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Pazour, Gregory

One or more keywords matched the following items that are connected to Pazour, Gregory

Item Type	Name
Academic Article	A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney.
Academic Article	Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease.
Academic Article	Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia.
Academic Article	Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome.
Academic Article	Disruption of IFT complex A causes cystic kidneys without mitotic spindle misorientation.
Concept	Kidney Diseases, Cystic
Academic Article	Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies.
Academic Article	Genetic link between renal birth defects and congenital heart disease.
Academic Article	Loss of Arf4 causes severe degeneration of the exocrine pancreas but not cystic kidney disease or retinal degeneration.
Academic Article	Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert?syndrome.
Academic Article	Ift25 is not a cystic kidney disease gene but is required for early steps of kidney development.
Academic Article	Cilia in cystic kidney and other diseases.

Search Criteria

Kidney Diseases Cystic