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Publications by Richard I Kelley
The 22-kD Peroxisomal Integral Membrane Protein in Zellweger Syndrome—Presence, Abundance, and Association With a Peroxisomal Thiolase Precursor Protein
Pediatric Research
Child Health
Pediatrics
Perinatology
Urine Carnitine Excretion in Secondary Carnitine Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Aberrant Subcellular Localization of Peroxisomal 3-Ketoacyl-CoA Thiolase in the Zellweger Syndrome and Rhizomelic Chondrodysplasia Punctata
Pediatric Research
Child Health
Pediatrics
Perinatology
Peroxisomal Membrane Protein Import Does Not Require Pex17p
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
PAS3, a Saccharomyces Cerevisiae Gene Encoding a Peroxisomal Integral Membrane Protein Essential for Peroxisome Biogenesis
Journal of Cell Biology
Medicine
Cell Biology
Síndrome Cerebrohepatorrenal De Zellweger: Una Enfermedad Peroxisomal
Revista Chilena de Pediatria
Child Health
Pediatrics
Perinatology
The Peroxisomal Membrane Protein Pex13p Shows a Novel Mode of SH3 Interaction
EMBO Journal
Immunology
Molecular Biology
Biochemistry
Microbiology
Neuroscience
Medicine
Genetics
Peroxisomal Biogenesis Disorders in Zellweger Syndrome Spectrum: Diagnosis, Monitoring and Treatment According to the Recommendations of the Global Foundation for Peroxisomal Disorders
CHILD`S HEALTH
Calmodulin Antagonist Affects Peroxisomal Functionality by Disrupting Both Peroxisomal Ca 2+ and Protein Import
Journal of Cell Science
Cell Biology
Brefeldin a Interferes With Peroxisomal Protein Sorting in the yeastHansenula Polymorpha
FEBS Letters
Genetics
Cell Biology
Molecular Biology
Biochemistry
Structural Biology
Biophysics
PER3, a Gene Required for Peroxisome Biogenesis inPichia Pastoris, Encodes a Peroxisomal Membrane Protein Involved in Protein Import
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology