Absmanner B - Search Results

1

ML3 is a NEDD8- and ubiquitin-modified protein.

Hakenjos JP, Bejai S, Ranftl Q, Behringer C, Vlot AC, Absmanner B, Hammes U, Heinzlmeir S, Kuster B, Schwechheimer C. Hakenjos JP, et al. Among authors: absmanner b. Plant Physiol. 2013 Sep;163(1):135-49. doi: 10.1104/pp.113.221341. Epub 2013 Jul 31. Plant Physiol. 2013. PMID: 23903439 Free PMC article.

2

Phloem development in nematode-induced feeding sites: the implications of auxin and cytokinin.

Absmanner B, Stadler R, Hammes UZ. Absmanner B, et al. Front Plant Sci. 2013 Jul 8;4:241. doi: 10.3389/fpls.2013.00241. eCollection 2013. Front Plant Sci. 2013. PMID: 23847644 Free PMC article.

3

Auxin efflux by PIN-FORMED proteins is activated by two different protein kinases, D6 PROTEIN KINASE and PINOID.

Zourelidou M, Absmanner B, Weller B, Barbosa IC, Willige BC, Fastner A, Streit V, Port SA, Colcombet J, de la Fuente van Bentem S, Hirt H, Kuster B, Schulze WX, Hammes UZ, Schwechheimer C. Zourelidou M, et al. Among authors: absmanner b. Elife. 2014 Jun 19;3:e02860. doi: 10.7554/eLife.02860. Elife. 2014. PMID: 24948515 Free PMC article.

4

Use of Xenopus laevis Oocytes to Study Auxin Transport.

Fastner A, Absmanner B, Hammes UZ. Fastner A, et al. Among authors: absmanner b. Methods Mol Biol. 2017;1497:259-270. doi: 10.1007/978-1-4939-6469-7_21. Methods Mol Biol. 2017. PMID: 27864772

5

Biochemical characterization, membrane association and identification of amino acids essential for the function of Alg11 from Saccharomyces cerevisiae, an alpha1,2-mannosyltransferase catalysing two sequential glycosylation steps in the formation of the lipid-linked core oligosaccharide.

Absmanner B, Schmeiser V, Kämpf M, Lehle L. Absmanner B, et al. Biochem J. 2010 Feb 9;426(2):205-17. doi: 10.1042/BJ20091121. Biochem J. 2010. PMID: 19929855

6

Biochemical characterization and membrane topology of Alg2 from Saccharomyces cerevisiae as a bifunctional alpha1,3- and 1,6-mannosyltransferase involved in lipid-linked oligosaccharide biosynthesis.

Kämpf M, Absmanner B, Schwarz M, Lehle L. Kämpf M, et al. Among authors: absmanner b. J Biol Chem. 2009 May 1;284(18):11900-12. doi: 10.1074/jbc.M806416200. Epub 2009 Mar 12. J Biol Chem. 2009. PMID: 19282279 Free PMC article.

7

A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.

Rind N, Schmeiser V, Thiel C, Absmanner B, Lübbehusen J, Hocks J, Apeshiotis N, Wilichowski E, Lehle L, Körner C. Rind N, et al. Among authors: absmanner b. Hum Mol Genet. 2010 Apr 15;19(8):1413-24. doi: 10.1093/hmg/ddq016. Epub 2010 Jan 15. Hum Mol Genet. 2010. PMID: 20080937

8

Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation.

Lefeber DJ, de Brouwer AP, Morava E, Riemersma M, Schuurs-Hoeijmakers JH, Absmanner B, Verrijp K, van den Akker WM, Huijben K, Steenbergen G, van Reeuwijk J, Jozwiak A, Zucker N, Lorber A, Lammens M, Knopf C, van Bokhoven H, Grünewald S, Lehle L, Kapusta L, Mandel H, Wevers RA. Lefeber DJ, et al. Among authors: absmanner b. PLoS Genet. 2011 Dec;7(12):e1002427. doi: 10.1371/journal.pgen.1002427. Epub 2011 Dec 29. PLoS Genet. 2011. PMID: 22242004 Free PMC article.

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