Frank Wolschendorf

4-Dihydromethyltrisporate dehydrogenase, an enzyme of the sex hormone pathway in Mucor mucedo, is constitutively transcribed but its activity is differently regulated in (+) and (-) mating types.

The growth rate of Mycobacterium smegmatis depends on sufficient porin-mediated influx of nutrients.

Porins are required for uptake of phosphates by Mycobacterium smegmatis.

Identification of two Mycobacterium smegmatis lipoproteins exported by a SecA2-dependent pathway.

Rv1698 of Mycobacterium tuberculosis represents a new class of channel-forming outer membrane proteins.

Hit-and-run stimulation: a novel concept to reactivate latent HIV-1 infection without cytokine gene induction.

Construction of unmarked deletion mutants in mycobacteria.

Copper resistance is essential for virulence of Mycobacterium tuberculosis.

Facts and fiction: cellular models for high throughput screening for HIV-1 reactivating drugs.

Kinase control prevents HIV-1 reactivation in spite of high levels of induced NF-κB activity.

Selected drugs with reported secondary cell-differentiating capacity prime latent HIV-1 infection for reactivation.

An AP-1 binding site in the enhancer/core element of the HIV-1 promoter controls the ability of HIV-1 to establish latent infection.

Copper-boosting compounds: a novel concept for antimycobacterial drug discovery.

Porins increase copper susceptibility of Mycobacterium tuberculosis.

Kinase control of latent HIV-1 infection: PIM-1 kinase as a major contributor to HIV-1 reactivation.

Copper complexation screen reveals compounds with potent antibiotic properties against methicillin-resistant Staphylococcus aureus.

Mycobacteria, metals, and the macrophage.

Stable Phenotypic Changes of the Host T Cells Are Essential to the Long-Term Stability of Latent HIV-1 Infection.

Disulfiram and Copper Ions Kill Mycobacterium tuberculosis in a Synergistic Manner.

RNAP II processivity is a limiting step for HIV-1 transcription independent of orientation to and activity of endogenous neighboring promoters.

Combinatorial phenotypic screen uncovers unrecognized family of extended thiourea inhibitors with copper-dependent anti-staphylococcal activity.

Protein Phosphatase, Mg2+/Mn2+-dependent 1A controls the innate antiviral and antibacterial response of macrophages during HIV-1 and Mycobacterium tuberculosis infection.

Development of a web-based tool for automated processing and cataloging of a unique combinatorial drug screen.

8-Hydroxyquinolines Are Boosting Agents of Copper-Related Toxicity in Mycobacterium tuberculosis.

Copper and Antibiotics: Discovery, Modes of Action, and Opportunities for Medicinal Applications.