Kenichi Yoshida

Kenichi Yoshida, G. Iguchi, Yutaka Takahashi, 2018, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Two Cases of Atezolizumab-Induced Hypophysitis

Kenichi Yoshida, G. Iguchi, Yutaka Takahashi, 2017, Journal of the Endocrine Society.

IGF-I induces senescence of hepatic stellate cells and limits fibrosis in a p53-dependent manner

Kenichi Yoshida, G. Iguchi, Yutaka Takahashi, 2016, Scientific Reports.

FBXL 16 is a novel E 2 F 1-regulated gene commonly upregulated in p 16 INK 4 Aand p 14 ARF-silenced HeLa cells

Kenichi Yoshida, Moe Tategu, Kazuyuki Sato, 2022 .

Hypoxic adaptation of leukemic cells infiltrating the CNS affords a therapeutic strategy targeting VEGFA.

S. Miyano, Y. Shiraishi, S. Ogawa, 2017, Blood.

Hypoxic adaptation of leukemic cells infiltrating the CNS affords a therapeutic strategy targeting VEGF Running Title: Hypoxic adaptation of leukemic cells in the CNS Authors and affiliations

Umeda, S. Miyano, Y. Shiraishi, 2017 .

Thymidine phosphorylase inhibits the expression of proapoptotic protein BNIP3.

Kenichi Yoshida, T. Furukawa, S. Akiyama, 2008, Biochemical and Biophysical Research Communications - BBRC.

TERT promoter mutations and chromosome 8p loss are characteristic of nonalcoholic fatty liver disease‐related hepatocellular carcinoma

S. Miyano, Y. Shiraishi, K. Chiba, 2016, International journal of cancer.

A prospective naturalistic multicentre study of intravenous medications in behavioural emergencies: Haloperidol versus flunitrazepam

Kenichi Yoshida, C. Usui, K. Hatta, 2010, Psychiatry Research.

Aprospectivenaturalisticmulticentrestudyofintravenousmedicationsinbehavioural emergencies: Haloperidol versus flunitrazepam☆

Kenichi Yoshida, C. Usui, K. Hatta, 2010 .

Current Awareness and Status of Transthoracic Echocardiography in Kumamoto Prefecture　― A Report of the Kumamoto Cardiovascular Echocardiography Standardization Project ―

Kenichi Yoshida, E. Yamamoto, K. Tsujita, 2020, Circulation Reports.

The destruction box of human Geminin is critical for proliferation and tumor growth in human colon cancer cells

Anindya Dutta, Kenichi Yoshida, I. Inoue, 2004, Oncogene.

The landscape of genetic aberrations in myxofibrosarcoma

L. Bullinger, S. Miyano, Y. Shiraishi, 2022, International journal of cancer.

Integrated Molecular Characterization of the Lethal Pediatric Cancer Pancreatoblastoma.

S. Miyano, T. Shimamura, Y. Shiraishi, 2018, Cancer research.

Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma Biallelic DICER1 mutations in sporadic PPB

S. Miyano, T. Shimamura, Y. Shiraishi, 2014 .

Gene expression levels of human shelterin complex and shelterin-associated factors regulated by the topoisomerase II inhibitors doxorubicin and etoposide in human cultured cells

Kenichi Yoshida, Masahiro Kato, M. Nakayama, 2013, Tumor Biology.

The influence of type 2 diabetes on serum GH and IGF-I levels in hospitalized Japanese patients.

Kenichi Yoshida, G. Iguchi, Yutaka Takahashi, 2016, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Identification of FAZF as a novel BMP2‐induced transcription factor during osteoblastic differentiation

Kenichi Yoshida, I. Inoue, R. Ikeda, 2007, Journal of cellular biochemistry.

Genetic and clinical characteristics of Japanese patients with sporadic somatotropinoma.

S. Yamada, Kenichi Yoshida, G. Iguchi, 2016, Endocrine journal.

The small heat shock protein alphaB-crystallin inhibits differentiation-induced caspase 3 activation and myogenic differentiation.

Kenichi Yoshida, T. Furukawa, S. Akiyama, 2006, Biological & pharmaceutical bulletin.

Oxidative stress augments pulmonary hypertension in chronically hypoxic mice overexpressing the oxidized LDL receptor.

Hong Wang, Kenichi Yoshida, Sayoko Ogura, 2013, American journal of physiology. Heart and circulatory physiology.

Novel DDX41 variants in Thai patients with myeloid neoplasms

S. Ogawa, Kenichi Yoshida, H. Makishima, 2019, International Journal of Hematology.

ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1‐RUNX1T1 and associated with a better prognosis

S. Miyano, Y. Shiraishi, K. Chiba, 2017, Genes, chromosomes & cancer.

Molecular and Functional Diversities of Cadherin and Protocadherin

T. Crow, D. Leckband, U. Wolfrum, 2010 .

Proof of Evidence: PPAR-induced ANGPTL4 in Lipid and Glucose Metabolism

Kenichi Yoshida, 2007 .

Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond–Blackfan anemia

S. Miyano, S. Ogawa, Kenichi Yoshida, 2020, Bone Marrow Transplantation.

Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria.

Satoru Miyano, Yuichi Shiraishi, Seishi Ogawa, 2014, The Journal of clinical investigation.

Detection of WIPI1 mRNA as an indicator of autophagosome formation

Kenichi Yoshida, S. Tsuyuki, Yusuke Kusama, 2014, Autophagy.

Delphinidin Induces Autolysosome as well as Autophagosome Formation and Delphinidin‐Induced Autophagy Exerts a Cell Protective Role

Kenichi Yoshida, S. Tsuyuki, Satoshi Akune, 2012, Journal of biochemical and molecular toxicology.

Isolated adrenocorticotropic hormone deficiency as a form of paraneoplastic syndrome

Kenichi Yoshida, G. Iguchi, Yutaka Takahashi, 2018, Pituitary.

Expression and tissue distribution of human X-linked armadillo repeat containing-6.

Kenichi Yoshida, Moe Tategu, Yusuke Kusama, 2010, Experimental and therapeutic medicine.

Accelerated Telomere Shortening in Acromegaly; IGF-I Induces Telomere Shortening and Cellular Senescence

S. Yamada, Kenichi Yoshida, G. Iguchi, 2015, PloS one.

Multi-omics analysis defines highly refractory RAS burdened immature subgroup of infant acute lymphoblastic leukemia

Nicola K. Wilson, H. Aburatani, B. Göttgens, 2022, Nature Communications.

