Lista de obras -

Aberrant somatic hypermutation and expression of activation-induced cytidine deaminase mRNA in mediastinal large B-cell lymphoma.

artículo científico publicado en 2005

Altered microRNA expression in folliculotropic and transformed mycosis fungoides.

artículo científico publicado en 2015

Calreticulin mutation specific CAL2 immunohistochemistry accurately identifies rare calreticulin mutations in myeloproliferative neoplasms

scientific article published on 31 December 2018

Catalog of genetic progression of human cancers: non-Hodgkin lymphoma.

artículo científico publicado en 2016

Chromatin mapping and single-cell immune profiling define the temporal dynamics of ibrutinib response in CLL

scientific article published on 29 January 2020

Clonal selection in the bone marrow involvement of follicular lymphoma.

artículo científico publicado en 2005

Concomitant 1p36 deletion and TNFRSF14 mutations in primary cutaneous follicle center lymphoma frequently expressing high levels of EZH2 protein

scientific article published on 01 June 2018

DNA and RNA isolated from tissues processed by microwave-accelerated apparatus MFX-800-3 are suitable for subsequent PCR and Q-RT-PCR amplification

artículo científico publicado en 2007

Discrepancy Between Low Levels of mTOR Activity and High Levels of P-S6 in Primary Central Nervous System Lymphoma May Be Explained by PAS Domain-Containing Serine/Threonine-Protein Kinase-Mediated Phosphorylation.

artículo científico publicado en 2018

Dissection of subclonal evolution by temporal mutation profiling in chronic lymphocytic leukemia patients treated with ibrutinib

scientific article published on 25 June 2019

EBNA3B-deficient EBV promotes B cell lymphomagenesis in humanized mice and is found in human tumors

artículo científico publicado en 2012

EZH2 Y641 mutations in follicular lymphoma.

artículo científico publicado en 2011

EZH2 is upregulated in the proliferation centers of CLL/SLL lymph nodes

artículo científico publicado en 2018

EZH2 mutations are frequent and represent an early event in follicular lymphoma

artículo científico publicado en 2013

Elevated expression of Cu, Zn-SOD and Mn-SOD mRNA in inflamed dental pulp tissue.

artículo científico publicado en 2007

Enhancer of zeste homologue 2 (EZH2) is a reliable immunohistochemical marker to differentiate malignant and benign hepatic tumors.

artículo científico publicado en 2012

Familial Acute Myeloid Leukemia and Myelodysplasia in Hungary

artículo científico publicado en 2017

Functional analysis of a breast cancer-associated FGFR2 single nucleotide polymorphism using zinc finger mediated genome editing

artículo científico publicado en 2013

Functional studies of chronic lymphocytic leukemia B cells expressing β2-integrin type complement receptors CR3 and CR4.

artículo científico publicado en 2017

GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML

artículo científico publicado en 2018

Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival.

artículo científico publicado en 2012

High-Throughput Copy Number Profiling by Digital Multiplex Ligation-Dependent Probe Amplification in Multiple Myeloma

artículo científico publicado en 2018

Highly variable clinical manifestations in a large family with a novel GATA2 mutation.

artículo científico publicado en 2013

Impact of the reactive microenvironment on the bone marrow involvement of follicular lymphoma.

artículo científico publicado en 2012

Increased Lipocalin 2 level may have important role in thrombotic events in patients with polycythemia vera and essential thrombocythemia

artículo científico publicado en 2016

Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma

artículo científico publicado en 2013

Juvenile myelomonocytic leukaemia presentation after preceding juvenile xanthogranuloma harbouring an identical somatic PTPN11 mutation

scientific article published on 18 June 2020

Low CD23 expression correlates with high CD38 expression and the presence of trisomy 12 in CLL.

artículo científico publicado en 2015

Myelodysplastic syndrome: 2011 and beyond

artículo científico publicado en 2011

P110α-mediated constitutive PI3K signaling limits the efficacy of p110δ-selective inhibition in mantle cell lymphoma, particularly with multiple relapse

artículo científico publicado en 2013

Prognostic significance and detection of the internal tandem duplication of the FLT3 gene in acute myeloid leukemia

artículo científico publicado en 2006

Quantitative assessment of JAK2 V617F and CALR mutations in Philadelphia negative myeloproliferative neoplasms

artículo científico publicado en 2018

ROR1 expression is not a unique marker of CLL

artículo científico publicado en 2011

Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma.

artículo científico publicado en 2015

Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigree

artículo científico publicado en 2017

Richter's and prolymphocytic transformation of chronic lymphocytic leukemia are associated with high mRNA expression of activation-induced cytidine deaminase and aberrant somatic hypermutation.

artículo científico publicado en 2006

Spatial clonal evolution leading to ibrutinib resistance and disease progression in chronic lymphocytic leukemia

scientific article published on 27 September 2018

State of the art molecular diagnostics and therapy of chronic lymphocytic leukaemia in the era of new targeted therapies

artículo científico publicado en 2017

Structural analysis of oval-cell-mediated liver regeneration in rats.

artículo científico publicado en 2012

The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants

artículo científico publicado en 2020

Thy-1 is expressed in hepatic myofibroblasts and not oval cells in stem cell-mediated liver regeneration.

