35 Publications

Mark all

[35]
2017 | Journal Article | PUB-ID: 2908778
Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase
Dhamale OP, Lawrence R, Wiegmann E, Shah BA, Al-Mafraji K, Lamanna WC, Lübke T, Dierks T, Boons G-J, Esko JD (2017)
ACS Chemical Biology 12(2): 367-373.
PUB | DOI | WoS | PubMed | Europe PMC
 
[34]
2017 | Journal Article | PUB-ID: 2909150 PUB | DOI | WoS | PubMed | Europe PMC
 
[33]
2016 | Journal Article | PUB-ID: 2905616
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
 
[32]
2014 | Journal Article | PUB-ID: 2699273
Molecular Characterization of Arylsulfatase G: EXPRESSION, PROCESSING, GLYCOSYLATION, TRANSPORT, AND ACTIVITY
Kowalewski B, Lübke T, Kollmann K, Braulke T, Reinheckel T, Dierks T, Damme M (2014)
The Journal of biological chemistry 289(40): 27992-28005.
PUB | DOI | WoS | PubMed | Europe PMC
 
[31]
2014 | Journal Article | PUB-ID: 2658538
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
 
[30]
2014 | Journal Article | PUB-ID: 2672894
Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1
Pan X, Grigoryeva L, Seyrantepe V, Peng J, Kollmann K, Tremblay J, Lavoie JL, Hinek A, Lübke T, Pshezhetsky AV (2014)
PLoS genetics 10(2): 1004146.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[29]
2013 | Journal Article | PUB-ID: 2623533
Cooperation of binding sites at the hydrophilic domain of cell-surface sulfatase Sulf1 allows for dynamic interaction of the enzyme with its substrate heparan sulfate
Milz F, Harder A, Neuhaus P, Breitkreuz-Korff O, Walhorn V, Lübke T, Anselmetti D, Dierks T (2013)
Biochim Biophys Acta 1830(11): 5287-5298.
PUB | DOI | WoS | PubMed | Europe PMC
 
[28]
2013 | Journal Article | PUB-ID: 2623550
Arylsulfatase K, a Novel Lysosomal Sulfatase
Wiegmann E, Westendorf E, Kalus I, Pringle TH, Lübke T, Dierks T (2013)
Journal of Biological Chemistry 288(42): 30019-30028.
PUB | DOI | WoS | PubMed | Europe PMC
 
[27]
2012 | Journal Article | 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
 
[26]
2012 | Journal Article | 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
 
[25]
2012 | Journal Article | 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
 
[24]
2011 | Journal Article | 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
 
[23]
2011 | Journal Article | 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
 
[22]
2010 | Journal Article | PUB-ID: 1939855
Erratum to: Rhesus macaque MHC class I molecules show differential subcellular localizations
Rosner C, Kruse PH, Lübke T, Walter L (2010)
Immunogenetics 62(6): 409-418.
PUB | DOI | WoS | PubMed | Europe PMC
 
[21]
2010 | Journal Article | PUB-ID: 2776186
Rhesus macaque MHC class I molecules show differential subcellular localizations
Rosner C, Kruse PH, Lübke T, Walter L (2010)
Immunogenetics 62(3): 149-158.
PUB | DOI | WoS | PubMed | Europe PMC
 
[20]
2010 | Journal Article | PUB-ID: 1939885
Mannose phosphorylation in health and disease
Kollmann K, Pohl S, Marschner K, Encarnacao M, Sakwa I, Tiede S, Poorthuis BJ, Lübke T, Müller-Loennies S, Storch S, Braulke T (2010)
European Journal of Cell Biology 89(1): 117-123.
PUB | DOI | WoS | PubMed | Europe PMC
 
[19]
2010 | Journal Article | 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
 
[18]
2009 | Journal Article | PUB-ID: 1939939
De novo sulfur SAD phasing of the lysosomal 66.3 kDa protein from mouse
Lakomek K, Dickmanns A, Mueller U, Kollmann K, Deuschl F, Berndt A, Lübke T, Ficner R (2009)
Acta Crystallographica Section D 65(3): 220-228.
PUB | DOI | WoS | PubMed | Europe PMC
 
[17]
2009 | Journal Article | PUB-ID: 1939981
Proteomics of the lysosome
Lübke T, Lobel P, Sleat DE (2009)
Biochimica et Biophysica Acta 1793(4): 625-635.
PUB | DOI | WoS | PubMed | Europe PMC
 
[16]
2009 | Journal Article | 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
 
