Pages that link to "Q41392247"

The following pages link to 5q-, twenty-five years later: a synopsis (Q41392247):

Displaying 45 items.

• The human GRAF gene is fused to MLL in a unique t(5;11)(q31;q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q (Q22254660) (← links)
• Deletions of PURA, at 5q31, and PURB, at 7p13, in myelodysplastic syndrome and progression to acute myelogenous leukemia (Q24291349) (← links)
• Deletion 5q31 in patients with stable, melphalan-treated multiple myeloma (Q28371600) (← links)
• Role of nucleophosmin in embryonic development and tumorigenesis (Q28591282) (← links)
• The role of lenalidomide in the management of myelodysplasia with del 5q. (Q33378398) (← links)
• Evolutionary conservation of zebrafish linkage group 14 with frequently deleted regions of human chromosome 5 in myeloid malignancies (Q34028179) (← links)
• Mutations of the Wilms tumor 1 gene (WT1) in older patients with primary cytogenetically normal acute myeloid leukemia: a Cancer and Leukemia Group B study (Q34052614) (← links)
• Insights into the biologic and molecular abnormalities in adult acute lymphocytic leukemia (Q34123842) (← links)
• Organization and expression of the SLC36 cluster of amino acid transporter genes (Q34310289) (← links)
• Rho GTPases in transformation and metastasis. (Q34554757) (← links)
• An efficient and robust statistical modeling approach to discover differentially expressed genes using genomic expression profiles (Q35033254) (← links)
• Oxidative stress and the myelodysplastic syndromes (Q35140206) (← links)
• Diagnostic application of FISH to hematological malignancies (Q35589218) (← links)
• Treatment with lenalidomide does not appear to increase the risk of progression in lower risk myelodysplastic syndromes with 5q deletion. A comparative analysis by the Groupe Francophone des Myelodysplasies (Q35717799) (← links)
• Important genes in the pathogenesis of 5q- syndrome and their connection with ribosomal stress and the innate immune system pathway (Q36417421) (← links)
• Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia (Q37140487) (← links)
• Multifaceted polo-like kinases: drug targets and antitargets for cancer therapy (Q37776652) (← links)
• Cytogenetic abnormalities in myelodysplastic syndrome: an overview (Q37888830) (← links)
• Molecular dissection of the 5q deletion in myelodysplastic syndrome (Q37937810) (← links)
• Review of therapeutic options and the management of patients with myelodysplastic syndromes (Q38095121) (← links)
• Distribution of breakpoints and fragment sizes in human chromosome 5 after heavy-ion bombardment (Q38477400) (← links)
• Characterization of psu dic(6;5)(p21.3;q13) with reverse chromosome painting in a patient with secondary myelodysplastic syndrome following treatment for multiple myeloma (Q38480900) (← links)
• Molecular cytogenetic analysis of the monoblastic cell line U937. karyotype clarification by G-banding, whole chromosome painting, microdissection and reverse painting, and comparative genomic hybridization (Q38487100) (← links)
• Fluorescence in situ hybridization confirmation of 5q deletions in patients with hematological malignancies. (Q38497622) (← links)
• A multimodal approach in the diagnosis of patients with hematopoietic disorders (Q38500953) (← links)
• Chromosome 5q deletion and epigenetic suppression of the gene encoding alpha-catenin (CTNNA1) in myeloid cell transformation (Q40198158) (← links)
• NPM1 gene deletions in myelodysplastic syndromes with 5q- and complex karyotype (Q42724172) (← links)
• Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype. (Q44117868) (← links)
• Myelodysplastic syndrome with chromosome 5 abnormalities: a nationwide survey in Japan (Q44125500) (← links)
• fgf1 is required for normal differentiation of erythrocytes in zebrafish primitive hematopoiesis (Q47073116) (← links)
• Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome (Q47981317) (← links)
• A unique clone involving multiple structural chromosome rearrangements in a myelodysplastic syndrome case (Q48360840) (← links)
• Exposure to myelotoxic agents and myelodysplasia: case-control study and correlation with clinicobiological findings (Q50860328) (← links)
• A novel 5q35.3 subtelomeric deletion syndrome. (Q52101982) (← links)
• Acute myeloid leukemia with t(5;11): two case reports. (Q54089095) (← links)
• Combined immunophenotyping and FISH identifies the involvement of B-cells in 5q- syndrome (Q63248775) (← links)
• Chronic myelomonocytic leukemia with t(7;11)(p15;p15) and NUP98/HOXA9 fusion (Q73191409) (← links)
• Coexisting myelodysplasia and myeloproliferative features in a single clone containing 5q-, Ph and i(17q) (Q73207902) (← links)
• Loss of heterozygosity on chromosome 5 in adults with acute lymphoblastic leukemia (Q73343616) (← links)
• Nodal marginal zone B-cell lymphoma with a novel t(X;5)(q28;q22): conventional and molecular cytogenetic analysis (Q73467032) (← links)
• 5q- syndrome presenting chronic myeloproliferative disorders-like manifestation: a case report (Q73801255) (← links)
• Philadelphia-positive chronic myelogenous leukemia with a 5q-- abnormality in a patient following interferon-alpha therapy (Q74095442) (← links)
• FISH investigation of 5q and 7q deletions in MDS/AML reveals hidden translocations, insertions and fragmentations of the same chromosomes (Q74789121) (← links)
• Isolation of yeast artificial chromosomes containing the entire transcriptional unit of the human FGF1 gene: a 720-kb contig spanning human chromosome 5q31.3-->q32 (Q77413294) (← links)
• Cryptic translocation t(5;11)(q35;p15.5) with involvement of the NSD1 and NUP98 genes without 5q deletion in childhood acute myeloid leukemia (Q78294890) (← links)