Lista de obras - Seishi Ogawa - Dominio Público Uruguay

A temporal shift of the evolutionary principle shaping intratumor heterogeneity in colorectal cancer

artículo científico publicado en 2018

Aberrant splicing and defective mRNA production induced by somatic spliceosome mutations in myelodysplasia

artículo científico publicado en 2018

Absence of a common founder mutation in patients with co-occurring myelodysplastic syndrome and plasma cell disorder

artículo científico publicado en 2020

Acquired initiating mutations in early hematopoietic cells of CLL patients

artículo científico publicado en 2014

Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome

scientific article published on 16 November 2020

BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders.

artículo científico publicado en 2013

BRCC3 mutations in myeloid neoplasms

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Clonal hematopoiesis in acquired aplastic anemia

artículo científico publicado en 2016

Combined Cohesin-Runx1 Deficiency Synergistically Perturbs Chromatin Looping and Causes Myelodysplastic Syndromes

scientific article published on 05 April 2020

Common Variable Immunodeficiency Caused by FANC Mutations

artículo científico publicado en 2017

Concurrent loss of Ezh2 and Tet2 cooperates in the pathogenesis of myelodysplastic disorders

artículo científico publicado en 2013

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

artículo científico publicado en 2017

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

scientific article published on 14 October 2020

Decreased RORC expression and downstream signaling in HTLV-1-associated Adult T-cell Lymphoma/Leukemia uncovers an antiproliferative IL17 link: a potential target for immunotherapy?

artículo científico publicado en 2018

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

scientific article published on 21 January 2019

Dynamics of clonal evolution in myelodysplastic syndromes

artículo científico publicado en 2016

Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype

artículo científico publicado en 2009

Frequent mutations that converge on the NFKBIZ pathway in ulcerative colitis

artículo científico publicado en 2019

Frequent pathway mutations of splicing machinery in myelodysplasia

artículo científico publicado en 2011

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

scientific article published on 25 January 2019

Gene expression and risk of leukemic transformation in myelodysplasia

artículo científico publicado en 2017

Genetic analysis of a case of Helicobacter pylori-uninfected intramucosal gastric cancer in a family with hereditary diffuse gastric cancer

artículo científico publicado en 2018

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

artículo científico publicado en 2020

Genetics of MDS

artículo científico publicado en 2019

Genomic Landscape of Esophageal Squamous Cell Carcinoma in a Japanese Population.

artículo científico publicado en 2016

Genomic profiling of adult acute lymphoblastic leukemia by single nucleotide polymorphism oligonucleotide microarray and comparison to pediatric acute lymphoblastic leukemia

artículo científico publicado en 2010

Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

artículo científico publicado en 2020

Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution

artículo científico publicado en 2016

Integrated molecular analysis of adult T cell leukemia/lymphoma.

artículo científico publicado en 2015

Integrated molecular analysis of clear-cell renal cell carcinoma

artículo científico publicado en 2013

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

scientific article published on 26 November 2019

MDS-related mutations in aplastic anemia.

artículo científico publicado en 2014

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

artículo científico publicado en 2019

Molecular pathogenesis of disease progression in MLL-rearranged AML

artículo científico publicado en 2018

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

artículo científico publicado en 2016

Patient-specific MDS-RS iPSCs define the mis-spliced transcript repertoire and chromatin landscape of SF3B1-mutant HSPCs

scientific article published on 01 May 2022

Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Profiling the inhibitory receptors LAG-3, TIM-3, and TIGIT in renal cell carcinoma reveals malignancy

artículo científico publicado en 2021

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

artículo científico publicado en 2019

Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms

artículo científico publicado en 2013

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

scientific article published on 18 September 2020

Resistance of KIR Ligand-Missing Leukocytes to NK Cells In Vivo in Patients with Acquired Aplastic Anemia

