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PEX13
E3 Ubiquitin Ligase SP1 Regulates Peroxisome Biogenesis in Arabidopsis
2014A Veenhuis Microbial Cell
Microduplication in the 2P16.1P15 Chromosomal Region Linked To
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 and Clinical Aspects of Zellweger Spectrum Patients with PEX1 Mutations H Rosewich, a Ohlenbusch, J Ga¨Rtner
Lysosomal Exocytosis Releases Pathogenic Α-Synuclein Species
Inheritest 500 PLUS
Comparative Genomics of Peroxisome Biogenesis Proteins: Making Sense of the PEX Mess
Generalised and Conditional Inactivation of Pex Genes in Mice ⁎ Myriam Baes A, , Paul P
E3 Ubiquitin Ligase SP1 Regulates Peroxisome Biogenesis In
Genetic Classification and Mutational Spectrum of More Than 600 Patients
Trypanosoma Brucei PEX 13S YG-Rich and SH3 Regions: Expression and Purification
Two Splice Variants of Human PEX19 Exhibit Distinct Functions in Peroxisomal Assembly
Peroksisomale Sykdommer V01
Knockdown of Hnrnpa0, a Del(5Q) Gene, Alters Myeloid Cell Fate In
Global Proteomic Profiling of Piscirickettsia Salmonis and Salmon
Identification of Pexl3p, a Peroxisomal Membrane Receptor for the PTS1
A Pex13 Knockout in Germ Cells Induces A
Top View
Blueprint Genetics Peroxisomal Disorders Panel
Chromosomal Contacts Connect Loci Associated with Autism, BMI and Head Circumference Phenotypes
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
Genetic Testing of Leukodystrophies Unraveling Extensive Heterogeneity
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
Recovery of PEX1-Gly843asp Peroxisome Dysfunction by Small-Molecule Compounds
Genetic and Molecular Bases of Peroxisome Biogenesis Disorders
2P15p16.1 Microdeletion Syndrome
Genepanel Mitochondrial Diseases Genepanel Paediatric Cardiomyopathy AARS2 AARS2 ABAT ABCC6 ACAD9 ABCC9 ACO2 ACAD8 AFG3L2 ACAD9
Genomic Unity® Prenatal Analysis
Genetics and Molecular Basis of Human Peroxisome Biogenesis Disorders☆
Universities of Leeds, Sheffield and York
The Structure and Function of Proline Recognition Domains
Identification of a Novel, Intraperoxisomal Pex14-Binding Site in Pex13
SSIEM Academy
Identification of Novel Genomic Imbalances in Saudi Patients with Congenital Heart Disease Zuhair N
POSITIVE RESULT Likely Pathogenic Variant Identified