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List of works by Søren W Gersting

Activation of Phenylalanine Hydroxylase Induces Positive Cooperativity toward the Natural Cofactor ⬇️

scientific article published on July 27, 2010

Bioluminescence Resonance Energy Transfer: An Emerging Tool for the Detection of Protein–Protein Interaction in Living Cells ⬇️

scientific article published on 01 January 2012

CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder

scientific article

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

scientific article published on 5 January 2017

Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency

scientific article published on 04 November 2021

Homooligomerization of ABCA3 and its functional significance

scientific article published on 21 June 2016

Identification of a New Fatty Acid Synthesis-Transport Machinery at the Peroxisomal Membrane ⬇️

scientific article published on January 2, 2012

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

scientific article published on 5 February 2018

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

scientific article published on April 2014

Isoform-specific domain organization determines conformation and function of the peroxisomal biogenesis factor PEX26

scientific article published on 23 October 2018

Loss of function in phenylketonuria is caused by impaired molecular motions and conformational instability

scientific article published on 5 June 2008

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

scientific article published on 16 January 2015

New insights into tetrahydrobiopterin pharmacodynamics from Pah enu1/2, a mouse model for compound heterozygous tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency

scientific article published on 10 August 2010

Novel pharmacological chaperones that correct phenylketonuria in mice.

scientific article

Pahenu1 is a mouse model for tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency and promotes analysis of the pharmacological chaperone mechanism in vivo

scientific article published on 23 February 2010

Phenotypic analysis of the pediatric immune response to SARS-CoV-2 by flow cytometry

scientific article published on 10 January 2022

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

scientific article published on September 8, 2010

Protein misfolding is the molecular mechanism underlying MCADD identified in newborn screening

scientific article

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

scientific article published on 13 May 2015

Rad50-CARD9 interactions link cytosolic DNA sensing to IL-1β production

scientific article published on 28 April 2014

Secondary BH4 deficiency links protein homeostasis to regulation of phenylalanine metabolism

scientific article published on 01 May 2018

The domain-specific and temperature-dependent protein misfolding phenotype of variant medium-chain acyl-CoA dehydrogenase

scientific article

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

scientific article published on 28 April 2011

Varicella zoster virus ORF25 gene product: an essential hub protein linking encapsidation proteins and the nuclear egress complex

scientific article published on 26 October 2011

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