artículo científico publicado en 2007

Treatment of refractory hairy cell leukemia with a BRAF-inhibitor: lessons to be learnt.

artículo científico publicado en 2014

[Change in paradigm in the treatment of pediatric acquired bone marrow failure syndromes in Hungary]

artículo científico publicado en 2018

[Chronic myelogenous leukemia: diagnosis and treatment].

artículo científico publicado en 2016

[Clinical and genetic background of familial myelodysplasia and acute myeloid leukemia].

artículo científico publicado en 2016

[Multiplex ligation-dependent probe amplification in oncohematological diagnostics and research]

scientific article published on 01 April 2018

[TP53 mutation analysis in chronic lymphocytic leukaemia].

artículo científico publicado en 2017

Lista de obras de

Aberrant somatic hypermutation and expression of activation-induced cytidine deaminase mRNA in mediastinal large B-cell lymphoma.

Altered microRNA expression in folliculotropic and transformed mycosis fungoides.

Calreticulin mutation specific CAL2 immunohistochemistry accurately identifies rare calreticulin mutations in myeloproliferative neoplasms

Catalog of genetic progression of human cancers: non-Hodgkin lymphoma.

Chromatin mapping and single-cell immune profiling define the temporal dynamics of ibrutinib response in CLL

Clonal selection in the bone marrow involvement of follicular lymphoma.

Concomitant 1p36 deletion and TNFRSF14 mutations in primary cutaneous follicle center lymphoma frequently expressing high levels of EZH2 protein

DNA and RNA isolated from tissues processed by microwave-accelerated apparatus MFX-800-3 are suitable for subsequent PCR and Q-RT-PCR amplification

Discrepancy Between Low Levels of mTOR Activity and High Levels of P-S6 in Primary Central Nervous System Lymphoma May Be Explained by PAS Domain-Containing Serine/Threonine-Protein Kinase-Mediated Phosphorylation.

Dissection of subclonal evolution by temporal mutation profiling in chronic lymphocytic leukemia patients treated with ibrutinib

EBNA3B-deficient EBV promotes B cell lymphomagenesis in humanized mice and is found in human tumors

EZH2 Y641 mutations in follicular lymphoma.

EZH2 is upregulated in the proliferation centers of CLL/SLL lymph nodes

EZH2 mutations are frequent and represent an early event in follicular lymphoma

Elevated expression of Cu, Zn-SOD and Mn-SOD mRNA in inflamed dental pulp tissue.

Enhancer of zeste homologue 2 (EZH2) is a reliable immunohistochemical marker to differentiate malignant and benign hepatic tumors.

Familial Acute Myeloid Leukemia and Myelodysplasia in Hungary

Functional analysis of a breast cancer-associated FGFR2 single nucleotide polymorphism using zinc finger mediated genome editing

Functional studies of chronic lymphocytic leukemia B cells expressing β2-integrin type complement receptors CR3 and CR4.

GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML

Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival.

High-Throughput Copy Number Profiling by Digital Multiplex Ligation-Dependent Probe Amplification in Multiple Myeloma

Highly variable clinical manifestations in a large family with a novel GATA2 mutation.

Impact of the reactive microenvironment on the bone marrow involvement of follicular lymphoma.

Increased Lipocalin 2 level may have important role in thrombotic events in patients with polycythemia vera and essential thrombocythemia

Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma

Juvenile myelomonocytic leukaemia presentation after preceding juvenile xanthogranuloma harbouring an identical somatic PTPN11 mutation

Low CD23 expression correlates with high CD38 expression and the presence of trisomy 12 in CLL.

Myelodysplastic syndrome: 2011 and beyond

P110α-mediated constitutive PI3K signaling limits the efficacy of p110δ-selective inhibition in mantle cell lymphoma, particularly with multiple relapse

Prognostic significance and detection of the internal tandem duplication of the FLT3 gene in acute myeloid leukemia

Quantitative assessment of JAK2 V617F and CALR mutations in Philadelphia negative myeloproliferative neoplasms

ROR1 expression is not a unique marker of CLL

Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma.

Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigree

Richter's and prolymphocytic transformation of chronic lymphocytic leukemia are associated with high mRNA expression of activation-induced cytidine deaminase and aberrant somatic hypermutation.

Spatial clonal evolution leading to ibrutinib resistance and disease progression in chronic lymphocytic leukemia

State of the art molecular diagnostics and therapy of chronic lymphocytic leukaemia in the era of new targeted therapies

Structural analysis of oval-cell-mediated liver regeneration in rats.

The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants

Thy-1 is expressed in hepatic myofibroblasts and not oval cells in stem cell-mediated liver regeneration.

Treatment of refractory hairy cell leukemia with a BRAF-inhibitor: lessons to be learnt.

[Change in paradigm in the treatment of pediatric acquired bone marrow failure syndromes in Hungary]

[Chronic myelogenous leukemia: diagnosis and treatment].

[Clinical and genetic background of familial myelodysplasia and acute myeloid leukemia].

[Multiplex ligation-dependent probe amplification in oncohematological diagnostics and research]

[TP53 mutation analysis in chronic lymphocytic leukaemia].