C. Escher

发表

Proteinase yscE, the yeast proteasome/multicatalytic‐multifunctional proteinase: mutants unravel its function in stress induced proteolysis and uncover its necessity for cell survival.

J. Kleinschmidt, D. Wolf, W Heinemeyer, 1991, The EMBO journal.

Sesquiterpene lactone containing Mexican Indian medicinal plants and pure sesquiterpene lactones as potent inhibitors of transcription factor NF‐κB

M. Schmitz, M. Heinrich, C. Escher, 1997, FEBS letters.

Extending the Limits of Quantitative Proteome Profiling with Data-Independent Acquisition and Application to Acetaminophen-Treated Three-Dimensional Liver Microtissues*

Oliver M. Bernhardt, Saša M. Miladinović, Roland Bruderer, 2015, Molecular & Cellular Proteomics.

Using iRT, a normalized retention time for more targeted measurement of peptides

John Chilton, Brendan MacLean, Lukas Reiter, 2012, Proteomics.

Optimized spectral library generation for HRM/DIA/SWATH as implemented within spectronaut

Oliver M. Bernhardt, Roland Bruderer, Tejas Gandhi, 2015 .

Cytotoxicity of pharmaceuticals found in aquatic systems: comparison of PLHC-1 and RTG-2 fish cell lines.

K. Fent, Daniel Caminada, C. Escher, 2006, Aquatic toxicology.

Proteinase yscE of yeast shows homology with the 20 S cylinder particles of Xenopus laevis

J. Kleinschmidt, D. Wolf, C. Escher, 1988, FEBS letters.

Proteinase yscE,theyeastproteasome/multicatalytic- multifunctional proteinase: mutantsunravel itsfunction instressinduced proteolysis anduncover itsnecessity forcell survival

W. Heinemeyer, J. Saidowsky, C. Escher, 1991 .

Reverse protein arrays as novel approach for protein quantification in muscular dystrophies

M. Ruegg, S. Frank, H. Lochmüller, 2010, Neuromuscular Disorders.

Induction of ER Stress by an AAV5 BDD FVIII Construct Is Dependent on the Strength of the Hepatic-Specific Promoter

Guoying Yu, J. Vowinckel, S. Bunting, 2020, Molecular therapy. Methods & clinical development.

Generation of recombinant antibody fragments for membrane protein crystallization.

Wei-Chun Kao, C. Hunte, C. Wirth, 2015, Methods in enzymology.

Proteomic profiling of Duchenne muscular dystrophy : protein patterns and candidate markers of disease

C. Escher, 2011 .

The Single Transmembrane Domains of Human Receptor Tyrosine Kinases Encode Self-Interactions

D. Schneider, Carmen Finger, Dirk Schneider, 2009, Science Signaling.

Encode Self-Interactions The Single Transmembrane Domains of Human Receptor Tyrosine Kinases

D. Schneider, Carmen Finger, C. Escher, 2009 .

Cell type-specific nuclear pores: a case in point for context-dependent stoichiometry of molecular machines

P. Bork, M. Beck, M. Iskar, 2013, Molecular systems biology.

Estrogenic activity of pharmaceuticals and pharmaceutical mixtures in a yeast reporter gene system.

K. Fent, Daniel Caminada, C. Escher, 2006, Reproductive toxicology.

Two GxxxG-like motifs facilitate promiscuous interactions of the human ErbB transmembrane domains.

D. Schneider, F. Cymer, C. Escher, 2009, Journal of molecular biology.

Transcriptomic, Proteomic, and Functional Long-Term Characterization of Multicellular Three-Dimensional Human Liver Microtissues

M. Ingelman-Sundberg, V. Lauschke, J. Kelm, 2018, Applied in vitro toxicology.

Some characteristics of hormone (pheromone) processing enzymes in yeast

D. Wolf, C. Escher, J. Wagner, 1987, FEBS letters.

Cell type-specific nuclear pores: a case in point for context-dependent stoichiometry of molecular machines

P. Bork, M. Iskar, A. Ori, 2013, Molecular systems biology.

Reverse protein arrays as novel approach for protein quantification in muscular dystrophies

M. Ruegg, S. Frank, H. Lochmüller, 2010, Neuromuscular Disorders.

Cell type-specific nuclear pores: a case in point for context-dependent stoichiometry of molecular machines

P. Bork, M. Iskar, A. Ori, 2013, Molecular systems biology.