Linked Life Data

10064019

Source:http://linkedlifedata.com/resource/pubmed/id/10064019

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1999-6-4
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0340-6245
pubmed:author
pubmed:issnType
Print
pubmed:volume
81
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
322-3
pubmed:dateRevised
2005-11-17
pubmed:meshHeading
pubmed-meshheading:10064019-Adult, pubmed-meshheading:10064019-Amino Acid Substitution, pubmed-meshheading:10064019-Biological Transport, pubmed-meshheading:10064019-Blood Coagulation Disorders, pubmed-meshheading:10064019-Carrier Proteins, pubmed-meshheading:10064019-Cell Membrane, pubmed-meshheading:10064019-DNA, Complementary, pubmed-meshheading:10064019-DNA Mutational Analysis, pubmed-meshheading:10064019-Female, pubmed-meshheading:10064019-Gene Expression, pubmed-meshheading:10064019-Gene Frequency, pubmed-meshheading:10064019-Genes, Recessive, pubmed-meshheading:10064019-Genotype, pubmed-meshheading:10064019-Humans, pubmed-meshheading:10064019-Male, pubmed-meshheading:10064019-Membrane Lipids, pubmed-meshheading:10064019-Membrane Proteins, pubmed-meshheading:10064019-Mutation, Missense, pubmed-meshheading:10064019-Phosphatidylserines, pubmed-meshheading:10064019-Phospholipid Transfer Proteins, pubmed-meshheading:10064019-Point Mutation, pubmed-meshheading:10064019-Polymerase Chain Reaction, pubmed-meshheading:10064019-RNA, Messenger, pubmed-meshheading:10064019-Syndrome
pubmed:year
1999
pubmed:articleTitle
Assessment of the expression of candidate human plasma membrane phospholipid scramblase in Scott syndrome cells.
pubmed:publicationType
Letter, Case Reports