and cultured cells using digoxigenin-labelled cRNA probes. This protocol can be applied for the detection of various transcripts present at a wide range of expression levels in the central nervous system. Cerebellar hybridization signals for transcripts estimated to be expressed at high (MBP, myelin basic protein), moderate (GluR1, subunit of AMPA/kainate sensitive glutamate receptors) and low (inositol polyphosphate-5-phosphatase) levels of abundance are demonstrated as examples. The sensitivity and cellular resolution were significantly improved by avoiding any ethanol treatment commonly used in other procedures. The localization of a labelled cell with respect to its environment is shown to be more easily assessed by counterstaining of the tissue with the nuclear dye Hoechst 33258. The present protocol can be combined with immunocytochemistry as demonstrated for glial fibrillary acidic protein (GFAP). All steps of the procedure, including preparation and labelling of the cRNA probes, pretreatment of tissue, hybridization and visualization of the labelled transcripts, are described in detail. read more read less

Topics:

In situ hybridization (55%)55% related to the paper, Digoxigenin (54%)54% related to the paper
1,175 Citations
Journal Article DOI: 10.1007/BF00306130
Differential staining of acid glycosaminoglycans (mucopolysaccharides) by Alcian blue in salt solutions
J. E. Scott1, J. Dorling1

Abstract:

The application of the “critical electrolyte concentration” (CEC) concept to the differentiation of acidic glycosaminglycans (mucopolysaccharides) is described. Alcian Blue 8GX stains with increasing selectivity as increasing amounts of magnesium chloride are incorporated into the dye solution. Model experiments with pure pol... The application of the “critical electrolyte concentration” (CEC) concept to the differentiation of acidic glycosaminglycans (mucopolysaccharides) is described. Alcian Blue 8GX stains with increasing selectivity as increasing amounts of magnesium chloride are incorporated into the dye solution. Model experiments with pure polyanions, or artifically carboxylated, phosphorylated and sulphated liver sections, showed that binding of dye to carboxylate or phosphate groups ceased at low electrolyte concentrations (< 0.3M) whereas dye continued to be held by sulphate ester groups at concentrations five to ten times as high. The similarity to the well established cetylpyridinium system for polyanion fractionation is discussed. Sections of tissues chosen to contain predominantly or characteristically carboxylated mucins, and/or sulphate ester polyanions showed a staining pattern entirely similar to the model sections. Goblet cell mucin in rat ileum stained at < 0.4M MgCl2, Cartilage at < 0.6M MgCl2, mast cells at < 0.75M, and corneal stroma at < 1.0M. These results are in agreement with the known contents of sialo-mucin, chondroitin sulphate, heparin and keratansulphate, respectively. The conditions in which this principle can be used in a practical technique are described. read more read less

Topics:

Staining (51%)51% related to the paper
982 Citations
Journal Article DOI: 10.1007/BF00316069
Quantitation of adipose conversion and triglycerides by staining intracytoplasmic lipids with Oil red O.

Abstract:

Cultured 3T3-F442A cells differentiate into adipocytes and accumulate lipid droplets in the cytoplasm. When fat cells are stained with Oil red O, the degree of staining seems to be proportional to the extent of cell differentiation. We report here a fast and simple method to quantitate the extent of adipose conversion by stai... Cultured 3T3-F442A cells differentiate into adipocytes and accumulate lipid droplets in the cytoplasm. When fat cells are stained with Oil red O, the degree of staining seems to be proportional to the extent of cell differentiation. We report here a fast and simple method to quantitate the extent of adipose conversion by staining the accumulated lipid with Oil red O and determining the amount of extracted dye at 510 nm. The results show that Oil red O specifically stains triglycerides and cholesteryl oleate but no other lipids. This technique is a valuable tool for processing large numbers of cell cultures or samples in which adipose differentiation and/or accumulated triglycerides is to be quantitated. read more read less

Topics:

Oil Red O (64%)64% related to the paper, Staining (56%)56% related to the paper, Adipose tissue (55%)55% related to the paper, Adipocyte (54%)54% related to the paper, Lipid droplet (54%)54% related to the paper
935 Citations
Journal Article DOI: 10.1007/BF00592566
Histochemical demonstration of heavy metals. A revised version of the sulphide silver method suitable for both light and electronmicroscopy
Gorm Danscher1

Abstract:

The three steps of the sulphide silver method have been examined: 1) Transformation of metals to metal sulphides; 2) Fixation and embedding or freezing of the tissue for sectioning; and 3) Deposition of metallic silver on the metal sulphides in a physical developer. Based on the results, a revised method is described and disc... The three steps of the sulphide silver method have been examined: 1) Transformation of metals to metal sulphides; 2) Fixation and embedding or freezing of the tissue for sectioning; and 3) Deposition of metallic silver on the metal sulphides in a physical developer. Based on the results, a revised method is described and discussed. It is particularly important 1) To maintain a sufficient but low concentration of sulphide ions during the perfusion; 2) To avoid using oxidating or acid fixatives; 3) To ensure low temperatures while embedding in paraffin or during polymerization of Epon; and 4) to use a slow-acting physical developer. Examples of the metal sulphide pattern from various tissues are presented. read more read less
744 Citations
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Histochemistry and Cell Biology format uses SPBASIC citation style.

Automatically format and order your citations and bibliography in a click.

SciSpace allows imports from all reference managers like Mendeley, Zotero, Endnote, Google Scholar etc.

Frequently asked questions

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

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

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

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

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

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

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

SciSpace's Histochemistry 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 Histochemistry 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 Histochemistry and Cell Biology?”

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

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

12. Is Histochemistry 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 Histochemistry 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 Histochemistry 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 Histochemistry and Cell Biology?

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

16. Can I download Histochemistry 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 Histochemistry 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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