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Pediatric Nephrology (Berlin, Germany)|April 2, 2011
Glomerular pathology in Alport syndrome: a molecular perspectiveDominic Cosgrove
Frontiers in Medicine|February 28, 2022
Molecular and Cellular Mechanisms Underlying the Initiation and Progression of Alport Glomerular PathologyDominic Cosgrove, Jacob Madison
The International Journal of Biochemistry & Cell Biology|November 19, 2013
Usher protein functions in hair cells and photoreceptorsDominic Cosgrove, Marisa Zallocchi
Matrix Biology : Journal of the International Society for Matrix Biology|August 31, 2016
Collagen IV diseases: A focus on the glomerular basement membrane in Alport syndromeDominic Cosgrove, Shiguang Liu
Biochemistry|August 24, 2005
Evidence for functional importance of usherin/fibronectin interactions in retinal basement membranesGautam Bhattacharya, Dominic Cosgrove
Biochemistry|January 12, 2010
Biochemical characterization of native Usher protein complexes from a vesicular subfraction of tracheal epithelial cellsMarisa Zallocchi, Joseph H Sisson, Dominic Cosgrove
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 5, 2012
Regulated vesicular trafficking of specific PCDH15 and VLGR1 variants in auditory hair cellsMarisa Zallocchi, Duane Delimont, Daniel T Meehan, et al.
Hearing Research|January 15, 2002
Strial marginal cells play a role in basement membrane homeostasis: in vitro and in vivo evidenceMichael Anne Gratton, Daniel T Meehan, Brendan J Smyth, et al.
Hearing Research|November 16, 2002
Usherin expression is highly conserved in mouse and human tissuesNicole Pearsall, Gautam Bhattacharya, Jim Wisecarver, et al.
Hearing Research|January 15, 2002
Localization and expression of usherin: a novel basement membrane protein defective in people with Usher's syndrome type IIaGautam Bhattacharya, Caroline Miller, William J Kimberling, et al.
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