Imbach T - Search Results

1

Improvement of dolichol-linked oligosaccharide biosynthesis by the squalene synthase inhibitor zaragozic acid.

Haeuptle MA, Welti M, Troxler H, Hülsmeier AJ, Imbach T, Hennet T. Haeuptle MA, et al. Among authors: imbach t. J Biol Chem. 2011 Feb 25;286(8):6085-91. doi: 10.1074/jbc.M110.165795. Epub 2010 Dec 23. J Biol Chem. 2011. PMID: 21183681 Free PMC article.

2

Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie.

Imbach T, Schenk B, Schollen E, Burda P, Stutz A, Grunewald S, Bailie NM, King MD, Jaeken J, Matthijs G, Berger EG, Aebi M, Hennet T. Imbach T, et al. J Clin Invest. 2000 Jan;105(2):233-9. doi: 10.1172/JCI8691. J Clin Invest. 2000. PMID: 10642602 Free PMC article.

3

Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic.

Imbach T, Grünewald S, Schenk B, Burda P, Schollen E, Wevers RA, Jaeken J, de Klerk JB, Berger EG, Matthijs G, Aebi M, Hennet T. Imbach T, et al. Hum Genet. 2000 May;106(5):538-45. doi: 10.1007/s004390000293. Hum Genet. 2000. PMID: 10914684

4

A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic.

Imbach T, Burda P, Kuhnert P, Wevers RA, Aebi M, Berger EG, Hennet T. Imbach T, et al. Proc Natl Acad Sci U S A. 1999 Jun 8;96(12):6982-7. doi: 10.1073/pnas.96.12.6982. Proc Natl Acad Sci U S A. 1999. PMID: 10359825 Free PMC article.

5

MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If.

Schenk B, Imbach T, Frank CG, Grubenmann CE, Raymond GV, Hurvitz H, Korn-Lubetzki I, Revel-Vik S, Raas-Rotschild A, Luder AS, Jaeken J, Berger EG, Matthijs G, Hennet T, Aebi M. Schenk B, et al. Among authors: imbach t. J Clin Invest. 2001 Dec;108(11):1687-95. doi: 10.1172/JCI13419. J Clin Invest. 2001. PMID: 11733564 Free PMC article.

6

Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesis.

Grünewald S, Imbach T, Huijben K, Rubio-Gozalbo ME, Verrips A, de Klerk JB, Stroink H, de Rijk-van Andel JF, Van Hove JL, Wendel U, Matthijs G, Hennet T, Jaeken J, Wevers RA. Grünewald S, et al. Among authors: imbach t. Ann Neurol. 2000 Jun;47(6):776-81. Ann Neurol. 2000. PMID: 10852543

7

Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG. First International Workshop on CDGS.

Aebi M, Helenius A, Schenk B, Barone R, Fiumara A, Berger EG, Hennet T, Imbach T, Stutz A, Bjursell C, Uller A, Wahlström JG, Briones P, Cardo E, Clayton P, Winchester B, Cormier-Dalre V, de Lonlay P, Cuer M, Dupré T, Seta N, de Koning T, Dorland L, de Loos F, Kupers L, et al. Aebi M, et al. Among authors: imbach t. Glycoconj J. 1999 Nov;16(11):669-71. doi: 10.1023/a:1017249723165. Glycoconj J. 1999. PMID: 11003549 No abstract available.

8

alpha1,3Fucosyltransferase VI is expressed in HepG2 cells and codistributed with beta1,4galactosyltransferase I in the golgi apparatus and monensin-induced swollen vesicles.

Borsig L, Imbach T, Höchli M, Berger EG. Borsig L, et al. Among authors: imbach t. Glycobiology. 1999 Nov;9(11):1273-80. doi: 10.1093/glycob/9.11.1273. Glycobiology. 1999. PMID: 10536043

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