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The molecular pathogenesis of the NUP98-HOXA9 fusion protein in acute myeloid leukemia

Leukemia, 2017-09, Vol.31 (9), p.2000-2005

2017

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Downregulation of specific miRNAs in hyperdiploid multiple myeloma mimics the oncogenic effect of IgH translocations occurring in the non-hyperdiploid subtype

Leukemia, 2013-04, Vol.27 (4), p.925-931

2013

Volltextzugriff (PDF)

P405: INHIBITION OF CKS1‐DEPENDENT PROTEOSTASIS REVEALS VULNERABILITIES IN LEUKAEMIC STEM CELLS WITH CONCOMITANT PROTECTION OF HEALTHY HAEMATOPOIETIC STEM CELLS

HemaSphere, 2022-06, Vol.6, p.305-306

2022

Volltextzugriff (PDF)

Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia

Leukemia, 2016-10, Vol.30 (10), p.2083-2086

2016

Volltextzugriff (PDF)

Abrogation of RUNX1 gene expression in de novo myelodysplastic syndrome with t(4;21)(q21;q22)

Haematologica (Roma), 2012-04, Vol.97 (4), p.534-537

2012

Volltextzugriff (PDF)

Proteomic and genomic integration identifies kinase and differentiation determinants of kinase inhibitor sensitivity in leukemia cells

Leukemia, 2017-12

2017

Volltextzugriff (PDF)

PF213 THE GENETIC LANDSCAPE OF FAMILIAL MDS/AML; RECURRING MUTATIONS IN THE RNA HELICASE DHX34 LEADING TO DEFECTS IN NONSENSE‐MEDIATED RNA DECAY

HemaSphere, 2019-06, Vol.3 (S1), p.58-n/a

2019

Volltextzugriff (PDF)

GATA2 deficiency syndrome: A compensatory mechanism gone awry?

British journal of haematology, 2024-08, Vol.205 (2), p.411-413

Rio‐Machin, Ana

2024

Volltextzugriff (PDF)

ATM serine/threonine kinase germline mutations in chronic lymphocytic leukaemia come in different flavours

British journal of haematology, 2022-11, Vol.199 (3), p.307-309

Rio‐Machin, Ana

2022

Volltextzugriff (PDF)

DDX41: the poster child for familial AML

Blood, 2022-08, Vol.140 (7), p.667-669

2022

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AML through the prism of molecular genetics

British journal of haematology, 2020-01, Vol.188 (1), p.49-62

2020

Volltextzugriff (PDF)

BPTF is required for c-MYC transcriptional activity and in vivo tumorigenesis

Nature communications, 2016-01, Vol.7 (1), p.10153-15, Article 10153

2016

Volltextzugriff (PDF)

Germline predisposition to haematological malignancies: Best practice consensus guidelines from the UK Cancer Genetics Group (UKCGG), CanGene‐CanVar and the NHS England Haematological Oncology Working Group

British journal of haematology, 2023-04, Vol.201 (1), p.25-34

2023

Volltextzugriff (PDF)

Endogenous retroviruses are a source of enhancers with oncogenic potential in acute myeloid leukaemia

Nature communications, 2020-07, Vol.11 (1), p.3506-3506, Article 3506

2020

Volltextzugriff (PDF)

Germline ERCC excision repair 6 like 2 (ERCC6L2) mutations lead to impaired erythropoiesis and reshaping of the bone marrow microenvironment

British journal of haematology, 2022-12, Vol.199 (5), p.754-764

2022

Volltextzugriff (PDF)

Genomic profiling reveals spatial intra-tumor heterogeneity in follicular lymphoma

Leukemia, 2018-05, Vol.32 (5), p.1261-1265

2018

Volltextzugriff (PDF)

Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene

JNCI : Journal of the National Cancer Institute, 2015-05, Vol.107 (5), p.1

2015

Volltextzugriff (PDF)

Transmission of diffuse large B-cell lymphoma by an allogeneic stem-cell transplant

Haematologica (Roma), 2019-04, Vol.104 (4), p.e174

2019

Volltextzugriff (PDF)

Myelodysplasia and liver disease extend the spectrum of RTEL1 related telomeropathies

