14 Publikationen

Alle markieren

[14]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124
Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice
Kruszewski K, Luellmann-Rauch R, Dierks T, Bartsch U, Damme M (2016)
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57(3): 1120-1131.
PUB | DOI | WoS | PubMed | Europe PMC
 
[13]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616 OA
A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease
Wolf H, Damme M, Stroobants S, D'Hooge R, Beck HC, Hermans-Borgmeyer I, Lüllmann-Rauch R, Dierks T, Lübke T (2016)
Disease Models & Mechanisms 9(9): 1015-1028.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[12]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2709463
Ataxia is the major neuropathological finding in Arylsulfatase G deficient mice: Similarities and dissimilarities to Sanfilippo disease (Mucopolysaccharidosis type III)
Kowalewski B, Heimann P, Ortkras T, Lüllmann-Rauch R, Sawada T, Walkley SU, Dierks T, Damme M (2015)
Human Molecular Genetics 24(7): 1856-1868.
PUB | DOI | WoS | PubMed | Europe PMC
 
[11]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2658538 OA
Loss of lysosomal membrane protein NCU-G1 in mice results in spontaneous liver fibrosis with accumulation of lipofuscin and iron in Kupffer cells
Kong XY, Nesset CK, Damme M, Loeberg E-M, Lübke T, Maehlen J, Andersson KB, Roos N, Thoresen GH, Rustan AC, Kase ET, et al. (2014)
Disease Models & Mechanisms 7(3): 351-362.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[10]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2484642 OA
Disruption of the Autophagy-Lysosome Pathway is Involved in Neuropathology of the nclf Mouse Model of Neuronal Ceroid Lipofuscinosis
Thelen M, Damme M, Schweizer M, Hagel C, Wong A, Cooper JD, Braulke T, Galliciotti G (2012)
PLOS ONE 7(4): e35493.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[9]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2471754
Mannose 6 dephosphorylation of lysosomal proteins mediated by Acid phosphatases acp2 and acp5
Makrypidi G, Damme M, Müller-Loennies S, Trusch M, Schmidt B, Schlüter H, Heeren J, Lübke T, Saftig P, Braulke T (2012)
Molecular and cellular biology 32(4): 774-782.
PUB | DOI | WoS | PubMed | Europe PMC
 
[8]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2529586
Lysosomal dysfunction causes neurodegeneration in mucolipidosis II 'knock-in' mice
Kollmann K, Damme M, Markmann S, Morelle W, Schweizer M, Hermans-Borgmeyer I, Rochert AK, Pohl S, Lübke T, Michalski J-C, Kakela R, et al. (2012)
Brain 135(9): 2661-2675.
PUB | DOI | WoS | PubMed | Europe PMC
 
[7]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022
Arylsulfatase G Inactivation Causes Loss of Heparan Sulfate 3-O-Sulfatase Activity and Mucopolysaccharidosis in Mice
Kowalewski B, Lamanna WC, Lawrence R, Damme M, Padva M, Stroobants S, Kalus I, Frese M-A, Lübke T, Lüllmann-Rauch R, D'Hooge R, et al. (2012)
Proc. Natl. Acad. Sci. USA 109(26): 10310-10315.
PUB | DOI | WoS | PubMed | Europe PMC
 
[6]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2352585
Disrupted in renal carcinoma 2 (DIRC2), a novel transporter of the lysosomal membrane, is proteolytically processed by cathepsin L.
Savalas LR, Gasnier B, Damme M, Lübke T, Wrocklage C, Debacker C, Jezeqou A, Reinheckel T, Hasilik A, Saftig P, Schröder B (2011)
Biochemical Journal 436(1): 113-121.
PUB | DOI | WoS | PubMed | Europe PMC
 
[5]
2011 | Zeitschriftenaufsatz | Im Druck | PUB-ID: 1940515
Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in alpha-mannosidosis
Damme M, Stroobants S, Walkley SU, Lüllmann-Rauch R, D'Hooge R, Fogh J, Saftig P, Lübke T, Blanz J (In Press)
Journal of Neuropathology & Experimental Neurology 70(1): 83-94.
PUB | DOI | WoS | PubMed | Europe PMC
 
[4]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902203
Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis.
Damme M, Morelle W, Schmidt B, Andersson C, Fogh J, Michalski J-C, Lübke T (2010)
Molecular and Cellular Biology 30(1): 273-283.
PUB | DOI | WoS | PubMed | Europe PMC
 
 
[2]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902143
NCU-G1 is a highly glycosylated integral membrane protein of the lysosome.
Schieweck O, Damme M, Schröder B, Hasilik A, Schmidt B, Lübke T (2009)
Biochemical Journal 422(1): 83-90.
PUB | DOI | WoS | PubMed | Europe PMC
 
[1]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940533
Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1
Kollmann K, Damme M, Deuschl F, Kahle J, D'Hooge R, Lüllmann-Rauch R, Lübke T (2009)
Febs Journal 276(5): 1356-1369.
PUB | DOI | WoS | PubMed | Europe PMC
 