Different Mutant Splicing Factors Cause Distinct Missplicing Events and Give Rise to Different Clinical Phenotypes in Myelodysplastic Syndromes

M. Cazzola, S. Miyano, Y. Shiraishi, 2015 .

Comprehensive Analysis of Aberrant RNA Splicing in Myelodysplastic Syndromes

M. Cazzola, S. Miyano, Y. Shiraishi, 2014 .

Poor Myocardial Compaction in a Patient with Recessive MYL2 Myopathy.

S. Ogawa, Kenichi Yoshida, R. Inuzuka, 2021, International heart journal.

Different In Vitro-Generated MUTZ-3-Derived Dendritic Cell Types Secrete Dexosomes with Distinct Phenotypes and Antigen Presentation Potencies

Kenichi Yoshida, Y. Ishigaki, S. Shimodaira, 2022, International journal of molecular sciences.

LYMPHOID NEOPLASIA Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma

A. Rosenwald, M. Ziepert, A. López-Guillermo, 2016 .

Adverse prognostic effect of homozygous TET2 mutation on the relapse risk of acute myeloid leukemia in patients of normal karyotype

M. Minden, S. Ogawa, Namshin Kim, 2015, Haematologica.

In Analogy to AML, MDS Can be Sub-Classified By Ancestral Mutations

S. Miyano, T. LaFramboise, Y. Shiraishi, 2014 .

Impact of Somatic Mutations on Outcome in Patients with MDS after Stem-Cell Transplantation

S. Miyano, Y. Shiraishi, K. Chiba, 2015 .

Somatic Mutations in Schinzel-Giedion Syndrome Gene SETBP1 Determine Progression in Myeloid Malignancies

S. Miyano, Y. Shiraishi, K. Chiba, 2012 .

Clinical and genetic characteristics of congenital sideroblastic anemia: comparison with myelodysplastic syndrome with ring sideroblast (MDS-RS)

S. Ogawa, Kenichi Yoshida, E. Ito, 2012, Annals of Hematology.

Acute megakaryoblastic leukemia with acquired trisomy 21 and GATA1 mutations in phenotypically normal children

Kenichi Yoshida, T. Toki, E. Ito, 2015, European Journal of Pediatrics.

S. Miyano, Y. Shiraishi, K. Chiba, 2018, Haematologica.

Bullous exudative retinal detachment due to infiltration of leukemic cells in a child with acute lymphoblastic leukemia

Tatsuo Yamaguchi, Kenichi Yoshida, I. Kato, 2010, International journal of hematology.

Hyperosmotic stress up-regulates the expression of major vault protein in SW620 human colon cancer cells.

Kenichi Yoshida, T. Furukawa, S. Akiyama, 2008, Experimental cell research.

The Detection of Immunity against WT1 and SMAD4P130L of EpCAM+ Cancer Cells in Malignant Pleural Effusion

Kenichi Yoshida, H. Sugiyama, Y. Niida, 2022, International journal of molecular sciences.

Multiple Salivary Cortisol Measurements Are a Useful Tool to Optimize Metyrapone Treatment in Patients with Cushing’s Syndromes Treatment: Case Presentations

Kenichi Yoshida, G. Iguchi, Yutaka Takahashi, 2018, Front. Endocrinol..

Identification of a homozygous JAK3 V674A mutation caused by acquired uniparental disomy in a relapsed early T-cell precursor ALL patient

S. Miyano, Y. Shiraishi, K. Chiba, 2015, International Journal of Hematology.

Successful treatment of hepatosplenic T-cell lymphoma with fludarabine, high-dose cytarabine and subsequent unrelated umbilical cord blood transplantation

S. Ogawa, M. Takagi, Kenichi Yoshida, 2021, International Journal of Hematology.

Kenichi Yoshida, G. Iguchi, Yutaka Takahashi, 2019, Pituitary.

Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations

S. Miyano, S. Ogawa, Y. Okuno, 2020, Human genome variation.

Gene Expression Changes During the Chondrogenic Differentiation of Human Mesenchymal Stem Cells

Kenichi Yoshida, I. Inoue, R. Ikeda, 2007 .

Identification of the ultrahigh-risk subgroup in neuroblastoma cases through DNA methylation analysis and its treatment exploiting cancer metabolism

H. Aburatani, S. Miyano, Hiromichi Suzuki, 2022, Oncogene.

Identification of epigallocatechin-3-gallate in green tea polyphenols as a potent inducer of p53-dependent apoptosis in the human lung cancer cell line A549.

Kenichi Yoshida, K. Sasaki, R. Yamauchi, 2009, Toxicology in vitro : an international journal published in association with BIBRA.

Patients with pheochromocytoma exhibit low aldosterone renin ratio-preliminary reports

Kenichi Yoshida, G. Iguchi, Yutaka Takahashi, 2020, BMC Endocrine Disorders.

Cell‐cycle‐dependent regulation of the human and mouse Tome‐1 promoters

Kenichi Yoshida, 2005, FEBS letters.

RUNX1 mutations in pediatric acute myeloid leukemia are associated with distinct genetic features and an inferior prognosis.

S. Miyano, Y. Shiraishi, S. Ogawa, 2018, Blood.

Gene regulatory network of unfolded protein response genes in endoplasmic reticulum stress

Kenichi Yoshida, Sayuri Takayanagi, Riga Fukuda, 2012, Cell stress & chaperones (Print).

SRSF2 is Mutated in 47.2% (77/163) of Chronic Myelomonocytic Leukemia (CMML) and Prognostically Favorable in Cases with Concomitant RUNX1 mutations

S. Ogawa, A. Kohlmann, T. Haferlach, 2011 .

Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency.

S. Ogawa, K. Matsuo, Kenichi Yoshida, 2021, Blood.

Mutational Spectrum Analysis of Interesting Correlation and Interrelationship Between RNA Splicing Pathway and Commonly Targeted Genes in Myelodysplastic Syndrome

S. Miyano, Y. Shiraishi, S. Ogawa, 2011 .

Recurrent Mutations of Multiple Components of Cohesin Complex in Myeloid Neoplasms

S. Ishikawa, H. Aburatani, K. Shirahige, 2012 .

Genetic Predispositions to Myeloid Neoplasms Caused By Germline DDX41 Mutations

Y. Kamatani, S. Miyano, T. Naoe, 2015 .

Olanzapine orally disintegrating tablet vs. risperidone oral solution in the treatment of acutely agitated psychotic patients.

Kenichi Yoshida, C. Usui, K. Hatta, 2008, General Hospital Psychiatry.

