Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2008-10-14
pubmed:abstractText
Mutations in the angiogenin gene, ANG, have been associated recently with familial and sporadic forms of amyotrophic lateral sclerosis (ALS). However, the cellular and molecular mechanisms that link ANG, a multidomain protein, to ALS are still unknown.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1538-3687
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
65
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1333-6
pubmed:dateRevised
2011-7-19
pubmed:meshHeading
pubmed-meshheading:18852347-Adult, pubmed-meshheading:18852347-Aged, pubmed-meshheading:18852347-Amyotrophic Lateral Sclerosis, pubmed-meshheading:18852347-Catalytic Domain, pubmed-meshheading:18852347-Central Nervous System, pubmed-meshheading:18852347-Cohort Studies, pubmed-meshheading:18852347-DNA Mutational Analysis, pubmed-meshheading:18852347-Female, pubmed-meshheading:18852347-France, pubmed-meshheading:18852347-Gene Frequency, pubmed-meshheading:18852347-Genetic Markers, pubmed-meshheading:18852347-Genetic Predisposition to Disease, pubmed-meshheading:18852347-Genetic Testing, pubmed-meshheading:18852347-Genotype, pubmed-meshheading:18852347-Humans, pubmed-meshheading:18852347-Male, pubmed-meshheading:18852347-Middle Aged, pubmed-meshheading:18852347-Mutation, pubmed-meshheading:18852347-Polymorphism, Single Nucleotide, pubmed-meshheading:18852347-Protein Structure, Tertiary, pubmed-meshheading:18852347-Ribonuclease, Pancreatic
pubmed:year
2008
pubmed:articleTitle
Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.
pubmed:affiliation
INSERM U930, Université François Rabelais Tours, CHRU de Tours, Faculté de Médecine, 10 boulevard Tonnellé, BP3223, 37032 Tours CEDEX, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't