425 results on '"Ohki, Kentaro"'
Search Results
52. A Hyperactive RelA/p65-Hexokinase 2 Signaling Axis Drives Primary Central Nervous System Lymphoma
53. On Recursive Quantum State Smoothing
54. Liver disease is frequently observed in Down syndrome patients with transient abnormal myelopoiesis
55. High PRDM16 expression identifies a prognostic subgroup of pediatric acute myeloid leukaemia correlated to FLT3-ITD, KMT2A-PTD, and NUP98-NSD1: the results of the Japanese Paediatric Leukaemia/Lymphoma Study Group AML-05 trial
56. Threshold theorem in isolated quantum dynamics with stochastic control errors.
57. A proposal of adaptive parameter tuning for robust stabilizing control of N–level quantum angular momentum systems
58. CSF3R and CALR mutations in paediatric myeloid disorders and the association of CSF3R mutations with translocations, including t(8; 21)
59. Treatment of pediatric lymphoma in Japan: Current status and plans for the future
60. phase III clinical trial evaluating efficacy and safety of minimal residual disease-based risk stratification for children with acute myeloid leukemia, incorporating a randomized study of gemtuzumab ozogamicin in combination with post-induction chemotherapy for non-low-risk patients (JPLSG-AML-20)
61. WT1 mutation in pediatric patients with acute myeloid leukemia: a report from the Japanese Childhood AML Cooperative Study Group
62. Genetic features of B‐cell lymphoblastic lymphoma withTCF3‐PBX1
63. Integrated Analysis of KIT Exon 17 Mutations and Flow-MRD Refines Risk Stratification in Pediatric Acute Myeloid Leukemia with RUNX1:: RUNX1T1
64. Acute myeloid leukaemia with myelodysplastic features in children: a report of Japanese Paediatric Leukaemia/Lymphoma Study Group
65. Langerhans cell histiocytosis with multifocal bone lesions: comparative clinical features between single and multi-systems
66. Genome-wide approach to identify second gene targets for malignant rhabdoid tumors using high-density oligonucleotide microarrays
67. Mutations of the GATA2 and CEBPA genes in paediatric acute myeloid leukaemia
68. SETBP1 mutations in juvenile myelomonocytic leukaemia and myelodysplastic syndrome but not in paediatric acute myeloid leukaemia
69. Clinical characteristics and outcomes of B-cell precursor ALL with MEF2Drearrangements: a retrospective study by the Ponte di Legno Childhood ALL Working Group
70. Droplet digital polymerase chain reaction assay for the detection of the minor clone of KIT D816V in paediatric acute myeloid leukaemia especially showing RUNX1‐RUNX1T1 transcripts
71. Genetic features of B‐cell lymphoblastic lymphoma with TCF3‐PBX1.
72. Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia
73. On a New Low-Rank Kalman-Bucy Filter and its Convergence Property
74. Mutational analyses of the ATP6V1B1 and ATP6V0A4 genes in patients with primary distal renal tubular acidosis
75. Aberrations of NEGR1 on 1p31 and MYEOV on 11q13 in neuroblastoma
76. A Hyperactive RelA/p65-Hexokinase 2 Signaling Axis Drives Primary Central Nervous System Lymphoma
77. ATRT-11. PREVALENCE OF GERMLINE VARIANTS IN SMARCB1 INCLUDING SOMATIC MOSAICISM IN AT/RT AND OTHER RHABDOID TUMORS
78. NUTM1-Rearranged Infant and Pediatric B Cell Precursor Acute Lymphoblastic Leukemia: A Good Prognostic Subtype Identified in a Collaborative International Study
79. High prevalence of SMARCB1 constitutional abnormalities including mosaicism in malignant rhabdoid tumors
80. B-Cell Precursor–Acute Lymphoblastic Leukemia With EBF1-PDGFRB Fusion Treated With Hematopoietic Stem Cell Transplantation and Imatinib: A Case Report and Literature Review
81. An invitation to quantum filtering and smoothing theory based on two inner products (Building Foundations for Quantum Statistical Modeling)
82. RUNX1 mutations in pediatric acute myeloid leukemia are associated with distinct genetic features and an inferior prognosis
83. Characteristics of genetic alterations of peripheral T‐cell lymphoma in childhood including identification of novel fusion genes: the Japan Children's Cancer Group (JCCG).
84. The Effect of Interim FDG-PET-guided Response-Adapted Therapy in Pediatric Patients with Hodgkin's Lymphoma (HL-14) : Protocol for a Phase II Study
85. DNA methylation-based classification reveals difference between pediatric T-cell acute lymphoblastic leukemia and normal thymocytes
86. Clinical Features of Pediatric Acute Myeloid Leukemia with TP53 and CDKN2A/2B copy Number Alterations
87. Acute Lymphoblastic Leukemia with Zinc-Finger Protein 384 (ZNF384)-Related Rearrangements: A Retrospective Analysis from the Ponte Di Legno Childhood ALL Working Group
88. Recurrent Gene Mutations in Pediatric Patients with AML By Targeted Sequencing ―the Jccg Study, JPLSG AML-05―
89. Significant Features of DNA Methylation at Bivalent Promotor and Repressed Polycomb Regions in Pediatric AML-the Jccg Study, JPLSG AML-05-
90. Patients aged less than 3 years with acute myeloid leukaemia characterize a molecularly and clinically distinct subgroup
91. Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndrome
92. Quantum smoother for open quantum systems driven by quantum jump-diffusion processes
93. A study of minimax LEQG control with constant-constrained Renyi divergence
94. Very late relapse cases of TCF3‐ZNF384 ‐positive acute lymphoblastic leukemia
95. Preface to Special Issue on The 5th Multi-symposium on Control Systems
96. Frequency of Common Copy-Number Variations at 15q11.2q13 in Sperm of Healthy Men
97. NUDT15variants confer high incidence of second malignancies in children with acute lymphoblastic leukemia
98. Impact of immunophenotypic characteristics on genetic subgrouping in childhood acute lymphoblastic leukemia: Tokyo Children's Cancer Study Group (TCCSG) study L04‐16.
99. Patients aged less than 3 years with acute myeloid leukaemia characterize a molecularly and clinically distinct subgroup.
100. Comprehensive Analysis of 343 Genes Using Targeted Sequencing Panel By Next-Generation Sequencer in 77 Pediatric AML Patients with Normal and Complex Karyotypes: Jccg Study, JPLSG AML-05
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