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Markus Damme
Markus Damme
Kiel University, Biochemistry
在 biochem.uni-kiel.de 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Guidelines for the use and interpretation of assays for monitoring autophagy
DJ Klionsky, K Abdelmohsen, A Abe, MJ Abedin, H Abeliovich, ...
Autophagy 12 (1), 1-222, 2016
13356*2016
Lassa virus entry requires a trigger-induced receptor switch
LT Jae, M Raaben, AS Herbert, AI Kuehne, AS Wirchnianski, TK Soh, ...
Science 344 (6191), 1506-1510, 2014
2952014
Absence of RNase H2 triggers generation of immunogenic micronuclei removed by autophagy
K Bartsch, K Knittler, C Borowski, S Rudnik, M Damme, K Aden, ...
Human molecular genetics 26 (20), 3960-3972, 2017
2092017
Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis
JK Götzl, K Mori, M Damme, K Fellerer, S Tahirovic, G Kleinberger, ...
Acta neuropathologica 127 (6), 845-860, 2014
2042014
In vivo evidence for lysosome depletion and impaired autophagic clearance in hereditary spastic paraplegia type SPG11
RE Varga, M Khundadze, M Damme, S Nietzsche, B Hoffmann, T Stauber, ...
PLoS genetics 11 (8), e1005454, 2015
1322015
Progranulin functions as a cathepsin D chaperone to stimulate axonal outgrowth in vivo
S Beel, M Moisse, M Damme, L De Muynck, W Robberecht, ...
Human molecular genetics 26 (15), 2850-2863, 2017
1262017
Autophagy in neuronal cells: general principles and physiological and pathological functions
M Damme, T Suntio, P Saftig, EL Eskelinen
Acta neuropathologica 129 (3), 337-362, 2015
1142015
Altered distribution of ATG9A and accumulation of axonal aggregates in neurons from a mouse model of AP-4 deficiency syndrome
R De Pace, M Skirzewski, M Damme, R Mattera, J Mercurio, AM Foster, ...
PLoS genetics 14 (4), e1007363, 2018
1012018
PLD3 and PLD4 are single-stranded acid exonucleases that regulate endosomal nucleic-acid sensing
AL Gavin, D Huang, C Huber, A Mårtensson, V Tardif, PD Skog, TR Blane, ...
Nature immunology 19 (9), 942-953, 2018
972018
Arylsulfatase G inactivation causes loss of heparan sulfate 3-O-sulfatase activity and mucopolysaccharidosis in mice
B Kowalewski, WC Lamanna, R Lawrence, M Damme, S Stroobants, ...
Proceedings of the National Academy of Sciences 109 (26), 10310-10315, 2012
952012
Enzyme replacement therapy with recombinant pro-CTSD (cathepsin D) corrects defective proteolysis and autophagy in neuronal ceroid lipofuscinosis
ARA Marques, A Di Spiezio, N Thießen, L Schmidt, J Grötzinger, ...
Autophagy 16 (5), 811-825, 2020
942020
Lysosomal dysfunction causes neurodegeneration in mucolipidosis II ‘knock-in’mice
K Kollmann, M Damme, S Markmann, W Morelle, M Schweizer, ...
Brain 135 (9), 2661-2675, 2012
912012
Plekhg5-regulated autophagy of synaptic vesicles reveals a pathogenic mechanism in motoneuron disease
P Lüningschrör, B Binotti, B Dombert, P Heimann, A Perez-Lara, C Slotta, ...
Nature communications 8 (1), 678, 2017
722017
Mannose 6-dephosphorylation of lysosomal proteins mediated by acid phosphatases Acp2 and Acp5
G Makrypidi, M Damme, S Müller-Loennies, M Trusch, B Schmidt, ...
Molecular and cellular biology, MCB. 06195-11, 2011
622011
A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans
S Khateb, B Kowalewski, N Bedoni, M Damme, N Pollack, A Saada, ...
Genetics in Medicine, 2018
582018
Gene disruption of Mfsd8 in mice provides the first animal model for CLN7 disease
M Damme, L Brandenstein, S Fehr, W Jankowiak, U Bartsch, M Schweizer, ...
Neurobiology of disease 65, 12-24, 2014
582014
The FTLD Risk Factor TMEM106B Regulates the Transport of Lysosomes at the Axon Initial Segment of Motoneurons
P Lüningschrör, G Werner, S Stroobants, S Kakuta, B Dombert, D Sinske, ...
Cell Reports 30 (10), 3506-3519. e6, 2020
492020
Loss of TMEM 106B potentiates lysosomal and FTLD‐like pathology in progranulin‐deficient mice
G Werner, M Damme, M Schludi, J Gnörich, K Wind, K Fellerer, B Wefers, ...
EMBO reports 21 (10), e50241, 2020
422020
Ubiquitin C-terminal hydrolase L1 (UCH-L1) loss causes neurodegeneration by altering protein turnover in the first postnatal weeks
AT Reinicke, K Laban, M Sachs, V Kraus, M Walden, M Damme, W Sachs, ...
Proceedings of the National Academy of Sciences 116 (16), 7963-7972, 2019
422019
Disrupted in renal carcinoma 2 (DIRC2), a novel transporter of the lysosomal membrane, is proteolytically processed by cathepsin L
LRT Savalas, B Gasnier, M Damme, T Lübke, C Wrocklage, C Debacker, ...
Biochemical Journal 439 (1), 113-128, 2011
402011
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