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「"Miyano S "[Author]」の検索結果

540件中 1件~20件表示    検索結果をPubMedで見る PubMedで見る

Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndrome.

Divergent lncRNA MYMLR regulates MYC by eliciting DNA looping and promoter-enhancer interaction.

Classification of patients with cold sensation by a review of systems database: A single-centre observational study.

Prediction of deficiency-excess pattern in Japanese Kampo medicine: Multi-centre data collection.

Appendiceal Perforation due to Migration of a Dental Instrument.

Genomic analysis of pancreatic juice DNA assesses malignant risk of intraductal papillary mucinous neoplasm of pancreas.

Massively parallel sequencing of tenosynovial giant cell tumors reveals novel CSF1 fusion transcripts and novel somatic CBL mutations.

Genome analysis of myelodysplastic syndromes among atomic bomb survivors in Nagasaki.

Molecular heterogeneity in peripheral T-cell lymphoma, not otherwise specified revealed by comprehensive genetic profiling.

Development of an MSI-positive colon tumor with aberrant DNA methylation in a PPAP patient.

The first case of elderly TCF3-HLF-positive B-cell acute lymphoblastic leukemia.

ALPHLARD-NT: Bayesian Method for Human Leukocyte Antigen Genotyping and Mutation Calling through Simultaneous Analysis of Normal and Tumor Whole-Genome Sequence Data.

Prognostic impact of circulating tumor DNA status post-allogeneic hematopoietic stem cell transplantation in AML and MDS.

A Bayesian model integration for mutation calling through data partitioning.

Seroprevalence of mumps before the introduction of mumps-containing vaccine in Lao PDR: results from a nationwide cross-sectional population-based survey.

Duplication of F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma.

Sensitivity analysis of agent-based simulation utilizing massively parallel computation and interactive data visualization.

Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients.

Frequent germline mutations of in sporadic subcutaneous panniculitis-like T-cell lymphoma.

Comprehensive analysis of genetic aberrations linked to tumorigenesis in regenerative nodules of liver cirrhosis.

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