Mayer, Matthias P. 1960-
Matthias P. Mayer
VIAF ID: 3924155044868972520007 ( Personal )
Permalink: http://viaf.org/viaf/3924155044868972520007
Preferred Forms
- 100 0 _ ‡a Matthias P. Mayer
- 100 1 _ ‡a Mayer, Matthias P. ‡d 1960-
4xx's: Alternate Name Forms (4)
5xx's: Related Names (3)
- 551 _ _ ‡a Heidelberg ‡4 ortw ‡4 https://d-nb.info/standards/elementset/gnd#placeOfActivity
- 510 2 _ ‡a Universität Heidelberg ‡b Zentrum für Molekulare Biologie ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 551 _ _ ‡a Zweibrücken ‡4 ortg ‡4 https://d-nb.info/standards/elementset/gnd#placeOfBirth
Works
Title | Sources |
---|---|
Conformational dynamics of the Hsp70 chaperone | |
Crucial HSP70 co-chaperone complex unlocks metazoan protein disaggregation | |
Development of mass spectrometric methods for tissue imaging and LC-based quantification of glycosphingolipids/gangliosides including Tay-Sachs disease based neuraminidase-deficient mouse models and human gut microbiota | |
Dynamics of Trigger Factor Interaction with Translating Ribosomes | |
Establishment of a multiple reaction monitoring assay for robust quantification of human glycosyltransferases in the endoplasmic reticulum | |
Hsp70 homolog Ssb affects ribosome biogenesis via the TORC1-Sch9 signaling pathway | |
The HSP70 molecular chaperone machines | |
Investigation of the regulation of Hsf1 activity by subcellular localization and posttranslational SUMOylation | |
Mechanismen der Proteinfaltung Molekulare Chaperone und ihr biotechnologisches Potential | |
Mechanisms of protein folding molecular chaperones and their application in biotechnology | |
Molecular mechanisms of the mammalian heat shock transcription factor Hsf1 | |
Multivalent contacts of the Hsp70 Ssb contribute to its architecture on ribosomes and nascent chain interaction | |
Targeted proteomics reveals quantitative differences in low-abundance glycosyltransferases of patients with congenital disorders of glycosylation | |
Unraveling metabolic mechanisms underlying the folate pathway and targeting antifolate resistance via synthetic lethality |