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Daneshyari Cancer Research Journas Latest Articles

Cancer Research Research Articles

Cryptic MLL-AF10 fusion caused by insertion of duplicated 5′ part of MLL into 10p12 in acute leukemia: a case report
Fulltext Access 4 Pages 2005
A clonal dic(16;21)(p13.1;p11.2)del(16)(q11.1), with gains of several chromosomes and monosomy 21, in a case of splenic hamartoma: evidence for its neoplastic, not hamartomatous, origin
Fulltext Access 4 Pages 2005
Cytogenetic and molecular cytogenetic studies of a variant of t(21;22), ins(22;21)(q12;q21q22), with a deletion of the 3′ EWSR1 gene in a patient with Ewing sarcoma
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BCR-ABL gene amplification and overexpression in a patient with chronic myeloid leukemia treated with imatinib
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Cytogenetic characterization of Ewing tumors with high-ploidy
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Trisomy 8 as the sole cytogenetic abnormality in a case of extraskeletal mesenchymal chondrosarcoma
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The value of fluorescence in situ hybridization in the diagnosis and prognosis of chronic lymphocytic leukemia
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SKY and genetic fingerprinting reveal a cross-contamination of the putative normal colon epithelial cell line NCOL-1
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Frequent allelic imbalances at 8p and 11q22 in oral and oropharyngeal epithelial dysplastic lesions
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Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia
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Acute myelogenous leukemia with tetrasomy 8 is a disease with a poor prognosis
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Chronic lymphocytic leukemia developing in a patient with chronic myeloid leukemia: evidence of distinct lineage-associated genomic events
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Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion
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Molecular cytogenetic characteristics of the human hepatocellular carcinoma cell line HCCLM3 with high metastatic potential: comparative genomic hybridization and multiplex fluorescence in situ hybridization
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Constitutional trisomy 8 mosaicism with myelodysplastic syndrome complicated by intestinal Behcet disease and antithrombin III deficiency
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The human Penumbra gene is mapped to a region on chromosome 7 frequently deleted in myeloid malignancies
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Live cell catapulting and recultivation does not change the karyotype of HCT116 tumor cells
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Ovarian cancer is a heterogeneous disease
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Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies
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A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies
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BCR/ABL rearrangement in two cases of Philadelphia chromosome negative chronic myeloid leukemia: deletion on the derivative chromosome 9 may or not be present
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Insertion (8;11) in a renal oncocytoma with multifocal transformation to chromophobe renal cell carcinoma
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Myeloid/natural killer cell precursor acute leukemia with tetraploidy
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Deletion 6q is not a characteristic marker of nodal lymphoplasmacytic lymphoma
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Random aneuploidy in neoplastic and pre-neoplastic diseases, multiple myeloma, and monoclonal gammopathy
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Rarity of IgH translocations in Waldenström macroglobulinemia
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Le récepteur à l'EGF et les cancers des voies aérodigestives supérieures
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Déplacements de la prostate et des vésicules séminales suite à l'uréthrographie : une étude par tomographie axiale
Fulltext Access 4 Pages 2005
SUBJECT INDEX
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Selectively desulfated heparin inhibits P-selectin-mediated adhesion of human melanoma cells
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SUBJECT INDEX
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SUBJECT INDEX
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SUBJECT INDEX
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SUBJECT INDEX
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The pheomelanin precursor 5-S-cysteinyldopa protects melanocytes from membrane damage induced by ultraviolet A radiation
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SUBJECT INDEX
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SUBJECT INDEX
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Association between the stages of cervical cancer and chromosome 1 aneusomy
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Cytogenetic findings in clear cell chondrosarcoma
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Development of a dual-color fluorescence in situ hybridization probe set on chromosome 6q to improve cytogenetic diagnosis of lymphoid malignancies
Fulltext Access 4 Pages 2005
Molecular and cytogenetic characterization of a novel rearrangement involving chromosomes 9, 12, and 17 resulting in ETV6 (TEL) and ABL fusion
Fulltext Access 4 Pages 2005
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders
Fulltext Access 4 Pages 2005
A functional single nucleotide polymorphism site detected in nasopharyngeal carcinoma-associated transforming gene Tx
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Karyotyping, immunophenotyping, and apoptosis analyses on human hematopoietic precursor cells derived from umbilical cord blood following long-term ex vivo expansion
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Mutational analysis of hSNF5/INI1 and TP53 genes in choroid plexus carcinomas
Fulltext Access 4 Pages 2005
Clonality analysis of cell lineages in acute myeloid leukemia with inversion 16
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Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes
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Genomic aberrations in plasma cell leukemia shown by interphase fluorescence in situ hybridization
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Inv(1)(p22q25) in chronic myeloproliferative disease: constitutional or clonal defect?
