Lista de obras - Motohiro Kato - Dominio Público Uruguay

A Cryptic NUP214-ABL1 Fusion in B-cell Precursor Acute Lymphoblastic Leukemia.

artículo científico publicado en 2017

A nonsense mutation of IDH1 in myelodysplastic syndromes and related disorders.

artículo científico publicado en 2010

A novel KMT2A-ACTN2 fusion in infant B-cell acute lymphoblastic leukemia

artículo científico publicado en 2019

A prospective study of allogeneic transplantation from unrelated donors for chronic granulomatous disease with target busulfan-based reduced-intensity conditioning

artículo científico publicado en 2018

Aberrant activation of ALK kinase by a novel truncated form ALK protein in neuroblastoma.

artículo científico publicado en 2012

Acute myeloid leukemia with mediastinal myeloid sarcoma refractory to acute myeloid leukemia therapy but responsive to L-asparaginase

artículo científico publicado en 2012

Acute promyelocytic leukemia with a cryptic insertion of RARA into TBL1XR1

artículo científico publicado en 2019

Adults with germline CBL mutation complicated with juvenile myelomonocytic leukemia at infancy

artículo científico publicado en 2016

Aggressive Transformation of Juvenile Myelomonocytic Leukemia Associated with Duplication of Oncogenic KRAS due to Acquired Uniparental Disomy

Allelotypes of lung adenocarcinomas featuring ALK fusion demonstrate fewer onco- and suppressor gene changes

artículo científico publicado en 2013

Allogeneic haematopoietic stem cell transplantation for infant acute lymphoblastic leukaemia with KMT2A (MLL) rearrangements: a retrospective study from the paediatric acute lymphoblastic leukaemia working group of the Japan Society for Haematopoiet

artículo científico publicado en 2014

Allogeneic hematopoietic stem cell transplantation for children and adolescents with high-risk cytogenetic AML: distinctly poor outcomes of FUS-ERG-positive cases

scientific article published on 29 June 2018

Analysis of the molecular mechanism underlying bone marrow necrosis with acute lymphoblastic leukemia.

artículo científico publicado en 2015

Association between Chiari malformation and bone marrow failure/myelodysplastic syndrome

artículo científico publicado en 2013

Atypical dyskeratosis congenita diagnosed using whole-exome sequencing.

artículo científico publicado en 2017

Bernard-Soulier syndrome caused by a hemizygous GPIbβ mutation and 22q11.2 deletion

Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma

artículo científico publicado en 2014

Blastic transformation of juvenile myelomonocytic leukemia caused by the copy number gain of oncogenic KRAS.

artículo científico publicado en 2017

CBL mutations in juvenile myelomonocytic leukemia and pediatric myelodysplastic syndrome

artículo científico publicado en 2010

Case series of pediatric acute leukemia without a peripheral blood abnormality, detected by magnetic resonance imaging

artículo científico publicado en 2011

Characterization of adenocarcinoma of the lung in a familial adenomatous polyposis patient

artículo científico publicado en 2008

Characterization of genetic lesions in rhabdomyosarcoma using a high-density single nucleotide polymorphism array

artículo científico publicado en 2013

Chromosomal abnormalities and novel disease-related regions in progression from Barrett's esophagus to esophageal adenocarcinoma

artículo científico publicado en 2009

Cisplatin-induced hearing loss: the need for a long-term evaluating system

artículo científico publicado en 2014

Clinical course of autologous recovery with chromosomal abnormalities after allogeneic hematopoietic stem cell transplantation

scientific article published on 09 December 2019

Clonal evolution mechanisms in NT5C2 mutant-relapsed acute lymphoblastic leukaemia

artículo científico publicado en 2018

Comparison of Outcomes for Pediatric Patients With Acute Myeloid Leukemia in Remission and Undergoing Allogeneic Hematopoietic Cell Transplantation With Myeloablative Conditioning Regimens Based on Either Intravenous Busulfan or Total Body Irradiati

artículo científico publicado en 2015

Comparison of chemotherapeutic agents as a myeloablative conditioning with total body irradiation for pediatric acute lymphoblastic leukemia: A study from the pediatric ALL working group of the Japan Society for Hematopoietic Cell Transplantation

artículo científico publicado en 2015

Comparison of clonazepam and levetiracetam in children for prevention of busulfan-induced seizure in hematopoietic stem cell transplantation

scientific article published on 20 December 2019

Comparison of intravenous with oral busulfan in allogeneic hematopoietic stem cell transplantation with myeloablative conditioning regimens for pediatric acute leukemia

artículo científico publicado en 2013

Consensus definitions of 14 severe acute toxic effects for childhood lymphoblastic leukaemia treatment: a Delphi consensus

