Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Bernd Groner

Lactogenic Hormone Activation of Stat5 and Transcription of the Β-Casein Gene in Mammary Epithelial Cells Is Independent of P42 ERK2 Mitogen-Activated Protein Kinase Activity

Journal of Biological Chemistry

English

Related publications

Epidermal Growth Factor Receptor, but Not C-erbB-2, Activation Prevents Lactogenic Hormone Induction of the Beta-Casein Gene in Mouse Mammary Epithelial Cells.

Molecular and Cellular Biology

Cell Biology

Molecular Biology

1990

English

The Nuclear Factor YY1 Participates in Repression of the Beta-Casein Gene Promoter in Mammary Epithelial Cells and Is Counteracted by Mammary Gland Factor During Lactogenic Hormone Induction.

Molecular and Cellular Biology

Cell Biology

Molecular Biology

1994

English

Serotonin Suppresses Β-Casein Expression via Inhibition of the Signal Transducer and Activator of Transcription 5 (STAT5) Protein Phosphorylation in Human Mammary Epithelial Cells McF-12a

Biological and Pharmaceutical Bulletin

Medicine

Pharmacology

Pharmaceutical Science

2014

English

The ERK2 Mitogen-Activated Protein Kinase Regulates the Timing of Oligodendrocyte Differentiation

Journal of Neuroscience

Neuroscience

2011

English

Activation of Mitogen-Activated Protein Kinases P42/44, P38, and Stress-Activated Protein Kinases in Myelo-Monocytic Cells byTreponemaLipoteichoic Acid

Journal of Biological Chemistry

English

Inhibition of MafA Transcriptional Activity and Human Insulin Gene Transcription by Interleukin-1β and Mitogen-Activated Protein Kinase Kinase Kinase in Pancreatic Islet Beta Cells

English

Selective Activation of P42 Mitogen-Activated Protein (MAP) Kinase in Murine B Lymphoma Cell Lines by Membrane Immunoglobulin Cross-Linking. Evidence for Protein Kinase C-Independent and -Dependent Mechanisms of Activation

English

Activation of Mitogen-Activated Protein Kinase by HO

Journal of Biological Chemistry

English

Fluid Shear Stress Activation of Egr-1 Transcription in Cultured Human Endothelial and Epithelial Cells Is Mediated via the Extracellular Signal-Related Kinase 1/2 Mitogen-Activated Protein Kinase Pathway.

Journal of Clinical Investigation

Medicine

1998

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Bernd Groner

Lactogenic Hormone Activation of Stat5 and Transcription of the Β-Casein Gene in Mammary Epithelial Cells Is Independent of P42 ERK2 Mitogen-Activated Protein Kinase Activity

Related publications

Epidermal Growth Factor Receptor, but Not C-erbB-2, Activation Prevents Lactogenic Hormone Induction of the Beta-Casein Gene in Mouse Mammary Epithelial Cells.

The Nuclear Factor YY1 Participates in Repression of the Beta-Casein Gene Promoter in Mammary Epithelial Cells and Is Counteracted by Mammary Gland Factor During Lactogenic Hormone Induction.

Serotonin Suppresses Β-Casein Expression via Inhibition of the Signal Transducer and Activator of Transcription 5 (STAT5) Protein Phosphorylation in Human Mammary Epithelial Cells McF-12a

The ERK2 Mitogen-Activated Protein Kinase Regulates the Timing of Oligodendrocyte Differentiation

Activation of Mitogen-Activated Protein Kinases P42/44, P38, and Stress-Activated Protein Kinases in Myelo-Monocytic Cells byTreponemaLipoteichoic Acid

Inhibition of MafA Transcriptional Activity and Human Insulin Gene Transcription by Interleukin-1β and Mitogen-Activated Protein Kinase Kinase Kinase in Pancreatic Islet Beta Cells

Selective Activation of P42 Mitogen-Activated Protein (MAP) Kinase in Murine B Lymphoma Cell Lines by Membrane Immunoglobulin Cross-Linking. Evidence for Protein Kinase C-Independent and -Dependent Mechanisms of Activation

Activation of Mitogen-Activated Protein Kinase by HO

Fluid Shear Stress Activation of Egr-1 Transcription in Cultured Human Endothelial and Epithelial Cells Is Mediated via the Extracellular Signal-Related Kinase 1/2 Mitogen-Activated Protein Kinase Pathway.