UB Paderborn / Katalog / Suche / in CDI

Spanish Guidelines for the use of targeted deep sequencing in myelodysplastic syndromes and chronic myelomonocytic leukaemia

British journal of haematology, 2020-03, Vol.188 (5), p.605-622

2020

Link zum Volltext

Verfügbarkeit prüfen

Diagnostic and prognostic contribution of targeted NGS in patients with triple‐negative myeloproliferative neoplasms

American journal of hematology, 2019-10, Vol.94 (10), p.E264-E267

2019

Link zum Volltext

Verfügbarkeit prüfen

Distinct mutational pattern of myelodysplastic syndromes with and without 5q– treated with lenalidomide

British journal of haematology, 2020-05, Vol.189 (4), p.e133-e137

2020

Link zum Volltext

Verfügbarkeit prüfen

Mutational signatures are markers of drug sensitivity of cancer cells

Nature communications, 2022-05, Vol.13 (1), p.2926-2926, Article 2926

2022

Link zum Volltext

Verfügbarkeit prüfen

Molecular landscape and clonal architecture of adult myelodysplastic/myeloproliferative neoplasms

Blood, 2020-10, Vol.136 (16), p.1851-1862

2020

Link zum Volltext

Verfügbarkeit prüfen

Targeted deep sequencing of CD34+ cells from peripheral blood can reproduce bone marrow molecular profile in myelodysplastic syndromes

American journal of hematology, 2018-06, Vol.93 (6), p.E152-E154

2018

Link zum Volltext

Verfügbarkeit prüfen

Analysis of Intratumoral Heterogeneity in Myelodysplastic Syndromes with Isolated del(5q) Using a Single Cell Approach

Cancers, 2021-02, Vol.13 (4), p.841

2021

Link zum Volltext

Verfügbarkeit prüfen

DNA methylation profile in chronic myelomonocytic leukemia associates with distinct clinical, biological and genetic features

Epigenetics, 2018-01, Vol.13 (1), p.8-18

2018

Link zum Volltext

Verfügbarkeit prüfen

Matching cell lines with cancer type and subtype of origin via mutational, epigenomic, and transcriptomic patterns

Science advances, 2020-07, Vol.6 (27)

2020

Link zum Volltext

Verfügbarkeit prüfen

TP53 Allelic State in Myelodysplastic Syndromes with 5q Deletion

Blood, 2022-11, Vol.140 (Supplement 1), p.6949-6951

2022

Link zum Volltext

Verfügbarkeit prüfen

Usefulness of a Sequencing Panel in Myeloproliferative Neoplasms Lacking Mutations in Driver Genes

Blood, 2017-12, Vol.130, p.1651-1651

2017

Link zum Volltext

Verfügbarkeit prüfen

Genomics improves risk stratification of adults with T-cell acute lymphoblastic leukemia enrolled in measurable residual disease-oriented trials

Haematologica (Roma), 2023-04, Vol.108 (4), p.969-980

2023

Link zum Volltext

Verfügbarkeit prüfen

Genomic Data Improves Prognostic Stratification in Adult T-Cell Acute Lymphoblastic Leukemia Patients Enrolled in Measurable Residual Disease-Oriented Trials

Blood, 2021-11, Vol.138 (Supplement 1), p.3486-3486

2021

Link zum Volltext

Verfügbarkeit prüfen

Genomics improves risk stratifi cation of adults with T-cell acute lymphoblastic leukemia enrolled in measurable residual disease-oriented trials

Haematologica (Roma), 2023-04, Vol.108 (4), p.969-980

2023

Link zum Volltext

Verfügbarkeit prüfen

Adverse prognostic impact of complex karyotype (≥3 cytogenetic alterations) in adult T-cell acute lymphoblastic leukemia (T-ALL)

Leukemia research, 2021-10, Vol.109, p.106612-106612, Article 106612

2021

Link zum Volltext

Verfügbarkeit prüfen

Application of Trusight Myeloid Panel on Whole Genome Amplified DNA in Myelodysplastic Syndrome Patients

Blood, 2016-12, Vol.128 (22), p.5519-5519

2016

Link zum Volltext

Verfügbarkeit prüfen

Genetic characterization of acute myeloid leukemia patients with mutations in IDH1/2 genes

Leukemia research, 2021-02, Vol.101, p.106492-106492, Article 106492

2021

Link zum Volltext

Verfügbarkeit prüfen

Poster: ALL-154: t(1;19)(q23;p13) TCF3-PBX1 May Not Be an Intermediate-Risk Subtype in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Patients Treated With MRD-Oriented Protocols from the PETHEMA Group

