المؤلفون: Allen, Edwin H A, Courtney, David G., Atkinson, Sarah D., Moore, Johnny E., Mairs, Laura, Poulsen, Ebbe Toftgaard, Schiroli, Davide, Maurizi, Eleonora, Cole, Christian, Hickerson, Robyn P., James, John, Murgatroyd, Helen, Smith, Frances J D, MacEwen, Carrie, Enghild, Jan J., Nesbit, M. Andrew, Leslie Pedrioli, Deena M., McLean, W. H Irwin, Moore, C. B Tara

المصدر: Allen , E H A , Courtney , D G , Atkinson , S D , Moore , J E , Mairs , L , Poulsen , E T , Schiroli , D , Maurizi , E , Cole , C , Hickerson , R P , James , J , Murgatroyd , H , Smith , F J D , MacEwen , C , Enghild , J J , Nesbit , M A , Leslie Pedrioli , D M , McLean , W H I & Moore , C B T 2016 , ' Keratin 12 missense mutation ....

مصطلحات موضوعية: /dk/atira/pure/subjectarea/asjc/1300/1311, Genetics, /dk/atira/pure/subjectarea/asjc/2700/2716, Genetics(clinical), /dk/atira/pure/subjectarea/asjc/1300/1312, Molecular Biology

وصف الملف: application/pdf

الإتاحة: https://doi.org/10.1093/hmg/ddw001Test
http://discovery.dundee.ac.uk/portal/en/research/keratin-12-missense-mutation-induces-the-unfolded-protein-response-and-apoptosis-in-meesmann-epithelial-corneal-dystrophyTest(830d49a4-2a6a-45ee-afb2-c3271122fbf1).html
http://hdl.handle.net/10588/830d49a4-2a6a-45ee-afb2-c3271122fbf1Test
http://discovery.dundee.ac.uk/ws/files/9964255/Hum._Mol._Genet._2016_Allen_1176_91.pdfTest
http://www.scopus.com/inward/record.url?scp=84960120804&partnerID=8YFLogxKTest

المؤلفون: Courtney, David G, Atkinson, Sarah D, Moore, Johnny E, Maurizi, Eleonora, Serafini, Chiara, Pellegrini, Graziella, Black, Graeme C, Manson, Forbes D, Yam, Gary H F, Macewen, Caroline J, Allen, Edwin H A, McLean, W H Irwin, Moore, C B Tara

المصدر: Courtney , D G , Atkinson , S D , Moore , J E , Maurizi , E , Serafini , C , Pellegrini , G , Black , G C , Manson , F D , Yam , G H F , Macewen , C J , Allen , E H A , McLean , W H I & Moore , C B T 2014 , ' Development of allele-specific gene-silencing siRNAs for TGFBI Arg124Cys in lattice corneal dystrophy type I. ' , Investigative ophthalmology & visual science , vol. 55 , no. 2 , pp. 977-985 . ....

مصطلحات موضوعية: RNA interference, TGFBI, allele discrimination, lattice corneal dystrophy, siRNA

الإتاحة: https://doi.org/10.1167/iovs.13-13279Test
https://research.manchester.ac.uk/en/publications/a7b41880-e915-450f-8712-32d90a587064Test
http://www.iovs.org/content/55/2/941.full.pdfTest

المؤلفون: Allen, Edwin H. A., Atkinson, Sarah D., Liao, Haihui, Moore, Jonathan E., Pedrioli, Deena M. Leslie, Smith, Frances J. D., McLean, William H. Irwin, Moore, C. B. Tara

المصدر: Allen , E H A , Atkinson , S D , Liao , H , Moore , J E , Pedrioli , D M L , Smith , F J D , McLean , W H I & Moore , C B T 2013 , ' Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophy ' Investigative Ophthalmology & Visual Science , vol 54 , no. 1 , pp. 494-502 . DOI:10.1167/iovs.12-10528

مصطلحات موضوعية: DISEASES, EPIDERMOLYSIS-BULLOSA SIMPLEX, CELL-LINE, RNAI THERAPEUTICS, GENE-THERAPY, KNOCKING, INCLUDING PACHYONYCHIA-CONGENITA, DISORDERS, INTERFERENCE, DELIVERY

الإتاحة: https://doi.org/10.1167/iovs.12-10528Test
http://discovery.dundee.ac.uk/portal/en/research/allelespecific-sirna-silencing-for-the-common-keratin-12-founder-mutation-in-meesmann-epithelial-corneal-dystrophyTest(654a4313-216b-4245-bc67-4d21562d46cb).html
http://hdl.handle.net/10588/654a4313-216b-4245-bc67-4d21562d46cbTest

المؤلفون: Allen, Edwin H. A., Courtney, David G., Atkinson, Sarah D., Moore, Johnny E., Mairs, Laura, Poulsen, Ebbe Toftgaard, Schiroli, Davide, Maurizi, Eleonora, Cole, Christian, Hickerson, Robyn P., James, John, Murgatroyd, Helen, Smith, Frances J. D., MacEwen, Carrie, Enghild, Jan J., Nesbit, M. Andrew, Pedrioli, Deena M. Leslie, McLean, W. H. Irwin, Moore, C. B. Tara

المصدر: Human Molecular Genetics; 3/15/2016, Vol. 25 Issue 6, p1176-1191, 16p

المؤلفون: Allen, Edwin H.

المصدر: American Review of Public Administration; Feb1968, Vol. 2 Issue 1, p33-35, 3p