Linked Life Data

21734084

Source:http://linkedlifedata.com/resource/pubmed/id/21734084

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2011-7-7
pubmed:abstractText
Mutations in the TRPC6 gene have been recently identified as the cause of late-onset autosomal-dominant focal segmental glomerulosclerosis (FSGS). To extend the screening, we analyzed TRPC6 in 33 Italian children with sporadic early-onset SRNS and three Italian families with adult-onset FSGS.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1555-905X
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
6
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1626-34
pubmed:meshHeading
pubmed-meshheading:21734084-Adolescent, pubmed-meshheading:21734084-Age of Onset, pubmed-meshheading:21734084-Amino Acid Sequence, pubmed-meshheading:21734084-Base Sequence, pubmed-meshheading:21734084-Calcium, pubmed-meshheading:21734084-Case-Control Studies, pubmed-meshheading:21734084-Child, pubmed-meshheading:21734084-Child, Preschool, pubmed-meshheading:21734084-DNA Mutational Analysis, pubmed-meshheading:21734084-Drug Resistance, pubmed-meshheading:21734084-Female, pubmed-meshheading:21734084-Fluorescent Antibody Technique, pubmed-meshheading:21734084-Genetic Predisposition to Disease, pubmed-meshheading:21734084-Glomerulosclerosis, Focal Segmental, pubmed-meshheading:21734084-HEK293 Cells, pubmed-meshheading:21734084-Humans, pubmed-meshheading:21734084-Infant, pubmed-meshheading:21734084-Italy, pubmed-meshheading:21734084-Kidney, pubmed-meshheading:21734084-Male, pubmed-meshheading:21734084-Membrane Proteins, pubmed-meshheading:21734084-Microscopy, Confocal, pubmed-meshheading:21734084-Molecular Sequence Data, pubmed-meshheading:21734084-Mutation, Missense, pubmed-meshheading:21734084-Nephrotic Syndrome, pubmed-meshheading:21734084-Pedigree, pubmed-meshheading:21734084-Phenotype, pubmed-meshheading:21734084-Polymerase Chain Reaction, pubmed-meshheading:21734084-Risk Assessment, pubmed-meshheading:21734084-Risk Factors, pubmed-meshheading:21734084-Steroids, pubmed-meshheading:21734084-TRPC Cation Channels, pubmed-meshheading:21734084-Transfection
pubmed:year
2011
pubmed:articleTitle
TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.
pubmed:affiliation
Department of Biomedical Sciences, University of Foggia, Viale Pinto, 1, 71100 Foggia, Italy. l.gesualdo@unifg.it.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't