Clinical lymphoma, myeloma and leukemia, 2021-09, Vol.21, p.S207-S207

2021

Link zum Volltext

Verfügbarkeit prüfen

ALL-154: t(1;19)(q23;p13) TCF3-PBX1 May Not Be an Intermediate-Risk Subtype in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Patients Treated With MRD-Oriented Protocols from the PETHEMA Group

Clinical lymphoma, myeloma and leukemia, 2021-09, Vol.21, p.S270-S271

2021

Link zum Volltext

Verfügbarkeit prüfen

In MDS Targeted Deep Sequencing of CD34+ Blood Cells but Not Peripheral Blood Mononuclear Cells Give Results Which Are Representative for Bone Marrow

Blood, 2016-12, Vol.128 (22), p.2383-2383

2016

Link zum Volltext

Verfügbarkeit prüfen

ALL-276: Complex Karyotype with ≥3 Cytogenetic Alterations is a New Marker of Worse Prognosis in Adult T-Cell Acute Lymphoblastic Leukemia (T-ALL)

Clinical lymphoma, myeloma and leukemia, 2020-09, Vol.20, p.S167-S168

2020

Link zum Volltext

Verfügbarkeit prüfen

Inspecting Targeted Deep Sequencing of Whole Genome Amplified DNA Versus Fresh DNA for Somatic Mutation Detection: A Genetic Study in Myelodysplastic Syndrome Patients

Biopreservation and biobanking, 2017-08, Vol.15 (4), p.360

2017

Link zum Volltext

Verfügbarkeit prüfen

Menü

Weitere Dienste

Einstellungen

Spanish Guidelines for the use of targeted deep sequencing in myelodysplastic syndromes and chronic myelomonocytic leukaemia

Diagnostic and prognostic contribution of targeted NGS in patients with triple‐negative myeloproliferative neoplasms

Distinct mutational pattern of myelodysplastic syndromes with and without 5q– treated with lenalidomide

Mutational signatures are markers of drug sensitivity of cancer cells

Molecular landscape and clonal architecture of adult myelodysplastic/myeloproliferative neoplasms

Targeted deep sequencing of CD34+ cells from peripheral blood can reproduce bone marrow molecular profile in myelodysplastic syndromes

Analysis of Intratumoral Heterogeneity in Myelodysplastic Syndromes with Isolated del(5q) Using a Single Cell Approach

DNA methylation profile in chronic myelomonocytic leukemia associates with distinct clinical, biological and genetic features

Matching cell lines with cancer type and subtype of origin via mutational, epigenomic, and transcriptomic patterns

TP53 Allelic State in Myelodysplastic Syndromes with 5q Deletion

Usefulness of a Sequencing Panel in Myeloproliferative Neoplasms Lacking Mutations in Driver Genes

Genomics improves risk stratification of adults with T-cell acute lymphoblastic leukemia enrolled in measurable residual disease-oriented trials

Genomic Data Improves Prognostic Stratification in Adult T-Cell Acute Lymphoblastic Leukemia Patients Enrolled in Measurable Residual Disease-Oriented Trials

Genomics improves risk stratifi cation of adults with T-cell acute lymphoblastic leukemia enrolled in measurable residual disease-oriented trials

Adverse prognostic impact of complex karyotype (≥3 cytogenetic alterations) in adult T-cell acute lymphoblastic leukemia (T-ALL)

Application of Trusight Myeloid Panel on Whole Genome Amplified DNA in Myelodysplastic Syndrome Patients

Genetic characterization of acute myeloid leukemia patients with mutations in IDH1/2 genes

Poster: ALL-154: t(1;19)(q23;p13) TCF3-PBX1 May Not Be an Intermediate-Risk Subtype in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Patients Treated With MRD-Oriented Protocols from the PETHEMA Group

ALL-154: t(1;19)(q23;p13) TCF3-PBX1 May Not Be an Intermediate-Risk Subtype in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Patients Treated With MRD-Oriented Protocols from the PETHEMA Group

Comparison of the Molecular Spectrum of Lenalidomide-Treated Myelodysplastic Syndrome with and without Del(5q)

In MDS Targeted Deep Sequencing of CD34+ Blood Cells but Not Peripheral Blood Mononuclear Cells Give Results Which Are Representative for Bone Marrow

ALL-276: Complex Karyotype with ≥3 Cytogenetic Alterations is a New Marker of Worse Prognosis in Adult T-Cell Acute Lymphoblastic Leukemia (T-ALL)

The Complete Mutatome and Clonal Architecture of Del(5q)

Inspecting Targeted Deep Sequencing of Whole Genome Amplified DNA Versus Fresh DNA for Somatic Mutation Detection: A Genetic Study in Myelodysplastic Syndrome Patients

Suchergebnisse filtern