Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Linda Cheung"'
Publikováno v:
Brazilian Journal of Anesthesiology (Elsevier)
The prone position is extensively used to improve oxygenation in patients with severe acute respiratory distress syndrome caused by SARS-CoV-2 pneumonia. Occasionally, these patients exhibit cardiac and respiratory functions so severely compromised t
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
Publikováno v:
Brain Research Reviews. 46:44-70
Sporadic Parkinson's disease (PD) is a common neurodegenerative disorder, characterized by the loss of midbrain dopamine neurons and Lewy body inclusions. It is thought to result from a complex interaction between multiple predisposing genes and envi
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, You Wei Peng, Mei Tian, Dominic Cosgrove, Weimin Wang, Linda Cheung, Marisa Zallocchi
Usher syndrome combines congenital hearing loss and retinitis pigmentosa (RP). Mutations in the whirlin gene (DFNB31/WHRN) cause a subtype of Usher syndrome (USH2D). Whirler mice have a defective whirlin gene. They have inner ear defects but usually
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::296b87695ad478a40eb8032a750720f5
https://europepmc.org/articles/PMC4408763/
https://europepmc.org/articles/PMC4408763/
Autor:
Sylvie Abouna, Michael Khan, Goran Mattsson, Stella Pelengaris, Linda Cheung, Luxian Zhou, Vasiliki Ifandi, Sevasti Zervou
Publikováno v:
Islets. 2(1)
c-Myc (Myc) is a mediator of glucotoxicity but could also independently compromise β-cell survival and function. We have shown that after Myc activation in adult β-cells in vivo, apoptosis is preceded by hyperglycemia, suggesting glucotoxicity migh
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