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Protein Subassemblies of the Helicobacter pylori Cag Type IV Secretion System Revealed by Localization and Interaction Studies

Journal of Bacteriology, 2008-03, Vol.190 (6), p.2161-2171

2008

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The leukemia-specific fusion gene ETV6/RUNX1 perturbs distinct key biological functions primarily by gene repression

PloS one, 2011-10, Vol.6 (10), p.e26348-e26348

2011

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Genomic breakpoint-specific monitoring of measurable residual disease in pediatric non-standard-risk acute myeloid leukemia

Haematologica (Roma), 2024-03, Vol.109 (3), p.740-750

2024

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High susceptibility to fatty liver disease in two-pore channel 2-deficient mice

Nature communications, 2014-08, Vol.5 (1), p.4699, Article 4699

2014

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Whole-genome sequencing of tetraploid potato varieties reveals different strategies for drought tolerance

Scientific reports, 2024-03, Vol.14 (1), p.5476-5476

2024

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Copy Number Changes and Allele Distribution Patterns of Chromosome 21 in B Cell Precursor Acute Lymphoblastic Leukemia

Cancers, 2021-09, Vol.13 (18), p.4597

2021

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Pilot study to identify missed opportunities for prevention of childhood tuberculosis

European journal of pediatrics, 2022-09, Vol.181 (9), p.3299-3307

2022

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ETV6/RUNX1-positive relapses evolve from an ancestral clone and frequently acquire deletions of genes implicated in glucocorticoid signaling

Blood, 2011-03, Vol.117 (9), p.2658-2667

2011

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The enigmatic role(s) of P2RY8-CRLF2

Oncotarget, 2017-11, Vol.8 (57), p.96466-96467

2017

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Aneuploidy in children with relapsed B‐cell precursor acute lymphoblastic leukaemia: clinical importance of detecting a hypodiploid origin of relapse

British journal of haematology, 2019-04, Vol.185 (2), p.266-283

2019

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Oscillometric pulse wave velocity estimated via the Mobil-O-Graph shows excellent accuracy in children, adolescents and young adults: an invasive validation study

Journal of hypertension, 2023-04, Vol.41 (4), p.597

2023

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Frequency and characterization of known and novel RHD variant alleles in 37 782 Dutch D‐negative pregnant women

British journal of haematology, 2016-05, Vol.173 (3), p.469-479

2016

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Genome-Wide Approach to Identify Quantitative Trait Loci for Drought Tolerance in Tetraploid Potato (Solanum tuberosum L.)

International journal of molecular sciences, 2021-06, Vol.22 (11), p.6123

2021

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Systematic mutagenesis of the Helicobacter pylori cag pathogenicity island: essential genes for CagA translocation in host cells and induction of interleukin‐8

Molecular microbiology, 2001-12, Vol.42 (5), p.1337-1348

2001

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Imatinib-induced long-term remission in a relapsed RCSD1-ABL1-positive acute lymphoblastic leukemia

Haematologica (Roma), 2016-08, Vol.101 (8), p.e332-e335

2016

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A novel sheathed surface organelle of the Helicobacter pylori cag type IV secretion system

Molecular microbiology, 2003-07, Vol.49 (1), p.219-234

2003

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Cyclic GMP and protein kinase G control a Src-containing mechanosome in osteoblasts

Science signaling, 2010-12, Vol.3 (153), p.ra91

2010

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Sputtered Iridium Oxide as Electrode Material for Subretinal Stimulation

Sensors and materials, 2020-09, Vol.32 (9), p.2903

2020

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Disruption of the vacuolar-type H+-ATPase complex in liver causes MTORC1-independent accumulation of autophagic vacuoles and lysosomes

Autophagy, 2017-04, Vol.13 (4), p.670-685

2017

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Treatment outcome of CRLF2-rearranged childhood acute lymphoblastic leukaemia: a comparative analysis of the AIEOP-BFM and UK NCRI-CCLG study groups

British journal of haematology, 2012-09, Vol.158 (6), p.772-777

2012

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Genetic alterations in glucocorticoid signaling pathway components are associated with adverse prognosis in children with relapsed ETV6/RUNX1-positive acute lymphoblastic leukemia

Leukemia & lymphoma, 2016-05, Vol.57 (5), p.1163-1173

2016

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Protein Subassemblies of the Helicobacter pylori Cag Type IV Secretion System Revealed by Localization and Interaction Studies

The leukemia-specific fusion gene ETV6/RUNX1 perturbs distinct key biological functions primarily by gene repression

Genomic breakpoint-specific monitoring of measurable residual disease in pediatric non-standard-risk acute myeloid leukemia

High susceptibility to fatty liver disease in two-pore channel 2-deficient mice

Molecular response to treatment redefines all prognostic factors in children and adolescents with B-cell precursor acute lymphoblastic leukemia: results in 3184 patients of the AIEOP-BFM ALL 2000 study

Whole-genome sequencing of tetraploid potato varieties reveals different strategies for drought tolerance

Copy Number Changes and Allele Distribution Patterns of Chromosome 21 in B Cell Precursor Acute Lymphoblastic Leukemia

Pilot study to identify missed opportunities for prevention of childhood tuberculosis

ETV6/RUNX1-positive relapses evolve from an ancestral clone and frequently acquire deletions of genes implicated in glucocorticoid signaling

The enigmatic role(s) of P2RY8-CRLF2

Small sizes and indolent evolutionary dynamics challenge the potential role of P2RY8-CRLF2–harboring clones as main relapse-driving force in childhood ALL

Aneuploidy in children with relapsed B‐cell precursor acute lymphoblastic leukaemia: clinical importance of detecting a hypodiploid origin of relapse

Oscillometric pulse wave velocity estimated via the Mobil-O-Graph shows excellent accuracy in children, adolescents and young adults: an invasive validation study

Frequency and characterization of known and novel RHD variant alleles in 37 782 Dutch D‐negative pregnant women

Genome-Wide Approach to Identify Quantitative Trait Loci for Drought Tolerance in Tetraploid Potato (Solanum tuberosum L.)

Systematic mutagenesis of the Helicobacter pylori cag pathogenicity island: essential genes for CagA translocation in host cells and induction of interleukin‐8

Imatinib-induced long-term remission in a relapsed RCSD1-ABL1-positive acute lymphoblastic leukemia

A novel sheathed surface organelle of the Helicobacter pylori cag type IV secretion system

Minimal Residual Disease Values Discriminate Between Low and High Relapse Risk in Children With B-Cell Precursor Acute Lymphoblastic Leukemia and an Intrachromosomal Amplification of Chromosome 21: The Austrian and German Acute Lymphoblastic Leukemia Berlin-Frankfurt-Münster (ALL-BFM) Trials

Cyclic GMP and protein kinase G control a Src-containing mechanosome in osteoblasts

Sputtered Iridium Oxide as Electrode Material for Subretinal Stimulation

Prospective use of molecular minimal residual disease for risk stratification in children and adolescents with acute lymphoblastic leukemia : Long-term results of the AIEOP-BFM ALL 2000 trial in Austria

Disruption of the vacuolar-type H+-ATPase complex in liver causes MTORC1-independent accumulation of autophagic vacuoles and lysosomes

Treatment outcome of CRLF2-rearranged childhood acute lymphoblastic leukaemia: a comparative analysis of the AIEOP-BFM and UK NCRI-CCLG study groups

Genetic alterations in glucocorticoid signaling pathway components are associated with adverse prognosis in children with relapsed ETV6/RUNX1-positive acute lymphoblastic leukemia

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