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GLB1
Epidemiology of Mucopolysaccharidoses Update
Novel Gene Fusions in Glioblastoma Tumor Tissue and Matched Patient Plasma
Vacuolated Lymphocytes, a Clinical Finding in GM1 Gangliosidosis
GM1 Gangliosidosis and Morquio B Disease
Revealing the Action Mechanisms of Dexamethasone on the Birth Weight
Clinica Chimica Acta 436 (2014) 112–120
Disorders of Sphingolipid Synthesis, Sphingolipidoses, Niemann-Pick Disease Type C and Neuronal Ceroid Lipofuscinoses
Metabolic Network-Based Stratification of Hepatocellular Carcinoma Reveals Three Distinct Tumor Subtypes
Transforming Growth Factor ß1-Mediated Functional Inhibition Of
Storage Disorders
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
D835a621d460bc7f1f92f1be9b4
Emerging Approaches for Fluorescence-Based Newborn Screening of Mucopolysaccharidoses
Bi-Functional Igg-Lysosomal Enzyme Fusion Proteins for Brain Drug Delivery Ruben J
Connectivity Mapping of Glomerular Proteins Identifies
Table S1. Genes Contributing to the Enrichment Scores of GSEA for Gene-Sets Down-Regulated in Adipose Tissue from Diabetic Compared with Non-Diabetic Co-Twins
Key Features in a New Murine Model of Human GM1-Gangliosidosis
Neurotrophic Effects of GM1 Ganglioside, NGF, and FGF2 On
Top View
Understanding Gene Therapy for GM1 Gangliosidosis Targeting the Genetic Cause of Disease
Expression and Purification of Human Lysosomal Β-Galactosidase from Pichia Pastoris
A Duplication in the Canine ß-Galactosidase Gene GLB1
Phenotyping and Genotyping of Skeletal Dysplasias Evolution of A
(A) Information on Patients Whose Tumors Were Used for Establishing PDX Models
GM1 Gangliosidosis: Review of Clinical, Molecular, and Therapeutic Aspects
Founder Mutation Causing Infantile GM1-Gangliosidosis in the Gypsy Population
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
1 Pharmacological Chaperones for the Mucopolysaccharidoses Juan
Online Supporting Information S2: Proteins in Each Negative Pathway
Genomic Unity® Prenatal Analysis
Oncogenic Effects of Germline Mutations in Lysosomal Storage Disease Genes
Supplementary Material
Mucopolysaccharidosis IV (Morquio Syndrome)
Identification and in Silico Analysis of GALNS Mutations Causing Morquio a Syndrome in Eight Consanguineous Families
Genetic Evaluation of Short Stature Laurie H
NRF2-Independent Regulation of Intestinal Constitutive Androstane Receptor by the Pro-Oxidants Cadmium and Isothiocyanate in Hugt1 Mice S
Galactosidase and Elastin Binding Protein in Lysosomal And
GLB1 Polyclonal Antibody Catalog Number PA5-49989 Product Data Sheet
Fetal Examination/Genetic Evaluation Information and Instructions
Diagnosis of Atelosteogenesis Type I
Characterization of a Murine Model of Mucopolysaccharidosis Type IIID: a Knockout Model Maryam Jamil Iowa State University
Nosology and Classification of Genetic Skeletal Disorders: 2015 Revision
Epidemiology of Mucopolysaccharidoses (MPS) in United States: Challenges and Opportunities Yana Puckett1*†, Alejandra Mallorga‑Hernández2† and Adriana M
Mucopolysaccharidosis IVA) Identifies 39 Novel GALNS Mutations
Diagnosis of Atelosteogenesis Type I Suggested by Fetal
Diagnosis of Mucopolysaccharidoses
Pharmacological Chaperones for Human Α-N-Acetylgalactosaminidase
Gene Expression Analyses Identify Narp Contribution in the Development of L-DOPA-Induced Dyskinesia
Phenotype Determining Alleles in GM1 Gangliosidosis Patients Bearing Novel GLB1 Mutations
Genomic Variability of the Mucopolysaccharidosis Complex in Southwestern Colombia
Individual Genome Sequence Gene List (By Disease)
CPT Code and Price List 2020 CPT Codes
Rare Mendelian Disorders Test Requisition Form
Inbred Mouse Strains Expression in Primary Immunocytes Across
Mis-Splicing of the GALNS Gene Resulting from Deep Intronic Mutations As a Cause of Morquio a Disease Anna Caciotti1†, Rodolfo Tonin1,2†, Matthew Mort3, David N
Keratan Sulfate Is a Linear Polymer the Basic Repeating Disaccharide Unit Within Keratan Sulfate Is 3Galβ1-4Glcnacβ1
Morquio a Syndrome-Associated Mutations: a Review of Alterations in the GALNS Gene and a New Locus-Specific Ad Tabase a Morrone
GLB1 Gene Galactosidase Beta 1
The Integrated RNA Landscape of Renal Preconditioning Against Ischemia-Reperfusion Injury
GM1 Gangliosidosis and Mucopolysaccharidosis Type IVB
UNIVERSITY of CALIFORNIA SAN DIEGO NRF2-Independent
Recombinant Human Β‑Galactosidase‑1/GLB1 Catalog Number: 6464-GH
Immune Reactivity to a Glb1 Homologue in a Highly Wheat-Sensitive Patient with Type 1 Diabetes and Celiac Disease
Morquio B Disease. Disease Characteristics and Treatment Options of a Distinct GLB1-Related Dysostosis Multiplex
Dual Positive and Negative Control of Chlamydomonas PII Signal
Identification of a Novel GLB1 Mutation in a Consanguineous Pakistani
Three Novel Beta-Galactosidase Gene Mutations in Han Chinese Patients