Calreticulin gene exon 9 frameshift mutations in patients with thrombocytosis.
about
Distinct clinical characteristics of myeloproliferative neoplasms with calreticulin mutations.High resolution melting analysis: a rapid and accurate method to detect CALR mutations.Stathmin 1 inhibition amplifies ruxolitinib-induced apoptosis in JAK2V617F cellsScreening PCR Versus Sanger Sequencing: Detection of CALR Mutations in Patients With ThrombocytosisCoexisting JAK2V617F and CALR Exon 9 Mutation in Essential ThrombocythemiaClinical Manifestation of Calreticulin Gene Mutations in Essential Thrombocythemia without Janus Kinase 2 and MPL Mutations: A Chinese Cohort Clinical Study.Coexistence of JAK2 and CALR mutations and their clinical implications in patients with essential thrombocythemia.Calreticulin gene mutations in myeloproliferative neoplasms without Janus kinase 2 mutations.Calreticulin mutations in myeloproliferative neoplasms and new methodology for their detection and monitoring.Calreticulin mutations in myeloproliferative neoplasms.Clinical validation of a multipurpose assay for detection and genotyping of CALR mutations in myeloproliferative neoplasms.Clinical relevance between CALR mutation and myeloproliferative neoplasms.JAK2, MPL, and CALR mutations in Chinese Han patients with essential thrombocythemia.Effect of conditioning regimens on graft failure in myelofibrosis: a retrospective analysis.Somatic mutations of calreticulin in a Brazilian cohort of patients with myeloproliferative neoplasms.Frequent CALR exon 9 alterations in JAK2 V617F-mutated essential thrombocythemia detected by high-resolution melting analysis.JAK2, CALR, and MPL mutation spectrum in Japanese patients with myeloproliferative neoplasms.CALR mutations in myeloproliferative neoplasms: hidden behind the reticulum.A rapid, highly accurate method for quantifying CALR mutant allele burden in persons with myeloproliferative neoplasms.Validation of a molecular diagnostic assay for CALR exon 9 indels in myeloproliferative neoplasms: identification of coexisting JAK2 and CALR mutations and a novel 9 bp deletion in CALR.EAGLE: Explicit Alternative Genome Likelihood Evaluator.Differential association of calreticulin type 1 and type 2 mutations with myelofibrosis and essential thrombocytemia: relevance for disease evolution
P2860
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P2860
Calreticulin gene exon 9 frameshift mutations in patients with thrombocytosis.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Calreticulin gene exon 9 frameshift mutations in patients with thrombocytosis.
@en
Calreticulin gene exon 9 frameshift mutations in patients with thrombocytosis.
@nl
type
label
Calreticulin gene exon 9 frameshift mutations in patients with thrombocytosis.
@en
Calreticulin gene exon 9 frameshift mutations in patients with thrombocytosis.
@nl
prefLabel
Calreticulin gene exon 9 frameshift mutations in patients with thrombocytosis.
@en
Calreticulin gene exon 9 frameshift mutations in patients with thrombocytosis.
@nl
P2093
P2860
P50
P356
P1433
P1476
Calreticulin gene exon 9 frameshift mutations in patients with thrombocytosis
@en
P2093
A Mitsidou
C Pierides
C Prokopiou
F Melanthiou
K A Nicolaou
K Barbouti
M Manoloukos
P2860
P2888
P304
P356
10.1038/LEU.2013.382
P577
2013-12-24T00:00:00Z
P5875
P6179
1023157935