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14 Publikationen

Alle markieren

[14]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124
Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice
Kruszewski K, Luellmann-Rauch R, Dierks T, Bartsch U, Damme M (2016)
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57(3): 1120-1131.
PUB | DOI | WoS | PubMed | Europe PMC
 
[13]
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616 OA
A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease
Wolf H, Damme M, Stroobants S, D'Hooge R, Beck HC, Hermans-Borgmeyer I, Lüllmann-Rauch R, Dierks T, Lübke T (2016)
Disease Models & Mechanisms 9(9): 1015-1028.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[12]
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2709463
Ataxia is the major neuropathological finding in Arylsulfatase G deficient mice: Similarities and dissimilarities to Sanfilippo disease (Mucopolysaccharidosis type III)
Kowalewski B, Heimann P, Ortkras T, Lüllmann-Rauch R, Sawada T, Walkley SU, Dierks T, Damme M (2015)
Human Molecular Genetics 24(7): 1856-1868.
PUB | DOI | WoS | PubMed | Europe PMC
 
[11]
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2658538 OA
Loss of lysosomal membrane protein NCU-G1 in mice results in spontaneous liver fibrosis with accumulation of lipofuscin and iron in Kupffer cells
Kong XY, Nesset CK, Damme M, Loeberg E-M, Lübke T, Maehlen J, Andersson KB, Roos N, Thoresen GH, Rustan AC, Kase ET, et al. (2014)
Disease Models & Mechanisms 7(3): 351-362.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[10]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2484642 OA
Disruption of the Autophagy-Lysosome Pathway is Involved in Neuropathology of the nclf Mouse Model of Neuronal Ceroid Lipofuscinosis
Thelen M, Damme M, Schweizer M, Hagel C, Wong A, Cooper JD, Braulke T, Galliciotti G (2012)
PLOS ONE 7(4): e35493.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[9]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2471754
Mannose 6 dephosphorylation of lysosomal proteins mediated by Acid phosphatases acp2 and acp5
Makrypidi G, Damme M, Müller-Loennies S, Trusch M, Schmidt B, Schlüter H, Heeren J, Lübke T, Saftig P, Braulke T (2012)
Molecular and cellular biology 32(4): 774-782.
PUB | DOI | WoS | PubMed | Europe PMC
 
[8]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2529586
Lysosomal dysfunction causes neurodegeneration in mucolipidosis II 'knock-in' mice
Kollmann K, Damme M, Markmann S, Morelle W, Schweizer M, Hermans-Borgmeyer I, Rochert AK, Pohl S, Lübke T, Michalski J-C, Kakela R, et al. (2012)
Brain 135(9): 2661-2675.
PUB | DOI | WoS | PubMed | Europe PMC
 
[7]
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022
Arylsulfatase G Inactivation Causes Loss of Heparan Sulfate 3-O-Sulfatase Activity and Mucopolysaccharidosis in Mice
Kowalewski B, Lamanna WC, Lawrence R, Damme M, Padva M, Stroobants S, Kalus I, Frese M-A, Lübke T, Lüllmann-Rauch R, D'Hooge R, et al. (2012)
Proc. Natl. Acad. Sci. USA 109(26): 10310-10315.
PUB | DOI | WoS | PubMed | Europe PMC
 
[6]
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2352585
Disrupted in renal carcinoma 2 (DIRC2), a novel transporter of the lysosomal membrane, is proteolytically processed by cathepsin L.
Savalas LR, Gasnier B, Damme M, Lübke T, Wrocklage C, Debacker C, Jezeqou A, Reinheckel T, Hasilik A, Saftig P, Schröder B (2011)
Biochemical Journal 436(1): 113-121.
PUB | DOI | WoS | PubMed | Europe PMC
 
[5]
2011 | Zeitschriftenaufsatz | Im Druck | PUB-ID: 1940515
Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in alpha-mannosidosis
Damme M, Stroobants S, Walkley SU, Lüllmann-Rauch R, D'Hooge R, Fogh J, Saftig P, Lübke T, Blanz J (In Press)
Journal of Neuropathology & Experimental Neurology 70(1): 83-94.
PUB | DOI | WoS | PubMed | Europe PMC
 
[4]
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902203
Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis.
Damme M, Morelle W, Schmidt B, Andersson C, Fogh J, Michalski J-C, Lübke T (2010)
Molecular and Cellular Biology 30(1): 273-283.
PUB | DOI | WoS | PubMed | Europe PMC
 
 
[2]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902143
NCU-G1 is a highly glycosylated integral membrane protein of the lysosome.
Schieweck O, Damme M, Schröder B, Hasilik A, Schmidt B, Lübke T (2009)
Biochemical Journal 422(1): 83-90.
PUB | DOI | WoS | PubMed | Europe PMC
 
[1]
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940533
Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1
Kollmann K, Damme M, Deuschl F, Kahle J, D'Hooge R, Lüllmann-Rauch R, Lübke T (2009)
Febs Journal 276(5): 1356-1369.
PUB | DOI | WoS | PubMed | Europe PMC
 

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