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Norrin
Norrin, Frizzled-4, and Lrp5 Signaling in Endothelial Cells Controls a Genetic Program for Retinal Vascularization
Identification of a Variant in NDP Associated with X-Linked Retinal Dysplasia in the English Cocker Spaniel Dog
Screening and Identification of Angiogenesis-Related Genes As Potential Novel Prognostic Biomarkers of Hepatocellular Carcinoma Through Bioinformatics Analysis
FZD4 Gene Frizzled Class Receptor 4
Interaction Between Retinoschisin and Norrin: Physical Or Functional Relationship?
Genome-Wide Occupancy Links Hoxa2 to Wnt–B-Catenin Signaling in Mouse Embryonic Development Ian J
International Union of Basic and Clinical Pharmacology. LXXX. the Class Frizzled Receptors□S
Norrie Disease
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Variants in the 3″UTR of SNCA Do Not Affect Mirna-433
Molecular Analysis of the Neuroprotective Role of Norrin for Photoreceptors in the Mammalian Retina
Studies to the Understanding of Cadasil. a Systematic Review
Mouse Models for Deafness: Lessons for the Human Inner Ear and Hearing Loss
NF-Кb-Regulated, Proinflammatory Mirnas in Alzheimer's Disease
Catenin Alpha 1 Mutations Cause Familial Exudative Vitreoretinopathy by Overactivating Norrin/Beta-Catenin Signaling
Norrin Mediates Tumor-Promoting and -Suppressive Effects in Glioblastoma Via Notch and Wnt
Genomic and Clinical Assessment of Norrie Disease
Whole-Gene Deletions of FZD4 Cause Familial Exudative Vitreoretinopathy
Top View
NDP Gene NDP, Norrin Cystine Knot Growth Factor
Structure of Human Frizzled5 by Fiducial- Assisted Cryo-EM Supports
Norrin Mediates Tumor-Promoting and -Suppressive Effects in Glioblastoma Via Notch and Wnt
Familial Exudative Vitreoretinopathy
Retinal Phenotype Genotype Correlation of Pediatric Patients
Nuclear Control of Lung Cancer Cells Migration, Invasion and Bioenergetics by Eukaryotic Translation Initiation Factor 3F
Interplay of the Norrin and Wnt7a/Wnt7b Signaling Systems in Blood–Brain Barrier and Blood–Retina Barrier Development and Maintenance
Predicting Human Disease Mutations and Identifying Drug Targets from Mouse Gene Knockout Phenotyping Campaigns Robert Brommage1,*, David R
Norrie Disease
High-Throughput Screening of Mouse Gene Knockouts Identifies Established and Novel Skeletal Phenotypes
Familial Exudative Vitreoretinopathy and Related Retinopathies
The Structural Biology of Canonical Wnt Signalling
Novel Norrie Disease Gene Mutations in Chinese Patients with Familial Exudative Vitreoretinopathy Li-Yun Jia* and Kai Ma