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18818701
Source:
http://linkedlifedata.com/resource/pubmed/id/18818701
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60
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0026882
,
umls-concept:C0150312
,
umls-concept:C0441712
,
umls-concept:C0812295
,
umls-concept:C1334291
,
umls-concept:C2826330
pubmed:issue
3
pubmed:dateCreated
2009-3-11
pubmed:grant
http://linkedlifedata.com/resource/pubmed/grant/K24 HL077522
,
http://linkedlifedata.com/resource/pubmed/grant/R01 HL082983
,
http://linkedlifedata.com/resource/pubmed/grant/U54 RR019391
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/8704895
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/JAK2 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Janus Kinase 2
,
http://linkedlifedata.com/resource/pubmed/chemical/MPL protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Thrombopoietin
,
http://linkedlifedata.com/resource/pubmed/chemical/STAT5 Transcription Factor
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1476-5551
pubmed:author
pubmed-author:GondekL PLP
,
pubmed-author:LowP SPS
,
pubmed-author:MaciejewskiJ PJP
,
pubmed-author:MohanS RSR
,
pubmed-author:SzpurkaHH
,
pubmed-author:TheilK SKS
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