About: Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome

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About: Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 1995

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1995 (uk) im Januar 1995 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 1995 (ast) artikull shkencor i botuar më 01 janar 1995 (sq) scientific article published on 01 January 1995 (en)
publication date	wds:Q71925303-9C50F053-FB92-48B6-9BF9-E1CD7B0367CF
publication date	1995-01-01 00:00:00Z (xsd:dateTime)
exact match	wds:Q71925303-D703CD97-9C6E-4A7B-AA17-DF73B49E2BBA
exact match	https://scigraph.springernature.com/pub.10.1007/bf00711367
cites work	wds:Q71925303-0A9283D7-46C3-4FDC-AE04-A3DEAD8880B4 wds:Q71925303-239EA6A5-E8E6-4AAC-8167-CDAF347D3D89 wds:Q71925303-2CA7967C-10DB-4779-ACB7-0F94E2CADEB5 wds:Q71925303-2D1F566E-1919-444B-81DB-457E971A3AE8 wds:Q71925303-37A8A496-76CF-46A1-935F-7381DE0AE91F wds:Q71925303-3C33ED7D-1DCD-4B26-81C2-AB0AC762A934 wds:Q71925303-3F92C806-8794-453E-AE74-312A310E59C8 wds:Q71925303-67525A41-005E-4057-A5B3-B9B99F9556E0 wds:Q71925303-747DF584-D3EB-4FDA-823F-0D0095153B86 wds:Q71925303-7782391A-387D-4A10-A49E-43BE443FA0BE wds:Q71925303-79499E84-4657-4527-AD80-9B630E12169A wds:Q71925303-798AB315-1E54-44CF-8882-D507C6DD8295 wds:Q71925303-810DD7D0-46D7-41C0-B1CB-DA655DD60E77 wds:Q71925303-85E06298-4A0C-417B-AD4C-44A980FF28FB wds:Q71925303-891DBF04-F234-43BC-84C4-F88ECCABC71D wds:Q71925303-8B17ABBF-EFEA-46AA-952A-0FE9ED835312 wds:Q71925303-A2FE0A6E-425D-46FE-8759-CFCD9E8269FB wds:Q71925303-A9124E1A-308C-4F14-B148-32F42C8A6341 wds:Q71925303-B1B1C8E0-2886-4626-B8DD-843CB9A93F60 wds:Q71925303-B35BA015-F3EA-44EE-B15F-EE948070BF76 wds:Q71925303-B3DFC4D0-DBB3-402C-A68D-4E1049B9FB12 wds:Q71925303-BB987C83-EEF8-49CC-A387-D2F9904ED7D8 wds:Q71925303-CA23F83D-73F6-4BBD-8AC0-619D3261F005 wds:Q71925303-EAA16E8D-7DD1-4133-860F-46B41006B51E
cites work	A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Replication and Transcription of Vertebrate Mitochondrial DNA Genomic sequencing mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases Sequence and organization of the human mitochondrial genome Changes in volume densities and distribution of mitochondria in rat skeletal muscle after chronic hypoxia Structure and variation of human ribosomal DNA: molecular analysis of cloned fragments Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion. Fatal infantile liver failure associated with mitochondrial DNA depletion Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease. Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy. The maturation of the inner membrane of foetal rat liver mitochondria Duplications of mitochondrial DNA in mitochondrial myopathy Defects of the mitochondrial respiratory chain complexes in three pediatric cases with hypotonia and cardiac involvement Deoxyribonucleic acid synthesis in the heart mitochondria after acute and exhaustive exercise Cytochrome c in Normal and Hypertrophied Heart Quantification of specific mRNA by flatbed scintillation counting of dual-labeled dot blots Report of the committee on human mitochondrial DNA. Congenital myotonic dystrophy: fiber type abnormalities in two cases Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: A new approach to the study of mitochondrial myopathies Muscle mitochondrial density after exhaustive exercise in dogs: prolonged restricted activity and retraining.
author name string	wds:Q71925303-1B5C28EB-83EE-43CD-ADCC-602F0B1D6B29 wds:Q71925303-3BA99F0F-EB34-4CC6-9016-180AA5475E65 wds:Q71925303-4B700C71-1AA2-45E4-A0C3-B98CD23DA930 wds:Q71925303-91802E90-3EA9-4D48-B210-8B9832FC3EA3 wds:Q71925303-9BF7DD34-D630-46E7-8F44-09AEAF7CD0BE wds:Q71925303-A8C369FE-C8D0-47D6-A5F9-461680FB1115 wds:Q71925303-F3E47260-D021-48B7-950F-EB581CE248A4
author name string	C Sewry G Brown F A Wijburg D Chretien K J Morten C G Potter T Bougeron
rdfs:label	Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (en) Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (nl) Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (sq)
skos:prefLabel	Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (en) Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (nl) Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (sq)
name	Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (en) Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (nl) Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (sq)
author	wds:Q71925303-D709437E-4FD1-4A1B-8AB5-0639D112B02A
author	Joanna Poulton
title	wds:Q71925303-08573C5F-1E07-4804-AB9E-2D3E1B2589A1
title	Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome (en)
page(s)	wds:Q71925303-141ACB09-CE06-47EE-96E4-6BAF28CB2830
page(s)	4-20
instance of	wds:Q71925303-4ABF756D-C2D9-4B3B-A01C-CE32D4F152CC
instance of	scholarly article
main subject	wds:Q71925303-0510D7EB-C209-4D6F-B9A6-B841DAD8F2D8
main subject	mitochondrial myopathy
PubMed ID	wds:Q71925303-67D8A003-878F-4250-A107-F6457FCAD242
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7623440
PubMed ID	7623440
published in	wds:Q71925303-07C4563D-639A-4AD1-A3AC-922C6A2364F2
published in	Journal of Inherited Metabolic Disease
issue	wds:Q71925303-BE6BCE59-84FB-46A2-8601-CFFEBDD061BD
volume	wds:Q71925303-6DADE05E-2F4F-4250-A5C7-3A2571B1CA78
issue	1

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