Showing 1 - 7 results of 7 for search 'Irwin McLean', query time: 0.03s Refine Results
  1. 1
    A lack of premature termination codon read-through efficacy of PTC124 (Ataluren) in a diverse array of reporter assays.

    A lack of premature termination codon read-through efficacy of PTC124 (Ataluren) in a diverse array of reporter assays. by Stuart P McElroy, Toshifumi Nomura, Leah S Torrie, Emma Warbrick, Ulrike Gartner, Gavin Wood, W H Irwin McLean

    Published 2013-01-01
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  2. 2
    Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort.

    Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort. by Santiago Rodriguez, Amanda J Hall, Raquel Granell, W H Irwin McLean, Alan D Irvine, Colin N A Palmer, George Davey Smith, John Henderson, Ian N M Day

    Published 2009-06-01
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  3. 3
    Improved annotation of 3' untranslated regions and complex loci by combination of strand-specific direct RNA sequencing, RNA-Seq and ESTs.

    Improved annotation of 3' untranslated regions and complex loci by combination of strand-specific direct RNA sequencing, RNA-Seq and ESTs. by Nicholas J Schurch, Christian Cole, Alexander Sherstnev, Junfang Song, Céline Duc, Kate G Storey, W H Irwin McLean, Sara J Brown, Gordon G Simpson, Geoffrey J Barton

    Published 2014-01-01
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  4. 4
    Gene-environment interaction in the onset of eczema in infancy: filaggrin loss-of-function mutations enhanced by neonatal cat exposure.

    Gene-environment interaction in the onset of eczema in infancy: filaggrin loss-of-function mutations enhanced by neonatal cat exposure. by Hans Bisgaard, Angela Simpson, Colin N A Palmer, Klaus Bønnelykke, Irwin McLean, Somnath Mukhopadhyay, Christian B Pipper, Liselotte B Halkjaer, Brian Lipworth, Jenny Hankinson, Ashley Woodcock, Adnan Custovic

    Published 2008-06-01
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  5. 5
    Generation and characterisation of keratin 7 (K7) knockout mice.

    Generation and characterisation of keratin 7 (K7) knockout mice. by Aileen Sandilands, Frances J D Smith, Declan P Lunny, Linda E Campbell, Kirsty M Davidson, Stephanie F MacCallum, Laura D Corden, Lesley Christie, Stewart Fleming, E Birgitte Lane, W H Irwin McLean

    Published 2013-01-01
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  6. 6
    Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophy.

    Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophy. by Haihui Liao, Alan D Irvine, Caroline J Macewen, Kathryn H Weed, Louise Porter, Laura D Corden, A Bethany Gibson, Jonathan E Moore, Frances J D Smith, W H Irwin McLean, C B Tara Moore

    Published 2011-01-01
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  7. 7
    Lysyl Hydroxylase 3 Localizes to Epidermal Basement Membrane and Is Reduced in Patients with Recessive Dystrophic Epidermolysis Bullosa.

    Lysyl Hydroxylase 3 Localizes to Epidermal Basement Membrane and Is Reduced in Patients with Recessive Dystrophic Epidermolysis Bullosa. by 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

    Published 2015-01-01
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