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Chromosome 7 abnormalities in acute megakaryoblastic leukemia associated with Down syndrome
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Risk of transmission of herpesviruses through cord blood transplantation
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A proline-90 residue unique to SUMO-4 prevents maturation and sumoylation
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Dual effects of copper-zinc superoxide dismutase
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Parallel development of cardiomyocytes and neurons in embryonic stem cell culture
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Insulin and IGF-I phosphorylate eNOS in HUVECs by a caveolin-1 dependent mechanism
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Tensile testing of a single ultrafine polymeric fiber
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Progrès thérapeutiques récents dans le mésothéliome malin primitif de la plèvre
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Cylindromes thoraciques
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SUBJECT INDEX
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Malignant neuroblastic tumors in adolescents
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Diversity in neuroblastomas and discrimination of the risk to progress
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Deletions of the 3′ BCR and 5′ ABL regions in patients with Philadelphia-positive chronic myeloid leukemia: a one-step process occurring in about 10% of the cases without any evidence of genetic instability in the target cells
Fulltext Access 4 Pages 2005
An intronic variant in the TP53 gene in a Brazilian woman with breast cancer
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Altered expression of neuronal nitric oxide synthase in the duodenum longitudinal muscle-myenteric plexus of obesity induced diabetes mouse: Implications on enteric neurodegeneration
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Regulatory T cells
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T-cell alloreactivity in hematopoietic stem cell transplantation
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Introduction to graft-versus-host disease
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Detection of Microchimerism by Minor Histocompatibility Antigen HA-1 Allele-Specific Nested Polymerase Chain Reaction
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The Evolution of the Evidence-Based Review: Evaluating the Science Enhances the Art of Medicine-Statement of the Steering Committee for Evidence-Based Reviews of the American Society for Blood and Marrow Transplantation
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Disclosure of competing financial interests and role of sponsors in phase III cancer trials
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Erosion of the principal investigator role in a climate of industry dominance
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Safety of gold in stapes surgery
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Protein layer coating method on metal surface by electrochemical process through genetical introduced tag
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Erratum to 'Locally delivered nanoencapsulated tyrphostin (AGL-2043) reduces neointima formation in balloon-injured rat carotid and stented porcine coronary arteries' [Biomaterials 26 (2005) 451-461]
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Biological fabrication of nacreous coating on titanium dental implant
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Transfer of nitric oxide from nitrovasodilators to free thiols-Evidence of two distinct stages
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NF-κB dependent cytokine levels in saliva of patients with oral preneoplastic lesions and oral squamous cell carcinoma
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Elevated levels of soluble interleukin-2 receptor in serum of patients with hematological or non-hematological malignancies
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ASPP-Apoptotic specific regulator of p53
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Allelic variation in the serotonin transporter (5HTT) gene contributes to idiopathic pulmonary hypertension in children
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Stereo-specificity for pro-(R) hydrogen of NAD(P)H during enzyme-catalyzed hydride transfer to CL-20
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Inhibition by adiponectin of IL-8 production by human macrophages upon coculturing with late apoptotic cells
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Unique complex between bacterial azurin and tumor-suppressor protein p53
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Urocortin: A cardiac protective peptide?
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Cystathionine β-synthase is enriched in the brains of Down's patients
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Structure of Thermus thermophilus type 2 isopentenyl diphosphate isomerase inferred from crystallography and molecular dynamics
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Direct measurement of the rupture force of single pair of decorin interactions
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Glimepiride activates eNOS with a mechanism Akt but not caveolin-1 dependent
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The effect of purmorphamine on osteoblast phenotype expression of human bone marrow mesenchymal cells cultured on titanium
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Development of efficient expression system for protein display on bacterial magnetic particles
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Deferoxamine photosensitizes cancer cells in vitro
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Isolated mouse liver mitochondria are devoid of glucokinase
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MicroRNA: Fine-tunes the function of genes in zebrafish
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Phosphorylation of cytochromes P450: First discovery of a posttranslational modification of a drug-metabolizing enzyme
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Molecular genetics of tyrosine 3-monooxygenase and inherited diseases
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Role of molecular oxygen in the bioluminescence of the firefly squid, Watasenia scintillans
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Aβ-polyacrolein aggregates: Novel mechanism of plastic formation in senile plaques
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Divergent effects of zinc depletion in brain vs non-brain endothelial cells
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Study of the peptide length and amino acid specific substitution in the antigenic activity of the chimeric synthetic peptides, containing the p19 core and gp46 envelope proteins of the HTLV-I virus
Fulltext Access 4 Pages 2005
Effect of serum on the down-regulation of CHOP-10 during differentiation of 3T3-L1 preadipocytes
Fulltext Access 4 Pages 2005
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