[15]
2009 | Journal Article | 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
 
[14]
2009 | Journal Article | PUB-ID: 1939923
Initial insight into the function of the lysosomal 66.3 kDa protein from mouse by means of X-ray crystallography
Lakomek K, Dickmanns A, Kettwig M, Urlaub H, Ficner R, Lübke T (2009)
BMC Structural Biology 9(1): 56-72.
PUB | DOI | WoS | PubMed | Europe PMC
 
[13]
2007 | Journal Article | PUB-ID: 1940006
Golgi GDP-fucose transporter-deficient mice mimic congenital disorder of glycosylation IIc/leukocyte adhesion deficiency II
Hellbusch C, Sperandio M, Frommhold D, Yakubenia S, Wild MK, Popovici D, Vestweber D, Gröne H-J, von Figura K, Lübke T, Körner C (2007)
Journal of Biological Chemistry 282(14): 10762-10772.
PUB | DOI | WoS | PubMed | Europe PMC
 
[12]
2007 | Journal Article | PUB-ID: 1939993
Mutational analysis of the HGSNAT gene in Italian patients with mucopolysaccharidosis IIIC (Sanfilippo C syndrome)
Fedele AO, Filocamo M, Di Rocco M, Sersale G, Lübke T, di Natale P, Cosma MP, Ballabio A (2007)
Human Mutation 28(5): 523.
PUB | DOI
 
[11]
2006 | Journal Article | PUB-ID: 1940030 PUB | DOI | WoS | PubMed | Europe PMC
 
[10]
2006 | Journal Article | PUB-ID: 1940045
Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality
Thiel C, Lübke T, Matthijs G, von Figura K, Körner C (2006)
Molecular and Cellular Biology 26(15): 5615-5620.
PUB | DOI | WoS | PubMed | Europe PMC
 
[9]
2006 | Journal Article | PUB-ID: 1940057
Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase
Tiede S, Storch S, Lübke T, Henrissat B, Bargal R, Raas-Rothschild A, Braulke T (2006)
Nature Medicine 11(10): 1109-1112.
PUB | DOI | WoS | PubMed | Europe PMC
 
[8]
2005 | Book Chapter | PUB-ID: 1940182
Lysosomal Proteome and Transcriptome
Lübke T, Landgrebe J (2005)
In: Lysosomes. Saftig P (Ed); Georgetown, Texas, USA: Landes Bioscience: 130-143.
PUB | DOI
 
[7]
2005 | Journal Article | PUB-ID: 1940072
Identification of novel lysosomal matrix proteins by proteome analysis
Kollmann K, Mutenda KE, Balleininger M, Eckermann E, von Figura K, Schmidt B, Lübke T (2005)
Proteomics 5(15): 3966-3978.
PUB | DOI | WoS | PubMed | Europe PMC
 
[6]
2002 | Journal Article | PUB-ID: 1940085
The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts
Hartmann D, de Strooper B, Serneels L, Craessaerts K, Herreman A, Annaert W, Umans L, Lübke T, Illert AL, von Figura K, Saftig P (2002)
Human Molecular Genetics 11(21): 2615-2624.
PUB
 
[5]
2002 | Journal Article | PUB-ID: 1940103
Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId
Hansske B, Thiel C, Lübke T, Hasilik M, Höning S, Peters V, Heidemann PH, Hoffmann GF, Berger EG, von Figura K, Körner C (2002)
Journal of Clinical Investigation 109(6): 725-733.
PUB
 
[4]
2001 | Journal Article | PUB-ID: 1940119
Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency
Lübke T, Marquardt T, Etzioni A, Hartmann E, von Figura K, Körner C (2001)
Nature Genetics 28(1): 73-76.
PUB
 
[3]
2001 | Dissertation | PUB-ID: 1940291 PUB
 
[2]
2000 | Journal Article | PUB-ID: 1940146
ModE-dependent molybdate regulation of the molybdenum cofactor operon moa in Escherichia coli
Andersson LA, McNairn E, Lübke T, Pau RN, Boxer DH (2000)
Journal of Bacteriology 182(24): 7035-7043.
PUB
 
[1]
1999 | Journal Article | PUB-ID: 1940173
A new type of carbohydrate-deficient glycoprotein syndrome due to a decreased import of GDP-fucose into the golgi
Lübke T, Marquardt T, von Figura K, Körner C (1999)
Journal of Biological Chemistry 274(37): 25986-25989.
PUB
 

