Molecular Characterization of the Human Cα-formylglycine-generating Enzyme

This publication has 32 references indexed in Scilit:

• Molecular and functional analysis ofSUMF1 mutations in multiple sulfatase deficiency
  Human Mutation, 2004
• The SNAREs vti1a and vti1b have distinct localization and SNARE complex partners
  European Journal of Cell Biology, 2002
• Deficiency of UDP-galactose:N-acetylglucosamine β-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId
  Journal of Clinical Investigation, 2002
• A new FAD-binding fold and intersubunit disulfide shuttle in the thiol oxidase Erv2p
  Nature Structural & Molecular Biology, 2001
• Characterization of Posttranslational Formylglycine Formation by Luminal Components of the Endoplasmic Reticulum
  Published by Elsevier ,2001
• Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency
  Nature Genetics, 2001
• Crystal Structure of an Enzyme-Substrate Complex Provides Insight into the Interaction between Human Arylsulfatase A and its Substrates During Catalysis
  Journal of Molecular Biology, 2001
• A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency
  Cell, 1995
• Studies on the transformation of intact yeast cells by the LiAc/SS‐DNA/PEG procedure
  Yeast, 1995
• A TECHNIQUE FOR ULTRACRYOTOMY OF CELL SUSPENSIONS AND TISSUES
  The Journal of cell biology, 1973