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- 1 Recent Natural Selection in Human Noncoding Sequences Heather A
- Hnrnp A2/B1 Modulates Epithelial-Mesenchymal Transition in Lung Cancer Cell Lines
- Mpdz Null Allele in an Avian Model of Retinal Degeneration and Mutations in Human Leber Congenital Amaurosis and Retinitis Pigmentosa
- Could Ion Channels-Encoding Or Related Genes Act As Modifier Of
- In Crb1 Causes Retinal Degeneration and Deregulates Expression of Pituitary Tumor Transforming Gene Pttg1
- Transcriptional Regulation of Cell Polarity in EMT and Cancer
- Cardiomyocyte Proliferation Prevents Failure in Pressure but Not Volume Overload”
- Spaceflight Influences Gene Expression, Photoreceptor
- Current Concepts of Genotype-Phenotype Correlations
- CRB1 Mutation Spectrum in Inherited Retinal Dystrophies
- Genetic Spectrum of Retinal Dystrophies in Tunisia Imen Habibi 1*, Yosra Falfoul2, Ahmed Turki2, Asma Hassairi2, Khaled El Matri 2, Ahmed Chebil2, Daniel F
- A Multi-Strategy Sequencing Workflow In
- Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal Retinoschisis
- Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal Retinoschisis
- Zebrafish Crb1, Localizing Uniquely to the Cell Membranes Around Cone
- Molecular and Clinical Analysis of 27 German Patients with Leber Congenital
- Comprehensive Rare Variant Analysis Using Whole Genome Sequencing To
- Novel Mutations in CRB1 and ABCA4 Genes Cause Leber Congenital Amaurosis and Stargardt Disease in a Swedish Family
- Defining Phenotype, Tropism, and Retinal Gene Therapy
- Phenotypic Variability in Patients with Retinal Dystrophies Due to Mutations in CRB1
- Gene Therapy Into Photoreceptors and Müller Glial Cells Restores Retinal Structure and Function in CRB1 Retinitis Pigmentosa Mouse Models
- A Clinical and Molecular Characterisation of CRB1-Associated Maculopathy
- CRB1-Related Leber Congenital Amaurosis: Reporting Novel Pathogenic Variants and a Brief Review on Mutations Spectrum
- Mutations in the CRB1 Gene Cause Leber Congenital Amaurosis
- The Correlation Between CRB1 Variants and the Clinical Severity Of
- Comprehensive Identification of Mrna Isoforms Reveals the Diversity of Neural Cell-Surface Molecules with Roles in Retinal Devel
- Multimodal Retinal Imaging and Microperimetry Reveal a Novel Phenotype and Potential Trial End Points in CRB1-Associated Retinopathies
- Mouse Crb1 Knockout Project (CRISPR/Cas9)
- CRB1 Gene Crumbs 1, Cell Polarity Complex Component
- The Genecards Suite Gil Stelzer Gene Information Consolidation