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Activated mineralocorticoid receptor regulates micro‐RNA‐29b in vascular smooth muscle cells

The FASEB journal, 2016-04, Vol.30 (4), p.1610-1622

2016

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EF Domains Are Sufficient for Nongenomic Mineralocorticoid Receptor Actions

The Journal of biological chemistry, 2008-03, Vol.283 (11), p.7109-7116

2008

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Mineralocorticoid receptor inhibits CREB signaling by calcineurin activation

The FASEB journal, 2010-06, Vol.24 (6), p.2010-2019

2010

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Aldosterone Stimulates Epidermal Growth Factor Receptor Expression

The Journal of biological chemistry, 2003-10, Vol.278 (44), p.43060-43066

2003

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Structural and molecular determinants of mineralocorticoid receptor signalling

British journal of pharmacology, 2022-07, Vol.179 (13), p.3103-3118

2022

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Modulation of transcriptional mineralocorticoid receptor activity by casein kinase 1

The FASEB journal, 2022-01, Vol.36 (1), p.e22059-n/a

2022

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Long‐term application of the aldosterone antagonist spironolactone prevents stiff endothelial cell syndrome

The FASEB journal, 2013-09, Vol.27 (9), p.3652-3659

2013

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The phosphatase calcineurin PP2BAβ mediates part of mineralocorticoid receptor transcriptional activity

The FASEB journal, 2012-06, Vol.26 (6), p.2327-2337

2012

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Mineralocorticoid receptor interaction with SP1 generates a new response element for pathophysiologically relevant gene expression

Nucleic acids research, 2013-09, Vol.41 (17), p.8045-8060

2013

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Feedforward activation of endothelial ENaC by high sodium

The FASEB journal, 2014-09, Vol.28 (9), p.4015-4025

2014

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Transactivation via the human glucocorticoid and mineralocorticoid receptor by therapeutically used steroids in CV-1 cells: a comparison of their glucocorticoid and mineralocorticoid properties

European journal of endocrinology, 2004-09, Vol.151 (3), p.397-406

2004

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PP2A attenuates cardiac response to LPS‐induced sepsis

The FASEB journal, 2010-04, Vol.24 (S1), p.793.7-793.7

2010

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A novel hierarchical prognostic model of AML solely based on molecular mutations

Blood, 2012-10, Vol.120 (15), p.2963-2972

2012

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Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1

Journal of clinical oncology, 2010-08, Vol.28 (24), p.3858-3865

2010

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Phase III Trial in Metastatic Gastroesophageal Adenocarcinoma with Fluorouracil, Leucovorin Plus Either Oxaliplatin or Cisplatin: A Study of the Arbeitsgemeinschaft Internistische Onkologie

Journal of clinical oncology, 2008-03, Vol.26 (9), p.1435-1442

2008

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High frequencies of SF3B1 and JAK2 mutations in refractory anemia with ring sideroblasts associated with marked thrombocytosis strengthen the assignment to the category of myelodysplastic/myeloproliferative neoplasms

Haematologica (Roma), 2013-02, Vol.98 (2), p.e15-e17

2013

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SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)

Blood, 2012-10, Vol.120 (15), p.3080-3088

2012

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Prognostic relevance of RUNX1 mutations in T-cell acute lymphoblastic leukemia

Haematologica (Roma), 2011-12, Vol.96 (12), p.1874-1877

2011

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Development and validation of a real-time quantification assay to detect and monitor BRAFV600E mutations in hairy cell leukemia

Blood, 2012-03, Vol.119 (13), p.3151-3154

2012

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Use of CBL exon 8 and 9 mutations in diagnosis of myeloproliferative neoplasms and myelodysplastic/myeloproliferative disorders: an analysis of 636 cases

Haematologica (Roma), 2012-12, Vol.97 (12), p.1890-1894

2012

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Ruxolitinib as potential targeted therapy for patients with JAK2 rearrangements

Haematologica (Roma), 2013-03, Vol.98 (3), p.404-408

2013

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Molecular analyses of 15,542 patients with suspected BCR-ABL1-negative myeloproliferative disorders allow to develop a stepwise diagnostic workflow

Haematologica (Roma), 2012-10, Vol.97 (10), p.1582-1585

2012

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Cell-Cell Contacts Prevent Anoikis in Primary Human Colonic Epithelial Cells

Gastroenterology (New York, N.Y. 1943), 2007-02, Vol.132 (2), p.587-600

2007

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Kurz kommentiert

Wirtschaftsdienst (Hamburg), 2015-04, Vol.95 (4), p.228-230

2015

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Activated mineralocorticoid receptor regulates micro‐RNA‐29b in vascular smooth muscle cells

EF Domains Are Sufficient for Nongenomic Mineralocorticoid Receptor Actions

Mineralocorticoid receptor inhibits CREB signaling by calcineurin activation

Aldosterone Stimulates Epidermal Growth Factor Receptor Expression

Structural and molecular determinants of mineralocorticoid receptor signalling

Modulation of transcriptional mineralocorticoid receptor activity by casein kinase 1

Long‐term application of the aldosterone antagonist spironolactone prevents stiff endothelial cell syndrome

The phosphatase calcineurin PP2BAβ mediates part of mineralocorticoid receptor transcriptional activity

Mineralocorticoid receptor interaction with SP1 generates a new response element for pathophysiologically relevant gene expression

Feedforward activation of endothelial ENaC by high sodium

Transactivation via the human glucocorticoid and mineralocorticoid receptor by therapeutically used steroids in CV-1 cells: a comparison of their glucocorticoid and mineralocorticoid properties

PP2A attenuates cardiac response to LPS‐induced sepsis

A novel hierarchical prognostic model of AML solely based on molecular mutations

Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1

Phase III Trial in Metastatic Gastroesophageal Adenocarcinoma with Fluorouracil, Leucovorin Plus Either Oxaliplatin or Cisplatin: A Study of the Arbeitsgemeinschaft Internistische Onkologie

High frequencies of SF3B1 and JAK2 mutations in refractory anemia with ring sideroblasts associated with marked thrombocytosis strengthen the assignment to the category of myelodysplastic/myeloproliferative neoplasms

SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)

Prognostic relevance of RUNX1 mutations in T-cell acute lymphoblastic leukemia

Development and validation of a real-time quantification assay to detect and monitor BRAFV600E mutations in hairy cell leukemia

Use of CBL exon 8 and 9 mutations in diagnosis of myeloproliferative neoplasms and myelodysplastic/myeloproliferative disorders: an analysis of 636 cases

Ruxolitinib as potential targeted therapy for patients with JAK2 rearrangements

Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype

Molecular analyses of 15,542 patients with suspected BCR-ABL1-negative myeloproliferative disorders allow to develop a stepwise diagnostic workflow

Cell-Cell Contacts Prevent Anoikis in Primary Human Colonic Epithelial Cells

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