C. Frank

发表

Does Rft1 flip an N-glycan lipid precursor?

Sumana Sanyal, A. Menon, C. Frank, 2008, Nature.

Congenital disorder of glycosylation (CDG) Ig: Report on a patient and review of the literature

T. Hennet, M. Aebi, M. Rocco, 2005, Journal of Inherited Metabolic Disease.

ALG9 mannosyltransferase is involved in two different steps of lipid-linked oligosaccharide biosynthesis.

M. Aebi, C. Frank, 2005, Glycobiology.

Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)

T. Hennet, M. Aebi, G. Matthijs, 2004, Journal of Medical Genetics.

CDG‐IL: An infant with a novel mutation in the ALG9 gene and additional phenotypic features

T. Hennet, M. Aebi, G. Matthijs, 2005, American journal of medical genetics. Part A.

Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik.

E. Berger, T. Hennet, M. Aebi, 2004, Human molecular genetics.

Synthesis of Stable Dolichylphosphomannose Analogues

M. Aebi, A. Vasella, C. Frank, 2004 .

Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih ( CDG-Ih ) ( ALG 8 deficiency )

T. Hennet, M. Aebi, G. Matthijs, 2004 .

Distinct Flippases Translocate Glycerophospholipids and Oligosaccharide Diphosphate Dolichols across the Endoplasmic Reticulum†

Sumana Sanyal, A. Menon, C. Frank, 2008, Biochemistry.

Two distinctly localized p-type ATPases collaborate to maintain organelle homeostasis required for glycoprotein processing and quality control.

D. Ng, Shilpa Vashist, Davis T W Ng, 2002, Molecular biology of the cell.

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

G. Raymond, E. Berger, T. Hennet, 2001, The Journal of clinical investigation.

ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg.

E. Berger, T. Hennet, M. Aebi, 2002, Human molecular genetics.

Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL.

E. Berger, T. Hennet, M. Aebi, 2004, American journal of human genetics.

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

G. Raymond, E. Berger, T. Hennet, 2001, The Journal of clinical investigation.