Author

A. Alder

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Microbiology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:biophysical modeling· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Approach:experimental assay· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:host-pathogen & immune response· 1 Organism:plant (other)· 1

Frequent Co-Authors

A. Passecker· 1 shared B. Liffner· 1 shared C. Loew· 1 shared D. I. Svergun· 1 shared D. W. Wilson· 1 shared G. J. Shami· 1 shared G. K. Heinemann· 1 shared H. Mertens· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperMicrobiology

A. Passecker

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Pfcerli2, a duplicated gene in the malaria parasite Plasmodium falciparum essential for invasion of erythrocytes as revealed by phylogenetic and cell biological analysis.

B. Liffner, J. M. Balbin, G. J. Shami, J. Strauss, S. Frolich, G. K. Heinemann, A. Alder, J. S. Wichers, L. Tilley, M. W. A. Dixon, T. W. Gilberger, D. W. Wilson

This study identifies PfCERLI2 as an essential protein for merozoite invasion in Plasmodium falciparum through phylogenetic and cell biological analysis.

Communications Biology · Feb 9, 2022Peer-reviewedMicrobiology

N-terminal phosphorylation regulates the activity of Glycogen Synthase Kinase 3 from Plasmodium falciparum

S. Pazicky, A. Alder, H. Mertens, D. I. Svergun, T. Gilberger, C. Loew

This study identifies N-terminal phosphorylation sites in PfGSK3 that regulate its activity through conformational changes, offering insights into malarial parasite biology.

bioRxiv · Jun 18, 2021Biochemistry

CRISPR/Cas9-engineered inducible gametocyte producer lines as a novel tool for basic and applied research on Plasmodium falciparum malaria transmission stages

S. D. Boltryk, A. Passecker, A. Alder, M. van de Vegte-Bolmer, R. W. Sauerwein, N. M. B. Brancucci, H.-P. Beck, T.-W. Gilberger, T. S. Voss

This paper develops CRISPR/Cas9-engineered inducible gametocyte producer lines for mass production of P. falciparum gametocytes, achieving 75% sexual commitment and enabling genetic studies of transmission stages.

bioRxiv · Oct 5, 2020 · PreprintMicrobiology