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CFHR4
Biomarker Discovery for Chronic Liver Diseases by Multi-Omics
Complement Factor H Deficiency and Endocapillary Glomerulonephritis Due to Paternal Isodisomy and a Novel Factor H Mutation
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New Functional and Structural Insights from Updated Mutational Databases for Complement Factor H, Factor I, Membrane Cofactor Protein and C3
Epistatic Interactions of Genetic Loci Associated with Age-Related
Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways
A Genome-Wide Association Study Identifies Key Modulators of Complement Factor H Binding to Malondialdehyde-Epitopes
Complement System in the Pathogenesis of Benign Lymphoepithelial Lesions of the Lacrimal Gland
The Impact of Complement Genes on the Risk of Late-Onset Alzheimer's
(12) Patent Application Publication (10) Pub. No.: US 2015/0050646A1 Hageman (43) Pub
Genetic Analysis of 400 Patients Refines Understanding And
Product Description SALSA® MLPA® Probemix P236-B1 CFH Region to Be Used with the MLPA General Protocol
Downloaded Phase II Hapmap Assuming Normality of the Distribution
Gene Expression Profiling of Peripheral Blood in Patients With
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CFHR Gene Variations Provide Insights in the Pathogenesis of the Kidney Diseases Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy
Recurrent Structural Variation, Clustered Sites of Selection, and Disease Risk for the Complement Factor H (CFH) Gene Family
Copy Number Variation in the Susceptibility to Systemic Lupus Erythematosus
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Recurrent Structural Variation, Clustered Sites of Selection, And
Rare Variants in the Complement Factor H–Related Protein 5 Gene Contribute to Genetic Susceptibility to Iga Nephropathy
Identification of Structural Variation in Chimpanzees Using Optical
Recent Findings in Genetic Research in AMD
Tissue Specificity of Human Disease Module
Prediction of Co-Expression Genes and Integrative Analysis of Gene
Complement in Age-Related Macular Degeneration: a Focus on Function
Variation of Complement Factor H and Mannan Binding Lectin in Human
The NEI/NCBI Dbgap Database: Genotypes and Haplotypes That May
A Transcriptome-Wide Association Study Based on 27 Tissues Identifies 106 Genes Potentially Relevant for Disease Pathology in Age-Related Macular Degeneration
Microsatellite Scanning of the Immunogenome for Associations with Graft-Versus-Host Disease Following Haematopoietic Stem Cell Transplantation
CFHR4 (NM 006684) Human Tagged ORF Clone Product Data
From Variants to Pathways: Interrogating the Genetic Architecture of Age-Related Macular Degeneration
Molecular Correlates of Metastasis by Systematic Pan-Cancer Analysis
SUPPLEMENTARY INFORMATION Increased Circulating Levels Of
A Mega-Analysis of Expression Quantitative Trait Loci (Eqtl) Provides Insight Into the Regulatory Architecture of Gene Expressio