Lübke T - Search Results

1

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, Lena Illert A, von Figura K, Saftig P. Hartmann D, et al. Among authors: lubke t. Hum Mol Genet. 2002 Oct 1;11(21):2615-24. doi: 10.1093/hmg/11.21.2615. Hum Mol Genet. 2002. PMID: 12354787

2

Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality.

Thiel C, Lübke T, Matthijs G, von Figura K, Körner C. Thiel C, et al. Among authors: lubke t. Mol Cell Biol. 2006 Aug;26(15):5615-20. doi: 10.1128/MCB.02391-05. Mol Cell Biol. 2006. PMID: 16847317 Free PMC article.

3

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. Lübke T, et al. Nat Genet. 2001 May;28(1):73-6. doi: 10.1038/ng0501-73. Nat Genet. 2001. PMID: 11326280

4

Molecular characterization of the hypothetical 66.3-kDa protein in mouse: lysosomal targeting, glycosylation, processing and tissue distribution.

Deuschl F, Kollmann K, von Figura K, Lübke T. Deuschl F, et al. Among authors: lubke t. FEBS Lett. 2006 Oct 16;580(24):5747-52. doi: 10.1016/j.febslet.2006.09.029. Epub 2006 Sep 22. FEBS Lett. 2006. PMID: 17007843 Free article.

Recently, we and others identified the 66.3-kDa protein as one of several putative novel lysosomal matrix proteins by analyzing mannose 6-phosphate receptors binding proteins [Kollmann K., Mutenda K.E., Balleininger M., Eckermann E., von Figura K., Schmidt B., Lubke T …

Recently, we and others identified the 66.3-kDa protein as one of several putative novel lysosomal matrix proteins by analyzing mannose 6-ph …

5

Golgi GDP-fucose transporter-deficient mice mimic congenital disorder of glycosylation IIc/leukocyte adhesion deficiency II.

Hellbusch CC, Sperandio M, Frommhold D, Yakubenia S, Wild MK, Popovici D, Vestweber D, Gröne HJ, von Figura K, Lübke T, Körner C. Hellbusch CC, et al. Among authors: lubke t. J Biol Chem. 2007 Apr 6;282(14):10762-72. doi: 10.1074/jbc.M700314200. Epub 2007 Feb 2. J Biol Chem. 2007. PMID: 17276979 Free article.

6

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. Lübke T, et al. J Biol Chem. 1999 Sep 10;274(37):25986-9. doi: 10.1074/jbc.274.37.25986. J Biol Chem. 1999. PMID: 10473542 Free article.

7

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. Hansske B, et al. Among authors: lubke t. J Clin Invest. 2002 Mar;109(6):725-33. doi: 10.1172/JCI14010. J Clin Invest. 2002. PMID: 11901181 Free PMC article.

8

Identification of novel lysosomal matrix proteins by proteome analysis.

Kollmann K, Mutenda KE, Balleininger M, Eckermann E, von Figura K, Schmidt B, Lübke T. Kollmann K, et al. Among authors: lubke t. Proteomics. 2005 Oct;5(15):3966-78. doi: 10.1002/pmic.200401247. Proteomics. 2005. PMID: 16145712

9

Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in α-mannosidosis.

Damme M, Stroobants S, Walkley SU, Lüllmann-Rauch R, D'Hooge R, Fogh J, Saftig P, Lübke T, Blanz J. Damme M, et al. Among authors: lubke t. J Neuropathol Exp Neurol. 2011 Jan;70(1):83-94. doi: 10.1097/NEN.0b013e31820428fa. J Neuropathol Exp Neurol. 2011. PMID: 21157375 Free PMC article.

10

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. Makrypidi G, et al. Among authors: lubke t. Mol Cell Biol. 2012 Feb;32(4):774-82. doi: 10.1128/MCB.06195-11. Epub 2011 Dec 12. Mol Cell Biol. 2012. PMID: 22158965 Free PMC article.

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