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Plos Medicine|March 3, 2006
Stage-specific action of matrix metalloproteinases influences progressive hereditary kidney diseaseMichael Zeisberg, Mona Khurana, Velidi H Rao, et al.
Hearing Research|April 3, 2020
Pericyte abnormalities precede strial capillary basement membrane thickening in Alport miceBrianna Dufek, Daniel T Meehan, Duane Delimont, et al.
The Journal of Pathology|December 21, 2023
Ramipril therapy in integrin α1-null, autosomal recessive Alport mice triples lifespan: mechanistic clues from RNA-seq analysisJacob Madison, Kevin Wilhelm, Daniel T Meehan, et al.
The American Journal of Pathology|February 9, 2008
Integrin alpha1beta1 regulates matrix metalloproteinases via P38 mitogen-activated protein kinase in mesangial cells: implications for Alport syndromeDominic Cosgrove, Daniel T Meehan, Duane Delimont, et al.
Kidney International|May 16, 2018
Lysyl oxidase like-2 contributes to renal fibrosis in Col4α3/Alport miceDominic Cosgrove, Brianna Dufek, Daniel T Meehan, et al.
Pediatric Nephrology (Berlin, Germany)|March 23, 2005
Dysregulation of renal MMP-3 and MMP-7 in canine X-linked Alport syndromeVelidi H Rao, George E Lees, Clifford E Kashtan, et al.
Plos One|August 22, 2020
RNA-seq analysis of gene expression profiles in isolated stria vascularis from wild-type and Alport mice reveals key pathways underling Alport strial pathogenesisBrianna Dufek, Daniel T Meehan, Duane Delimont, et al.
Kidney International|April 5, 2003
Increased expression of MMP-2, MMP-9 (type IV collagenases/gelatinases), and MT1-MMP in canine X-linked Alport syndrome (XLAS)Velidi H Rao, George E Lees, Clifford E Kashtan, et al.
The Journal of Pathology|May 31, 2023
Dual inhibition of the endothelin and angiotensin receptor ameliorates renal and inner ear pathologies in Alport miceDominic Cosgrove, Michael Anne Gratton, Jacob Madison, et al.
Plos One|April 8, 2014
EIAV-based retinal gene therapy in the shaker1 mouse model for usher syndrome type 1B: development of UshStatMarisa Zallocchi, Katie Binley, Yatish Lad, et al.
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