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- Hsc70/Stub1 Promotes the Removal of Individual Oxidatively Stressed Peroxisomes ✉ Bo-Hua Chen1,2,3, Yao-Jen Chang 2, Steven Lin 2,4 & Wei Yuan Yang1,2,4
- Zellweger Spectrum Disorder
- Recovery of PEX1-Gly843asp Peroxisome Dysfunction by Small-Molecule Compounds
- Blueprint Genetics Peroxisomal Disorders Panel
- Peroxisome Quality Control and Dysregulated Lipid Metabolism in Neurodegenerative Diseases Doo Sin Jo1,Nayeonpark2 and Dong-Hyung Cho1,2
- PEX1 Mutations in Complementation Group 1 of Zellweger Spectrum Patients Correlate with Severity of Disease
- Glycosome Biogenesis in Trypanosomes : Identification And
- Case Report Chinese Boy with Normal Initial Peroxisomal Blood Assays: a Diagnostic Pitfall in the Workup for Infantile Refsum Disease
- Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
- HHS Public Access Author Manuscript
- Genetic and Molecular Bases of Peroxisome Biogenesis Disorders
- Genomic Unity® Prenatal Analysis
- Disruption of a PEX1–PEX6 Interaction Is the Most Common Cause of the Neurologic Disorders Zellweger Syndrome, Neonatal Adreno
- Uva-DARE (Digital Academic Repository)
- Peroxisome Biogenesis Disorders in the Zellweger Spectrum: an Overview of Current Diagnosis, Clinical Manifestations, and Treatment Guidelines
- EGL Test Description
- A Computational Interactome and Functional Annotation for the Human 5 Proteome
- Zellweger Spectrum Disorders
- Peroxisome Metabolism in Cancer
- Supplementary Table 4. Gene-Set Differential Expression Analysis of TKI Resistance Sample (R2) Versus Pre-TKI Sample (R1) Using Rnaseq Exon Expression Data
- Molecular Snapshots of the Pex1/6 AAA&Plus
- PEX1 Gene Peroxisomal Biogenesis Factor 1
- Inbred Mouse Strains Expression in Primary Immunocytes Across
- Heimler Syndrome Is Caused by Hypomorphic Mutations in The
- Attractor Metafeatures and Their Application in Biomolecular Data Analysis
- Genetic Variation in Radiation-Induced Cell Death
- A Chinese Newborn with Zellweger Syndrome and Compound Heterozygous Mutations Novel in the PEX1 Gene: a Case Report and Literature Review
- Zellweger Syndrome Spectrum