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Copy number analysis identifies tumor suppressive lncRNAs in human osteosarcoma

artículo científico publicado en 2017

Cytokine Profiles in Pericardial Effusion in a Down Syndrome Infant with Transient Abnormal Myelopoiesis

artículo científico publicado en 2017

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

scientific article published on 15 November 2019

Delayed short-term administration of granulocyte colony-stimulating factor is a good mobilization strategy for harvesting autologous peripheral blood stem cells in pediatric patients with solid tumors

artículo científico publicado en 2013

Deletion of the TNFAIP3/A20 gene detected by FICTION analysis in classical Hodgkin lymphoma

artículo científico publicado en 2012

Diplotype analysis of NUDT15 variants and 6-mercaptopurine sensitivity in pediatric lymphoid neoplasms

artículo científico publicado en 2018

Donor cell-derived hematological malignancies after allogeneic hematopoietic stem cell transplantation

artículo científico

Exploration of the genetic basis of GVHD by genetic association studies

artículo científico publicado en 2009

Favorable outcome in non-infant children with MLL-AF4-positive acute lymphoblastic leukemia: a report from the Tokyo Children's Cancer Study Group

artículo científico publicado en 2015

Frequent inactivation of A20 in B-cell lymphomas

artículo científico publicado en 2009

Frequent loss of HLA alleles associated with copy number-neutral 6pLOH in acquired aplastic anemia

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

Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms

artículo científico publicado en 2009

Genome-wide approach to identify second gene targets for malignant rhabdoid tumors using high-density oligonucleotide microarrays

artículo científico publicado en 2014

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

artículo científico publicado en 2015

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

Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome

artículo científico publicado en 2016

Hematopoietic Stem Cell Transplantation for Progressive Combined Immunodeficiency and Lymphoproliferation in Activated PI3K <delta> Syndrome Type 1.

artículo científico publicado en 2018

Hepatoblastoma in a Patient with Sotos Syndrome

Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations

artículo científico publicado en 2008

High prevalence of SMARCB1 constitutional abnormalities including mosaicism in malignant rhabdoid tumors

scientific article published on 26 March 2020

High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray

artículo científico publicado en 2009

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

artículo científico publicado en 2007

How to manage pediatric oncologic emergencies: Imaging diagnosis

artículo científico publicado en 2019

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

artículo científico publicado en 2014

Imatinib use immediately before stem cell transplantation in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: Results from Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) Study Ph(+) ALL04

artículo científico publicado en 2015

Impact of graft-versus-host disease on relapse and survival after allogeneic stem cell transplantation for pediatric leukemia

article published in 2018

Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma

artículo científico publicado en 2015

Integrated molecular characterization of the lethal pediatric cancer pancreatoblastoma

artículo científico publicado en 2017

Interstitial deletion of 13q14.13-q32.3 presenting with Arima syndrome and bilateral retinoblastoma

Kasabach-Merritt phenomenon: a report of 11 cases from a single institution

artículo científico publicado en 2013

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

artículo científico publicado en 2016

Long-term survivor of relapsed stage IV malignant rhabdoid tumor of the kidney

MYC amplification as a prognostic marker of early-stage lung adenocarcinoma identified by whole genome copy number analysis.

artículo científico publicado en 2010

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

artículo científico publicado en 2008

Mutational and functional genetics mapping of chemotherapy resistance mechanisms in relapsed acute lymphoblastic leukemia

artículo científico publicado en 2020

Mutational landscape, clonal evolution patterns, and role of RAS mutations in relapsed acute lymphoblastic leukemia

artículo científico publicado en 2016

NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity

scientific journal article

Nationwide study of pediatric B-cell precursor acute lymphoblastic leukemia with chromosome 8q24/MYC rearrangement in Japan

artículo científico publicado en 2020

Nationwide survey of pediatric hypodiploid acute lymphoblastic leukemia in Japan

artículo científico publicado en 2019

No impact of high-dose cytarabine and asparaginase as early intensification with intermediate-risk paediatric acute lymphoblastic leukaemia: results of randomized trial TCCSG study L99-15.

artículo científico publicado en 2013

Oncogenic mutations of ALK kinase in neuroblastoma

artículo científico publicado en 2008

Outcome of pediatric acute lymphoblastic leukemia with very late relapse: a retrospective analysis by the Tokyo Children's Cancer Study Group (TCCSG).

artículo científico publicado en 2014

Partial monosomy of 10p and duplication of another chromosome in two patients

Perioperative management of severe congenital protein C deficiency.

artículo científico publicado en 2017

Phase II/III study in children and adolescents with newly diagnosed B-cell precursor acute lymphoblastic leukemia: protocol for a nationwide multicenter trial in Japan.

artículo científico publicado en 2018

Preclinical evaluation of NUDT15-guided thiopurine therapy and its effects on toxicity and anti-leukemic efficacy.

artículo científico publicado en 2018

Preoperative diagnosis of clear cell sarcoma of the kidney by detection of BCOR internal tandem duplication in circulating tumor DNA

artículo científico publicado en 2018

Prevalence and prognostic impact of allelic imbalances associated with leukemic transformation of Philadelphia chromosome-negative myeloproliferative neoplasms

artículo científico publicado en 2010

Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7

artículo científico publicado en 2020

Prognostic impact of gained chromosomes in high-hyperdiploid childhood acute lymphoblastic leukaemia: a collaborative retrospective study of the Tokyo Children's Cancer Study Group and Japan Association of Childhood Leukaemia Study

Prognostic significance of leukopenia in childhood acute lymphoblastic leukemia

scientific article published on 24 January 2014

Prophylactic administration of prothrombin complex concentrates for congenital prothrombin deficiency with a novel frameshift mutation, prothrombin saitama

artículo científico publicado en 2012

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

artículo científico publicado en 2017

RecurrentRARBTranslocations in Acute Promyelocytic Leukemia LackingRARATranslocation

artículo científico publicado en 2018

Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese.

artículo científico publicado en 2018

Relapse of leukemia with loss of mismatched HLA resulting from uniparental disomy after haploidentical hematopoietic stem cell transplantation

artículo científico publicado en 2010

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

artículo científico publicado en 2009

Safety of Live Attenuated High-Titer Varicella-Zoster Virus Vaccine in Pediatric Allogeneic Hematopoietic Stem Cell Transplantation Recipients

artículo científico publicado en 2015

Salvage allogeneic stem cell transplantation in patients with pediatric myelodysplastic syndrome and myeloproliferative neoplasms

artículo científico publicado en 2014

Salvage therapy for children with relapsed or refractory Philadelphia chromosome-positive acute lymphoblastic leukemia

artículo científico publicado en 2017

Simple evaluation method for CYP3A4 induction from human hepatocytes; The relative factor approach with an induction detection limit concentration based on the Emax model.

artículo científico publicado en 2017

Somatic MECOM mosaicism in a patient with congenital bone marrow failure without a radial abnormality.

artículo científico publicado en 2018

Spontaneous improvement of chronic immune thrombocytopenia in children: experience of 56 patients at a single institute

artículo científico publicado en 2012

Successful treatment of systemic EBV positive T-cell lymphoma of childhood using the SMILE regimen.

artículo científico publicado en 2018

Susceptibility to 6-MP toxicity conferred by a NUDT15 variant in Japanese children with acute lymphoblastic leukaemia

artículo científico publicado en 2015

Systemic lupus erythematosus presenting with mixed-type fulminant autoimmune hemolytic anemia

scholarly article by Yoko Hirano et al published 19 February 2016 in Pediatrics International

The effect of the order of total body irradiation and chemotherapy on graft-versus-host disease

artículo científico publicado en 2014

The effects of inherited NUDT15 polymorphisms on thiopurine active metabolites in Japanese children with acute lymphoblastic leukemia

artículo científico publicado en 2017

Transmission of chromosomally integrated human herpesvirus 6 via cord blood transplantation

artículo científico publicado en 2016

Treatment and biology of pediatric acute lymphoblastic leukemia

artículo científico publicado en 2017

Treatment outcome of children with acute lymphoblastic leukemia: the Tokyo Children's Cancer Study Group (TCCSG) Study L04-16.

artículo científico publicado en 2018

Treatment outcomes of adolescent acute lymphoblastic leukemia treated on Tokyo Children's Cancer Study Group (TCCSG) clinical trials

artículo científico publicado en 2014

Unrelated cord blood and bone marrow transplantation in pediatric leukemia

Variegated clonality and rapid emergence of new molecular lesions in xenografts of acute lymphoblastic leukemia are associated with drug resistance

artículo científico publicado en 2014

Voriconazole-micafungin combination therapy for acute lymphoblastic leukemia

artículo científico publicado en 2010

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

artículo científico publicado en 2016

Whole-genome profiling of chromosomal aberrations in hepatoblastoma using high-density single-nucleotide polymorphism genotyping microarrays

artículo científico publicado en 2008

[Leukemia and lymphoma]

artículo científico publicado en 2010

[Pediatric acute lymphoblastic leukemia: update on pathophysiology and management]

artículo científico publicado en 2018

[Severe aplastic anemia following living-donor liver transplantation for fluminant hepatitis]

artículo científico publicado en 2012

[Significance of A20 in B-cell lymphomas]

artículo científico publicado en 2011

Lista de obras de Motohiro Kato

A Cryptic NUP214-ABL1 Fusion in B-cell Precursor Acute Lymphoblastic Leukemia.

A nonsense mutation of IDH1 in myelodysplastic syndromes and related disorders.

A novel KMT2A-ACTN2 fusion in infant B-cell acute lymphoblastic leukemia

A prospective study of allogeneic transplantation from unrelated donors for chronic granulomatous disease with target busulfan-based reduced-intensity conditioning

Aberrant activation of ALK kinase by a novel truncated form ALK protein in neuroblastoma.

Acute myeloid leukemia with mediastinal myeloid sarcoma refractory to acute myeloid leukemia therapy but responsive to L-asparaginase

Acute promyelocytic leukemia with a cryptic insertion of RARA into TBL1XR1

Adults with germline CBL mutation complicated with juvenile myelomonocytic leukemia at infancy

Aggressive Transformation of Juvenile Myelomonocytic Leukemia Associated with Duplication of Oncogenic KRAS due to Acquired Uniparental Disomy

Allelotypes of lung adenocarcinomas featuring ALK fusion demonstrate fewer onco- and suppressor gene changes

Allogeneic haematopoietic stem cell transplantation for infant acute lymphoblastic leukaemia with KMT2A (MLL) rearrangements: a retrospective study from the paediatric acute lymphoblastic leukaemia working group of the Japan Society for Haematopoiet

Allogeneic hematopoietic stem cell transplantation for children and adolescents with high-risk cytogenetic AML: distinctly poor outcomes of FUS-ERG-positive cases

Analysis of the molecular mechanism underlying bone marrow necrosis with acute lymphoblastic leukemia.

Association between Chiari malformation and bone marrow failure/myelodysplastic syndrome

Atypical dyskeratosis congenita diagnosed using whole-exome sequencing.

Bernard-Soulier syndrome caused by a hemizygous GPIbβ mutation and 22q11.2 deletion

Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma

Blastic transformation of juvenile myelomonocytic leukemia caused by the copy number gain of oncogenic KRAS.

CBL mutations in juvenile myelomonocytic leukemia and pediatric myelodysplastic syndrome

Case series of pediatric acute leukemia without a peripheral blood abnormality, detected by magnetic resonance imaging

Characterization of adenocarcinoma of the lung in a familial adenomatous polyposis patient

Characterization of genetic lesions in rhabdomyosarcoma using a high-density single nucleotide polymorphism array

Chromosomal abnormalities and novel disease-related regions in progression from Barrett's esophagus to esophageal adenocarcinoma

Cisplatin-induced hearing loss: the need for a long-term evaluating system

Clinical course of autologous recovery with chromosomal abnormalities after allogeneic hematopoietic stem cell transplantation

Clonal evolution mechanisms in NT5C2 mutant-relapsed acute lymphoblastic leukaemia

Comparison of Outcomes for Pediatric Patients With Acute Myeloid Leukemia in Remission and Undergoing Allogeneic Hematopoietic Cell Transplantation With Myeloablative Conditioning Regimens Based on Either Intravenous Busulfan or Total Body Irradiati