Haematologica (Roma), 2017-08, Vol.102 (8), p.e293

2017

Volltextzugriff (PDF)

SH2B3 GERMLINE MUTATION CAUSE A MULTISYSTEM DISORDER WITH PREDISPOSITION TO MYELOPROLIFERATIVE NEOPLASMS

EJC paediatric oncology, 2023-12, Vol.2, p.100042, Article 100042

2023

Volltextzugriff (PDF)

Inherited predisposition to MDS/AML

HemaSphere, 2018-06, Vol.2 (S2), p.12-14

2018

Volltextzugriff (PDF)

MAPK8‐mediated stabilization of SP1 is essential for RUNX1‐RUNX1T1 – driven leukaemia

British journal of haematology, 2016-03, Vol.172 (5), p.807-810

2016

Volltextzugriff (PDF)

Integrative phosphoproteomics defines two biologically distinct groups of KMT2A rearranged acute myeloid leukaemia with different drug response phenotypes

Signal transduction and targeted therapy, 2023-02, Vol.8 (1), p.80-80, Article 80

2023

Volltextzugriff (PDF)

Germline ETV6 variants: not ALL created equally

Blood, 2021-01, Vol.137 (3), p.288-289

2021

Volltextzugriff (PDF)

Familial CEBPA -mutated acute myeloid leukemia

Seminars in hematology, 2017-04, Vol.54 (2), p.87-93

2017

Volltextzugriff (PDF)

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The molecular pathogenesis of the NUP98-HOXA9 fusion protein in acute myeloid leukemia

Downregulation of specific miRNAs in hyperdiploid multiple myeloma mimics the oncogenic effect of IgH translocations occurring in the non-hyperdiploid subtype

P405: INHIBITION OF CKS1‐DEPENDENT PROTEOSTASIS REVEALS VULNERABILITIES IN LEUKAEMIC STEM CELLS WITH CONCOMITANT PROTECTION OF HEALTHY HAEMATOPOIETIC STEM CELLS

Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia

Abrogation of RUNX1 gene expression in de novo myelodysplastic syndrome with t(4;21)(q21;q22)

Proteomic and genomic integration identifies kinase and differentiation determinants of kinase inhibitor sensitivity in leukemia cells

PF213 THE GENETIC LANDSCAPE OF FAMILIAL MDS/AML; RECURRING MUTATIONS IN THE RNA HELICASE DHX34 LEADING TO DEFECTS IN NONSENSE‐MEDIATED RNA DECAY

GATA2 deficiency syndrome: A compensatory mechanism gone awry?

ATM serine/threonine kinase germline mutations in chronic lymphocytic leukaemia come in different flavours

DDX41: the poster child for familial AML

AML through the prism of molecular genetics

BPTF is required for c-MYC transcriptional activity and in vivo tumorigenesis

Germline predisposition to haematological malignancies: Best practice consensus guidelines from the UK Cancer Genetics Group (UKCGG), CanGene‐CanVar and the NHS England Haematological Oncology Working Group

Endogenous retroviruses are a source of enhancers with oncogenic potential in acute myeloid leukaemia

Germline ERCC excision repair 6 like 2 (ERCC6L2) mutations lead to impaired erythropoiesis and reshaping of the bone marrow microenvironment

Genomic profiling reveals spatial intra-tumor heterogeneity in follicular lymphoma

Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene

Transmission of diffuse large B-cell lymphoma by an allogeneic stem-cell transplant

Myelodysplasia and liver disease extend the spectrum of RTEL1 related telomeropathies

SH2B3 GERMLINE MUTATION CAUSE A MULTISYSTEM DISORDER WITH PREDISPOSITION TO MYELOPROLIFERATIVE NEOPLASMS

Inherited predisposition to MDS/AML

MAPK8‐mediated stabilization of SP1 is essential for RUNX1‐RUNX1T1 – driven leukaemia

Integrative phosphoproteomics defines two biologically distinct groups of KMT2A rearranged acute myeloid leukaemia with different drug response phenotypes

Germline ETV6 variants: not ALL created equally

Familial CEBPA -mutated acute myeloid leukemia

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