Linked Life Data

14720311

Source:http://linkedlifedata.com/resource/pubmed/id/14720311

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2004-1-14
pubmed:abstractText
Mitochondrial encephalomyopathies are clinically and genetically heterogeneous because mitochondria are the products of 2 genomes: mitochondrial DNA (mtDNA) and nuclear DNA (nDNA). Among the mendelian-inherited mitochondrial diseases are defects of intergenomic communication, disorders due to nDNA mutations that cause depletion and multiple deletions of mtDNA.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1074-7931
pubmed:author
pubmed:issnType
Print
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
8-17
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:14720311-Adolescent, pubmed-meshheading:14720311-Adult, pubmed-meshheading:14720311-Aldehyde-Lyases, pubmed-meshheading:14720311-Brain, pubmed-meshheading:14720311-Cachexia, pubmed-meshheading:14720311-Child, pubmed-meshheading:14720311-Child, Preschool, pubmed-meshheading:14720311-Co-Repressor Proteins, pubmed-meshheading:14720311-DNA, Mitochondrial, pubmed-meshheading:14720311-DNA Mutational Analysis, pubmed-meshheading:14720311-Dementia, pubmed-meshheading:14720311-Deoxyuridine, pubmed-meshheading:14720311-Female, pubmed-meshheading:14720311-Gastrointestinal Motility, pubmed-meshheading:14720311-Humans, pubmed-meshheading:14720311-Infant, pubmed-meshheading:14720311-Magnetic Resonance Imaging, pubmed-meshheading:14720311-Male, pubmed-meshheading:14720311-Middle Aged, pubmed-meshheading:14720311-Mitochondrial Diseases, pubmed-meshheading:14720311-Mitochondrial Encephalomyopathies, pubmed-meshheading:14720311-Point Mutation, pubmed-meshheading:14720311-Repressor Proteins, pubmed-meshheading:14720311-Thymidine Phosphorylase
pubmed:year
2004
pubmed:articleTitle
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes.
pubmed:affiliation
Department of Neurology, Columbia University College of Physicians & Surgeons, New York, NY, USA. mh29@columbia.edu
pubmed:publicationType
Journal Article, Review