Lübke T - Search Results

1

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.

2

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.

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

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.

5

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 …

6

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.

7

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

8

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

9

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. Kollmann K, et al. Among authors: lubke t. FEBS J. 2009 Mar;276(5):1356-69. doi: 10.1111/j.1742-4658.2009.06877.x. FEBS J. 2009. PMID: 19187242 Free article.

10

NCU-G1 is a highly glycosylated integral membrane protein of the lysosome.

Schieweck O, Damme M, Schröder B, Hasilik A, Schmidt B, Lübke T. Schieweck O, et al. Among authors: lubke t. Biochem J. 2009 Jul 29;422(1):83-90. doi: 10.1042/BJ20090567. Biochem J. 2009. PMID: 19489740

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