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3. Quantification of escape from X chromosome inactivation with single-cell omics data reveals heterogeneity across cell types and tissues

7. DOCK2 is involved in the host genetics and biology of severe COVID-19

8. The whole blood transcriptional regulation landscape in 465 COVID-19 infected samples from Japan COVID-19 Task Force

9. Common progenitor origin for Rosai–Dorfman disease and clear cell sarcoma.

10. Application of targeted nanopore sequencing for the screening and determination of structural variants in patients with Lynch syndrome

11. Generation of a p16 Reporter Mouse and Its Use to Characterize and Target p16high Cells In Vivo

14. KMT2C expression and DNA homologous recombination repair factors in lung cancers with a high-grade fetal adenocarcinoma component

15. Clinical and prognostic features of Langerhans cell histiocytosis in adults

17. A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

18. Combined burden and functional impact tests for cancer driver discovery using DriverPower

19. Integrative pathway enrichment analysis of multivariate omics data

20. Pathway and network analysis of more than 2500 whole cancer genomes

21. Divergent mutational processes distinguish hypoxic and normoxic tumours

22. Genomic footprints of activated telomere maintenance mechanisms in cancer

23. Case report: Common clonal origin of concurrent langerhans cell histiocytosis and acute myeloid leukemia

24. Genetic analysis of low-grade adenosquamous carcinoma of the breast that progressed to high-grade metaplastic carcinoma

27. Role of the Orphan Transporter SLC35E1 in the Nuclear Egress of Herpes Simplex Virus 1

28. Repeated Lineage Switches in an Elderly Case of Refractory B-Cell Acute Lymphoblastic Leukemia With MLL Gene Amplification: A Case Report and Literature Review

29. Anti-inflammatory effects of ruxolitinib on chronic neutrophilic leukemia harboring CSF3R-T618I mutation with bilateral renal abscesses

30. DOCK2 is involved in the host genetics and biology of severe COVID-19

31. Japan COVID-19 Task Force: a nation-wide consortium to elucidate host genetics of COVID-19 pandemic in Japan

32. Comprehensive molecular analysis of genomic profiles and PD-L1 expression in lung adenocarcinoma with a high-grade fetal adenocarcinoma component

33. Pan-cancer analysis of whole genomes

34. Senolysis by glutaminolysis inhibition ameliorates various age-associated disorders

35. Annotations of Recurrent Structural Variant Events in Pan-cancer Whole Genome Data for Precision Medicine

36. Successful Clinical Sequencing by Molecular Tumor Board in an Elderly Patient With Refractory Sézary Syndrome

38. Association of single nucleotide polymorphisms in the NRF2 promoter with vascular stiffness with aging

39. Variant analysis of prostate cancer in Japanese patients and a new attempt to predict related biological pathways

41. An Unusually Short Latent Period of Therapy-Related Myeloid Neoplasm Harboring a Rare MLL-EP300 Rearrangement: Case Report and Literature Review

42. Genomic Analysis of Therapy-Related Myeloid Neoplasms and Tracking of the Founder Clone By Circulating Tumor DNA

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

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

45. DOCK2is involved in the host genetics and biology of severe COVID-19

46. Artificial Intelligence Guided Precision Medicine Approach to Hematological Disease

47. Prognostic Impact of Circulating Tumor DNA Status Post-Allogeneic Hematopoietic Stem Cell Transplantation in Acute Myeloid Leukemia and Myelodysplastic Syndrome

48. Cell-lineage level–targeted sequencing to identify acute myeloid leukemia with myelodysplasia-related changes

50. Different clonal dynamics of chronic myeloid leukaemia between bone marrow and the central nervous system

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