Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jasbani H. S. Dayal"'
Autor:
Patrizia Cammareri, Aidan M. Rose, David F. Vincent, Jun Wang, Ai Nagano, Silvana Libertini, Rachel A. Ridgway, Dimitris Athineos, Philip J. Coates, Angela McHugh, Celine Pourreyron, Jasbani H. S. Dayal, Jonas Larsson, Simone Weidlich, Lindsay C. Spender, Gopal P. Sapkota, Karin J. Purdie, Charlotte M. Proby, Catherine A. Harwood, Irene M. Leigh, Hans Clevers, Nick Barker, Stefan Karlsson, Catrin Pritchard, Richard Marais, Claude Chelala, Andrew P. South, Owen J. Sansom, Gareth J. Inman
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-14 (2016)
Cutaneous squamous cell carcinomas is a growing problem but the driver genes causing this remain poorly defined. Here, the authors demonstrate that inactivating driver mutations in TGFBR1 and TGFBR2occur in vemurafenib-induced and sporadic cutaneous
Externí odkaz:
https://doaj.org/article/007e4295faa9467ba2f947c4d342dc0a
Autor:
Stephen A Watt, Jasbani H S Dayal, Sheila Wright, Megan Riddle, Celine Pourreyron, James R McMillan, Roy M Kimble, Marco Prisco, Ulrike Gartner, Emma Warbrick, W H Irwin McLean, Irene M Leigh, John A McGrath, Julio C Salas-Alanis, Jakub Tolar, Andrew P South
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0137639 (2015)
Recessive dystrophic epidermolysis bullosa (RDEB) is caused by mutations in COL7A1 resulting in reduced or absent type VII collagen, aberrant anchoring fibril formation and subsequent dermal-epidermal fragility. Here, we identify a significant decrea
Externí odkaz:
https://doaj.org/article/2a4b58a6374444fe9124646dfdeb503e
Autor:
Jasbani H S, Dayal, Clare L, Cole, Celine, Pourreyron, Stephen A, Watt, Yok Zuan, Lim, Julio C, Salas-Alanis, Dedee F, Murrell, John A, McGrath, Bruno, Stieger, Colin, Jahoda, Irene M, Leigh, Andrew P, South
Publikováno v:
Journal of cell science. 127(Pt 4)
Type VII collagen is the main component of anchoring fibrils, structures that are integral to basement membrane homeostasis in skin. Mutations in the gene encoding type VII collagen COL7A1 cause recessive dystrophic epidermolysis bullosa (RDEB) an in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f8cbb99318d25f4d205c44401684bc8
https://pubmed.ncbi.nlm.nih.gov/24357722
https://pubmed.ncbi.nlm.nih.gov/24357722