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PEX16
Common Variants in SOX-2 and Congenital Cataract Genes Contribute to Age-Related Nuclear Cataract
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Aneuploidy: Using Genetic Instability to Preserve a Haploid Genome?
Supplementary Material
Limited Survival and Impaired Hepatic Fasting Metabolism in Mice with Constitutive Rag Gtpase Signaling
Sec16b Is Involved in the Endoplasmic Reticulum Export of the Peroxisomal Membrane Biogenesis Factor Peroxin 16 (Pex16) in Mammalian Cells
Construction of a Natural Panel of 11P11.2 Deletions and Further Delineation of the Critical Region Involved in Potocki–Shaffer Syndrome
Inheritest 500 PLUS
Hamdan Medical Journal 2012; 5:313–326 (
The Neuroprotective Role of the GM1 Oligosaccharide, Ii3neu5ac-Gg4, In
Renoprotective Effect of Combined Inhibition of Angiotensin-Converting Enzyme and Histone Deacetylase
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Genetic Classification and Mutational Spectrum of More Than 600 Patients
Peroxisomal Biogenesis Is Genetically and Biochemically Linked to Carbohydrate Metabolism in Drosophila and Mouse
Two Splice Variants of Human PEX19 Exhibit Distinct Functions in Peroxisomal Assembly
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Peroksisomale Sykdommer V01
Gnomad Lof Supplement
Top View
Structural and Functional Roles of Ether Lipids John M
Ubiquitin Signals Autophagic Degradation of Cytosolic Proteins and Peroxisomes
Blueprint Genetics Peroxisomal Disorders Panel
Trifunctional Lipid Probes for Comprehensive Studies of Single Lipid Species in Living Cells
Peroxisome Quality Control and Dysregulated Lipid Metabolism in Neurodegenerative Diseases Doo Sin Jo1,Nayeonpark2 and Dong-Hyung Cho1,2
Functional Characterization of the Human Peroxins PEX3 and PEX19, Proteins Essential for Early Peroxisomal Membrane Biogenesis
Glycosome Biogenesis in Trypanosomes : Identification And
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
The Alterations of Mitochondrial Function During NAFLD Progression—An Independent Effect of Mitochondrial ROS Production
Genetic and Molecular Bases of Peroxisome Biogenesis Disorders
A Homozygous Mutation in PEX16 Identified by Whole-Exome
De Novo Truncating Variants in PHF21A Cause Intellectual Disability and Craniofacial Anomalies
Genetics and Molecular Basis of Human Peroxisome Biogenesis Disorders☆
Clinical Utility of Genetic Testing in the Precision Diagnosis and Management of Pediatric Patients with Kidney and Urinary Tract Diseases
Diagnostic Genetic Testing Requisition
SSIEM Academy
Determination of the Functions of Rab32, Rab38, and Their Effector Myosin Vc