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PEX26
The Peroxisomal PTS1-Import Defect of PEX1- Deficient Cells Is Independent of Pexophagy in Saccharomyces Cerevisiae
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
Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome
Table S8. Positively Selected Genes (Psgs) Identified in Glyptosternoid and Yellowhead Catfish Lineages
Recovery of PEX1-Gly843asp Associated Peroxisome Dysfunction by Flavonoid Compounds in Fibroblasts from Zellweger Spectrum Patients
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Hamdan Medical Journal 2012; 5:313–326 (
Downloaded Per Proteome Cohort Via the Web- Site Links of Table 1, Also Providing Information on the Deposited Spectral Datasets
SSIEM Classification of Inborn Errors of Metabolism 2011
Targeting of the Tail-Anchored Peroxisomal Membrane Proteins PEX26 and PEX15 Occurs Through C-Terminal PEX19-Binding Sites
Lineage-Specific Effector Signatures of Invariant NKT Cells Are Shared Amongst Δγ T, Innate Lymphoid, and Th Cells
Peroksisomale Sykdommer V01
An Integrative Genomic Analysis of the Longshanks Selection Experiment for Longer Limbs in Mice
Structural Mapping of Missense Mutations in the Pex1/Pex6 Complex
Ubiquitin Signals Autophagic Degradation of Cytosolic Proteins and Peroxisomes
Recovery of PEX1-Gly843asp Peroxisome Dysfunction by Small-Molecule Compounds
Blueprint Genetics Peroxisomal Disorders Panel
Top View
Liver Diseases Genetic Testing Program
Gene Symbol Genbank MCF7-T MCF-F De
Peroxisome Quality Control and Dysregulated Lipid Metabolism in Neurodegenerative Diseases Doo Sin Jo1,Nayeonpark2 and Dong-Hyung Cho1,2
Effect of Redox-Cycling Agents on Nitric Oxide Synthase Activity In
Theranostics Selective Autophagy of Intracellular Organelles: Recent
Doç. Dr. Serdar Ceylaner
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
Supplementary Table 2. List of the Genes Implicated in Known Gld and Early Onset Hereditary Spastic Paraplegia Tested in Our Series
Genomic Unity® Prenatal Analysis
Clinical Utility of Genetic Testing in the Precision Diagnosis and Management of Pediatric Patients with Kidney and Urinary Tract Diseases
Publikationspromotion Guder P
Peroxisome Biogenesis Disorders in the Zellweger Spectrum: an Overview of Current Diagnosis, Clinical Manifestations, and Treatment Guidelines
PEX26 Gene Genotype-Phenotype Correlation in Neonates with Zellweger Syndrome
SSIEM Academy
A Pex1 Missense Mutation Improves Peroxisome Function in a Subset Of
Common Variants in Mendelian Kidney Disorder Genes and Their Association with Renal Function And
The Association of Germline Variants with Chronic Lymphocytic Leukemia
Identification of a Homozygous PEX26 Mutation in a Heimler Syndrome