Literature DB >> 7837759

Normal N-oligosaccharyltransferase activity in fibroblasts from patients with carbohydrate-deficient glycoprotein syndrome.

R Knauer1, L Lehle, F Hanefeld, K von Figura.   

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Year:  1994        PMID: 7837759     DOI: 10.1007/bf00711588

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


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  15 in total

1.  Carbohydrate-deficient glycoprotein (CDG) syndrome--a new variant, type III.

Authors:  H Stibler; B Westerberg; F Hanefeld; B Hagberg
Journal:  Neuropediatrics       Date:  1993-02       Impact factor: 1.947

2.  The specific site of tunicamycin inhibition in the formation of dolichol-bound N-acetylglucosamine derivatives.

Authors:  L Lehle; W Tanner
Journal:  FEBS Lett       Date:  1976-11-15       Impact factor: 4.124

3.  Enzymatic N-glycosylation of synthetic Asn--X--Thr containing peptides.

Authors:  C Ronin; S Bouchilloux; C Granier; J van Rietschoten
Journal:  FEBS Lett       Date:  1978-12-01       Impact factor: 4.124

4.  Oligosaccharyltransferase activity is associated with a protein complex composed of ribophorins I and II and a 48 kd protein.

Authors:  D J Kelleher; G Kreibich; R Gilmore
Journal:  Cell       Date:  1992-04-03       Impact factor: 41.582

5.  Conformational aspects of N-glycosylation of proteins. Studies with linear and cyclic peptides as probes.

Authors:  E Bause; H Hettkamp; G Legler
Journal:  Biochem J       Date:  1982-06-01       Impact factor: 3.857

6.  Biosynthesis and characterization of large dolichyl diphosphate-linked oligosaccharides in Saccharomyces cerevisiae.

Authors:  L Lehle; W Tanner
Journal:  Biochim Biophys Acta       Date:  1978-03-01

7.  Sugar chains of serum transferrin from patients with carbohydrate deficient glycoprotein syndrome. Evidence of asparagine-N-linked oligosaccharide transfer deficiency.

Authors:  K Yamashita; H Ideo; T Ohkura; K Fukushima; I Yuasa; K Ohno; K Takeshita
Journal:  J Biol Chem       Date:  1993-03-15       Impact factor: 5.157

8.  N-Glycosylation of yeast proteins. Characterization of the solubilized oligosaccharyl transferase.

Authors:  C B Sharma; L Lehle; W Tanner
Journal:  Eur J Biochem       Date:  1981-05

9.  The yeast WBP1 is essential for oligosaccharyl transferase activity in vivo and in vitro.

Authors:  S te Heesen; B Janetzky; L Lehle; M Aebi
Journal:  EMBO J       Date:  1992-06       Impact factor: 11.598

10.  Yeast Wbp1p and Swp1p form a protein complex essential for oligosaccharyl transferase activity.

Authors:  S te Heesen; R Knauer; L Lehle; M Aebi
Journal:  EMBO J       Date:  1993-01       Impact factor: 11.598

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  7 in total

1.  Carbohydrate-deficient glycoprotein syndrome type V: deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferase.

Authors:  C Körner; R Knauer; U Holzbach; F Hanefeld; L Lehle; K von Figura
Journal:  Proc Natl Acad Sci U S A       Date:  1998-10-27       Impact factor: 11.205

2.  Carbohydrate-deficient glycoprotein syndrome type I: determination of the oligosaccharide structure of newly synthesized glycoproteins by analysis of calnexin binding.

Authors:  T Marquardt; K Ullrich; R Niehues; H G Koch; E Harms
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

3.  A novel cerebello-ocular syndrome with abnormal glycosylation due to abnormalities in dolichol metabolism.

Authors:  Eva Morava; Ron A Wevers; Vincent Cantagrel; Lies H Hoefsloot; Lihadh Al-Gazali; Jeroen Schoots; Arno van Rooij; Karin Huijben; Connie M A van Ravenswaaij-Arts; Marjolein C J Jongmans; Jolanta Sykut-Cegielska; Georg F Hoffmann; Peter Bluemel; Maciej Adamowicz; Jeroen van Reeuwijk; Bobby G Ng; Jorieke E H Bergman; Hans van Bokhoven; Christian Körner; Dusica Babovic-Vuksanovic; Michel A Willemsen; Joseph G Gleeson; Ludwig Lehle; Arjan P M de Brouwer; Dirk J Lefeber
Journal:  Brain       Date:  2010-09-17       Impact factor: 13.501

4.  Analysis of glycosylation in CDG-Ia fibroblasts by fluorophore-assisted carbohydrate electrophoresis: implications for extracellular glucose and intracellular mannose 6-phosphate.

Authors:  Ningguo Gao; Jie Shang; Mark A Lehrman
Journal:  J Biol Chem       Date:  2005-02-11       Impact factor: 5.157

5.  Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development.

Authors:  J Tan; J Dunn; J Jaeken; H Schachter
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025

6.  Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies.

Authors:  Dirk J Lefeber; Johannes Schönberger; Eva Morava; Mailys Guillard; Karin M Huyben; Kiek Verrijp; Olga Grafakou; Athanasios Evangeliou; Frank W Preijers; Panagiota Manta; Jef Yildiz; Stephanie Grünewald; Martha Spilioti; Christa van den Elzen; Dominique Klein; Daniel Hess; Hisashi Ashida; Jan Hofsteenge; Yusuke Maeda; Lambert van den Heuvel; Martin Lammens; Ludwig Lehle; Ron A Wevers
Journal:  Am J Hum Genet       Date:  2009-07-02       Impact factor: 11.025

7.  Mannose corrects altered N-glycosylation in carbohydrate-deficient glycoprotein syndrome fibroblasts.

Authors:  K Panneerselvam; H H Freeze
Journal:  J Clin Invest       Date:  1996-03-15       Impact factor: 14.808

  7 in total

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