Lista de obras - Tetsuichi Yoshizato - Dominio Público Uruguay

A novel genetic and morphologic phenotype of ARID2-mediated myelodysplasia

artículo científico publicado en 2017

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

artículo científico publicado en 2018

Aberrant PD-L1 expression through 3'-UTR disruption in multiple cancers.

artículo científico publicado en 2016

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

artículo científico publicado en 2018

Age-related remodelling of oesophageal epithelia by mutated cancer drivers

artículo científico publicado en 2019

Chronologic analysis of clonal evolution in acquired aplastic anemia and sMDS

artículo científico publicado en 2016

Clinical significance of serum-soluble interleukin-2 receptor in patients with follicular lymphoma.

artículo científico

Clonally related diffuse large B-cell lymphoma and interdigitating dendritic cell sarcoma sharing translocation

artículo científico publicado en 2018

Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria.

artículo científico publicado en 2014

Disseminated tuberculosis following unrelated cord blood transplantation for refractory peripheral T-cell lymphoma: Clinical role of serum procalcitonin levels.

artículo científico publicado en 2011

Dynamics of clonal evolution in myelodysplastic syndromes

artículo científico publicado en 2016

Effects of universal vs bedside leukoreductions on the alloimmunization to platelets and the platelet transfusion refractoriness.

artículo científico publicado en 2014

Frequent mutations that converge on the NFKBIZ pathway in ulcerative colitis

artículo científico publicado en 2019

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

Gene mutations in bone marrow failure syndromes

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2020

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

Molecular classification and diagnostics of upper urinary tract urothelial carcinoma

artículo científico publicado en 2021

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

Mutational landscape and clonal architecture in grade II and III gliomas

artículo científico publicado en 2015

Nilotinib-induced hypothyroidism in a patient with chronic myeloid leukemia

artículo científico publicado en 2011

Origins of myelodysplastic syndromes after aplastic anemia

artículo científico publicado en 2017

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

artículo científico publicado en 2017

Prognostic relevance of genetic alterations in diffuse lower-grade gliomas

artículo científico publicado en 2017

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

artículo científico publicado en 2017

Pulmonary mucormycosis with embolism: two autopsied cases of acute myeloid leukemia

artículo científico publicado en 2014

Recurrent somatic mutations underlie corticotropin-independent Cushing's syndrome.

artículo científico publicado en 2014

Simple but powerful prognostic scoring model for MALT lymphoma: a retrospective study

artículo científico publicado en 2012

Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia

artículo científico publicado en 2015

Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms

artículo científico publicado en 2016

Sustained clonal hematopoiesis by HLA-lacking hematopoietic stem cells without driver mutations in aplastic anemia

scientific article published on 01 May 2018

Telomere attrition and candidate gene mutations preceding monosomy 7 in aplastic anemia

artículo científico publicado en 2014

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

artículo científico publicado en 2015

[Impact of genetic alterations on prognosis in myelodysplastic syndrome patients undergoing stem cell transplantation]

artículo científico publicado en 2019

[Significance of somatic mutations on the prognosis of myelodysplastic syndromes]

artículo científico publicado en 2018

Lista de obras de Tetsuichi Yoshizato

A novel genetic and morphologic phenotype of ARID2-mediated myelodysplasia

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

Aberrant PD-L1 expression through 3'-UTR disruption in multiple cancers.

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

Age-related remodelling of oesophageal epithelia by mutated cancer drivers

Chronologic analysis of clonal evolution in acquired aplastic anemia and sMDS

Clinical significance of serum-soluble interleukin-2 receptor in patients with follicular lymphoma.

Clonally related diffuse large B-cell lymphoma and interdigitating dendritic cell sarcoma sharing translocation

Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria.

Disseminated tuberculosis following unrelated cord blood transplantation for refractory peripheral T-cell lymphoma: Clinical role of serum procalcitonin levels.

Dynamics of clonal evolution in myelodysplastic syndromes

Effects of universal vs bedside leukoreductions on the alloimmunization to platelets and the platelet transfusion refractoriness.

Frequent mutations that converge on the NFKBIZ pathway in ulcerative colitis

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

Gene expression and risk of leukemic transformation in myelodysplasia

Gene mutations in bone marrow failure syndromes

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

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

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

Molecular classification and diagnostics of upper urinary tract urothelial carcinoma

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

Molecular pathogenesis of disease progression in MLL-rearranged AML

Mutational landscape and clonal architecture in grade II and III gliomas

Nilotinib-induced hypothyroidism in a patient with chronic myeloid leukemia

Origins of myelodysplastic syndromes after aplastic anemia

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

Prognostic relevance of genetic alterations in diffuse lower-grade gliomas

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

Pulmonary mucormycosis with embolism: two autopsied cases of acute myeloid leukemia

Recurrent somatic mutations underlie corticotropin-independent Cushing's syndrome.

Simple but powerful prognostic scoring model for MALT lymphoma: a retrospective study

Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia

Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms

Sustained clonal hematopoiesis by HLA-lacking hematopoietic stem cells without driver mutations in aplastic anemia

Telomere attrition and candidate gene mutations preceding monosomy 7 in aplastic anemia

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

[Impact of genetic alterations on prognosis in myelodysplastic syndrome patients undergoing stem cell transplantation]

[Significance of somatic mutations on the prognosis of myelodysplastic syndromes]