Taylor & Francis

Small GTPases Template

Write in a clean editor, then format for Small GTPases in one click — DocuGuru applies the official Taylor & Francis template with author–year references and exports a submission-ready PDF plus the editable LaTeX source. Free to start.

About the Small GTPases format

Small GTPases is a peer-reviewed journal published by Taylor & Francis, covering Cellular transport and secretion, Protein Kinase Regulation and GTPase Signaling, Cellular Mechanics and Interactions.

PublisherTaylor & Francis
Reference styleAuthor–year (Chicago, T&F)
Author–year — (Smith, 2023) in the text
Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Small GTPases 12 (3): 45–58.

Formats any DOI in Small GTPases style. No sign-up.

Publishes research inCellular transport and secretion Protein Kinase Regulation and GTPase Signaling Cellular Mechanics and Interactions Microtubule and mitosis dynamics Cell Adhesion Molecules Research
ISSN2154-1248
Citation impact (2-yr)3.33
h-index68
i10-index403
Total citations19,336
Top institutions publishing hereCentre National de la Recherche Scientifique
Journal websitewww.tandfonline.com
You getA submission-ready PDF and the editable LaTeX source — ready to submit.

Papers published in Small GTPases per year

40
2013
44
2014
32
2015
107
2016
104
2017
20
2018
18
2019
16
2020
24
2021
6
2022
5
2023
3
2024

Citation impact of Small GTPases by publication year

1.2K
2013
4.1K
2014
987
2015
4.3K
2016
3.4K
2017
383
2018
363
2019
308
2020
293
2021
42
2022
25
2023
8
2024

Citations each year’s papers have accumulated so far — the most recent years are still building up.

Most-cited papers in Small GTPases

Ras history

Adrienne D. Cox, Channing J. Der · 1 Jul 2010

Although the roots of Ras sprouted from the rich history of retrovirus research, it was the discovery of mutationally activated RAS genes in human cancer in 1982 that stimulated an intensive research effort to understand Ras protein structure, biochemistry and biology. While the ultimate goal has been developing anti-Ras drugs for cancer treatment, discoveries from…

Biology and biogenesis of shed microvesicles

Christopher Tricarico, James Clancy, Crislyn D’Souza‐Schorey · 5 Aug 2016

The ability of cells to transmit bioactive molecules to recipient cells and the extracellular environment is a fundamental requirement for both normal physiology and disease pathogenesis. It has traditionally been thought that soluble factors released from cells were responsible for this cellular signaling but recent research has revealed a fundamental role for microvesicles in this…

Rho GTPases: Regulation and roles in cancer cell biology

Raquel Brandão Haga, Anne J. Ridley · 15 Sep 2016

Rho GTPases are well known for their roles in regulating cell migration, and also contribute to a variety of other cellular responses. They are subdivided into 2 groups: typical and atypical. The typical Rho family members, including RhoA, Rac1 and Cdc42, cycle between an active GTP-bound and inactive GDP-bound conformation, and are regulated by GEFs,…

Rho-associated coiled-coil containing kinases (ROCK)

Linda Julian, Michael F. Olson · 3 Apr 2014

Rho-associated coiled-coil containing kinases (ROCK) were originally identified as effectors of the RhoA small GTPase. (1)(-) (5) They belong to the AGC family of serine/threonine kinases (6) and play vital roles in facilitating actomyosin cytoskeleton contractility downstream of RhoA and RhoC activation. Since their discovery, ROCK kinases have been extensively studied, unveiling their manifold functions…

New insights into the function of Rab GTPases in the context of exosomal secretion

Lionel Blanc, Michel Vidal · 31 Jan 2017

In the last two decades, extracellular vesicle-mediated communication between cells has become a major field in cell biology. However, the function of extracellular vesicles is far from clear, especially due to the disparity of released vesicles by cells. Basically, one must consider vesicles budding from the cell plasma membrane (ectosomes) and vesicles released upon fusion…

Small GTPases template — frequently asked questions

How do I write a paper in the Small GTPases format?
In DocuGuru you write your manuscript in a normal editor — no LaTeX setup required — and select the Small GTPases template. When you export, DocuGuru compiles the paper into the official Taylor & Francis format and hands you a submission-ready PDF along with the editable LaTeX source.
What reference style does Small GTPases use?
Small GTPases uses Author–year (Chicago, T&F) references, shown as author–year markers such as (Smith, 2023) in the text. DocuGuru formats every in-text citation and the reference list in this exact style automatically. A reference appears like this: Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Small GTPases 12 (3): 45–58.
Do I need to know LaTeX to submit to Small GTPases?
No. DocuGuru generates the interact LaTeX class and compiles the PDF for you in the background, so you get a Taylor & Francis-ready Small GTPases document without writing any LaTeX. If you do want it, the LaTeX source is included in the export.
Can I import an existing draft into the Small GTPases template?
Yes. Paste or upload your current manuscript — Word, LaTeX, Markdown, or plain text — and DocuGuru reflows it into the Small GTPases format with correct headings, figures, tables, and author–year citations.
Who publishes Small GTPases?
Small GTPases is a multidisciplinary journal published by Taylor & Francis. DocuGuru's Small GTPases template matches Taylor & Francis's official submission format.
Can I export a submission-ready Small GTPases PDF?
Yes — DocuGuru produces a PDF built with the official Small GTPases template (the interact class) that is ready to submit to Taylor & Francis, together with the matching LaTeX source files.
How much does the Small GTPases template cost?
You can start writing in the Small GTPases template for free. Exporting the final submission-ready Small GTPases PDF and LaTeX source is part of DocuGuru's paid plans — see the app for current pricing.
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