The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotype

S. Ogawa, K. Matsuo, Y. Okuno, 2016, British journal of haematology.

Molecular Defects In BRCC3 Complex, a Novel Pathogenic Pathway In MDS

S. Miyano, Y. Shiraishi, K. Chiba, 2013 .

Whole Exome Sequencing to Predict Response to Hypomethylating Agents in MDS

S. Miyano, Y. Shiraishi, K. Chiba, 2012 .

Integrated molecular analysis of adult T cell leukemia/lymphoma

H. Aburatani, O. Nureki, T. Kawaguchi, 2015, Nature Genetics.

TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups

P. Campbell, M. Cazzola, D. Neuberg, 2019, Leukemia.

A diagnostic pitfall in IgG4-related hypophysitis: infiltration of IgG4-positive cells in the pituitary of granulomatosis with polyangiitis

Kenichi Yoshida, G. Iguchi, Yutaka Takahashi, 2015, Pituitary.

Identification of Two New DBA Genes, RPS27 and RPL27, by Whole-Exome Sequencing in Diamond-Blackfan Anemia Patients

S. Miyano, Y. Shiraishi, K. Chiba, 2012 .

Transcription of the Geminin gene is regulated by a negative-feedback loop

J. Voncken, Kenichi Yoshida, M. Ohtsubo, 2014, Molecular biology of the cell.

Hematopoietic lineage distribution and evolutionary dynamics of clonal hematopoiesis

B. Dörken, C. Schmitt, L. Bullinger, 2018, Leukemia.

Acute loss of transcription factor E2F1 induces mitochondrial biogenesis in Hela cells

Kenichi Yoshida, D. Kang, R. Hayashi, 2006, Journal of cellular physiology.

Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia

S. Miyano, Y. Shiraishi, K. Chiba, 2013, Nature Genetics.

Somatic SETBP1 mutations in myeloid malignancies

S. Miyano, Y. Shiraishi, K. Chiba, 2013, Nature Genetics.

Clinical Heterogeneity of Acquired Idiopathic Isolated Adrenocorticotropic Hormone Deficiency

Kenichi Yoshida, K. Iida, G. Iguchi, 2021, Frontiers in Endocrinology.

Autologous Induced Stem‐Cell–Derived Retinal Cells for Macular Degeneration: Brief Report

Takashi Daimon, Shinya Yamanaka, Shigeki Tanishima, 2017, The New England journal of medicine.

Profiling of somatic mutations in acute myeloid leukemia with FLT3-ITD at diagnosis and relapse.

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Blood.

Germline loss-of-function SAMD9 and SAMD9L alterations in adult myelodysplastic syndromes.

F. Solé, T. LaFramboise, S. Ogawa, 2018, Blood.

Gain-of-function IKBKB mutation causes human combined immune deficiency

T. Andrews, S. Miyano, M. Field, 2018, The Journal of experimental medicine.

Somatic RHOA mutation in angioimmunoblastic T cell lymphoma

O. Nureki, S. Miyano, Y. Shiraishi, 2014, Nature Genetics.

Comprehensive analysis of expression pattern and promoter regulation of human autophagy-related genes

Kenichi Yoshida, N. Kimura, Kazuyuki Sato, 2009, Apoptosis.

Frequent structural variations involving programmed death ligands in Epstein-Barr virus-associated lymphomas

P. Gaulard, S. Miyano, Y. Shiraishi, 2019, Leukemia.

KLF1 mutation E325K induces cell cycle arrest in erythroid cells differentiated from congenital dyserythropoietic anemia patient-specific induced pluripotent stem cells.

S. Ogawa, Y. Okuno, Kenichi Yoshida, 2019, Experimental hematology.

Title Splicing factor mutations and cancer

S. Ogawa, Kenichi Yoshida, 2018 .

Splicing factor mutations and cancer

S. Ogawa, Kenichi Yoshida, 2014, Wiley interdisciplinary reviews. RNA.

Tracing the development of acute myeloid leukemia in CBL syndrome.

K. Döhner, S. Miyano, Y. Shiraishi, 2014, Blood.

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

K. Kinoshita, S. Miyano, Y. Shiraishi, 2019, Haematologica.

SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML).

S. Ogawa, A. Kohlmann, T. Haferlach, 2012, Blood.

NOTCH1 pathway activating mutations and clonal evolution in pediatric T‐cell acute lymphoblastic leukemia

S. Miyano, Y. Shiraishi, S. Ogawa, 2019, Cancer science.

Molecular classification and diagnostics of upper urinary tract urothelial carcinoma.

H. Aburatani, A. Lenis, H. Kume, 2021, Cancer cell.

Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms.

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Cancer cell.

Genomic landscape of liposarcoma

Christoph, O. Myklebost, S. Miyano, 2015, Oncotarget.

Whole‐exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia

S. Miyano, Y. Shiraishi, K. Chiba, 2016, British journal of haematology.

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

T. Miyazaki, S. Miyano, Y. Shiraishi, 2019, Leukemia.

Recurrent SPI1 (PU.1) fusions in high-risk pediatric T cell acute lymphoblastic leukemia

S. Miyano, T. Shimamura, Y. Shiraishi, 2017, Nature Genetics.

MicroRNA as a Modulator of Cell Proliferation and Senescence: Role in Lung Cancer Cells

Kenichi Yoshida, K. Miyata, M. Sekiguchi, 2013 .

Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution

Satoru Miyano, Yuichi Shiraishi, Teppei Shimamura, 2016, PLoS genetics.

Two Aldehyde Clearance Systems Are Essential to Prevent Lethal Formaldehyde Accumulation in Mice and Humans

Nicola K. Wilson, B. Göttgens, N. Wilson, 2020, Molecular cell.

Frequent Genetic Alterations in Immune Checkpoint-Related Genes in Intravascular Large B-Cell Lymphoma.

S. Miyano, Y. Shiraishi, K. Chiba, 2020, Blood.

Genetic and transcriptional landscape of plasma cells in POEMS syndrome

O. Ohara, S. Miyano, Y. Shiraishi, 2019, Leukemia.

Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic Leukemia

S. Miyano, Y. Shiraishi, S. Ogawa, 2015, PloS one.

Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma.

S. Miyano, T. Shimamura, Y. Shiraishi, 2014, Cancer research.

Clonal evidence for the development of neuroblastoma with extensive copy‐neutral loss of heterozygosity arising in a mature teratoma

S. Ogawa, J. Takita, Kenichi Yoshida, 2021, Cancer science.

Association of high-risk neuroblastoma classification based on expression profiles with differentiation and metabolism

S. Miyano, Hiromichi Suzuki, S. Ogawa, 2021, PloS one.

Dysregulation of Epstein-Barr Virus Infection in Hypomorphic ZAP70 Mutation

S. Miyano, Y. Shiraishi, K. Chiba, 2018, The Journal of infectious diseases.

Loss of DNA Damage Response in Neuroblastoma and Utility of a PARP Inhibitor

S. Miyano, S. Ogawa, Y. Hayashi, 2017, Journal of the National Cancer Institute.

Ring sideroblasts in AML are associated with adverse risk characteristics and have a distinct gene expression pattern.

