Toward a Gene Therapy for Dominant Disease: Validation of an RNA Interference-Based Mutation-Independent Approach von Kiang, Anna-Sophia, Palfi, Arpad, Ader, Marius, Kenna, Paul F, Millington-Ward, Sophia, Clark, Gerry, Kennan, Avril, O'reilly, Mary, Tam, Lawrence C T, Aherne, Aileen, McNally, Niamh, Humphries, Pete, Farrar, G Jane

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TH6.7 Direct Streaming of Acute Surgical Patients to an Advanced Nurse Practitioner-led Service: A Prospective Audit of a Pilot Service to Improve Patient Flow von Riley, Anna, Aherne, Aileen, Box, Joe, Grady, Natalie, Maria, Jashmin, Chan, Anthony

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Light in retinitis pigmentosa von Kennan, Avril, Aherne, Aileen, Humphries, Pete

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Molecular recruitment as a basis for negative dominant inheritance? Propagation of misfolding in oligomers of IMPDH1, the mutated enzyme in the RP10 form of retinitis pigmentosa von Wang, Xiao-tao, Mion, Brian, Aherne, Aileen, Engel, Paul C.

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Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10) von Tam, Lawrence C.S., Kiang, Anna-Sophia, Kennan, Avril, Kenna, Paul F., Chadderton, Naomi, Ader, Marius, Palfi, Arpad, Aherne, Aileen, Ayuso, Carmen, Campbell, Matthew, Reynolds, Alison, McKee, Alex, Humphries, Marian M., Farrar, G. Jane, Humphries, Pete

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On the molecular pathology of neurodegeneration in IMPDH1-based retinitis pigmentosa von Aherne, Aileen, Kennan, Avril, Kenna, Paul F., McNally, Niamh, Lloyd, David G., Alberts, Ian L., Kiang, Anna-Sophia, Humphries, Marian M., Ayuso, Carmen, Engel, Paul C., Gu, Jing Jin, Mitchell, Beverly S., Farrar, G. Jane, Humphries, Pete

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Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wil... von KENNAN, Avril, AHERNE, Aileen, KENNA, Paul F, FARRAR, G. Jane, HUMPHRIES, Pete, PALFI, Arpad, HUMPHRIES, Marian, MCKEE, Alex, STITT, Alan, SIMPSON, David A. C, DEMTRODER, Karin, ORNTOFT, Torben, AYUSO, Carmen

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METHODS AND REAGENTS FOR TREATING AUTOSOMAL DOMINANT DISEASES OF THE EYE von AHERNE, AILEEN, KENNAN, AVRIL, HUMPHRIES, PETER, FARRAR, JANE, KENNA, PAUL, MCNALLY, NIAMH

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Molecular Mechanisms of Photoreceptor Degeneration in RP Caused by IMPDH1 Mutations von Aherne, Aileen, Kennan, Avril, Kenna, Paul F., McNally, Niamh, Farrar, G. Jane, Humphries, Pete

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METHODS AND REAGENTS FOR TREATING DISEASE von AHERNE, AILEEN, KENNAN, AVRIL, HUMPHRIES, PETER, FARRAR, JANE, KENNA, PAUL, MCNALLY, NIAMH

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