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PEX6
Ophthalmic Manifestations of Heimler Syndrome Due to PEX6 Mutations
Propranolol-Mediated Attenuation of MMP-9 Excretion in Infants with Hemangiomas
The Peroxisomal PTS1-Import Defect of PEX1- Deficient Cells Is Independent of Pexophagy in Saccharomyces Cerevisiae
Spectrum of PEX1 and PEX6 Variants in Heimler Syndrome
Common Variants in SOX-2 and Congenital Cataract Genes Contribute to Age-Related Nuclear Cataract
Peroxisomal Disorders and Their Mouse Models Point to Essential Roles of Peroxisomes for Retinal Integrity
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Full Disclosure Forms
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Perkinelmer Genomics
Geneseq PLUS
SSIEM Classification of Inborn Errors of Metabolism 2011
Peroksisomale Sykdommer V01
The Pex1/Pex6 Complex Is a Heterohexameric AAA+ Motor With
Structural Mapping of Missense Mutations in the Pex1/Pex6 Complex
Genes for Spinocerebellar Ataxia with Blindness and Deafness (SCABD/SCAR3, MIM# 271250 and SCABD2)
Ubiquitin Signals Autophagic Degradation of Cytosolic Proteins and Peroxisomes
Zellweger Spectrum Disorder
Top View
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
Theranostics Selective Autophagy of Intracellular Organelles: Recent
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
An Arabidopsis Indole-3-Butyric Acid-Response Mutant Defective in PEROXIN6, an Apparent Atpase Implicated in Peroxisomal Function
Genetic and Molecular Bases of Peroxisome Biogenesis Disorders
Next Generation Sequencing (NGS)
PEX6: an Imaging Overlap Between Peroxisomal and Lysosomal Storage Diseases
Genomic Unity® Prenatal Analysis
A Clinical Evaluation Tool for SNP Arrays, Especially for Autosomal Recessive Conditions in Offspring of Consanguineous Parents
Disruption of a PEX1–PEX6 Interaction Is the Most Common Cause of the Neurologic Disorders Zellweger Syndrome, Neonatal Adreno
Peroxisome Biogenesis Disorders in the Zellweger Spectrum: an Overview of Current Diagnosis, Clinical Manifestations, and Treatment Guidelines
SSIEM Academy
A Pex1 Missense Mutation Improves Peroxisome Function in a Subset Of
Table S2.Pdf