E. van den Berg, Y. Shiraishi, S. Ogawa, 2019, Blood advances.

Recurrent somatic mutations underlie corticotropin-independent Cushing’s syndrome

O. Nureki, H. Kume, Y. Homma, 2014, Science.

Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation

S. Ogawa, Y. Shiozawa, Kenichi Yoshida, 2018, Genes, chromosomes & cancer.

Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients.

S. Miyano, Y. Shiraishi, K. Chiba, 2013, Blood.

Unbiased Detection of Driver Mutations in Extramammary Paget Disease

S. Miyano, Y. Shiraishi, K. Chiba, 2020, Clinical Cancer Research.

Quality Verification with a Cluster−Controlled Manufacturing System to Generate Monocyte−Derived Dendritic Cells

Kenichi Yoshida, Y. Ishigaki, Yuka Nakamura, 2021, Vaccines.

S. Tsunoda, S. Miyano, K. Mimori, 2019, Nature.

Genetic and clinical landscape of breast cancers with germline BRCA1/2 variants

S. Miyano, Y. Shiraishi, K. Chiba, 2020, Communications Biology.

Genetic and clinical landscape of breast cancers with germline BRCA1/2 variants

S. Miyano, Y. Shiraishi, K. Chiba, 2020, Communications biology.

Deep sequencing in cancer research.

S. Ogawa, Kenichi Yoshida, M. Sanada, 2013, Japanese journal of clinical oncology.

Physiological Srsf2 P95H expression causes impaired hematopoietic stem cell functions and aberrant RNA splicing in mice.

S. Ogawa, H. Nakauchi, Y. Shiozawa, 2018, Blood.

Acromegaly caused by a somatotroph adenoma in patient with neurofibromatosis type 1.

Kenichi Yoshida, K. Kosaki, G. Iguchi, 2019, Endocrine journal.

Integrated multiomics analysis of hepatoblastoma unravels its heterogeneity and provides novel druggable targets

S. Miyano, T. Shimamura, Y. Shiraishi, 2020, npj Precision Oncology.

The E‐Id Protein Axis Specifies Adaptive Lymphoid Cell Identity and Suppresses Thymic Innate Lymphoid Cell Development

S. Ogawa, Yin C Lin, C. Murre, 2017, Immunity.

Differential expression of individual transcript variants of PD-1 and PD-L2 genes on Th-1/Th-2 status is guaranteed for prognosis prediction in PCNSL

S. Ogawa, Kenichi Yoshida, Y. Iwadate, 2019, Scientific Reports.

Conditional expression of MCM7 increases tumor growth without altering DNA replication activity

Kenichi Yoshida, I. Inoue, 2003, FEBS letters.

Role of Donor Clonal Hematopoiesis in Allogeneic Hematopoietic Stem-Cell Transplantation.

L. Bullinger, M. Heuser, F. Thol, 2019, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia.

S. Miyano, B. Dumitriu, Y. Shiraishi, 2015, The New England journal of medicine.

Genomic landscape and clonal evolution of acute myeloid leukemia with t(8;21): an international study on 331 patients.

L. Bullinger, M. Heuser, F. Thol, 2019, Blood.

BRCC3 mutations in myeloid neoplasms

H. Aburatani, S. Miyano, Y. Shiraishi, 2015, Haematologica.

Description of longitudinal tumor evolution in a case of multiply relapsed clear cell sarcoma of the kidney

S. Miyano, Y. Shiraishi, S. Ogawa, 2021, Cancer reports.

Integrated molecular profiling of juvenile myelomonocytic leukemia.

H. Aburatani, S. Miyano, Y. Shiraishi, 2018, Blood.

Elucidation of gene function based on the animal genomics

Kenichi Yoshida, K. Maruyama, 2005 .

Landscape of driver mutations and their clinical impacts in pediatric B-cell precursor acute lymphoblastic leukemia.

S. Miyano, Y. Shiraishi, K. Chiba, 2020, Blood advances.

Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia

S. Miyano, M. Heuser, F. Thol, 2022, Blood cancer discovery.

Recent Advances in MicroRNA Expression Profiling towards a Molecular Anatomy of Tumorigenesis and Applications for Diagnosis, Prognosis, and Therapeutics

Kenichi Yoshida, H. Ohdaira, Hiroaki Ohdaira, 2011 .

A subset of microRNAs potentially acts as a convergent hub for upstream transcription factors in cancer cells.

Kenichi Yoshida, H. Ohdaira, T. Sasaki, 2010, Oncology reports.

Molecular pathogenesis of disease progression in MLL-rearranged AML

S. Miyano, Y. Shiraishi, S. Ogawa, 2018, Leukemia.

Prognostic relevance of integrated genetic profiling in adult T-cell leukemia/lymphoma.

O. Nureki, S. Miyano, T. Shibata, 2015, Blood.

The landscape of somatic mutations in Down syndrome–related myeloid disorders

S. Miyano, Y. Shiraishi, K. Chiba, 2013, Nature Genetics.

Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantation.

S. Miyano, Y. Shiraishi, K. Chiba, 2017, Blood.

Impact of genetic alterations in stem-cell transplantation for myelodysplasia and secondary acute myeloid leukemia Short title: Genetic alterations in myelodysplasia with HCT

S. Miyano, Y. Shiraishi, K. Chiba, 2017 .

Defective Epstein–Barr virus in chronic active infection and haematological malignancy

Masahiro Yoshida, S. Miyano, M. Seto, 2019, Nature Microbiology.

Characterization of estrogen-induced F-box protein FBXO45.

Kenichi Yoshida, 2005, Oncology reports.

Studies on the Mechanisms of Pollen Embryogenesis (III) : Mitotic Responses of the Pollen to Varied Sucrose Concentrations and the Process of Embryoid Formation in Tobacco Anther Culture

Kenichi Yoshida, S. Misoo, M. Matsubayashi, 1979 .

Replication from oriP of Epstein-Barr Virus Requires Human ORC and Is Inhibited by Geminin

Anindya Dutta, Kenichi Yoshida, J. Wohlschlegel, 2001, Cell.

PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus

S. Miyano, Y. Shiraishi, K. Chiba, 2016, International Journal of Hematology.

Fusion partner-specific mutation profiles and KRAS mutations as adverse prognostic factors in MLL-rearranged AML.

