Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Daniel T. Meehan"'
Autor:
Jacob Madison, Kevin Wilhelm, Daniel T Meehan, Duane Delimont, Gina Samuelson, Dominic Cosgrove
Publikováno v:
The Journal of Pathology. 258:26-37
Publikováno v:
The American Journal of Pathology. 183(4):1269-1280
Alport syndrome, hereditary glomerulonephritis with hearing loss, results from mutations in type IV collagen COL4A3, COL4A4, or COL4A5 genes. The mechanism for delayed glomerular disease onset is unknown. Comparative analysis of Alport mice and CD151
Autor:
Greg A. Perry, Stacie O'Brien, Taina Pihlajaniemi, Duane Delimont, Dominic Cosgrove, Hongmin Tu, Daniel T. Meehan, Marisa Zallocchi, Jameel Dennis
Publikováno v:
The American Journal of Pathology. 177:2527-2540
Alport syndrome is a common hereditary basement membrane disorder caused by mutations in the collagen IV α3, α4, or α5 genes that results in progressive glomerular and interstitial renal disease. Interstitial monocytes that accumulate in the renal
Autor:
Richard M. Tempero, Duane Delimont, Velidi H. Rao, Daniel T. Meehan, Kathyrn D. Rodgers, Marisa Zallocchi, Xiwu Chen, Ambra Pozzi, Dominic Cosgrove
Publikováno v:
The American Journal of Pathology. 172:761-773
Previous work has shown that integrin α1-null Alport mice exhibit attenuated glomerular disease with decreased matrix accumulation and live much longer than strain-matched Alport mice. However, the mechanism underlying this observation is unknown. H
Publikováno v:
The American Journal of Pathology. 166:1465-1474
Alport syndrome results from mutations in genes encoding collagen α3(IV), α4(IV), or α5(IV) and is characterized by progressive glomerular disease associated with a high-frequency sensorineural hearing loss. Earlier studies of a gene knockout mous
Autor:
Dominic Cosgrove, Raghu Kalluri, Aldo Amatucci, Phillip Gotwals, Daniel T. Meehan, Victor E. Kotelianski, Humphrey Gardner, Karen Bovard, Amy Gilroy, Caroline Miller, Kathryn D. Rodgers
Publikováno v:
Scopus-Elsevier
Alport syndrome is a genetic disorder resulting from mutations in type IV collagen genes. The defect results in pathological changes in kidney glomerular and inner-ear basement membranes. In the kidney, progressive glomerulonephritis culminates in tu
Autor:
Dominic Cosgrove, Takashi Wada, Motowo Nakajima, Michael Ann Gratton, Daniel T. Meehan, Velidi H. Rao, Duane Delimont
Alport syndrome is a glomerular basement membrane (GBM) disease caused by mutations in type IV collagen genes. A unique irregular thickening and thinning of the GBM characterizes the progressive glomerular pathology. The metabolic imbalances responsi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::371f381e2b9c7df9972b59d6b9c9af78
https://europepmc.org/articles/PMC1698763/
https://europepmc.org/articles/PMC1698763/