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Lipschutz, Joshua
One or more keywords matched the following items that are connected to Lipschutz, Joshua
Item TypeName
Concept Zebrafish Proteins
Concept Zebrafish
Academic Article The exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypes.
Academic Article Cdc42 deficiency causes ciliary abnormalities and cystic kidneys.
Academic Article Exocyst Sec10 protects renal tubule cells from injury by EGFR/MAPK activation and effects on endocytosis.
Academic Article Wnt5a is necessary for normal kidney development in zebrafish and mice.
Academic Article A possible zebrafish model of polycystic kidney disease: knockdown of wnt5a causes cysts in zebrafish kidneys.
Academic Article Dynamin Binding Protein (Tuba) Deficiency Inhibits Ciliogenesis and Nephrogenesis in Vitro and in Vivo.
Academic Article A post-developmental genetic screen for zebrafish models of inherited liver disease.
Academic Article Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.
Academic Article Arl13b and the exocyst interact synergistically in ciliogenesis.
Academic Article The exocyst is required for photoreceptor ciliogenesis and retinal development.
Academic Article Targeting Neph1 and ZO-1 protein-protein interaction in podocytes prevents podocyte injury and preserves glomerular filtration function.
Academic Article Zebrafish as models to study ciliopathies of the eye and kidney.
Academic Article The Retinol-Binding Protein Receptor 2 (Rbpr2) Is Required for Photoreceptor Survival and Visual Function in the Zebrafish.
Academic Article The exocyst acting through the primary cilium is necessary for renal ciliogenesis, cystogenesis, and tubulogenesis.
Academic Article Defects in the Exocyst-Cilia Machinery Cause Bicuspid Aortic Valve Disease and Aortic Stenosis.
Academic Article Conditional Loss of the Exocyst Component Exoc5 in Retinal Pigment Epithelium (RPE) Results in RPE Dysfunction, Photoreceptor Cell Degeneration, and Decreased Visual Function.
Academic Article A Functional Binding Domain in the Rbpr2 Receptor Is Required for Vitamin A Transport, Ocular Retinoid Homeostasis, and Photoreceptor Cell Survival in Zebrafish.
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  • Zebrafish