Search

Filter Publications

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35 Data Publications

Mark all

[35]
2017 | Journal Article | PUB-ID: 2908778
Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase
Dhamale OP, Lawrence R, Wiegmann E, Shah BA, Al-Mafraji K, Lamanna WC, Lübke T, Dierks T, Boons G-J, Esko JD (2017)
ACS Chemical Biology 12(2): 367-373.
PUB | DOI | WoS | PubMed | Europe PMC
 
[34]
2017 | Journal Article | PUB-ID: 2909150 PUB | DOI | WoS | PubMed | Europe PMC
 
[33]
2016 | Journal Article | PUB-ID: 2905616
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
 
[32]
2014 | Journal Article | PUB-ID: 2699273
Molecular Characterization of Arylsulfatase G: EXPRESSION, PROCESSING, GLYCOSYLATION, TRANSPORT, AND ACTIVITY
Kowalewski B, Lübke T, Kollmann K, Braulke T, Reinheckel T, Dierks T, Damme M (2014)
The Journal of biological chemistry 289(40): 27992-28005.
PUB | DOI | WoS | PubMed | Europe PMC
 
[31]
2014 | Journal Article | PUB-ID: 2658538
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
 
[30]
2014 | Journal Article | PUB-ID: 2672894
Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1
Pan X, Grigoryeva L, Seyrantepe V, Peng J, Kollmann K, Tremblay J, Lavoie JL, Hinek A, Lübke T, Pshezhetsky AV (2014)
PLoS genetics 10(2): 1004146.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
[29]
2013 | Journal Article | PUB-ID: 2623533
Cooperation of binding sites at the hydrophilic domain of cell-surface sulfatase Sulf1 allows for dynamic interaction of the enzyme with its substrate heparan sulfate
Milz F, Harder A, Neuhaus P, Breitkreuz-Korff O, Walhorn V, Lübke T, Anselmetti D, Dierks T (2013)
Biochim Biophys Acta 1830(11): 5287-5298.
PUB | DOI | WoS | PubMed | Europe PMC
 
[28]
2013 | Journal Article | PUB-ID: 2623550
Arylsulfatase K, a Novel Lysosomal Sulfatase
Wiegmann E, Westendorf E, Kalus I, Pringle TH, Lübke T, Dierks T (2013)
Journal of Biological Chemistry 288(42): 30019-30028.
PUB | DOI | WoS | PubMed | Europe PMC
 
[27]
2012 | Journal Article | 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
 
[26]
2012 | Journal Article | 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
 
[25]
2012 | Journal Article | 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
 
[24]
2011 | Journal Article | 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
 
[23]
2011 | Journal Article | 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
 
[22]
2010 | Journal Article | PUB-ID: 1939855
Erratum to: Rhesus macaque MHC class I molecules show differential subcellular localizations
Rosner C, Kruse PH, Lübke T, Walter L (2010)
Immunogenetics 62(6): 409-418.
PUB | DOI | WoS | PubMed | Europe PMC
 
[21]
2010 | Journal Article | PUB-ID: 2776186
Rhesus macaque MHC class I molecules show differential subcellular localizations
Rosner C, Kruse PH, Lübke T, Walter L (2010)
Immunogenetics 62(3): 149-158.
PUB | DOI | WoS | PubMed | Europe PMC
 
[20]
2010 | Journal Article | PUB-ID: 1939885
Mannose phosphorylation in health and disease
Kollmann K, Pohl S, Marschner K, Encarnacao M, Sakwa I, Tiede S, Poorthuis BJ, Lübke T, Müller-Loennies S, Storch S, Braulke T (2010)
European Journal of Cell Biology 89(1): 117-123.
PUB | DOI | WoS | PubMed | Europe PMC
 
[19]
2010 | Journal Article | 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
 
[18]
2009 | Journal Article | PUB-ID: 1939939
De novo sulfur SAD phasing of the lysosomal 66.3 kDa protein from mouse
Lakomek K, Dickmanns A, Mueller U, Kollmann K, Deuschl F, Berndt A, Lübke T, Ficner R (2009)
Acta Crystallographica Section D 65(3): 220-228.
PUB | DOI | WoS | PubMed | Europe PMC
 
[17]
2009 | Journal Article | PUB-ID: 1939981
Proteomics of the lysosome
Lübke T, Lobel P, Sleat DE (2009)
Biochimica et Biophysica Acta 1793(4): 625-635.
PUB | DOI | WoS | PubMed | Europe PMC
 
[16]
2009 | Journal Article | 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
 
