Lommel M - Search Results

1

Protein O-mannosylation is crucial for E-cadherin-mediated cell adhesion.

Lommel M, Winterhalter PR, Willer T, Dahlhoff M, Schneider MR, Bartels MF, Renner-Müller I, Ruppert T, Wolf E, Strahl S. Lommel M, et al. Proc Natl Acad Sci U S A. 2013 Dec 24;110(52):21024-9. doi: 10.1073/pnas.1316753110. Epub 2013 Dec 2. Proc Natl Acad Sci U S A. 2013. PMID: 24297939 Free PMC article.

2

Protein O-mannosylation: conserved from bacteria to humans.

Lommel M, Strahl S. Lommel M, et al. Glycobiology. 2009 Aug;19(8):816-28. doi: 10.1093/glycob/cwp066. Epub 2009 May 9. Glycobiology. 2009. PMID: 19429925 Review.

3

O-glycosylation of the non-canonical T-cadherin from rabbit skeletal muscle by single mannose residues.

Winterhalter PR, Lommel M, Ruppert T, Strahl S. Winterhalter PR, et al. Among authors: lommel m. FEBS Lett. 2013 Nov 15;587(22):3715-21. doi: 10.1016/j.febslet.2013.09.041. Epub 2013 Oct 7. FEBS Lett. 2013. PMID: 24113656 Free article.

4

Protein O-Mannosylation in the Murine Brain: Occurrence of Mono-O-Mannosyl Glycans and Identification of New Substrates.

Bartels MF, Winterhalter PR, Yu J, Liu Y, Lommel M, Möhrlen F, Hu H, Feizi T, Westerlind U, Ruppert T, Strahl S. Bartels MF, et al. Among authors: lommel m. PLoS One. 2016 Nov 3;11(11):e0166119. doi: 10.1371/journal.pone.0166119. eCollection 2016. PLoS One. 2016. PMID: 27812179 Free PMC article.

5

Protein O-mannosylation is crucial for human mesencyhmal stem cells fate.

Ragni E, Lommel M, Moro M, Crosti M, Lavazza C, Parazzi V, Saredi S, Strahl S, Lazzari L. Ragni E, et al. Among authors: lommel m. Cell Mol Life Sci. 2016 Jan;73(2):445-58. doi: 10.1007/s00018-015-2007-y. Epub 2015 Aug 6. Cell Mol Life Sci. 2016. PMID: 26245304 Free PMC article.

6

Aberrant processing of the WSC family and Mid2p cell surface sensors results in cell death of Saccharomyces cerevisiae O-mannosylation mutants.

Lommel M, Bagnat M, Strahl S. Lommel M, et al. Mol Cell Biol. 2004 Jan;24(1):46-57. doi: 10.1128/MCB.24.1.46-57.2004. Mol Cell Biol. 2004. PMID: 14673142 Free PMC article.

7

Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality.

Willer T, Prados B, Falcón-Pérez JM, Renner-Müller I, Przemeck GK, Lommel M, Coloma A, Valero MC, de Angelis MH, Tanner W, Wolf E, Strahl S, Cruces J. Willer T, et al. Among authors: lommel m. Proc Natl Acad Sci U S A. 2004 Sep 28;101(39):14126-31. doi: 10.1073/pnas.0405899101. Epub 2004 Sep 21. Proc Natl Acad Sci U S A. 2004. PMID: 15383666 Free PMC article.

8

POMT2, a key enzyme in Walker-Warburg syndrome: somatic sPOMT2, but not testis-specific tPOMT2, is crucial for mannosyltransferase activity in vivo.

Lommel M, Willer T, Strahl S. Lommel M, et al. Glycobiology. 2008 Aug;18(8):615-25. doi: 10.1093/glycob/cwn042. Epub 2008 May 19. Glycobiology. 2008. PMID: 18490429

9

POMT1 is essential for protein O-mannosylation in mammals.

Lommel M, Willer T, Cruces J, Strahl S. Lommel M, et al. Methods Enzymol. 2010;479:323-42. doi: 10.1016/S0076-6879(10)79018-2. Methods Enzymol. 2010. PMID: 20816174

10

A conserved acidic motif is crucial for enzymatic activity of protein O-mannosyltransferases.

Lommel M, Schott A, Jank T, Hofmann V, Strahl S. Lommel M, et al. J Biol Chem. 2011 Nov 18;286(46):39768-75. doi: 10.1074/jbc.M111.281196. Epub 2011 Sep 28. J Biol Chem. 2011. PMID: 21956107 Free PMC article.

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