Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata

Enhanced response of T lymphocytes from Pgap3 knockout mouse: Insight into roles of fatty acid remodeling of GPI anchored proteins

(2011) Hidekazu Murakami et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Molecular and clinical findings and diagnostic flowchart of peroxisomal diseases

(2011) Nobuyuki Shimozawa   BRAIN & DEVELOPMENT

Peroxisomes, lipid metabolism and lipotoxicity

(2010) R.J.A. Wanders et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS

Structural remodeling of GPI anchors during biosynthesis and after attachment to proteins

(2009) Morihisa Fujita et al.   FEBS LETTERS

Defects in myelination, paranode organization and Purkinje cell innervation in the ether lipid-deficient mouse cerebellum

(2009) Andre Teigler et al.   HUMAN MOLECULAR GENETICS

Spectrum ofPEX6mutations in Zellweger syndrome spectrum patients

(2009) Merel S. Ebberink et al.   HUMAN MUTATION

Wnt Signaling Is Regulated by Endoplasmic Reticulum Retention

(2009) J. Susie Zoltewicz et al.   PLoS One

Peroxisome dependency of alkyl-containing GPI-anchor biosynthesis in the endoplasmic reticulum

(2009) N. Kanzawa et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Biosynthesis, Remodelling and Functions of Mammalian GPI-anchored Proteins: Recent Progress

(2008) T. Kinoshita et al.   JOURNAL OF BIOCHEMISTRY

The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway

(2008) Takashi Matsuzaki et al.   JOURNAL OF CELL BIOLOGY