Tara S 2nd Assignment To Bcp

Peer-Reviewed Publications

Campbell, M. and Cassidy, P.S. and O'Callaghan, J. and Crosbie, D.E. and Humphries, P., Manipulating ocular endothelial tight junctions: Applications in treatment of retinal disease pathology and ocular hypertension, Progress in Retinal and Eye Research, 62, 2018, p120-133

O'Callaghan, J. and Cassidy, P.S. and Humphries, P., Open-angle glaucoma: therapeutically targeting the extracellular matrix of the conventional outflow pathway, Expert opinion on therapeutic targets, 21, (11), 2017, p1037-1050

Farrar, G.J. and Carrigan, M. and Dockery, A. and Millington-Ward, S. and Palfi, A. and Chadderton, N. and Humphries, M. and Kiang, A.S. and Kenna, P.F. and Humphries, P., Toward an elucidation of the molecular genetics of inherited retinal degenerations, Human Molecular Genetics, 26, (R1), 2017, pR2-R11

Tam L.C.S, Reina-Torres E, Sherwood J.M, Cassidy P.S, Crosbie D.E, LÃ"tjen-Drecoll E, FlÃ"gel-Koch C, Perkumas K, Humphries M.M, Kiang A.-S, O'Callaghan J, Callanan J.J, Read A.T, Ethier C.R, O'Brien C, Lawrence M, Campbell M, Stamer W.D, Overby D.R, Humphries P, Enhancement of outflow facility in the murine eye by targeting selected tight-junctions of Schlemm's canal endothelia, Scientific Reports, 7, 2017, p40717-

Hanlon, K.S. and Chadderton, N. and Palfi, A. and Fernandez, A.B. and Humphries, P. and Kenna, P.F. and Millington-Ward, S. and Farrar, G.J., A novel retinal ganglion cell promoter for utility in AAV vectors, Frontiers in Neuroscience, 11, (SEP), 2017

O'Callaghan, J. and Crosbie, D.E. and Cassidy, P.S. and Sherwood, J.M. and FlÃŒgel-Koch, C. and LÃŒtjen-Drecoll, E. and Humphries, M.M. and Reina-Torres, E. and Wallace, D. and Kiang, A.-S. and Campbell, M. and Stamer, W.D. and Overby, D.R. and O'Brien, C. and Tam, L.C.S. and Humphries, P., Therapeutic potential of AAV-mediated MMP-3 secretion from corneal endothelium in treating glaucoma, Human Molecular Genetics, 26, (7), 2017, p1230-1246

Dockery, A. and Stephenson, K. and Keegan, D. and Wynne, N. and Silvestri, G. and Humphries, P. and Kenna, P.F. and Carrigan, M. and Farrar, G.J., Target 5000: Target capture sequencing for inherited retinal degenerations, Genes, 8, (11), 2017, p304-

Carrigan M, Duignan E, Malone C.P.G, Stephenson K, Saad T, McDermott C, Green A, Keegan D, Humphries P, Kenna P.F, Farrar G.J, Panel-Based population next-generation sequencing for inherited retinal degenerations, Scientific Reports, 6, 2016, p33248 -

Carrigan M, Duignan E, Humphries P, Palfi A, Kenna P.F, Jane Farrar G, A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration, British Journal of Ophthalmology, 100, (4), 2016, p501 - 504

Doyle SL, López FJ, Celkova L, Brennan K, Mulfaul K, Ozaki E, Kenna PF, Kurali E, Hudson N, Doggett T, Ferguson TA, Humphries P, Adamson P, Campbell M, IL-18 Immunotherapy for Neovascular AMD: Tolerability and Efficacy in Nonhuman Primates., Invest Ophthalmol Vis Sci, 56, (9), 2015, p5424-30

Palfi Arpad, Chadderton Naomi, O'reilly Mary, Nagel-Wolfrum Kerstin, Wolfrum Uwe, Bennett Jean, Humphries Peter, Kenna Paul, Millington-Ward Sophia, Farrar Jane, Efficient gene delivery to photoreceptors using AAV2/rh10 and rescue of the Rhoâ, '/â, ' mouse , Molecular Therapy-Methods & Clinical Development , 2 , 2015, p15016 -

Tanimoto, N., Sothilingam, V., Kondo, M., (...), Humphries, P., Seeliger, M.W., Electroretinographic assessment of rod- and cone-mediated bipolar cell pathways using flicker stimuli in mice, Scientific Reports, 5, 2015, p10731-

Doyle SL, López FJ, Humphries P, Adamson P, Campbell M, Author Response: The Role of IL-18 in the Treatment of AMD., Invest Ophthalmol Vis Sci, 56, (3), 2015, p8237-8

Doyle, S.L., Adamson, P., López, F.J., Humphries, P., Campbell, M. , Interleukin-18 bioactivity and dose: Data interpretation at a crossroads, Investigative Ophthalmology and Visual Science, 55, (12), 2014, p8349

Ozaki, E., Campbell, M., Kiang, A.S., (...), Doyle, S.L., Humphries, P. , Inflammation in age-related macular degeneration., Advances in experimental medicine and biology, 801, 2014, p229-235

Nguyen, A.T., Campbell, M., Kiang, A.S., Humphries, M.M., Humphries, P. , Current therapeutic strategies for P23H RHO-linked RP., Advances in experimental medicine and biology, 801, 2014, p471-476

Campbell, M., Doyle, S., Humphries, P. , IL-18: A new player in immunotherapy for age-related macular degeneration?, Expert Review of Clinical Immunology, 10, (10), 2014, p1273-1275

Kiang, A.S., Humphries, M.M., Campbell, M., Humphries, P. , Antioxidant therapy for retinal disease., Advances in experimental medicine and biology, 801, 2014, p783-789