S. Miyano, Y. Shiraishi, K. Chiba, 2020, Blood advances.

Paraneoplastic hypereosinophilic syndrome associated with IL3‐IgH positive acute lymphoblastic leukemia

S. Miyano, Y. Shiraishi, K. Chiba, 2018, Pediatric blood & cancer.

Frequent germline mutations of HAVCR2 in sporadic subcutaneous panniculitis-like T-cell lymphoma.

S. Miyano, Y. Shiraishi, K. Chiba, 2019, Blood advances.

Genomic analysis of clonal origin of Langerhans cell histiocytosis following acute lymphoblastic leukaemia

S. Miyano, Y. Shiraishi, K. Chiba, 2016, British journal of haematology.

DNA methylation-based classification reveals difference between pediatric T-cell acute lymphoblastic leukemia and normal thymocytes

S. Miyano, Y. Shiraishi, Hiromichi Suzuki, 2019, Leukemia.

De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome.

N. Kenmochi, S. Miyano, Y. Shiraishi, 2018, American journal of human genetics.

Geminin organizes the molecular platform to balance cellular proliferation and differentiation.

Kenichi Yoshida, 2007, Frontiers in bioscience : a journal and virtual library.

Peptide binding to Geminin and inhibitory for DNA replication.

Kenichi Yoshida, I. Inoue, 2004, Biochemical and biophysical research communications.

Clinical utility of target capture‐based panel sequencing in hematological malignancies: A multicenter feasibility study

K. Karube, Y. Shiraishi, S. Ogawa, 2020, Cancer science.

Genomon ITDetector: a tool for somatic internal tandem duplication detection from cancer genome sequencing data

Satoru Miyano, Yuichi Shiraishi, Kenichi Chiba, 2015, Bioinform..

Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome.

P. Campbell, P. Vyas, E. Papaemmanuil, 2019, Cancer cell.

Loss of function mutations in RPL27 and RPS27 identified by whole‐exome sequencing in Diamond‐Blackfan anaemia

N. Kenmochi, S. Miyano, Y. Shiraishi, 2015, British journal of haematology.

Biallelic DICER 1 mutations in sporadic PPB 2 Financial support

S. Miyano, T. Shimamura, Y. Shiraishi, 2014 .

Molecular and Cellular Pathobiology Biallelic DICER 1 Mutations in Sporadic Pleuropulmonary Blastoma

S. Miyano, T. Shimamura, Y. Shiraishi, 2014 .

Revised version 2 ) Biallelic DICER 1 mutations in sporadic pleuropulmonary blastoma Running title Biallelic DICER 1 mutations in sporadic PPB

S. Miyano, T. Shimamura, Y. Shiraishi, 2014 .

A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India

S. Ogawa, Y. Okuno, Kenichi Yoshida, 2019, Human mutation.

Afoundervariant in theSouthAsianpopulation leads toahigh prevalence of FANCL Fanconi anemia cases in India

S. Ogawa, Y. Okuno, Kenichi Yoshida, 2019 .

Variegated RHOA mutations in adult T-cell leukemia/lymphoma.

O. Nureki, S. Miyano, Y. Totoki, 2016, Blood.

PRPF8 Defects Cause Missplicing in Myeloid Malignancies

Seishi Ogawa, Bartlomiej Przychodzen, Amina Kurtovic-Kozaric, 2014, Leukemia.

Novel neuroblastoma amplified sequence (NBAS) mutations in a Japanese boy with fever-triggered recurrent acute liver failure

S. Miyano, Y. Shiraishi, K. Chiba, 2019, Human Genome Variation.

GATA2 and secondary mutations in familial myelodysplastic syndromes and pediatric myeloid malignancies

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Haematologica.

The ex vivo production of ammonia predicts l-asparaginase biological activity in children with acute lymphoblastic leukemia

Kenichi Yoshida, A. Manabe, A. Ohara, 2009, International journal of hematology.

Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia

S. Ogawa, K. Matsuo, Y. Okuno, 2018, Annals of Hematology.

Erratum: Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome (Cancer Cell (2019) 36(2) (123–138.e10), (S1535610819302983), (10.1016/j.ccell.2019.06.007))

P. Campbell, P. Vyas, E. Papaemmanuil, 2019 .

Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome.

P. Campbell, P. Vyas, E. Papaemmanuil, 2019, Cancer cell.

Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome

S. Miyano, Y. Shiraishi, S. Ogawa, 2020, Pediatric blood & cancer.

Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia

S. Miyano, S. Ogawa, Kenichi Yoshida, 2022, EJHaem.

BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders.

D. Birnbaum, S. Miyano, Y. Shiraishi, 2013, Blood.

Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Journal of Clinical Immunology.

A novel thymoma-associated autoimmune disease: Anti-PIT-1 antibody syndrome

Kenichi Yoshida, G. Iguchi, Yutaka Takahashi, 2017, Scientific Reports.

Frequent mutations that converge on the NFKBIZ pathway in ulcerative colitis

H. Ikeuchi, S. Hirota, S. Miyano, 2019, Nature.

Genomic analysis of multiple myeloma using targeted capture sequencing in the Japanese cohort

S. Miyano, Y. Shiraishi, K. Chiba, 2020, British journal of haematology.

Autonomous feedback loop of RUNX1-p53-CBFB in acute myeloid leukemia cells

S. Ogawa, H. Sugiyama, Kenichi Yoshida, 2017, Scientific Reports.

Single-cell analysis based dissection of clonality in myelofibrosis

L. Bullinger, Y. Shiraishi, S. Ogawa, 2019, Nature Communications.

Systems Biology-Based Identification of Crosstalk between E2F Transcription Factors and the Fanconi Anemia Pathway

Kenichi Yoshida, T. Arauchi, Hiroki Nakagawa, 2007, Gene Regulation and Systems Biology.

Single-cell analysis based dissection of clonality in myelofibrosis

L. Bullinger, Y. Shiraishi, S. Ogawa, 2019, Nature Communications.

Defective Epstein–Barr virus in chronic active infection and haematological malignancy

Masahiro Yoshida, S. Miyano, M. Seto, 2019, Nature Microbiology.

Clonal selection in xenografted TAM recapitulates the evolutionary process of myeloid leukemia in Down syndrome.

S. Miyano, Y. Shiraishi, S. Ogawa, 2013, Blood.

Publisher Correction: Defective Epstein–Barr virus in chronic active infection and haematological malignancy

Masahiro Yoshida, S. Miyano, M. Seto, 2019, Nature Microbiology.

