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Heme controls ferroportin1 (FPN1) transcription involving Bach1, Nrf2 and a MARE/ARE sequence motif at position −7007 of the FPN1 promoter

Haematologica (Roma), 2010-08, Vol.95 (8), p.1261-1268

2010

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The favorable effect of activating NOTCH1 receptor mutations on long-term outcome in T-ALL patients treated on the ALL-BFM 2000 protocol can be separated from FBXW7 loss of function

Leukemia, 2010-12, Vol.24 (12), p.2005-2013

2010

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HFE and ALK3 act in the same signaling pathway

Free radical biology & medicine, 2020-11, Vol.160, p.501-505

2020

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Maternal iron status in early pregnancy and DNA methylation in offspring: an epigenome-wide meta-analysis

Clinical epigenetics, 2022-05, Vol.14 (1), p.59, Article 59

2022

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Efficacy and safety of deferasirox in non-thalassemic patients with elevated ferritin levels after allogeneic hematopoietic stem cell transplantation

Bone marrow transplantation (Basingstoke), 2016-01, Vol.51 (1), p.89-95

2016

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Identification of a genetically defined ultra-high-risk group in relapsed pediatric T-lymphoblastic leukemia

Blood cancer journal (New York), 2017-02, Vol.7 (2), p.e523-e523

2017

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A new paradigm to understand and treat diabetic neuropathy

Experimental and clinical endocrinology & diabetes, 2014-04, Vol.122 (4), p.201

2014

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Iron accelerates cardiovascular disease: The importance of maintaining iron balance

Atherosclerosis, 2016-09, Vol.252, p.e241-e242

2016

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S108: PEDIATRIC T‐ ALL RELAPSE: CONSTITUTIONAL CANCER PREDISPOSITION AND HYPERMUTATATOR PHENOTYPES

HemaSphere, 2022-06, Vol.6, p.9-10

2022

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Iron refractory iron deficiency anemia

Haematologica (Roma), 2013-06, Vol.98 (6), p.845-853

2013

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S277: HYPOFERREMIA CAUSED BY FERROPORTIN DOWNREGULATION IS REGULATED BY NFКB THROUGH HDAC‐DEPENDENT MECHANISMS

HemaSphere, 2022-06, Vol.6, p.178-179

2022

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The murine growth differentiation factor 15 is not essential for systemic iron homeostasis in phlebotomized mice

Haematologica (Roma), 2013-03, Vol.98 (3), p.444-447

2013

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S274: A NOVEL SUBTYPE OF ANEMIA CAUSED BY MUTATIONS IN TFRC GENE

HemaSphere, 2022-06, Vol.6, p.175-176

2022

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NOTCH1 activation clinically antagonizes the unfavorable effect of PTEN inactivation in BFM-treated children with precursor T-cell acute lymphoblastic leukemia

Haematologica (Roma), 2013-06, Vol.98 (6), p.928-936

2013

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Pediatric T-cell lymphoblastic leukemia evolves into relapse by clonal selection, acquisition of mutations and promoter hypomethylation

Haematologica (Roma), 2015-11, Vol.100 (11), p.1442

2015

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Comparison of Fluorescent Tag DNA Labeling Methods Used for Expression Analysis by DNA Microarrays

BioTechniques, 2002-09, Vol.33 (3), p.620-630

2002

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Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosis

Nature genetics, 2003-05, Vol.34 (1), p.102-107

2003

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High CD45 surface expression determines relapse risk in children with precursor B-cell and T-cell acute lymphoblastic leukemia treated according to the ALL-BFM 2000 protocol

Haematologica (Roma), 2014-01, Vol.99 (1), p.103

2014

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Balancing Acts: Molecular Control of Mammalian Iron Metabolism

Cell, 2004-04, Vol.117 (3), p.285-297

2004

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Hereditary hyperferritinemia cataract syndrome--the first family in Germany

Zeitschrift fur Gastroenterologie, 2009-12, Vol.47 (12), p.1211

2009

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A sensitive array for microRNA expression profiling (miChip) based on locked nucleic acids (LNA)

RNA (Cambridge), 2006-05, Vol.12 (5), p.913-920

2006

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Cystic Fibrosis (CF) Newborn Screening (NBS) – Comparison of an IRT-PAP with an IRT-DNA based protocol in a German population

Journal of cystic fibrosis, 2009, Vol.8, p.S9-S9

2009

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HFE Downregulates Iron Uptake From Transferrin and Induces Iron-Regulatory Protein Activity in Stably Transfected Cells

Blood, 1999-12, Vol.94 (11), p.3915-3921

1999

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Heme controls ferroportin1 (FPN1) transcription involving Bach1, Nrf2 and a MARE/ARE sequence motif at position −7007 of the FPN1 promoter

The favorable effect of activating NOTCH1 receptor mutations on long-term outcome in T-ALL patients treated on the ALL-BFM 2000 protocol can be separated from FBXW7 loss of function

HFE and ALK3 act in the same signaling pathway

Maternal iron status in early pregnancy and DNA methylation in offspring: an epigenome-wide meta-analysis

Efficacy and safety of deferasirox in non-thalassemic patients with elevated ferritin levels after allogeneic hematopoietic stem cell transplantation

Identification of a genetically defined ultra-high-risk group in relapsed pediatric T-lymphoblastic leukemia

A new paradigm to understand and treat diabetic neuropathy

Iron accelerates cardiovascular disease: The importance of maintaining iron balance

S108: PEDIATRIC T‐ ALL RELAPSE: CONSTITUTIONAL CANCER PREDISPOSITION AND HYPERMUTATATOR PHENOTYPES

Iron refractory iron deficiency anemia

S277: HYPOFERREMIA CAUSED BY FERROPORTIN DOWNREGULATION IS REGULATED BY NFКB THROUGH HDAC‐DEPENDENT MECHANISMS

The murine growth differentiation factor 15 is not essential for systemic iron homeostasis in phlebotomized mice

S274: A NOVEL SUBTYPE OF ANEMIA CAUSED BY MUTATIONS IN TFRC GENE

The activating STAT5B N642H mutation is a common abnormality in pediatric T-cell acute lymphoblastic leukemia and confers a higher risk of relapse

NOTCH1 activation clinically antagonizes the unfavorable effect of PTEN inactivation in BFM-treated children with precursor T-cell acute lymphoblastic leukemia

Pediatric T-cell lymphoblastic leukemia evolves into relapse by clonal selection, acquisition of mutations and promoter hypomethylation

Comparison of Fluorescent Tag DNA Labeling Methods Used for Expression Analysis by DNA Microarrays

Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosis

High CD45 surface expression determines relapse risk in children with precursor B-cell and T-cell acute lymphoblastic leukemia treated according to the ALL-BFM 2000 protocol

Consensus Statement on the definition and classification of metabolic hyperferritinaemia

Balancing Acts: Molecular Control of Mammalian Iron Metabolism

Hereditary hyperferritinemia cataract syndrome--the first family in Germany

A sensitive array for microRNA expression profiling (miChip) based on locked nucleic acids (LNA)

Cystic Fibrosis (CF) Newborn Screening (NBS) – Comparison of an IRT-PAP with an IRT-DNA based protocol in a German population

HFE Downregulates Iron Uptake From Transferrin and Induces Iron-Regulatory Protein Activity in Stably Transfected Cells

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