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Daneshyari Molecular Biology Journas Latest Articles

Molecular Biology Research Articles

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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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
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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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Chromosome 7 abnormalities in acute megakaryoblastic leukemia associated with Down syndrome
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Cryptic MLL-AF10 fusion caused by insertion of duplicated 5′ part of MLL into 10p12 in acute leukemia: a case report
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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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Association between the stages of cervical cancer and chromosome 1 aneusomy
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Asymmetric expression of Syndecan-2 in early chick embryogenesis
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Amino acid cotransporter SLC3A2 is selectively expressed in the early proximal segment of Xenopus pronephric kidney nephrons
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Keyword Index
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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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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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Development of a dual-color fluorescence in situ hybridization probe set on chromosome 6q to improve cytogenetic diagnosis of lymphoid malignancies
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Molecular and cytogenetic characterization of a novel rearrangement involving chromosomes 9, 12, and 17 resulting in ETV6 (TEL) and ABL fusion
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Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders
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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
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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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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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Genotoxic and cytotoxic effects in the bone marrow of rats exposed to a low dose of paraquat via the dermal route
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Germline mutations of the MYH gene in Japanese patients with multiple colorectal adenomas
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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
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An intronic variant in the TP53 gene in a Brazilian woman with breast cancer
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Risk of transmission of herpesviruses through cord blood transplantation
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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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Mutation research, genetic toxicology and environmental mutagenesis
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Pengawetan Spermatozoa Menggunakan Metode Pengeringbekuan
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Efek Antiinflamasi Beberapa Tumbuhan Umbelliferae
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In Vitro Fertilization and Embryo Development of Vitrified Ovine Oocytes Stressed in Sucrose
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Kloning DNA Genom Pengapit Transposon dari Mutan Nonpatogenik Xanthomonas axonopodis pv. glycines M715
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In Vitro Development of Ovine Embryos Following Maturation Under Limited CO2
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Bioakumulasi Logam Berat oleh Beberapa Galur Bradyrhizobium japonicum
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Musa sebagai Model Genom
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Ekspresi Gen GFDD4-1 pada Physcomitrella patens dan Gen Homolog pada Arabidopsis thaliana dalam Respons terhadap Cekaman Abiotik
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Subject Index
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Erratum to “High-throughput quantification of phosphatidylcholine and sphingomyelin by electrospray ionization tandem mass spectrometry coupled with isotope corrections algorithm” [Biochimica et Biophysics Acta, 1686 (2004) 108-117]
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Direct evidence in vivo of impaired macrophage-specific reverse cholesterol transport in ATP-binding cassette transporter A1-deficient mice
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Phosphorylation of cytochromes P450: First discovery of a posttranslational modification of a drug-metabolizing enzyme
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Cytogenetic findings in clear cell chondrosarcoma
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Effect of the pancreatic digestion with liberase versus collagenase on the yield, function and viability of neonatal rat pancreatic islets
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Effects of short-term fasting on energy reserves of vampire bats (Desmodus rotundus)
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Noncovalent interaction of MNSFbeta, a ubiquitin-like protein, with histone 2A
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Contents of Volume 142
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Young Scientist Award Session
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E3 Teaching Technology Posters
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P8 Leaf Metabolism and Development
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P5 Protein-Protein Interactions
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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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Exercise might favor reverse cholesterol transport and lipoprotein clearance: Potential mechanism for its anti-atherosclerotic effects
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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
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Effect of serum on the down-regulation of CHOP-10 during differentiation of 3T3-L1 preadipocytes
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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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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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