Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2009-3-11
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1476-5551
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
23
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
610-4
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:18818701-Aged, pubmed-meshheading:18818701-Aged, 80 and over, pubmed-meshheading:18818701-Algorithms, pubmed-meshheading:18818701-Amino Acid Substitution, pubmed-meshheading:18818701-Anemia, Refractory, pubmed-meshheading:18818701-Chromosomes, Human, Pair 1, pubmed-meshheading:18818701-Humans, pubmed-meshheading:18818701-Janus Kinase 2, pubmed-meshheading:18818701-Loss of Heterozygosity, pubmed-meshheading:18818701-Middle Aged, pubmed-meshheading:18818701-Mutation, Missense, pubmed-meshheading:18818701-Phenotype, pubmed-meshheading:18818701-Phosphorylation, pubmed-meshheading:18818701-Point Mutation, pubmed-meshheading:18818701-Polymorphism, Single Nucleotide, pubmed-meshheading:18818701-Protein Processing, Post-Translational, pubmed-meshheading:18818701-Receptors, Thrombopoietin, pubmed-meshheading:18818701-STAT5 Transcription Factor, pubmed-meshheading:18818701-Thrombocytosis, pubmed-meshheading:18818701-Uniparental Disomy
pubmed:year
2009
pubmed:articleTitle
UPD1p indicates the presence of MPL W515L mutation in RARS-T, a mechanism analogous to UPD9p and JAK2 V617F mutation.
pubmed:publicationType
Letter, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural