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B Schenk

Research Profile

Disorders

Congenital Disorders of Glycosylation

Phenomena

Glycosylation

Chemicals & Drugs

Concepts & Ideas

Molecular Sequence Data

Physiology

Mutation

Genes & Molecular Sequences

Anatomy

Living Beings

Saccharomyces cerevisiae

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Publications

TOP 3
B Schenk; T Imbach; Christian G Frank; Claudia E Grubenmann; Gerald V Raymond; Haggit Hurvitz; isabelle korn-lubetzki; S Revel-Vik; A Raas-Rotschild; A S Luder; Jaak Jaeken; Eric G Berger; Gert Matthijs; Thierry Hennet; Markus Aebi
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If.
B Schenk; Fabiana Fernandez; Charles J Waechter
The ins(ide) and out(side) of dolichyl phosphate biosynthesis and recycling in the endoplasmic reticulum.
B Schenk; Jeffrey S Rush; Charles J Waechter; Markus Aebi
An alternative cis-isoprenyltransferase activity in yeast that produces polyisoprenols with chain lengths similar to mammalian dolichols.

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All Publications

2001: B Schenk; T Imbach; Christian G Frank; Claudia E Grubenmann; Gerald V Raymond; Haggit Hurvitz; isabelle korn-lubetzki; S Revel-Vik; A Raas-Rotschild; A S Luder; Jaak Jaeken; Eric G Berger; Gert Matthijs; Thierry Hennet; Markus Aebi
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If.
The Journal of clinical investigation 2001;108(11):1687-95.
2001: B Schenk; Fabiana Fernandez; Charles J Waechter
The ins(ide) and out(side) of dolichyl phosphate biosynthesis and recycling in the endoplasmic reticulum.
Glycobiology 2001;11(5):61R-70R.
2001: B Schenk; Jeffrey S Rush; Charles J Waechter; Markus Aebi
An alternative cis-isoprenyltransferase activity in yeast that produces polyisoprenols with chain lengths similar to mammalian dolichols.
Glycobiology 2001;11(1):89-98.
2000: T Imbach; Stephanie Grünewald; B Schenk; Patricie Burda; Els Schollen; Ron A Wevers; Jaak Jaeken; J B C de Klerk; Eric G Berger; Gert Matthijs; Markus Aebi; Thierry Hennet
Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic.
Human genetics 2000;106(5):538-45.
2000: T Imbach; B Schenk; Els Schollen; Patricie Burda; A Stutz; S Grunewald; N M Bailie; M D King; Jaak Jaeken; Gert Matthijs; Eric G Berger; Markus Aebi; Thierry Hennet
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie.
The Journal of clinical investigation 2000;105(2):233-9.
1999: Markus Aebi; ari Helenius; B Schenk; R Barone; A Fiumara; Eric G Berger; Thierry Hennet; T Imbach; A Stutz; Cecilia Bjursell; A Uller; Jan Wahlström; Paz Briones; E Cardo; Peter Clayton; Bryan Winchester; V Cormier-Dalre; Pascale de Lonlay; Maryvonne Cuer; Thierry Dupré; Nathalie Seta; Tom J de Koning; Lambertus Dorland; F de Loos; L Kupers
Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG. First International Workshop on CDGS.
Glycoconjugate journal 1999;16(11):669-71.

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