Johan Palmfeldt
Johan Palmfeldt
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Influence of culture pH on survival of Lactobacillus reuteri subjected to freeze-drying
J Palmfeldt, B Hahn-Hägerdal
International Journal of Food Microbiology 55 (1-3), 235-238, 2000
Optimisation of initial cell concentration enhances freeze-drying tolerance of Pseudomonas chlororaphis
J Palmfeldt, P Rådström, B Hahn-Hägerdal
Cryobiology 47 (1), 21-29, 2003
Candidate hippocampal biomarkers of susceptibility and resilience to stress in a rat model of depression
K Henningsen, J Palmfeldt, S Christiansen, I Baiges, S Bak, ON Jensen, ...
Molecular & Cellular Proteomics 11 (7), M111. 016428-1-M111. 016428-12, 2012
Targeting sortilin in immune cells reduces proinflammatory cytokines and atherosclerosis
MB Mortensen, M Kjolby, S Gunnersen, JV Larsen, J Palmfeldt, E Falk, ...
The Journal of clinical investigation 124 (12), 5317-5322, 2014
Riboflavin-responsive and-non-responsive mutations in FAD synthase cause multiple acyl-CoA dehydrogenase and combined respiratory-chain deficiency
RKJ Olsen, E Koňaříková, TA Giancaspero, S Mosegaard, V Boczonadi, ...
The American journal of human genetics 98 (6), 1130-1145, 2016
Lipogenesis is decreased by grape seed proanthocyanidins according to liver proteomics of rats fed a high fat diet
I Baiges, J Palmfeldt, C Blade, N Gregersen, L Arola
Molecular & Cellular Proteomics 9 (7), 1499-1513, 2010
Profiling of long non-coding RNAs identifies LINC00958 and LINC01296 as candidate oncogenes in bladder cancer
AK Seitz, LL Christensen, E Christensen, K Faarkrog, MS Ostenfeld, ...
Scientific reports 7 (1), 395, 2017
Decreased expression of the mitochondrial matrix proteases Lon and ClpP in cells from a patient with hereditary spastic paraplegia (SPG13)
J Hansen, TJ Corydon, J Palmfeldt, A Dürr, B Fontaine, MN Nielsen, ...
Neuroscience 153 (2), 474-482, 2008
The Hsp60-(p. V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo
P Bross, S Naundrup, J Hansen, MN Nielsen, JH Christensen, ...
Journal of Biological Chemistry 283 (23), 15694-15700, 2008
Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency
N Cornelius, FE Frerman, TJ Corydon, J Palmfeldt, P Bross, N Gregersen, ...
Human molecular genetics 21 (15), 3435-3448, 2012
Mitochondrial fatty acid oxidation and the electron transport chain comprise a multifunctional mitochondrial protein complex
Y Wang, J Palmfeldt, N Gregersen, AM Makhov, JF Conway, M Wang, ...
Journal of Biological Chemistry 294 (33), 12380-12391, 2019
STAT3 associates with vacuolar H+-ATPase and regulates cytosolic and lysosomal pH
B Liu, J Palmfeldt, L Lin, A Colaço, KKB Clemmensen, J Huang, F Xu, ...
Cell research 28 (10), 996-1012, 2018
The Hsp60 folding machinery is crucial for manganese superoxide dismutase folding and function
R Magnoni, J Palmfeldt, J Hansen, JH Christensen, TJ Corydon, P Bross
Free radical research 48 (2), 168-179, 2014
Urinary NGAL, cystatin C, β2-microglobulin, and osteopontin significance in hydronephrotic children
MG Madsen, R Nørregaard, J Palmfeldt, LH Olsen, J Frøkiær, ...
Pediatric nephrology 27, 2099-2106, 2012
Quantitative proteomics reveals cellular targets of celastrol
J Hansen, J Palmfeldt, S Vang, TJ Corydon, N Gregersen, P Bross
PLoS One 6 (10), e26634, 2011
Proteomics of human mitochondria
J Palmfeldt, P Bross
Mitochondrion 33, 2-14, 2017
Mitochondrial proteomics—a tool for the study of metabolic disorders
N Gregersen, J Hansen, J Palmfeldt
Journal of inherited metabolic disease 35, 715-726, 2012
Epidermal growth factor and monocyte chemotactic peptide-1: potential biomarkers of urinary tract obstruction in children with hydronephrosis
MG Madsen, R Nørregaard, J Palmfeldt, LH Olsen, J Frøkiær, ...
Journal of pediatric urology 9 (6), 838-845, 2013
Late onset motoneuron disorder caused by mitochondrial Hsp60 chaperone deficiency in mice
R Magnoni, J Palmfeldt, JH Christensen, M Sand, F Maltecca, TJ Corydon, ...
Neurobiology of Disease 54, 12-23, 2013
Effects of a Mutation in the HSPE1 Gene Encoding the Mitochondrial Co-chaperonin HSP10 and Its Potential Association with a Neurological and Developmental …
AS Bie, P Fernandez-Guerra, RID Birkler, S Nisemblat, D Pelnena, X Lu, ...
Frontiers in molecular biosciences 3, 65, 2016
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