Comparison of chemotherapeutic agents as a myeloablative conditioning with total body irradiation for pediatric acute lymphoblastic leukemia: A study from the pediatric ALL working group of the Japan Society for Hematopoietic Cell Transplantation

Comparison of clonazepam and levetiracetam in children for prevention of busulfan-induced seizure in hematopoietic stem cell transplantation

Comparison of intravenous with oral busulfan in allogeneic hematopoietic stem cell transplantation with myeloablative conditioning regimens for pediatric acute leukemia

Consensus definitions of 14 severe acute toxic effects for childhood lymphoblastic leukaemia treatment: a Delphi consensus

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

Copy number analysis identifies tumor suppressive lncRNAs in human osteosarcoma

Cytokine Profiles in Pericardial Effusion in a Down Syndrome Infant with Transient Abnormal Myelopoiesis

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

Delayed short-term administration of granulocyte colony-stimulating factor is a good mobilization strategy for harvesting autologous peripheral blood stem cells in pediatric patients with solid tumors

Deletion of the TNFAIP3/A20 gene detected by FICTION analysis in classical Hodgkin lymphoma

Diplotype analysis of NUDT15 variants and 6-mercaptopurine sensitivity in pediatric lymphoid neoplasms

Donor cell-derived hematological malignancies after allogeneic hematopoietic stem cell transplantation

Exploration of the genetic basis of GVHD by genetic association studies

Favorable outcome in non-infant children with MLL-AF4-positive acute lymphoblastic leukemia: a report from the Tokyo Children's Cancer Study Group

Frequent inactivation of A20 in B-cell lymphomas

Frequent loss of HLA alleles associated with copy number-neutral 6pLOH in acquired aplastic anemia

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

Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms

Genome-wide approach to identify second gene targets for malignant rhabdoid tumors using high-density oligonucleotide microarrays

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

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

Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome

Hematopoietic Stem Cell Transplantation for Progressive Combined Immunodeficiency and Lymphoproliferation in Activated PI3K <delta> Syndrome Type 1.

Hepatoblastoma in a Patient with Sotos Syndrome

Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations

High prevalence of SMARCB1 constitutional abnormalities including mosaicism in malignant rhabdoid tumors

High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

How to manage pediatric oncologic emergencies: Imaging diagnosis

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

Imatinib use immediately before stem cell transplantation in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: Results from Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) Study Ph(+) ALL04

Impact of graft-versus-host disease on relapse and survival after allogeneic stem cell transplantation for pediatric leukemia

Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma

Integrated molecular characterization of the lethal pediatric cancer pancreatoblastoma

Interstitial deletion of 13q14.13-q32.3 presenting with Arima syndrome and bilateral retinoblastoma

Kasabach-Merritt phenomenon: a report of 11 cases from a single institution

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

Long-term survivor of relapsed stage IV malignant rhabdoid tumor of the kidney

MYC amplification as a prognostic marker of early-stage lung adenocarcinoma identified by whole genome copy number analysis.

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

Mutational and functional genetics mapping of chemotherapy resistance mechanisms in relapsed acute lymphoblastic leukemia

Mutational landscape, clonal evolution patterns, and role of RAS mutations in relapsed acute lymphoblastic leukemia

NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity

Nationwide study of pediatric B-cell precursor acute lymphoblastic leukemia with chromosome 8q24/MYC rearrangement in Japan

Nationwide survey of pediatric hypodiploid acute lymphoblastic leukemia in Japan

No impact of high-dose cytarabine and asparaginase as early intensification with intermediate-risk paediatric acute lymphoblastic leukaemia: results of randomized trial TCCSG study L99-15.

Oncogenic mutations of ALK kinase in neuroblastoma

Outcome of pediatric acute lymphoblastic leukemia with very late relapse: a retrospective analysis by the Tokyo Children's Cancer Study Group (TCCSG).

Partial monosomy of 10p and duplication of another chromosome in two patients

Perioperative management of severe congenital protein C deficiency.

Phase II/III study in children and adolescents with newly diagnosed B-cell precursor acute lymphoblastic leukemia: protocol for a nationwide multicenter trial in Japan.

Preclinical evaluation of NUDT15-guided thiopurine therapy and its effects on toxicity and anti-leukemic efficacy.