BCL6 locus is hypermethylated in angioimmunoblastic T-cell lymphoma

S. Ogawa, Kenichi Yoshida, K. Izutsu, 2017, International Journal of Hematology.

Lineage tracing of human development through somatic mutations

P. Campbell, L. Moore, A. Cvejic, 2021, Nature.

Molecular studies reveal MLL-MLLT10/AF10 and ARID5B-MLL gene fusions displaced in a case of infantile acute lymphoblastic leukemia with complex karyotype

S. Miyano, Y. Shiraishi, K. Chiba, 2017, Oncology letters.

Early detection and evolution of preleukemic clones in therapy-related myeloid neoplasms following autologous SCT.

S. Miyano, E. van den Berg, Y. Shiraishi, 2018, Blood.

Correction: Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution

H. Aburatani, S. Yachida, Yutaka Suzuki, 2017, PLoS genetics.

Integration of hepatitis B virus DNA into the myeloid/lymphoid or mixed‐lineage leukemia (MLL4) gene and rearrangements of MLL4 in human hepatocellular carcinoma

Takehide Asano, Yoshiki Murakami, Ituro Inoue, 2008, Human mutation.

Transcriptional regulation of human chromatin assembly factor ASF1.

Kenichi Yoshida, R. Hayashi, Yuya Goto, 2007, DNA and cell biology.

Dendritic Cells Pre-Pulsed with Wilms’ Tumor 1 in Optimized Culture for Cancer Vaccination

Kenichi Yoshida, H. Sugiyama, S. Shimodaira, 2020, Pharmaceutics.

ANRIL is implicated in the regulation of nucleus and potential transcriptional target of E2F1.

Kenichi Yoshida, I. Inoue, A. Tajima, 2010, Oncology reports.

Abstract 3294: Clonal evolution and integral analysis of hepatoblastoma

S. Miyano, S. Ogawa, Y. Hayashi, 2015 .

Germline DDX41 mutations define a unique subtype of myeloid neoplasms.

Y. Kamatani, M. Cazzola, S. Miyano, 2022, Blood.

The quality of life in acromegalic patients with biochemical remission by surgery alone is superior to that in those with pharmaceutical therapy without radiotherapy, using the newly developed Japanese version of the AcroQoL

Kenichi Yoshida, G. Iguchi, Yutaka Takahashi, 2015, Pituitary.

Pan-Myeloid Leukemia Analysis: Machine Learning-Based Approach to Predict Phenotype and Clinical Outcomes Using Mutation Data

P. A. Futreal, S. Ogawa, Jianhua Zhang, 2018, Blood.

Corrigendum: Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia (Leukemia (2016) 30 (1672-1681) DOI: 10.1038/leu.2016.69)

Madan, Tengyu Ma, S. Miyano, 2016 .

Cyclophosphamide^|^mdash;associated cardiomyopathy after allogeneic hematopoietic stem cell transplantation from a sibling donor for refractory cytopenia of childhood

S. Ogawa, M. Fukayama, J. Takita, 2014 .

Aggressive transformation of anaplastic large cell lymphoma with increased number of ALK-translocated chromosomes

S. Miyano, Y. Shiraishi, K. Chiba, 2015, International Journal of Hematology.

Case of type 1 diabetes mellitus following interferon β-1a treatment for multiple sclerosis.

Kenichi Yoshida, Yoshio Nakamura, M. Shimodahira, 2012, Internal medicine.

Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes

S. Miyano, Y. Shiraishi, K. Chiba, 2017, Genetics in Medicine.

Polymorphisms in the prostaglandin E2 receptor subtype 2 gene confer susceptibility to aspirin-intolerant asthma: a candidate gene approach.

T. Nakajima, Kenichi Yoshida, S. Goto, 2004, Human molecular genetics.

Transcriptional co-factor CDCA4 participates in the regulation of JUN oncogene expression.

Reiko Hayashi, Moe Tategu, Kenichi Yoshida, 2008, Biochimie.

Expression of MCM10 and TopBP1 is regulated by cell proliferation and UV irradiation via the E2F transcription factor

Ituro Inoue, Kenichi Yoshida, Kenichi Yoshida, 2004, Oncogene.

ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia

S. Miyano, S. Ogawa, Kenichi Yoshida, 2016, Haematologica.

Puma is a novel target of soy isoflavone genistein but is dispensable for genistein-induced cell fate determination.

Kenichi Yoshida, T. Arauchi, Hiroki Nakagawa, 2008, Molecular nutrition & food research.

Variations in infection sites and mortality rates among patients in intensive care units with severe sepsis and septic shock in Japan

H. Okudera, Kenichi Yoshida, N. Takeyama, 2019, Journal of Intensive Care.

Detection of the G17V RHOA Mutation in Angioimmunoblastic T-Cell Lymphoma and Related Lymphomas Using Quantitative Allele-Specific PCR

S. Ogawa, Y. Shiozawa, Kenichi Yoshida, 2014, PloS one.

Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol‐3‐OH kinase &dgr; syndrome type 1

O. Ohara, S. Ogawa, H. Kanegane, 2019, The Journal of allergy and clinical immunology.

Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations

S. Ogawa, Y. Okuno, Kenichi Yoshida, 2020, Human Genome Variation.

Angiopoietin-like protein 4 is a potent hyperlipidemia-inducing factor in mice and inhibitor of lipoprotein lipase Published, JLR Papers in Press, September 16, 2002. DOI 10.1194/jlr.C200010-JLR200

Kenichi Yoshida, Mitsuru Ono, H. Furukawa, 2002, Journal of Lipid Research.

Tobacco smoking and somatic mutations in human bronchial epithelium

M. Stratton, P. Campbell, A. Menzies, 2020, Nature.

Development of QSAR models for prediction of fish bioconcentration factors using physicochemical properties and molecular descriptors with machine learning algorithms

Yoshiyuki Kobayashi, Kenichi Yoshida, Kenichi Yoshida, 2021, Ecol. Informatics.

Identification of a novel cell-cycle-induced MCM family protein MCM9.

Kenichi Yoshida, Kenichi Yoshida, 2005, Biochemical and biophysical research communications.

Identification and characterization of human ZNF18 gene in silico.

Kenichi Yoshida, 2005, International Journal of Molecular Medicine.

Comparative genomics on MCM8 orthologous genes reveals the transcriptional regulation by transcription factor E2F.

Ryuji Ikeda, Yuya Goto, Reiko Hayashi, 2006, Gene.

Localization and mechanism of nephrocalcinosis in pseudo-Bartter's syndrome.

Kenichi Yoshida, T. Fujita, A. Tojo, 2010, Kidney international.

Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma.

A. Rosenwald, M. Ziepert, A. López-Guillermo, 2016, Blood.

Quantitative structure-property relationships for the calculation of the soil adsorption coefficient using machine learning algorithms with calculated chemical properties from open-source software.

Yoshiyuki Kobayashi, Kenichi Yoshida, Kenichi Yoshida, 2020, Environmental research.

