Gersting SW - Search Results

1

Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathy.

Braun F, Abed A, Sellung D, Rogg M, Woidy M, Eikrem O, Wanner N, Gambardella J, Laufer SD, Haas F, Wong MN, Dumoulin B, Rischke P, Mühlig A, Sachs W, von Cossel K, Schulz K, Muschol N, Gersting SW, Muntau AC, Kretz O, Hahn O, Rinschen MM, Mauer M, Bork T, Grahammer F, Liang W, Eierhoff T, Römer W, Hansen A, Meyer-Schwesinger C, Iaccarino G, Tøndel C, Marti HP, Najafian B, Puelles VG, Schell C, Huber TB. Braun F, et al. Among authors: gersting sw. J Clin Invest. 2023 Jun 1;133(11):e157782. doi: 10.1172/JCI157782. J Clin Invest. 2023. PMID: 37014703 Free PMC article.

2

Phenylketonuria as a model for protein misfolding diseases and for the development of next generation orphan drugs for patients with inborn errors of metabolism.

Muntau AC, Gersting SW. Muntau AC, et al. Among authors: gersting sw. J Inherit Metab Dis. 2010 Dec;33(6):649-58. doi: 10.1007/s10545-010-9185-4. Epub 2010 Sep 8. J Inherit Metab Dis. 2010. PMID: 20824346 Review.

3

The interplay between genotype, metabolic state and cofactor treatment governs phenylalanine hydroxylase function and drug response.

Staudigl M, Gersting SW, Danecka MK, Messing DD, Woidy M, Pinkas D, Kemter KF, Blau N, Muntau AC. Staudigl M, et al. Among authors: gersting sw. Hum Mol Genet. 2011 Jul 1;20(13):2628-41. doi: 10.1093/hmg/ddr165. Epub 2011 Apr 28. Hum Mol Genet. 2011. PMID: 21527427 Free article.

4

Bioluminescence resonance energy transfer: an emerging tool for the detection of protein-protein interaction in living cells.

Gersting SW, Lotz-Havla AS, Muntau AC. Gersting SW, et al. Methods Mol Biol. 2012;815:253-63. doi: 10.1007/978-1-61779-424-7_19. Methods Mol Biol. 2012. PMID: 22130997

5

Innovative strategies to treat protein misfolding in inborn errors of metabolism: pharmacological chaperones and proteostasis regulators.

Muntau AC, Leandro J, Staudigl M, Mayer F, Gersting SW. Muntau AC, et al. Among authors: gersting sw. J Inherit Metab Dis. 2014 Jul;37(4):505-23. doi: 10.1007/s10545-014-9701-z. Epub 2014 Apr 1. J Inherit Metab Dis. 2014. PMID: 24687294 Review.

6

Mapping the functional landscape of frequent phenylalanine hydroxylase (PAH) genotypes promotes personalised medicine in phenylketonuria.

Danecka MK, Woidy M, Zschocke J, Feillet F, Muntau AC, Gersting SW. Danecka MK, et al. Among authors: gersting sw. J Med Genet. 2015 Mar;52(3):175-85. doi: 10.1136/jmedgenet-2014-102621. Epub 2015 Jan 16. J Med Genet. 2015. PMID: 25596310

7

Quantification of mevalonate-5-phosphate using UPLC-MS/MS for determination of mevalonate kinase activity.

Reitzle L, Maier B, Stojanov S, Teupser D, Muntau AC, Vogeser M, Gersting SW. Reitzle L, et al. Among authors: gersting sw. Clin Biochem. 2015 Aug;48(12):781-7. doi: 10.1016/j.clinbiochem.2015.05.007. Epub 2015 May 13. Clin Biochem. 2015. PMID: 25982894

8

Homooligomerization of ABCA3 and its functional significance.

Frixel S, Lotz-Havla AS, Kern S, Kaltenborn E, Wittmann T, Gersting SW, Muntau AC, Zarbock R, Griese M. Frixel S, et al. Among authors: gersting sw. Int J Mol Med. 2016 Aug;38(2):558-66. doi: 10.3892/ijmm.2016.2650. Epub 2016 Jun 21. Int J Mol Med. 2016. PMID: 27352740

9

Disease-causing mutations affecting surface residues of mitochondrial glutaryl-CoA dehydrogenase impair stability, heteromeric complex formation and mitochondria architecture.

Schmiesing J, Lohmöller B, Schweizer M, Tidow H, Gersting SW, Muntau AC, Braulke T, Mühlhausen C. Schmiesing J, et al. Among authors: gersting sw. Hum Mol Genet. 2017 Feb 1;26(3):538-551. doi: 10.1093/hmg/ddw411. Hum Mol Genet. 2017. PMID: 28062662

10

Inborn errors of metabolism and the human interactome: a systems medicine approach.

Woidy M, Muntau AC, Gersting SW. Woidy M, et al. Among authors: gersting sw. J Inherit Metab Dis. 2018 May;41(3):285-296. doi: 10.1007/s10545-018-0140-0. Epub 2018 Feb 5. J Inherit Metab Dis. 2018. PMID: 29404805 Free PMC article. Review.

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