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Organelle Contact Sites

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Cover of 'Organelle Contact Sites'

Table of Contents

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    Book Overview
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    Chapter 1 Organelle Communication at Membrane Contact Sites (MCS): From Curiosity to Center Stage in Cell Biology and Biomedical Research
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    Chapter 2 Over Six Decades of Discovery and Characterization of the Architecture at Mitochondria-Associated Membranes (MAMs)
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    Chapter 3 Regulation of Mitochondrial Dynamics and Autophagy by the Mitochondria-Associated Membrane
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    Chapter 4 Endoplasmic Reticulum-Mitochondria Communication Through Ca2+ Signaling: The Importance of Mitochondria-Associated Membranes (MAMs)
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    Chapter 5 Ceramide Transport from the Endoplasmic Reticulum to the Trans Golgi Region at Organelle Membrane Contact Sites
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    Chapter 6 Endoplasmic Reticulum – Plasma Membrane Crosstalk Mediated by the Extended Synaptotagmins
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    Chapter 7 Endoplasmic Reticulum-Plasma Membrane Contacts Regulate Cellular Excitability
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    Chapter 8 The Lipid Droplet and the Endoplasmic Reticulum
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    Chapter 9 Role of Intra- and Inter-mitochondrial Membrane Contact Sites in Yeast Phospholipid Biogenesis
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    Chapter 10 Discovery and Roles of ER-Endolysosomal Contact Sites in Disease
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    Chapter 11 Alzheimer Disease
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    Chapter 12 Mitochondrial-Associated Membranes in Parkinson’s Disease
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    Chapter 13 Role of Endoplasmic Reticulum-Mitochondria Communication in Type 2 Diabetes
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    Chapter 14 Mitochondria–Endoplasmic Reticulum Contact Sites Mediate Innate Immune Responses
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    Chapter 15 Hepatitis C Virus Replication
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    Chapter 16 Hijacking of Membrane Contact Sites by Intracellular Bacterial Pathogens
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    Chapter 17 Alterations in Ca2+ Signalling via ER-Mitochondria Contact Site Remodelling in Cancer
Attention for Chapter 15: Hepatitis C Virus Replication
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Citations

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Chapter title
Hepatitis C Virus Replication
Chapter number 15
Book title
Organelle Contact Sites
Published in
Advances in experimental medicine and biology, January 2017
DOI 10.1007/978-981-10-4567-7_15
Pubmed ID
Book ISBNs
978-9-81-104566-0, 978-9-81-104567-7
Authors

Tetsuro Suzuki, Suzuki, Tetsuro

Abstract

Viruses use synthetic mechanism and organelles of the host cells to facilitate their replication and make new viruses. Host's ATP provides necessary energy. Hepatitis C virus (HCV) is a major cause of liver disease. Like other positive-strand RNA viruses, the HCV genome is thought to be synthesized by the replication complex, which consists of viral- and host cell-derived factors, in tight association with structurally rearranged vesicle-like cytoplasmic membranes. The virus-induced remodeling of subcellular membranes, which protect the viral RNA from nucleases in the cytoplasm, promotes efficient replication of HCV genome. The assembly of HCV particle involves interactions between viral structural and nonstructural proteins and pathways related to lipid metabolisms in a concerted fashion. Association of viral core protein, which forms the capsid, with lipid droplets appears to be a prerequisite for early steps of the assembly, which are closely linked with the viral genome replication. This review presents the recent progress in understanding the mechanisms for replication and assembly of HCV through its interactions with organelles or distinct organelle-like structures.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 101 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Gambia 1 <1%
Brazil 1 <1%
Unknown 99 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 19 19%
Student > Bachelor 17 17%
Researcher 15 15%
Student > Master 14 14%
Student > Doctoral Student 6 6%
Other 12 12%
Unknown 18 18%
Readers by discipline Count As %
Medicine and Dentistry 19 19%
Biochemistry, Genetics and Molecular Biology 17 17%
Agricultural and Biological Sciences 16 16%
Immunology and Microbiology 14 14%
Chemistry 4 4%
Other 10 10%
Unknown 21 21%