artículo científico publicado en 2020

SF3B1-mutant myelodysplastic syndrome as a distinct disease subtype - A Proposal of the International Working Group for the Prognosis of Myelodysplastic Syndromes (IWG-PM)

artículo científico publicado en 2020

SNP array analysis of tyrosine kinase inhibitor-resistant chronic myeloid leukemia identifies heterogeneous secondary genomic alterations

artículo científico publicado en 2009

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

artículo científico publicado en 2012

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

scientific article published on 11 January 2019

The BRG1/SOX9 axis is critical for acinar cell-derived pancreatic tumorigenesis

article by Motoyuki Tsuda et al published 1 August 2018 in Journal of Clinical Investigation

The transcription factor E2A activates multiple enhancers that drive Rag expression in developing T and B cells

artículo científico publicado en 2020

Unbiased Detection of Driver Mutations in Extramammary Paget Disease

artículo científico publicado en 2020

Lista de obras de Seishi Ogawa

A temporal shift of the evolutionary principle shaping intratumor heterogeneity in colorectal cancer

Aberrant splicing and defective mRNA production induced by somatic spliceosome mutations in myelodysplasia

Absence of a common founder mutation in patients with co-occurring myelodysplastic syndrome and plasma cell disorder

Acquired initiating mutations in early hematopoietic cells of CLL patients

Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome

BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders.

BRCC3 mutations in myeloid neoplasms

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

Clonal hematopoiesis in acquired aplastic anemia

Combined Cohesin-Runx1 Deficiency Synergistically Perturbs Chromatin Looping and Causes Myelodysplastic Syndromes

Common Variable Immunodeficiency Caused by FANC Mutations

Concurrent loss of Ezh2 and Tet2 cooperates in the pathogenesis of myelodysplastic disorders

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

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

Decreased RORC expression and downstream signaling in HTLV-1-associated Adult T-cell Lymphoma/Leukemia uncovers an antiproliferative IL17 link: a potential target for immunotherapy?

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

Dynamics of clonal evolution in myelodysplastic syndromes

Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype

Frequent mutations that converge on the NFKBIZ pathway in ulcerative colitis

Frequent pathway mutations of splicing machinery in myelodysplasia

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

Gene expression and risk of leukemic transformation in myelodysplasia

Genetic analysis of a case of Helicobacter pylori-uninfected intramucosal gastric cancer in a family with hereditary diffuse gastric cancer

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

Genetics of MDS

Genomic Landscape of Esophageal Squamous Cell Carcinoma in a Japanese Population.

Genomic profiling of adult acute lymphoblastic leukemia by single nucleotide polymorphism oligonucleotide microarray and comparison to pediatric acute lymphoblastic leukemia

Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution

Integrated molecular analysis of adult T cell leukemia/lymphoma.

Integrated molecular analysis of clear-cell renal cell carcinoma

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

MDS-related mutations in aplastic anemia.

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

Molecular pathogenesis of disease progression in MLL-rearranged AML

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

Patient-specific MDS-RS iPSCs define the mis-spliced transcript repertoire and chromatin landscape of SF3B1-mutant HSPCs

Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency

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

Profiling the inhibitory receptors LAG-3, TIM-3, and TIGIT in renal cell carcinoma reveals malignancy

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

Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms

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

Resistance of KIR Ligand-Missing Leukocytes to NK Cells In Vivo in Patients with Acquired Aplastic Anemia

SF3B1-mutant myelodysplastic syndrome as a distinct disease subtype - A Proposal of the International Working Group for the Prognosis of Myelodysplastic Syndromes (IWG-PM)

SNP array analysis of tyrosine kinase inhibitor-resistant chronic myeloid leukemia identifies heterogeneous secondary genomic alterations

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

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

The BRG1/SOX9 axis is critical for acinar cell-derived pancreatic tumorigenesis

The transcription factor E2A activates multiple enhancers that drive Rag expression in developing T and B cells

Unbiased Detection of Driver Mutations in Extramammary Paget Disease