about
ACTN1 mutations cause congenital macrothrombocytopeniaIntegrated molecular analysis of clear-cell renal cell carcinoma.Inherited and Somatic Defects in DDX41 in Myeloid NeoplasmsIntegrated Multiregional Analysis Proposing a New Model of Colorectal Cancer EvolutionFrequent pathway mutations of splicing machinery in myelodysplasiaLoss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing dataGenomon ITDetector: a tool for somatic internal tandem duplication detection from cancer genome sequencing data.Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia.Common Variable Immunodeficiency Caused by FANC Mutations.Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantationFrequent somatic mutations in epigenetic regulators in newly diagnosed chronic myeloid leukemia.Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria.Detection of the G17V RHOA mutation in angioimmunoblastic T-cell lymphoma and related lymphomas using quantitative allele-specific PCR.Acquired initiating mutations in early hematopoietic cells of CLL patients.PRPF8 defects cause missplicing in myeloid malignancies.Autologous Induced Stem-Cell-Derived Retinal Cells for Macular Degeneration.Clonal evolution in myelodysplastic syndromesRecurrent mutations in multiple components of the cohesin complex in myeloid neoplasms.Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia.Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma.Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic Leukemia.Identification of cell-type-specific mutations in nodal T-cell lymphomas.Profiling of somatic mutations in acute myeloid leukemia with FLT3-ITD at diagnosis and relapse.Genomic landscape of liposarcoma.Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents.Somatic SETBP1 mutations in myeloid malignanciesComprehensive mutational analysis of primary and relapse acute promyelocytic leukemia.BRCC3 mutations in myeloid neoplasms.Landscape of genetic lesions in 944 patients with myelodysplastic syndromes.Variegated RHOA mutations in adult T-cell leukemia/lymphoma.Recurrent genetic defects on chromosome 5q in myeloid neoplasms.Deep sequencing in cancer research.Splicing factor mutations and cancer.Acute megakaryoblastic leukemia with acquired trisomy 21 and GATA1 mutations in phenotypically normal children.Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients.Aberrant PD-L1 expression through 3'-UTR disruption in multiple cancers.Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma.Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms.
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Kenichi Yoshida
@ast
Kenichi Yoshida
@en
Kenichi Yoshida
@es
Kenichi Yoshida
@nl
Kenichi Yoshida
@sl
كينيتشي يوشيدا
@ar
type
label
Kenichi Yoshida
@ast
Kenichi Yoshida
@en
Kenichi Yoshida
@es
Kenichi Yoshida
@nl
Kenichi Yoshida
@sl
كينيتشي يوشيدا
@ar
prefLabel
Kenichi Yoshida
@ast
Kenichi Yoshida
@en
Kenichi Yoshida
@es
Kenichi Yoshida
@nl
Kenichi Yoshida
@sl
كينيتشي يوشيدا
@ar
P106
P31
P496
0000-0003-4612-2778