Clinical and biologic implications of recurrent genomic aberrations in myeloma.
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Deficient spindle assembly checkpoint in multiple myelomaPrognostic significance of copy-number alterations in multiple myelomaCriteria for diagnosis, staging, risk stratification and response assessment of multiple myelomaOverexpression of transcripts originating from the MMSET locus characterizes all t(4;14)(p16;q32)-positive multiple myeloma patientsAntibody-based targeting of FGFR3 in bladder carcinoma and t(4;14)-positive multiple myeloma in miceDrug resistance in multiple myeloma: latest findings and new concepts on molecular mechanisms.Clinical and biological significance of RAS mutations in multiple myeloma.Molecular Mechanisms of p53 Deregulation in Cancer: An Overview in Multiple MyelomaIdentification of ID-1 as a potential target gene of MMSET in multiple myelomaAdvances in understanding prognosis in myeloma.Impact of high-risk classification by FISH: an eastern cooperative oncology group (ECOG) study E4A03.Combining fluorescent in situ hybridization data with ISS staging improves risk assessment in myeloma: an International Myeloma Working Group collaborative project.Chromosome 1 amplification has similar prognostic value to del(17p13) and t(4;14)(p16;q32) in multiple myeloma patients: analysis of real-life data from the Polish Myeloma Study Group.Plasma cell leukemia.How I treat plasma cell leukemia.Identification of novel pathogenic copy number aberrations in multiple myeloma: the Malaysian contextNovel therapies in multiple myeloma for newly diagnosed nontransplant candidatesAnticancer Role of PPARgamma Agonists in Hematological Malignancies Found in the Vasculature, Marrow, and Eyes.Identification and expression of MMSA-8, and its clinical significance in multiple myeloma.Clinical implications of c-maf expression in plasma cells from patients with multiple myeloma.p53 abnormalities and potential therapeutic targeting in multiple myeloma.Expression of CD99 in Multiple Myeloma: A Clinicopathologic and Immunohistochemical Study of 170 Cases.Implications of heterogeneity in multiple myeloma.Risk of progression and survival in multiple myeloma relapsing after therapy with IMiDs and bortezomib: a multicenter international myeloma working group study.Combining information regarding chromosomal aberrations t(4;14) and del(17p13) with the International Staging System classification allows stratification of myeloma patients undergoing autologous stem cell transplantation.The t(14;20) is a poor prognostic factor in myeloma but is associated with long-term stable disease in monoclonal gammopathies of undetermined significanceLenalidomide in multiple myeloma: an evidence-based review of its role in therapy.A critical role for the NFkB pathway in multiple myeloma.Mapping of chromosome 1p deletions in myeloma identifies FAM46C at 1p12 and CDKN2C at 1p32.3 as being genes in regions associated with adverse survival.International Myeloma Working Group molecular classification of multiple myeloma: spotlight review.Correlation between array-comparative genomic hybridization-defined genomic gains and losses and survival: identification of 1p31-32 deletion as a prognostic factor in myeloma.Monoclonal gammopathy of undetermined significance and smoldering multiple myeloma: a review of the current understanding of epidemiology, biology, risk stratification, and management of myeloma precursor disease.SAMSN1 is a tumor suppressor gene in multiple myeloma.The molecular classification of multiple myelomaArsenic trioxide-mediated growth inhibition of myeloma cells is associated with an extrinsic or intrinsic signaling pathway through activation of TRAIL or TRAIL receptor 2.Predictive value of post-transplant bone marrow plasma cell percent in multiple myeloma patients undergone autologous transplantation.Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.Dilemmas in treating smoldering multiple myeloma.Prognostic value and efficacy evaluation of novel drugs for cytogenetic aberrations in multiple myeloma: a meta-analysis.Retrospective analysis of genetic abnormalities and survival in 131 patients with multiple myeloma.
P2860
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P2860
Clinical and biologic implications of recurrent genomic aberrations in myeloma.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
Clinical and biologic implications of recurrent genomic aberrations in myeloma.
@en
Clinical and biologic implications of recurrent genomic aberrations in myeloma.
@nl
type
label
Clinical and biologic implications of recurrent genomic aberrations in myeloma.
@en
Clinical and biologic implications of recurrent genomic aberrations in myeloma.
@nl
prefLabel
Clinical and biologic implications of recurrent genomic aberrations in myeloma.
@en
Clinical and biologic implications of recurrent genomic aberrations in myeloma.
@nl
P2093
P50
P1433
P1476
Clinical and biologic implications of recurrent genomic aberrations in myeloma.
@en
P2093
Brian Van Ness
David Harrington
Emily Blood
Gordon W Dewald
Kimberly J Henderson
Martin M Oken
Montserrat Rue
Philip R Greipp
Richard J Bailey
Scott A Van Wier
P304
P356
10.1182/BLOOD-2002-10-3017
P407
P577
2003-02-06T00:00:00Z