992 results on '"Seto, Masao"'
Search Results
202. Abstract 131: Biological effect of miR-210 overexpression on renal carcinoma cells
203. Nodal Relapse After Helicobacter pylori Eradication in a Patient With Primary Localized Gastric Mucosa-Associated Lymphoid Tissue Lymphoma
204. Array Comparative Genomic Hybridization Revealed Polyclonality In Acute Type Adult T-Cell Leukemia/Lymphoma and PTCL NOS
205. MicroRNA-375 Is Downregulated in Gastric Carcinomas and Regulates Cell Survival by Targeting PDK1 and 14-3-3ζ
206. Expression of the c-kit Protein in Human Solid Tumors and in Corresponding Fetal and Adult Normal Tissues
207. Metric learning for DNA microarray data analysis
208. Cytotoxic Molecule (CM)-Positive Classical Hodgkin Lymphoma: a Clinicopathologic Study in Comparison with Nodal Peripheral T-Cell Lymphoma of Not Otherwise Specified Type Possessing CM Expression.
209. Alcohol Drinking, Smoking, Past History of Gastroduodenal Ulcer, Height, and Risk of API2-MALT1 Fusion Positive and Negative Gastric MALT Lymphoma Among Japanese.
210. NK-Cell Lymphoma Shares Strikingly Similar Molecular Features with a Distinct Set of γδ T-Cell Lymphoma and Identification of Aurora Kinase A Inhibitor as a Novel Therapeutic Agent.
211. Association of Alcohol Intake and Smoking with Malignant Lymphoma Risk in Japanese: A Hospital-Based Case-Control Study at Aichi Cancer Center
212. Array Comparative Genomic Hybridization Analysis of PTCL-U Reveals a Distinct Subgroup with Genetic Alterations Similar to Lymphoma-Type Adult T-Cell Leukemia/Lymphoma
213. A Part of Acute-Type ATLL Cases Has Genomic Imbalance in Common with Lymphoma-Type ATLL
214. Molecular Signatures to Improve Diagnosis, Prognostication and Identification of Oncogenic Pathways in Peripheral T and NK Cell Lymphoma.
215. 2. Etiological Mechanism (Gene Abnormalities)
216. TNFAIP3is the target gene of chromosome band 6q23.3-q24.1 loss in ocular adnexal marginal zone B cell lymphoma
217. Gain-of-Function Mutations and Copy Number Increases of Notch2 in Diffuse Large B-Cell Lymphoma.
218. Array CGH Analysis for PTCL-U Revealed a Distinct Subgroup with Pathological and Clinical Relevance.
219. Ocular Adnexal Marginal Zone B Cell Lymphoma Has Characteristic Deletion at Chromosome Band 6q23.3-24.1 Whose Target Is TNFAIP3.
220. Genome-wide array-based comparative genomic hybridization of ocular marginal zone B cell lymphoma: Comparison with pulmonary and nodal marginal zone B cell lymphoma
221. PD6-2-2: Genomic profiling of malignant pleural mesothelioma with array-based comparative genomic hybridization
222. Chromosomal imbalances are associated with outcome ofHelicobacter pylorieradication in t(11;18)(q21;q21) negative gastric mucosa-associated lymphoid tissue lymphomas
223. Genetic abnormalities involved in t(12;21) TEL?AML1 acute lymphoblastic leukemia: Analysis by means of array-based comparative genomic hybridization
224. Downregulation of NDUFB6 due to 9p24.1-p13.3 loss is implicated in metastatic clear cell renal cell carcinoma.
225. CD10−MUM1+ follicular lymphoma lacks BCL2 gene translocation and shows characteristic biologic and clinical features
226. The Synergistic Action of the microRNA-17 Cluster with c-MYC in Aggressive Cancer Development.
227. Non-Coding RNA without ORF Is Overexpressed in Diffuse Large B-Cell Lymphoma with t(1;14)(p33;q32) Translocation.
228. Genomic Imbalances Are Associated with Outcome of Helicobacter pylori Eradication in t(11;18)(q21;q21)-Negative Gastric MALT Lymphomas.
229. Array CGH Analysis for PTCL-U Revealed Two Genetically Distinct Subgroups.
230. Expression profiling analysis of the CD5+ diffuse large B‐cell lymphoma subgroup: Development of a CD5 signature
231. Characterization of target genes at the 2p15–16 amplicon in diffuse large B‐cell lymphoma
232. Genomewide array-based comparative genomic hybridization analysis of acute promyelocytic leukemia
233. Array CGH Reveals Clonal Evolution of Adult T-Cell Leukemia/Lymphoma.
234. MALT1 contains nuclear export signals and regulates cytoplasmic localization of BCL10
235. Identification ofCCND3andBYSLas Candidate Targets for the 6p21 Amplification in Diffuse Large B-Cell Lymphoma
236. Defining Second-Hit Genetic Abnormalities Involved in the t(12; 21) TEL-AML1 Acute Lymphoblastic Leukemia by Array-Based Comparative Genomic Hybridization.
237. A microRNA Cluster as a Target of Genomic Amplification in B-Cell Lymphomas.
238. Identification of Target Gene at 2p15 Amplification in DLBCL Using Contig Array CGH.
239. Identification of Subtype-Specific Genomic Alterations of Acute and Lymphoma Types of Adult T-Cell Leukemia/Lymphoma.
240. API2-MALT1 fusion protein induces transcriptional activation of the API2 gene through NF-κB binding elements: Evidence for a positive feed-back loop pathway resulting in unremitting NF-κB activation
241. Genome‐wide array‐based comparative genomic hybridization of natural killer cell lymphoma/leukemia: Different genomic alteration patterns of aggressive NK‐cell leukemia and extranodal Nk/T‐cell lymphoma, nasal type
242. BMI-1 Is Highly Expressed in M0-Subtype Acute Myeloid Leukemia
243. Differential expression of cytokines, chemokines and their receptors in follicular lymphoma and reactive follicular hyperplasia: Assessment by complementary DNA microarray
244. Genome-wide array-based CGH for mantle cell lymphoma: identification of homozygous deletions of the proapoptotic gene BIM
245. Highly efficient delivery of p16 antitumor peptide into aggressive leukemia/lymphoma cells using a novel transporter system
246. Gastric MALT Lymphomas Are Divided Into Three Groups Based on Responsiveness to Helicobacter Pylori Eradication and Detection of API2-MALT1 Fusion
247. Methylenetetrahydrofolate reductase gene (MTHFR) polymorphisms and reduced risk of malignant lymphoma
248. Contig Array CGH at 3p14.2 Points to the FHIT Gene as the Deleted Gene in Diffuse Large B Cell Lymphoma.
249. Array CGH Analysis for Target Genes at 6p21 Amplification Region in Diffuse Large B-Cell Lymphoma.
250. Genome-Wide Array-Based CGH for Mantle Cell Lymphoma: Precise Mapping of Genomic Aberrations and Identification of Novel Candidate Genes.
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