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PEX12
PEX2 Is the E3 Ubiquitin Ligase Required for Pexophagy During Starvation
Fig. S1
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
Supp Table 6.Pdf
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
LRP1 Regulates Peroxisome Biogenesis and Cholesterol
Inheritest 500 PLUS
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
Protein Homeostasis Networks and the Use of Yeast to Guide Interventions in Alzheimer’S Disease
Genetic Classification and Mutational Spectrum of More Than 600 Patients
PEX12 Gene Novel Mutation: a Case Report on Iranian Girl Withchildhood Onset Peroxisomal Disorder: Pseudo ALD?
Discerning the Role of Foxa1 in Mammary Gland
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
Transcriptome Profiling Reveals the Complexity of Pirfenidone Effects in IPF
Peroksisomale Sykdommer V01
Top View
Imputed Gene Associations Identify Replicable Trans-Acting Genes Enriched in Transcription Pathways and Complex Traits
Orsetti Et Al. Table S1
A Pex13 Knockout in Germ Cells Induces A
Blueprint Genetics Peroxisomal Disorders Panel
The Novel Interacting Partners of Viperin and Their Role in Establishing a Host Antiviral State
Liver Diseases Genetic Testing Program
Supplementary Data
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
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
Bee Gootjes Üf
Genetic and Molecular Bases of Peroxisome Biogenesis Disorders
Genepanel Mitochondrial Diseases Genepanel Paediatric Cardiomyopathy AARS2 AARS2 ABAT ABCC6 ACAD9 ABCC9 ACO2 ACAD8 AFG3L2 ACAD9
Genomic Unity® Prenatal Analysis
Clinical Utility of Genetic Testing in the Precision Diagnosis and Management of Pediatric Patients with Kidney and Urinary Tract Diseases
Identification of Novel Mutations in PEX2, PEX6, PEX10, PEX12 And
Gene Symbol Genbank MCF7-T MCF7-F Description
SSIEM Academy