Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Linda Cheung"'
Autor:
Shiguang Liu, Duane Delimont, Brianna Dufek, Michael Anne Gratton, Linda Cheung, Wenping Song, Grady Phillips, Daniel T. Meehan, Dominic Cosgrove
Publikováno v:
Kidney International. 90:300-310
Recent work demonstrates that Alport glomerular disease is mediated through a biomechanical strain-sensitive activation of mesangial actin dynamics. This occurs through a Rac1/CDC42 cross-talk mechanism that results in the invasion of the subcapillar
Autor:
Linda Cheung, Bridget Speller, Bruce G. Robinson, Claire McBride, Ronald J. Koenig, Roderick J. Clifton-Bligh, John Wentworth, Kenneth G. Wilhelm, Vitomir Tasevski, Diana L. Learoyd, Amy Y. M. Au, Marinella Messina
Publikováno v:
Endocrinology. 147:367-376
Follicular thyroid carcinomas are associated with a chromosomal translocation that fuses the thyroid-specific transcription factor paired box gene 8 (PAX8) with the nuclear receptor peroxisome proliferator-activated receptor gamma (PPARgamma). This s
Autor:
Anthony J. Gill, John Wentworth, Leigh Delbridge, Roderick J. Clifton-Bligh, Bruce G. Robinson, Linda Cheung, Marinella Messina, Jeanette Philips, Adele Clarkson, Diana L. Learoyd
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 88:354-357
Chromosomal translocations encoding fusion oncoproteins are common in hematological malignancies, sarcomas, and papillary thyroid carcinomas. A recent study of follicular thyroid carcinomas reported a novel chromosomal translocation, t(2;3)(q13;p25),
Autor:
Duane Delimont, Velidi H. Rao, Dominic Cosgrove, Steven C. Sansom, Marisa Zallocchi, Linda Cheung, J. David Holzclaw, Daniel T. Meehan
Publikováno v:
Kidney international. 76(9)
Alport glomerular disease is associated with dysregulation of pro-inflammatory cytokines and matrix metalloproteinases, promoting progressive glomerulonephritis. Changes in composition and structure of Alport GBM resulting from mutations in type IV c
Autor:
Kyriacos A. Mitrophanous, Michelle Kelleher, Yatish Lad, Linda Cheung, Weimin Wang, Vicky Scripps, Katie Binley, Marisa Zallocchi, You Wei Peng, Peter Widdowson, Dominic Cosgrove, S. Iqball, Scott Ellis, James Miskin, Julie Loader, Duane Delimont
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e94272 (2014)
PLoS ONE
PLoS ONE
Usher syndrome type 1B is a combined deaf-blindness condition caused by mutations in the MYO7A gene. Loss of functional myosin VIIa in the retinal pigment epithelia (RPE) and/or photoreceptors leads to blindness. We evaluated the impact of subretinal