Retinopathy induced in mice by targeted disruption of the rhodopsin gene von Humphries, Marian M., Rancourt, Derrick, Farrar, G. Jane, Kenna, Paul, Hazel, Mark, Bush, Ronald A., Sieving, Paul A., Sheils, Denise M., Creighton, Peter, Erven, Alexandra, Boros, Andras, Gulya, Karoly, Capecchi, Mario R., Humphries, Peter

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Gene-based therapies for dominantly inherited retinopathies von Farrar, G J, Millington-Ward, S, Chadderton, N, Humphries, P, Kenna, P F

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On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention von Farrar, G. Jane, Kenna, Paul F., Humphries, Peter

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On the Molecular Genetics of Retinitis Pigmentosa von Humphries, Peter, Kenna, Paul, Farrar, G. Jane

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Localizing Multiple X Chromosome-Linked Retinitis Pigmentosa Loci Using Multilocus Homogeneity Tests von Ott, Jurg, Bhattacharya, Shomi, Chen, J. D., Denton, Michael J., Donald, Jenny, Dubay, Christopher, Farrar, G. Jane, Fishman, Gerald A., Frey, Daniel, Gal, Andreas, Humphries, Peter, Jay, B., Jay, Marcelle, Litt, Michael, Machler, Marco, Musarella, Maria, Neugebauer, Meinhard, Naussbaum, Robert L., Terwilliger, Joseph D., Weleber, Richard G., Wirth, Brunhilde, Wong, Fulton, Worton, Ronald G., Wright, Alan F.

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Strategems in Vitro for Gene Therapies Directed to Dominant Mutations von Millington-Ward, Sophia, O'Neill, Brian, Tuohy, Gearoid, Al-Jandal, Najma, Kiang, Anna-Sophia, Kenna, Paul F., Palfi, Arpad, Hayden, Patrick, Mansergh, Fiona, Kennan, Avril, Humphries, Peter, Farrar, G. Jane

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Ribozyme-Based Therapeutic Approaches for Autosomal Dominant Retinitis Pigmentosa von O'Neill, Brian, Millington-Ward, Sophia, O'Reilly, Mary, Tuohy, Gearoid, Kiang, Anna-Sophia, Kenna, Paul F, Humphries, Peter, Farrar, G. Jane

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A novel Asp380Ala mutation in the GLC1A/myocilin gene in a family with juvenile onset primary open angle glaucoma von Kennan, A M, Mansergh, F C, Fingert, J H, Clark, T, Ayuso, C, Kenna, P F, Humphries, P, Farrar, G J

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Structural and Functional Rescue of Murine Rod Photoreceptors by Human Rhodopsin Transgene von McNally, Niamh, Kenna, Paul, Humphries, Marian M., Hobson, Audrey H., Khan, Noheed W., Bush, Ron A., Sieving, Paul A., Humphries, Peter, Farrar, G. Jane

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Retinitis Pigmentosa and Progressive Sensorineural Hearing Loss Caused by a C12258A Mutation in the Mitochondrial MTTS2 Gene von Mansergh, Fiona C., Millington-Ward, Sophia, Kennan, Avril, Kiang, Anna-Sophia, Humphries, Marian, Farrar, G. Jane, Humphries, Peter, Kenna, Paul F.

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Emerging therapeutic approaches for osteogenesis imperfecta von Millington-Ward, Sophia, McMahon, Helena P., Farrar, G. Jane

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A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa von Farrar, G. Jane, Kenna, Paul, Jordan, Siobhán A., Kumar-Singh, Rajendra, Humphries, Marian M., Sharp, Elizabeth M., Sheils, Denise M., Humphries, Peter

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Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness von Kenna, Paul, Mansergh, Fiona, Millington-Ward, Sophia, Erven, Alexandra, Kumar-Singh, Rajendra, Brennan, Rosemary, Farrar, G Jane, Humphries, Peter

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Assignment of a Gene for Autosomal Recessive Retinitis Pigmentosa (RP12) to Chromosome 1q31-q32.1 in an Inbred and Genetically Heterogeneous Disease Population von van Soest, Simone, van den Born, L.Ingeborgh, Gal, Andreas, Farrar, G.Jane, Bleeker-Wagemakers, Liesbeth M., Westerveld, Andries, Humphries, Peter, Sandkuijl, Lodewijk A., Bergen, Arthur A.B.

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Efficacy of Codelivery of Dual AAV2/5 Vectors in the Murine Retina and Hippocampus von PALFI, Arpad, CHADDERTON, Naomi, MCKEE, Alex G, FERNANDEZ, Alfonso Blanco, HUMPHRIES, Peter, KENNA, Paul F, FARRAR, G. Jane

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Murine model of autosomal dominant retinitis pigmentosa generated by targeted deletion at codon 307 of the rds–peripherin gene von McNally, Niamh, Kenna, Paul F., Rancourt, Derrick, Ahmed, Tanweer, Stitt, Alan, Colledge, William H., Lloyd, David G., Palfi, Arpad, O'Neill, Brian, Humphries, Marian M., Humphries, Peter, Farrar, G. Jane

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Validation in mesenchymal progenitor cells of a mutation-independent ex vivo approach to gene therapy for osteogenesis imperfecta von Millington-Ward, Sophia, Allers, Carolina, Tuohy, Gearóid, Conget, Paulette, Allen, Danny, McMahon, Helena P., Kenna, Paul F., Humphries, Peter, Farrar, G. Jane

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Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability von Corradi, Zelia, Khan, Mubeen, Hitti-Malin, Rebekkah, Mishra, Ketan, Whelan, Laura, Cornelis, Stéphanie S., Hoyng, Carel B., Kämpjärvi, Kati, Klaver, Caroline C.W., Liskova, Petra, Stöhr, Heidi, Weber, Bernhard H.F., Banfi, Sandro, Farrar, G. Jane, Sharon, Dror, Zernant, Jana, Allikmets, Rando, Dhaenens, Claire-Marie, Cremers, Frans P.M.

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Lack of evidence for genetic heterogeneity in Best vitelliform macular dystrophy von Mansergh, F, Meitinger, T, Rodolph, G, Humphries, P, Farrar, G J

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Autosomal dominant Retinitis Pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked family von Farrar, G.J., Findlay, J.B.C., Kumar-Singh, R., Kenna, P., Humphries, M.M., Sharpe, E., Humphries, P.

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