Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Su M. Lwin"'
Autor:
Farzin Farzaneh, Anna E. Martinez, Magdalena Martinez-Queipo, Havinder Hara, Wei Wang, Adrian J. Thrasher, Alya Abdul-Wahab, Jemima E. Mellerio, Alex Virasami, Su M. Lwin, Waseem Qasim, John A. McGrath, Farhatullah Syed, Dale Moulding, Neil J. Sebire, John I. Harper, Wei Li Di, Tendai Kadiyirire, Anastasia Petrova, Catina Bernadis, M. Zamiri, Dyanne Rampling
Publikováno v:
Human gene therapy. 30(9)
Netherton syndrome (NS) is a rare autosomal recessive skin disorder caused by mutations in SPINK5. It is a debilitating condition with notable mortality in the early years of life. There is no cura...
Autor:
Emanuele de Rinaldis, Dusko Ilic, Magdalena Martinez-Queipo, Sabrina Zeddies, Alka Saxena, Ineke Slaper-Cortenbach, Sophia Aristodemou, Lu Liu, Su M. Lwin, James R. McMillan, Anna E. Martinez, Chrysanthi Ainali, John A. McGrath, Kasper Westinga, Gabriela Petrof, Alyson Guy, Marcel P. H. van den Broek, Rashida Pramanik, Francesco Dazzi, Venu Pullabhatla, Rosamund Nuamah, Linda Ozoemena, Salma Ayis, John B. Mee, Sonia Serrano, Clarisse Maurin, Jemima E. Mellerio, Ellie Rashidghamat, Alexandros Onoufriadis, Tendai Kadiyirire
Publikováno v:
Journal of the American Academy of Dermatology. 83(2)
Background Recessive dystrophic epidermolysis bullosa (RDEB) is a hereditary blistering disorder due to a lack of type VII collagen. At present, treatment is mainly supportive. Objectives To determine whether intravenous allogeneic bone marrow–deri
Autor:
Michael Antoniou, Sophia Aristodemou, Alain Hovnanian, Christos Georgiadis, Mei Chen, Su M. Lwin, M. Titeux, S. Miskinyte, Rashida Pramanik, Waseem Qasim, Lucas Chan, Rachel Phillips, Jakub Tolar, Wei Li Di, John A. McGrath, Adrian J. Thrasher, Christos Tziotzios, Linda Ozoemena, Alyson Guy, Alya Abdul-Wahab, Fiona Reid, James R. McMillan, Magdalena Martinez-Queipo, Lu Liu, Fernando Larcher, Jemima E. Mellerio, Johann W. Bauer, Patricia A. Lovell, Marcela Del Rio, Sonia Serrano, Clarisse Maurin, Anastasia Petrova, Farhatullah Syed, Alexandros Onoufriadis, Tendai Kadiyirire, Ellie Rashidghamat, Maria Elstad, Racheal Rowles, Farzin Farzaneh, John B. Mee, Elizabeth Orrin
BACKGROUND: Recessive dystrophic epidermolysis bullosa (RDEB) is a severe form of skin fragility disorder due to mutations in COL7A1 encoding basement membrane type VII collagen (C7), the main constituent of anchoring fibrils (AFs) in skin. We develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3df16e09632564610c72d70991aa6380
http://hdl.handle.net/10044/1/74451
http://hdl.handle.net/10044/1/74451
Autor:
Damilola Fajuyigbe, Richard Baker, Su M. Lwin, Antony R. Young, Desmond J. Tobin, Robert Sarkany, Brian Diffey
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 32(7)
Epidermal DNA damage, especially to the basal layer, is an established cause of keratinocyte cancers (KCs). Large differences in KC incidence (20- to 60-fold) between white and black populations are largely attributable to epidermal melanin photoprot