Anne Grünewald
Anne Grünewald
University of Luxembourg
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PINK1 loss-of-function mutations affect mitochondrial complex I activity via NdufA10 ubiquinone uncoupling
VA Morais, D Haddad, K Craessaerts, PJ De Bock, J Swerts, S Vilain, ...
Science 344 (6180), 203-207, 2014
2322014
Mutations in PINK1 and Parkin impair ubiquitination of Mitofusins in human fibroblasts
A Rakovic, A Grünewald, J Kottwitz, N Brüggemann, PP Pramstaller, ...
PloS one 6 (3), e16746, 2011
1952011
Phosphatase and Tensin Homolog (PTEN)-induced Putative Kinase 1 (PINK1)-dependent Ubiquitination of Endogenous Parkin Attenuates Mitophagy STUDY IN HUMAN PRIMARY FIBROBLASTS …
A Rakovic, K Shurkewitsch, P Seibler, A Grünewald, A Zanon, J Hagenah, ...
Journal of Biological Chemistry 288 (4), 2223-2237, 2013
1862013
Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness
SB Wortmann, FM Vaz, T Gardeitchik, LELM Vissers, GH Renkema, ...
Nature genetics 44 (7), 797-802, 2012
1602012
Mutant Parkin impairs mitochondrial function and morphology in human fibroblasts
A Grünewald, L Voges, A Rakovic, M Kasten, H Vandebona, ...
PloS one 5 (9), e12962, 2010
1392010
Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?
K Hedrich, J Hagenah, A Djarmati, A Hiller, T Lohnau, K Lasek, ...
Archives of neurology 63 (6), 833-838, 2006
1322006
Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients
A Rakovic, A Grünewald, P Seibler, A Ramirez, N Kock, S Orolicki, ...
Human molecular genetics 19 (16), 3124-3137, 2010
1282010
Differential effects of PINK1 nonsense and missense mutations on mitochondrial function and morphology
A Grünewald, ME Gegg, JW Taanman, RH King, N Kock, C Klein, ...
Experimental neurology 219 (1), 266-273, 2009
1202009
Myoclonus‐dystonia: significance of large SGCE deletions
A Grünewald, A Djarmati, K Lohmann‐Hedrich, K Farrell, JA Zeller, ...
Human mutation 29 (2), 331-332, 2008
1172008
Mitochondrial DNA Depletion in Respiratory Chain–Deficient P arkinson Disease Neurons
A Grünewald, KA Rygiel, PD Hepplewhite, CM Morris, M Picard, ...
Annals of neurology 79 (3), 366-378, 2016
1042016
ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome
A Grünewald, B Arns, P Seibler, A Rakovic, A Münchau, A Ramirez, ...
Neurobiology of aging 33 (8), 1843. e1-1843. e7, 2012
1022012
Bee venom and its component apamin as neuroprotective agents in a Parkinson disease mouse model
D Alvarez-Fischer, C Noelker, F Vulinović, A Grünewald, C Chevarin, ...
PLoS One 8 (4), e61700, 2013
912013
Bioenergetic consequences of PINK1 mutations in Parkinson disease
AY Abramov, M Gegg, A Grunewald, NW Wood, C Klein, AHV Schapira
PLoS One 6 (10), e25622, 2011
882011
A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis
MC Rocha, JP Grady, A Grünewald, A Vincent, PF Dobson, RW Taylor, ...
Scientific reports 5, 15037, 2015
852015
Genetics of Parkinson's disease
KR Kumar, A Djarmati-Westenberger, A Grünewald
Seminars in neurology 31 (05), 433-440, 2011
752011
New insights into the complex role of mitochondria in Parkinson’s disease
A Grünewald, KR Kumar, CM Sue
Progress in neurobiology 177, 73-93, 2019
722019
Next-Generation Phenotyping Using the Parkin Example: Time to Catch Up With Genetics
A Grünewald, M Kasten, A Ziegler, C Klein
JAMA neurology 70 (9), 1186-1191, 2013
612013
SCNT-derived ESCs with mismatched mitochondria trigger an immune response in allogeneic hosts
T Deuse, D Wang, M Stubbendorff, R Itagaki, A Grabosch, LC Greaves, ...
Cell Stem Cell 16 (1), 33-38, 2015
512015
Targeted next generation sequencing in SPAST-negative hereditary spastic paraplegia
KR Kumar, NF Blair, H Vandebona, C Liang, K Ng, DM Sharpe, ...
Journal of neurology 260 (10), 2516-2522, 2013
502013
Genome‐wide association study in musician's dystonia: A risk variant at the arylsulfatase G locus?
K Lohmann, A Schmidt, A Schillert, S Winkler, A Albanese, F Baas, ...
Movement Disorders 29 (7), 921-927, 2014
492014
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