Joachim Geyer

Full Professor, Head of Department

Justus Liebig University

Germany

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Joachim Geyer is a Full Professor and Head of Department at Justus Liebig Universität Gießen, Germany. His research focuses on bile acid transport and interactions with viral proteins, as well as the intracrine formation of steroid hormones in various cell lines. Recent articles include studies on bile acid reabsorption inhibitors, the Na+/taurocholate co-transporting polypeptide's role in hepatitis B virus entry, and the physiological implications of steroid transporters.

Articles (15)

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2025

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2021

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2021

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2021

Collaborators (2)

Giuliano Ciarimboli

University Hospital Münster

GERMANY

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John Ziebuhr

Professor

Justus Liebig University

GERMANY

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Joachim Geyer

Research Interests

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Articles (15)

Carrier cross-reactivities of the bile acid reabsorption inhibitors elobixibat, linerixibat, maralixibat, and odevixibat

Interaction between W41 of the hepatitis B virus preS1 surface peptide and Y146/F274 of the cellular receptor molecule Na+/taurocholate co-transporting polypeptide is essential for virus entry

Fluorescent 4-Nitrobenzo-2-oxa-1,3-diazole-Coupled Bile Acids as Probe Substrates of Hepatic and Intestinal Bile Acid Transporters of the Solute Carrier Families SLC10 and SLCO

Intracrine Formation of Steroid Hormones in Breast Cancer, Epidermal Keratinocyte, Dermal Fibroblast, and Adipocyte Cell Lines Measured by LC-MS/MS

Structure–Activity Relationships and Target Selectivity of Phenylsulfonylamino-Benzanilide Inhibitors Based on S1647 at the SLC10 Carriers ASBT, NTCP, and SOAT

Interactions of Na+/taurocholate cotransporting polypeptide with host cellular proteins upon hepatitis B and D virus infection: novel potential targets for antiviral therapy

The Rauischholzhausen Transport Colloquium: membrane proteins from structure to function

Role of the Sodium-Dependent Organic Anion Transporter (SOAT/SLC10A6) in Physiology and Pathophysiology

IFITM3 Interacts with the HBV/HDV Receptor NTCP and Modulates Virus Entry and Infection

Tyrosine 146 of the Human Na+/Taurocholate Cotransporting Polypeptide (NTCP) Is Essential for Its Hepatitis B Virus (HBV) Receptor Function and HBV Entry into Hepatocytes

Urinary cortisol metabolites are reduced in MDR1 mutant dogs in a pilot targeted GC‐MS urinary steroid hormone metabolome analysis

Multitasking Na+/Taurocholate Cotransporting Polypeptide (NTCP) as a Drug Target for HBV Infection: From Protein Engineering to Drug Discovery

Identification of Novel HBV/HDV Entry Inhibitors by Pharmacophore- and QSAR-Guided Virtual Screening

Hepatitis D Virus Entry Inhibitors Based on Repurposing Intestinal Bile Acid Reabsorption Inhibitors

Long-term trans-inhibition of the hepatitis B and D virus receptor NTCP by taurolithocholic acid

Collaborators (2)

Giuliano Ciarimboli

John Ziebuhr

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