Mitochondria: From Physiology to Pathology (Record no. 2983092)

MARC details
000 -LEADER
fixed length control field 04073naaaa2200781uu 4500
001 - CONTROL NUMBER
control field https://directory.doabooks.org/handle/20.500.12854/76954
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220714163558.0
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number books978-3-0365-2152-7
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9783036521510
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9783036521527
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.3390/books978-3-0365-2152-7
Terms of availability doi
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title English
042 ## - AUTHENTICATION CODE
Authentication code dc
072 #7 - SUBJECT CATEGORY CODE
Subject category code GP
Source bicssc
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Bruni, Francesco
Relator code edt
9 (RLIN) 1577016
245 10 - TITLE STATEMENT
Title Mitochondria: From Physiology to Pathology
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc Basel, Switzerland
Name of publisher, distributor, etc MDPI - Multidisciplinary Digital Publishing Institute
Date of publication, distribution, etc 2021
300 ## - PHYSICAL DESCRIPTION
Extent 1 electronic resource (196 p.)
506 0# - RESTRICTIONS ON ACCESS NOTE
Terms governing access Open Access
Source of term star
Standardized terminology for access restriction Unrestricted online access
520 ## - SUMMARY, ETC.
Summary, etc Mitochondria play an increasingly central role in the context of cellular physiology. These organelles possess their own genome (mtDNA), which is functionally coordinated with the nuclear genome. Mitochondrial gene expression is mediated by molecular processes (replication, transcription, translation, and assembly of respiratory chain complexes) that all take place within the mitochondria. Several aspects of mtDNA expression have already been well characterized, but many more either are under debate or have yet to be discovered. Understanding the molecular processes occurring in mitochondria also has clinical relevance. Dysfunctions affecting these important metabolic 'hubs' are associated with a whole range of severe disorders, known as mitochondrial diseases. In recent years, significant progress has been made to understand the pathogenic mechanisms underlying mitochondrial dysfunction; however, to date, mitochondrial diseases are complex genetic disorders without any effective therapy. Current therapeutic strategies and clinical trials are aimed at mitigating clinical manifestations and slowing the disease progression to improve the quality of life of patients. The goal of the Special Issue 'Mitochondria: from Physiology to Pathology' published in Life (ISSN: 2075-1729) was to collect research and review articles covering the physiological and pathological aspects related to mtDNA maintenance and gene expression, mitochondrial biogenesis, protein import, organelle metabolism, and quality control.
540 ## - TERMS GOVERNING USE AND REPRODUCTION NOTE
Terms governing use and reproduction Creative Commons
-- https://creativecommons.org/licenses/by/4.0/
-- cc
-- https://creativecommons.org/licenses/by/4.0/
546 ## - LANGUAGE NOTE
Language note English
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Research & information: general
Source of heading or term bicssc
9 (RLIN) 928234
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Uncontrolled term atherosclerosis
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Uncontrolled term carotid intima-media thickness
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Uncontrolled term mitochondrial mutations
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Uncontrolled term cardiovascular risk factors
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Uncontrolled term mitochondria
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Uncontrolled term mtDNA
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Uncontrolled term cristae
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Uncontrolled term mitochondrial fission
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Uncontrolled term mitochondrial fusion
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Uncontrolled term mitochondrial diseas
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Uncontrolled term mitochondrial dynamics
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Uncontrolled term mitoenergetics
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Uncontrolled term mitosteroidogenesis
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Uncontrolled term LH
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Uncontrolled term cAMP
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Uncontrolled term Leydig cell
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Uncontrolled term mitochondrial DNA segregation
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Uncontrolled term heteroplasmy
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Uncontrolled term selective elimination
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Uncontrolled term mitophagy
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Uncontrolled term mitochondrial engineered nucleases
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Uncontrolled term kinases
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Uncontrolled term phosphorylation
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Uncontrolled term disease
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Uncontrolled term PINK1
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Uncontrolled term Parkinson's disease
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Uncontrolled term mitochondria homeostasis
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Uncontrolled term Cterm
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Uncontrolled term MELAS
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Uncontrolled term transmitochondrial cybrids
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Uncontrolled term aminoacyl-tRNA synthetases
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Uncontrolled term LARS2
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Uncontrolled term mitochondrial disease
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Uncontrolled term therapeutic peptides
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Uncontrolled term FAD synthase
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Uncontrolled term FAD1
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Uncontrolled term mitochondria localization
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Uncontrolled term Saccharomyces cerevisiae
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Uncontrolled term mRNA
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Uncontrolled term mitochondrial localization motif
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Uncontrolled term n/a
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Bruni, Francesco
Relator code oth
9 (RLIN) 1577016
856 40 - ELECTRONIC LOCATION AND ACCESS
Host name www.oapen.org
Uniform Resource Identifier <a href="https://mdpi.com/books/pdfview/book/4545">https://mdpi.com/books/pdfview/book/4545</a>
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Public note DOAB: download the publication
856 40 - ELECTRONIC LOCATION AND ACCESS
Host name www.oapen.org
Uniform Resource Identifier <a href="https://directory.doabooks.org/handle/20.500.12854/76954">https://directory.doabooks.org/handle/20.500.12854/76954</a>
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Public note DOAB: description of the publication
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