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PEX11B
Bilateral Gene Interaction Hierarchy Analysis of the Cell Death Gene
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
1Q21.1 Deletion and a Rare Functional Polymorphism in Siblings with Thrombocytopenia-Absent Radius–Like Phenotypes
Prenatal Detection of TAR Syndrome in a Fetus with Compound Inheritance of an RBM8A SNP and a 334‑Kb Deletion: a Case Report
Inheritest 500 PLUS
LOXL2-Mediated H3K4 Oxidation Reduces Chromatin Accessibility in Triple-Negative Breast Cancer Cells
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
High Incidence of Recurrent Copy Number Variants in Patients with Isolated and Syndromic Mullerian Aplasia
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Peroksisomale Sykdommer V01
Copy Number Variant Syndromes Are Frequent in Schizophrenia: Progressing Towards A
Blueprint Genetics Peroxisomal Disorders Panel
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Expanding the Phenotype of Reciprocal 1Q21.1 Deletions and Duplications: a Case Series Martina Busè1* , Helenia C
Immunity Resolution of Inflammation and Airway Diversity in Expression with Critical Roles in Macrophage Populations Reveals
Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
Top View
Brain Peroxisomes Doriane Trompier, A
Clinical Utility of Genetic Testing in the Precision Diagnosis and Management of Pediatric Patients with Kidney and Urinary Tract Diseases
Peroxisome Biogenesis Disorders in the Zellweger Spectrum: an Overview of Current Diagnosis, Clinical Manifestations, and Treatment Guidelines
Genomic Analysis of Human Spinal Deformity and Characterization of a Zebrafish Disease Model Jillian Gwen Buchan Washington University in St
STO (%) % O (STO) Slices of 12Μm Thickness After Equilibration to -20 C
Proximal Microdeletions and Microduplications of 1Q21.1 Contribute to Variable Abnormal Phenotypes
Supporting Information
Interplay Between Zika Virus and Peroxisomes During Infection
EGL Test Description
Complex Genetics of Radial Ray Deficiencies: Screening of a Cohort of 54 Patients
Viperin Interacts with PEX19 to Mediate Peroxisomal Augmentation of the Innate Antiviral Response
Dichloroacetate Prevents Cisplatin-Induced Nephrotoxicity Without Compromising Cisplatin Anticancer Properties
Responsive Nuclear Proteins in Collecting Duct Cells
Peroxisomes Protect Lymphoma Cells from HDAC Inhibitor-Mediated Apoptosis
Evidence of Chromosomal Domains Containing Co-Expressed Genes—A Study of 130 Invasive Ductal Breast Carcinomas
Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract As an Early Feature
Inbred Mouse Strains Expression in Primary Immunocytes Across
Variants in the 1Q21 Risk Region Are Associated with a Visual Endophenotype of Autism and Schizophrenia
RUNX1-EVI1 Disrupts Lineage Determination and the Cell Cycle by Interfering with RUNX1 and EVI1 Driven Gene Regulatory Networks
The Peroxisome: an Update on Mysteries 2.0
Long Term Response to Circulating Angiogenic Cells, Unstimulated Or Atherosclerotic Pre-Conditioned, in Critical Limb Ischemic Mice
Expression Pattern and Biological Significance of the Lncrna ST3GAL6-AS1 in Multiple Myeloma
Medfødte Leversykdommer