[15]
2009 | Journal Article | 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
 
[14]
2009 | Journal Article | PUB-ID: 1939923
Initial insight into the function of the lysosomal 66.3 kDa protein from mouse by means of X-ray crystallography
Lakomek K, Dickmanns A, Kettwig M, Urlaub H, Ficner R, Lübke T (2009)
BMC Structural Biology 9(1): 56-72.
PUB | DOI | WoS | PubMed | Europe PMC
 
[13]
2007 | Journal Article | PUB-ID: 1940006
Golgi GDP-fucose transporter-deficient mice mimic congenital disorder of glycosylation IIc/leukocyte adhesion deficiency II
Hellbusch C, Sperandio M, Frommhold D, Yakubenia S, Wild MK, Popovici D, Vestweber D, Gröne H-J, von Figura K, Lübke T, Körner C (2007)
Journal of Biological Chemistry 282(14): 10762-10772.
PUB | DOI | WoS | PubMed | Europe PMC
 
[12]
2007 | Journal Article | PUB-ID: 1939993
Mutational analysis of the HGSNAT gene in Italian patients with mucopolysaccharidosis IIIC (Sanfilippo C syndrome)
Fedele AO, Filocamo M, Di Rocco M, Sersale G, Lübke T, di Natale P, Cosma MP, Ballabio A (2007)
Human Mutation 28(5): 523.
PUB | DOI
 
[11]
2006 | Journal Article | PUB-ID: 1940030 PUB | DOI | WoS | PubMed | Europe PMC
 
[10]
2006 | Journal Article | PUB-ID: 1940045
Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality
Thiel C, Lübke T, Matthijs G, von Figura K, Körner C (2006)
Molecular and Cellular Biology 26(15): 5615-5620.
PUB | DOI | WoS | PubMed | Europe PMC
 
[9]
2006 | Journal Article | PUB-ID: 1940057
Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase
Tiede S, Storch S, Lübke T, Henrissat B, Bargal R, Raas-Rothschild A, Braulke T (2006)
Nature Medicine 11(10): 1109-1112.
PUB | DOI | WoS | PubMed | Europe PMC
 
[8]
2005 | Book Chapter | PUB-ID: 1940182
Lysosomal Proteome and Transcriptome
Lübke T, Landgrebe J (2005)
In: Lysosomes. Saftig P (Ed); Georgetown, Texas, USA: Landes Bioscience: 130-143.
PUB | DOI
 
[7]
2005 | Journal Article | PUB-ID: 1940072
Identification of novel lysosomal matrix proteins by proteome analysis
Kollmann K, Mutenda KE, Balleininger M, Eckermann E, von Figura K, Schmidt B, Lübke T (2005)
Proteomics 5(15): 3966-3978.
PUB | DOI | WoS | PubMed | Europe PMC
 
[6]
2002 | Journal Article | PUB-ID: 1940085
The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts
Hartmann D, de Strooper B, Serneels L, Craessaerts K, Herreman A, Annaert W, Umans L, Lübke T, Illert AL, von Figura K, Saftig P (2002)
Human Molecular Genetics 11(21): 2615-2624.
PUB
 
[5]
2002 | Journal Article | PUB-ID: 1940103
Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId
Hansske B, Thiel C, Lübke T, Hasilik M, Höning S, Peters V, Heidemann PH, Hoffmann GF, Berger EG, von Figura K, Körner C (2002)
Journal of Clinical Investigation 109(6): 725-733.
PUB
 
[4]
2001 | Journal Article | PUB-ID: 1940119
Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency
Lübke T, Marquardt T, Etzioni A, Hartmann E, von Figura K, Körner C (2001)
Nature Genetics 28(1): 73-76.
PUB
 
[3]
2001 | Dissertation | PUB-ID: 1940291 PUB
 
[2]
2000 | Journal Article | PUB-ID: 1940146
ModE-dependent molybdate regulation of the molybdenum cofactor operon moa in Escherichia coli
Andersson LA, McNairn E, Lübke T, Pau RN, Boxer DH (2000)
Journal of Bacteriology 182(24): 7035-7043.
PUB
 
[1]
1999 | Journal Article | PUB-ID: 1940173
A new type of carbohydrate-deficient glycoprotein syndrome due to a decreased import of GDP-fucose into the golgi
Lübke T, Marquardt T, von Figura K, Körner C (1999)
Journal of Biological Chemistry 274(37): 25986-25989.
PUB
 

Search

Filter Publications

Display / Sort

Export / Embed