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- Distinct CDH3 Mutations Cause Ectodermal Dysplasia, Ectrodactyly, Macular Dystrophy
- Cadherin Superfamily Genes: Functions, Genomic Organization, and Neurologic Diversity
- CDH16/1071) NBP2-45157-0.1Mg
- Kidney Side Population Reveals Multilineage Potential and Renal Functional Capacity but Also Cellular Heterogeneity
- Identification of Hub Genes in Diabetic Kidney Disease Via Multiple-Microarray Analysis
- An Oncogenic Mechanism for Mutant FGFR3 Erica Di Martino1, Gavin Kelly2, Jo-An Roulson3, and Margaret A
- Epithelial Notch Signaling Regulates Interstitial Fibrosis Development in the Kidneys of Mice and Humans
- Sorting out a Promiscuous Superfamily: Towards Cadherin Connectomics
- Pax8 Controls Thyroid Follicular Polarity Through Cadherin-16 Petrina Koumarianou1, Gonzalo Goméz-López2 and Pilar Santisteban1,*
- Supplemental Data Progression of Human Bronchioloalveolar
- Beyond N-Cadherin, Relevance of Cadherins 5, 6 and 17 in Cancer Progression and Metastasis
- Quantitative Proteomics of MDCK Cells Identify Unrecognized Roles of Clathrin Adaptor AP-1 in Polarized Distribution of Surface Proteins
- Kindlin-2 in Sertoli Cells Is Essential for Testis Development and Male
- An RGD Motif Present in Cadherin 17 Induces Integrin Activation and Tumor Growth
- Transcriptomic and Proteomic Profiling Provides Insight Into
- Figure S1. Frequency Distribution of the Expression Levels of the Six Cell Adhesion Molecules. Skewed Distribution Was Observed
- Article Proteomic Analysis of Urinary Microvesicles and Exosomes In
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