Gene regulatory network of unfolded protein response genes in endoplasmic reticulum stress

Kenichi Yoshida, Sayuri Takayanagi, Riga Fukuda, 2012, Cell Stress and Chaperones.

Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia

S. Miyano, Y. Shiraishi, K. Chiba, 2017, Pediatric blood & cancer.

EPOR/JAK/STAT Signaling Pathway As Therapeutic Target of Acute Erythroid Leukemia

S. Miyano, M. Heuser, F. Thol, 2021, Blood.

Remission clone in acute myeloid leukemia shows growth advantage after chemotherapy but is distinct from leukemic clone.

Zhaolei Zhang, S. Ogawa, Kenichi Yoshida, 2019, Experimental hematology.

Genome-wide DNA methylation analysis in pediatric acute myeloid leukemia

S. Miyano, Y. Shiraishi, S. Ogawa, 2022, Blood advances.

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

S. Miyano, Y. Shiraishi, S. Ogawa, 2019, Journal of Gastroenterology.

Metachronous anaplastic sarcoma of the kidney and thyroid follicular carcinoma as manifestations of DICER1 abnormalities.

S. Ogawa, J. Takita, Kenichi Yoshida, 2017, Human pathology.

Dysregulation of DNA Methylation Involves in Progression of Myeloid Leukemia in Down Syndrome

S. Ogawa, Kenichi Yoshida, T. Toki, 2015 .

A Possible Association Between a Nucleotide‐Binding Domain LRR‐Containing Protein Family PYD‐Containing Protein 1 Mutation and an Autoinflammatory Disease Involving Liver Cirrhosis

S. Ogawa, J. Takita, Kenichi Yoshida, 2021, Hepatology.

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

Y. Hayashi, N. Matsumoto, Kenichi Yoshida, 2021, British journal of haematology.

Procedure for Liquid Chromatographic Determination of Thiamphenicol in Bovine Serum and Milk

Kenichi Yoshida, F. Kondo, 1994 .

Recurrent CCND3 mutations in MLL-rearranged acute myeloid leukemia.

S. Miyano, Y. Shiraishi, K. Chiba, 2018, Blood advances.

Characteristics and outcomes of bacteremia among ICU-admitted patients with severe sepsis

H. Okudera, Kenichi Yoshida, N. Takeyama, 2020, Scientific Reports.

Profiling of molecular pathways regulated by microRNA 601

Kenichi Yoshida, Hiroki Nakagawa, Hiroaki Ohdaira, 2009, Comput. Biol. Chem..

Invariant patterns of clonal succession determine specific clinical features of myelodysplastic syndromes

S. Miyano, T. LaFramboise, Y. Shiraishi, 2019, Nature Communications.

Fibroblast cell shape and adhesion in vitro is altered by overexpression of the 7a and 7b isoforms of protocadherin 7, but not the 7c isoform.

Kenichi Yoshida, 2003, Cellular & molecular biology letters.

BCOR and BCORL 1 mutations in myelodysplastic syndromes and related disorders

D. Birnbaum, S. Miyano, Y. Shiraishi, 2013 .

Single cell genotyping of exome sequencing-identified mutations to characterize the clonal composition and evolution of inv(16) AML in a CBL mutated clonal hematopoiesis.

S. Ogawa, Kenichi Yoshida, R. Claus, 2016, Leukemia research.

Ischemia enhances translocation of connexin43 and gap junction intercellular communication, thereby propagating contraction band necrosis after reperfusion.

Kenichi Yoshida, K. Unuma, Kaori Shintani-Ishida, 2009, Circulation journal : official journal of the Japanese Circulation Society.

Augmentation of the ubiquitin-mediated proteolytic system by F-box and additional motif-containing proteins (Review).

Kenichi Yoshida, Kazuyuki Sato, 2010, International journal of oncology.

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

S. Miyano, Y. Shiraishi, K. Chiba, 2019, Cancer science.

Comprehensive genetic analysis of pediatric germ cell tumors identifies potential drug targets

S. Miyano, Y. Shiraishi, K. Chiba, 2020, Communications biology.

Frequent mutations in HLA and related genes in extranodal NK/T cell lymphomas

S. Miyano, Y. Shiraishi, K. Chiba, 2020, Leukemia & lymphoma.

Common Variable Immunodeficiency Caused by FANC Mutations

O. Ohara, S. Miyano, Y. Shiraishi, 2017, Journal of Clinical Immunology.

Der(1;7)(q10;p10) Presents with a Unique Genetic Profile and Frequent ETNK1 Mutations in Myeloid Neoplasms

S. Miyano, Y. Shiraishi, S. Ogawa, 2021, Blood.

Somatic Mosaicism for a NRAS Mutation Associates with Disparate Clinical Features in RAS-associated Leukoproliferative Disease: a Report of Two Cases

S. Miyano, S. Ogawa, H. Kanegane, 2015, Journal of Clinical Immunology.

Significance of body temperature in elderly patients with sepsis

H. Okudera, Kenichi Yoshida, N. Takeyama, 2020, Critical Care.

Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia

S. Miyano, Y. Shiraishi, S. Ogawa, 2021, Haematologica.

TP53 and RB1 alterations characterize poor prognostic subgroups in pediatric acute myeloid leukemia

S. Miyano, Y. Shiraishi, S. Ogawa, 2023, Genes, chromosomes & cancer.

UBTF‐internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia

S. Miyano, Y. Shiraishi, S. Ogawa, 2022, Genes, chromosomes & cancer.

Genetic Background of Chronic Active Epstein-Barr Virus Disease

S. Miyano, Y. Shiraishi, K. Chiba, 2017 .

Frequent Activating Somatic Alterations in T-Cell Receptor / NF-κb Signaling in Adult T-Cell Leukemia/Lymphoma

S. Miyano, Y. Totoki, T. Shibata, 2015 .

FBXL16 is a novel E2F1-regulated gene commonly upregulated in p16INK4A- and p14ARF-silenced HeLa cells.

Kenichi Yoshida, Moe Tategu, Kazuyuki Sato, 2009, International journal of oncology.

marrow failure in Japanese Fanconi anemia patients Variant ALDH2 is associated with accelerated progression of bone

S. Miyano, Y. Shiraishi, K. Chiba, 2013 .

S. Miyano, S. Ogawa, H. Kanegane, 2015, Journal of Clinical Immunology.

Clonal Hematopoiesis: Cell of Origin, Lineage Repartition and Dynamic Evolution during Chemotherapy

B. Dörken, C. Schmitt, S. Ogawa, 2017 .

Atypical dyskeratosis congenita diagnosed using whole‐exome sequencing

Y. Shiraishi, S. Ogawa, J. Takita, 2017, Pediatrics International.

Landscape of genetic lesions in 944 patients with myelodysplastic syndromes

C Haferlach, H Aburatani, S Miyano, 2013, Leukemia.

