Virus Internalization

"Virus Internalization" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

The entering of cells by viruses following VIRUS ATTACHMENT. This is achieved by ENDOCYTOSIS, by direct MEMBRANE FUSION of the viral membrane with the CELL MEMBRANE, or by translocation of the whole virus across the cell membrane.

Descriptor ID	D053586
MeSH Number(s)	G06.920.881
Concept/Terms	Virus Internalization Virus Internalization Internalization, Virus Virus Entry Entry, Virus Virus Membrane Fusion Virus Membrane Fusion Viral Membrane Fusion Fusion, Viral Membrane Membrane Fusion, Viral

Below are MeSH descriptors whose meaning is more general than "Virus Internalization".

Biological Sciences [G]
Microbiological Phenomena [G06]
Virus Physiological Phenomena [G06.920]
Virus Internalization [G06.920.881]

Below are MeSH descriptors whose meaning is related to "Virus Internalization".

Below are MeSH descriptors whose meaning is more specific than "Virus Internalization".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Virus Internalization" by people in this website by year, and whether "Virus Internalization" was a major or minor topic of these publications.

Bar chart showing 21 publications over 13 distinct years, with a maximum of 3 publications in 2014

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2007	0	1	1
2008	1	1	2
2009	1	1	2
2010	1	1	2
2012	0	1	1
2013	0	1	1
2014	2	1	3
2015	1	1	2
2017	1	1	2
2018	1	0	1
2019	1	0	1
2022	0	2	2
2023	0	1	1

Below are the most recent publications written about "Virus Internalization" by people in Profiles.

Wang Z, Sharda N, Omtri RS, Li L, Kandimalla KK. Amyloid-Beta Peptides 40 and 42 Employ Distinct Molecular Pathways for Cell Entry and Intracellular Transit at the Blood-Brain Barrier Endothelium. Mol Pharmacol. 2023 Nov; 104(5):203-213.

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Wang W, Yang F, Lin J, Muthusamy S, Du S, Mullen M, Garba F, Wang W, Liu X, Li T, Yang Z, Ding X, Aikhionbare F, Gao X, Wang Z, Liu X, Yao X. Modeling of COVID-19 disease disparity in gastric organoids reveals the spatiotemporal dynamics of SARS-CoV-2 infectivity. J Mol Cell Biol. 2022 05 20; 14(2).

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Mondal T, Shivange G, Habieb A, Tushir-Singh J. A Feasible Alternative Strategy Targeting Furin Disrupts SARS-CoV-2 Infection Cycle. Microbiol Spectr. 2022 02 23; 10(1):e0236421.

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Strange DP, Jiyarom B, Pourhabibi Zarandi N, Xie X, Baker C, Sadri-Ardekani H, Shi PY, Verma S. Axl Promotes Zika Virus Entry and Modulates the Antiviral State of Human Sertoli Cells. mBio. 2019 07 16; 10(4).

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Dong XH, Ho MH, Liu B, Hildreth J, Dash C, Goodwin JS, Balasubramaniam M, Chen CH, Xie H. Role of Porphyromonas gingivalis outer membrane vesicles in oral mucosal transmission of HIV. Sci Rep. 2018 06 11; 8(1):8812.

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Ruedas JB, Ladner JT, Ettinger CR, Gummuluru S, Palacios G, Connor JH. Spontaneous Mutation at Amino Acid 544 of the Ebola Virus Glycoprotein Potentiates Virus Entry and Selection in Tissue Culture. J Virol. 2017 08 01; 91(15).

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Calton CM, Bronnimann MP, Manson AR, Li S, Chapman JA, Suarez-Berumen M, Williamson TR, Molugu SK, Bernal RA, Campos SK. Translocation of the papillomavirus L2/vDNA complex across the limiting membrane requires the onset of mitosis. PLoS Pathog. 2017 May; 13(5):e1006200.

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Lamers SL, Rose R, Ndhlovu LC, Nolan DJ, Salemi M, Maidji E, Stoddart CA, McGrath MS. The meningeal lymphatic system: a route for HIV brain migration? J Neurovirol. 2016 06; 22(3):275-81.

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Torres L, Ortiz T, Tang Q. Enhancement of herpes simplex virus (HSV) infection by seminal plasma and semen amyloids implicates a new target for the prevention of HSV infection. Viruses. 2015 Apr 20; 7(4):2057-73.

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Hsieh SC, Wu YC, Zou G, Nerurkar VR, Shi PY, Wang WK. Highly conserved residues in the helical domain of dengue virus type 1 precursor membrane protein are involved in assembly, precursor membrane (prM) protein cleavage, and entry. J Biol Chem. 2014 Nov 28; 289(48):33149-60.

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