Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor

Current protocols in molecular biology

1988 • 4,543 citations

An analysis of vertebrate mRNA sequences: intimations of translational control.

1991 • 1,655 citations

A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase.

1991 • 629 citations

PAS7 encodes a novel yeast member of the WD-40 protein family essential for import of 3-oxoacyl-CoA thiolase, a PTS2-containing protein, into peroxisomes.

1994 • 295 citations

Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting

1991 • 288 citations

The Kinetics of Catalase Synthesis and Destruction in Vivo

1962 • 279 citations

Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1.

1990 • 226 citations

Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome

1984 • 192 citations

The import receptor for the peroxisomal targeting signal 2 (PTS2) in Saccharomyces cerevisiae is encoded by the PAS7 gene.

1996 • 181 citations

Targeting of human catalase to peroxisomes is dependent upon a novel COOH-terminal peroxisomal targeting sequence.

1996 • 167 citations

The Kinetics of Disappearance of Labeled Leucine from the Free Leucine Pool and Rat Liver and Its Effect on the Apparent Turnover of Catalase and Other Hepatic Proteins

1971 • 158 citations

Development of a highly efficient expression cDNA cloning system: application to oncogene isolation.

1991 • 145 citations

PEB1 (PAS7) in Saccharomyces cerevisiae encodes a hydrophilic, intra-peroxisomal protein that is a member of the WD repeat family and is essential for the import of thiolase into peroxisomes.

1995 • 140 citations

Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders

1995 • 120 citations

Differential protein import deficiencies in human peroxisome assembly disorders.

1994 • 117 citations

Peb1p (Pas7p) is an intraperoxisomal receptor for the NH2-terminal, type 2, peroxisomal targeting sequence of thiolase: Peb1p itself is targeted to peroxisomes by an NH2-terminal peptide.

1996 • 100 citations

Comparative genomics, genome cross-referencing and XREFdb

1995 • 77 citations

Aberrant Subcellular Localization of Peroxisomal 3-Ketoacyl-CoA Thiolase in the Zellweger Syndrome and Rhizomelic Chondrodysplasia Punctata

1990 • 65 citations

Novel peroxisome clustering mutants and peroxisome biogenesis mutants of Saccharomyces cerevisiae.

1993 • 58 citations

Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular trageting. Analysis of the marmoset and rabbit genes

1992 • 53 citations

Acyl-CoA: dihydroxyacetone phosphate acyltransferase in human skin fibroblasts: study of its properties using a new assay method

1986 • 47 citations

Peroxisome Structure, Function, and Biogenesis—Human Patients and Yeast Mutants Show Strikingly Similar Defects in Peroxisome Biogenesis

1995 • 37 citations

Rhizomelic chondrodysplasia punctata: Biochemical studies of peroxisomes isolated from cultured skin fibroblasts

1991 • 26 citations

[10] Dihydroxyacetone phosphate acyltransferase

1992 • 19 citations