Long-term outcome of 6-month maintenance chemotherapy for acute lymphoblastic leukemia in children

S. Miyano, Y. Shiraishi, K. Chiba, 2017, Leukemia.

Identification of cell-type-specific mutations in nodal T-cell lymphomas

S. Miyano, K. Ohshima, Y. Shiraishi, 2017, Blood Cancer Journal.

Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents

M. Stratton, F. Artiguenave, L. Alexandrov, 2016, Nature Communications.

Postazacitidine clone size predicts long-term outcome of patients with myelodysplastic syndromes and related myeloid neoplasms

S. Miyano, T. Naoe, E. Papaemmanuil, 2023, Blood advances.

Clonal evolution in myelodysplastic syndromes

S. Miyano, Y. Shiraishi, K. Chiba, 2017, Nature Communications.

Evolutionary histories of breast cancer and related clones

S. Miyano, Y. Shiraishi, K. Chiba, 2023, Nature.

Donor cell-derived transient abnormal myelopoiesis as a specific complication of umbilical cord blood transplantation

S. Miyano, Y. Shiraishi, K. Chiba, 2018, Bone Marrow Transplantation.

Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele

S. Miyano, Y. Shiraishi, K. Chiba, 2016, Blood Cancer Journal.

Frequent ZNF217 mutations lead to transcriptional deregulation of interferon signal transduction via altered chromatin accessibility in B cell lymphoma

W. Klapper, A. López-Guillermo, G. Ott, 2023, Leukemia.

Characteristics and outcomes of bacteremia among ICU-admitted patients with severe sepsis

H. Okudera, Kenichi Yoshida, N. Takeyama, 2020, Scientific Reports.

Recombinant Human-Soluble Thrombomodulin Contributes to Reduced Mortality in Sepsis Patients With Severe Respiratory Failure: A Retrospective Observational Study Using a Multicenter Dataset

Kenichi Yoshida, M. Hayakawa, K. Ono, 2019, Shock.

PPM1D and DNMT3A Mutations in Myelodysplasia and Clonal Hematopoiesis

Y. Kamatani, S. Miyano, Y. Shiraishi, 2019, Blood.

Novel Molecular Pathogenesis and Therapeutic Target in Acute Erythroid Leukemia

S. Miyano, M. Heuser, F. Thol, 2019, Blood.

Childhood acute myeloid leukemia with 5q deletion and HNRNPH1-MLLT10 fusion: the first case report

S. Ogawa, J. Takita, Kenichi Yoshida, 2022, Blood Advances.

Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic Leukemia

S. Miyano, Y. Shiraishi, S. Ogawa, 2015, PloS one.

Acute loss of DP1, but not DP2, induces p53 mRNA and augments p21Waf1/Cip1 and senescence

Kenichi Yoshida, K. Miyata, T. Sasaki, 2012, Cell biochemistry and function.

Geminin as a molecular target for the development of new anticancer drugs.

Kenichi Yoshida, 2006, Mini-Reviews in Medical Chemistry.

Comprehensive genetic analysis of pediatric germ cell tumors identifies potential drug targets

S. Miyano, Y. Shiraishi, K. Chiba, 2020, Communications Biology.

mutations in adult T-cell leukemia / lymphoma

O. Nureki, S. Miyano, Y. Totoki, 2015 .

Landscape of Genetic Alterations in Adult T-Cell Leukemia/Lymphoma

H. Aburatani, O. Nureki, S. Miyano, 2014 .

Recurrent genetic defects on chromosome 7q in myeloid neoplasms

S. Miyano, Y. Shiraishi, K. Chiba, 2014, Leukemia.

Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma

H. Aburatani, S. Miyano, T. Shimamura, 2015, Nature Communications.

Genomic landscape of liposarcoma

O. Myklebost, Y. Shiraishi, K. Chiba, 2015, OncoTarget.

Deep sequencing in cancer research.

S. Ogawa, Kenichi Yoshida, M. Sanada, 2013, Japanese journal of clinical oncology.

Modification of cellular and humoral immunity by somatically reverted T cells in X-linked lymphoproliferative syndrome type 1.

S. Miyano, Y. Shiraishi, K. Chiba, 2019, The Journal of allergy and clinical immunology.

Normal neutrophil myosin IIA localization in an immunofluorescence analysis can rule out MYH9 disorders

S. Miyano, Y. Shiraishi, K. Chiba, 2013, Journal of thrombosis and haemostasis : JTH.

Somatic Mosaicism for a NRAS Mutation Associates with Disparate Clinical Features in RAS-associated Leukoproliferative Disease: a Report of Two Cases

S. Miyano, S. Ogawa, H. Kanegane, 2015, Journal of Clinical Immunology.

Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma

H. Aburatani, S. Miyano, Y. Shiraishi, 2015, Nature Communications.

Loss of function mutations in RPL27 and RPS27 identified by whole‐exome sequencing in Diamond‐Blackfan anaemia

N. Kenmochi, S. Miyano, Y. Shiraishi, 2015, British journal of haematology.

Oxidative stress augments pulmonary hypertension in chronically hypoxic mice overexpressing the oxidized LDL receptor.

Hong Wang, Kenichi Yoshida, S. Mu, 2013, American journal of physiology. Heart and circulatory physiology.

Genomon ITDetector: a tool for somatic internal tandem duplication detection from cancer genome sequencing data

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Bioinform..

Role of Donor Clonal Hematopoiesis in Allogeneic Hematopoietic Stem-Cell Transplantation.

L. Bullinger, M. Heuser, F. Thol, 2019, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Thymidine phosphorylase inhibits the expression of proapoptotic protein BNIP3.

Kenichi Yoshida, T. Furukawa, S. Akiyama, 2008, Biochemical and biophysical research communications.

TAL1 Super Enhancer Aberration and Stil-TAL1 Fusion in Pediatric T Cell Acute Lymphoblastic Leukemia

S. Miyano, Y. Shiraishi, K. Chiba, 2016 .

Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients.

S. Miyano, Y. Shiraishi, K. Chiba, 2013, Blood.

Array CGH identifies copy number changes in 11% of 520 MDS patients with normal karyotype and uncovers prognostically relevant deletions

S. Ogawa, T. Haferlach, S. Schnittger, 2016, Leukemia.

Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia.

S. Miyano, B. Dumitriu, Y. Shiraishi, 2015, The New England journal of medicine.

GATA2 and secondary mutations in familial myelodysplastic syndromes and pediatric myeloid malignancies

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Haematologica.