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Anzahl der Publikationen: 7
Zeitschriftenartikel
Lotz-Havla, Amelie S.; Woidy, Mathias; Guder, Philipp; Schmiesing, Jessica; Erdmann, Ralf; Waterham, Hans R.; Muntau, Ania C. und Gersting, Soren W.
(4. November 2021):
Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency.
In: Frontiers in Genetics, Bd. 12, 726174
[PDF, 2MB]
Lotz-Havla, Amelie S.; Woidy, Mathias; Guder, Philipp; Friedel, Caroline C.; Klingbeil, Julian M.; Bulau, Ana-Maria; Schultze, Anja; Dahmen, Ilona; Noll-Puchta, Heidi; Kemp, Stephan; Erdmann, Ralf; Zimmer, Ralf; Muntau, Ania C. und Gersting, Soren W.
(2021):
iBRET Screen of the ABCD1 Peroxisomal Network and Mutation-Induced Network Perturbations.
In: Journal of Proteome Research, Bd. 20, Nr. 9: S. 4366-4380
Guder, Philipp; Lotz-Havla, Amelie S.; Woidy, Mathias; Reiss, Dunja D.; Danecka, Marta K.; Schatz, Ulrich A.; Becker, Marc; Ensenauer, Regina; Pagel, Philipp; Buettner, Lars; Muntau, Ania C. und Gersting, Soren W.
(2019):
Isoform-specific domain organization determines conformation and function of the peroxisomal biogenesis factor PEX26.
In: Biochimica et Biophysica Acta-Molecular Cell Research, Bd. 1866, Nr. 3: S. 518-531
Woidy, Mathias; Muntau, Ania C. und Gersting, Soren W.
(2018):
Inborn errors of metabolism and the human interactome: a systems medicine approach.
In: Journal of Inherited Metabolic Disease, Bd. 41, Nr. 3: S. 285-296
Eichinger, Anna; Danecka, Marta K.; Moeglich, Tamara; Borsch, Julia; Woidy, Mathias; Büttner, Lars; Muntau, Ania C. und Gersting, Soren W.
(2018):
Secondary BH4 deficiency links protein homeostasis to regulation of phenylalanine metabolism.
In: Human Molecular Genetics, Bd. 27, Nr. 10: S. 1732-1742
Schmiesing, Jessica; Lohmöller, Benjamin; Schweizer, Michaela; Tidow, Henning; Gersting, Soren W.; Muntau, Ania C.; Braulke, Thomas und Muehlhausen, Chris
(2017):
Disease-causing mutations affecting surface residues of mitochondrial glutaryl-CoA dehydrogenase impair stability, heteromeric complex formation and mitochondria architecture.
In: Human Molecular Genetics, Bd. 26, Nr. 3: S. 538-551
Jank, Johanna M.; Maier, Esther M.; Reiss, Dunja D.; Haslbeck, Martin; Kemter, Kristina F.; Truger, Marietta S.; Sommerhoff, Christian P.; Ferdinandusse, Sacha; Wanders, Ronald J.; Gersting, Soren W. und Muntau, Ania C.
(2014):
The Domain-Specific and Temperature-Dependent Protein Misfolding Phenotype of Variant Medium-Chain acyl-CoA Dehydrogenase.
In: PLOS ONE 9(4), e93852 [PDF, 1MB]
In: PLOS ONE 9(4), e93852 [PDF, 1MB]