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- Molecular Structures of the Eukaryotic Retinal Importer ABCA4 Fangyu Liu1,2†, James Lee1, Jue Chen1,3*
- Gene Expression Profiling of ABC Transporters in Dermal Fibroblasts Of
- Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
- Role of ABCA7 in Human Health and in Alzheimer's Disease
- An Overview of the Genetics of ABCA4 Retinopathies, an Evolving Story
- Genetic Spectrum of ABCA4-Associated Retinal Degeneration in Poland
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- Functional Characterization of ABCA4 Missense Variants Linked to Stargardt Macular Degeneration
- Biophysical Studies of the First Nucleotide Binding Domain of Sulfonylurea Receptor 2A to Assess the Significance of Phosphorylation and Mutations
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- ABCA4 Gene Screening in a Chinese Cohort with Stargardt Disease
- Structural Basis of Substrate Recognition And
- ABCA7 Frameshift Deletion Associated with Alzheimer Disease in African Americans
- Functional Significance of Conserved Cysteines in the Extracellular Loops
- Report Mutations in the ABCA4 (ABCR)
- Realtime Ready Plate Layout ABC Transporter Panel, 96
- The Effect on Retinal Structure and Function of 15 Specific ABCA4
- The Human ATP-Binding Cassette (ABC) Transporter Superfamily
- A Computational Approach from Gene to Structure Analysis of the Human ABCA4 Transporter Involved in Genetic Retinal Diseases
- Novel Mutations in CRB1 and ABCA4 Genes Cause Leber Congenital Amaurosis and Stargardt Disease in a Swedish Family
- (ABCC1) and Human MRP2 (ABCC2) Expression
- Discovery of Regulatory Elements in Human ATP-Binding Cassette Transporters Through Expression Quantitative Trait Mapping
- ABC A-Subfamily Transporters: Structure, Function and Disease ⁎ Wolfgang E
- Polymorphisms of ATP-Binding Cassette, Sub-Family A, Member 4 (Rs560426 and Rs481931) and Non-Syndromic Cleft Lip/Palate: a Meta-Analysis
- Taqman® Human ABC Transporter Array
- The ABCA4 Gene and Age-Related Macular Degenerationinnocence Or
- ABCA4 Heterozygosity
- Development of a Bile Acid-Related Gene Signature for Predicting Survival in Patients with Hepatocellular Carcinoma
- The CFTR Corrector, VX-809 (Lumacaftor), Rescues ABCA4 Trafficking Mutants: a Potential Treatment for Stargardt Disease
- Identification of Ectodysplasin-A Receptor Gene Deletion at 2Q12.2 and a Potential Autosomal MR Locus
- Abcc6 Deficiency in Mice Leads to Altered ABC Transporter Gene Expression in Metabolic Active Tissues Bettina Ibold1, Isabel Faust1, Janina Tiemann1, Theo G
- ABCA4 Rabbit Pab
- DNA Nanoparticle-Mediated ABCA4 Delivery Rescues Stargardt Dystrophy in Mice
- Microarray-Based Detection of Multidrug Resistance in Human Tumor Cells by Expression Profiling of ATP-Binding Cassette Transporter Genes
- ABCA4 Is an N-Retinylidene- Phosphatidylethanolamine and Phosphatidylethanolamine Importer