Tanimoto, N., Sothilingam, V., Gloeckner, G., (...), Biel, M., Seeliger, M.W. , Auditory event-related signals in mouse ERG recordings, Documenta Ophthalmologica, 128, (1), 2014, p25-32

Daiger, S.P., Bowne, S.J., Sullivan, L.S., (...), Chen, R., Li, Y. , Application of next-generation sequencing to identify genes and mutations causing autosomal dominant retinitis pigmentosa (adRP)., Advances in experimental medicine and biology, 801, 2014, p123-129

Campbell, M., Doyle, S.L., Ozaki, E., (...), Humphries, M.M., Humphries, P. , An overview of the involvement of interleukin-18 in degenerative retinopathies., Advances in experimental medicine and biology, 801, 2014, p409-415

Doyle, SL, Ozaki, E, Brennan, K, Humphries, MM, Mulfaul, K, Keaney, J, Kenna, PF, Maminishkis, A, Kiang, AS, Saunders, SP, Hams, E, Lavelle, EC, Gardiner, C, Fallon, PG, Adamson, P, Humphries, P, Campbell, M, IL-18 Attenuates Experimental Choroidal Neovascularization as a Potential Therapy for Wet Age-Related Macular Degeneration, SCIENCE TRANSLATIONAL MEDICINE, 6, 2014, p230-

N Chadderton, A Palfi, S Millington-Ward, O Gobbo, N Overlack, M Carrigan, M O'Reilly, M Campbell, C Ehrhardt, U Wolfrum, P Humphries, PF Kenna, GJ Farrar, Intravitreal delivery of AAV-NDI1 provides functional benefit in a murine model of Leber hereditary optic neuropathy, Eur J Hum Genet, 21, (1), 2013, p62-68

Campbell M, Humphries MM, Humphries P, Barrier modulation in drug delivery to the retina., Methods in molecular biology (Clifton, N.J.), 935, 2013, p371-80

Czekaj M, Haas J, Gebhardt M, Müller-Reichert T, Humphries P, Farrar J, Bartsch U, Ader M, In vitro expanded stem cells from the developing retina fail to generate photoreceptors but differentiate into myelinating oligodendrocytes., PloS one, 7, (7), 2012, pe41798

Nguyen AT, Campbell M, Kenna PF, Kiang AS, Tam L, Humphries MM, Humphries P, Calpain and photoreceptor apoptosis., Advances in experimental medicine and biology, 723, 2012, p547-52

Palfi, A., Chadderton, N., McKee, A.G., Blanco Fernandez, A., Humphries, P., Kenna, P.F., Farrar, G.J., Efficacy of codelivery of dual AAV2/5 vectors in the murine retina and hippocampus, Human Gene Therapy, 23, (8), 2012, p847-858

Tam LC, Kiang AS, Campbell M, Keaney J, Farrar GJ, Humphries MM, Kenna PF, Humphries P, Protein misfolding and potential therapeutic treatments in inherited retinopathies., Advances in experimental medicine and biology, 723, 2012, p567-72

Fischer MD, Huber G, Paquet-Durand F, Humphries P, Redmond TM, Grimm C, Seeliger MW, In vivo assessment of rodent retinal structure using spectral domain optical coherence tomography., Advances in experimental medicine and biology, 723, 2012, p489-94

Hanrahan F, Campbell M, Nguyen AT, Suzuki M, Kiang AS, Tam LC, Gobbo OL, Dhubhghaill SN, Humphries MM, Kenna PF, Humphries P, On further development of barrier modulation as a technique for systemic ocular drug delivery., Advances in experimental medicine and biology, 723, 2012, p155-9

Farrar GJ, Millington-Ward S, Chadderton N, Humphries P, Kenna PF, Gene-based therapies for dominantly inherited retinopathies., Gene therapy, 19, (2), 2012, p137-44

Campbell M, Humphries P, The blood-retina barrier: tight junctions and barrier modulation., Advances in experimental medicine and biology, 763, 2012, p70-84

Hanrahan, F, Campbell, M, Nguyen, AT, Suzuki, M, Kiang, AS, Tam, LC, Gobbo, OL, Dhubhghaill, SN, Humphries, MM, Kenna, PF, Humphries, P, LaVail, MM, Ash, JD, Anderson, RE, Hollyfield, JG, Grimm, C, On Further Development of Barrier Modulation as a Technique for Systemic Ocular Drug Delivery, RETINAL DEGENERATIVE DISEASES, 723, 2012, p155-159

Humphries MM, Kenna PF, Campbell M, Tam LC, Nguyen AT, Farrar GJ, Botto M, Kiang AS, Humphries P, C1q enhances cone photoreceptor survival in a mouse model of autosomal recessive retinitis pigmentosa., European journal of human genetics : EJHG, 20, (1), 2012, p64-8

Doyle SL, Campbell M, Ozaki E, Salomon RG, Mori A, Kenna PF, Farrar GJ, Kiang AS, Humphries MM, Lavelle EC, O'Neill LA, Hollyfield JG, Humphries P, NLRP3 has a protective role in age-related macular degeneration through the induction of IL-18 by drusen components., Nature medicine, 18, (5), 2012, p791-798

Campbell M, Hanrahan F, Gobbo OL, Kelly ME, Kiang AS, Humphries MM, Nguyen AT, Ozaki E, Keaney J, Blau CW, Kerskens CM, Cahalan SD, Callanan JJ, Wallace E, Grant GA, Doherty CP, Humphries P, Targeted suppression of claudin-5 decreases cerebral oedema and improves cognitive outcome following traumatic brain injury., Nature communications, 3, 2012, p849

Campbell M, Humphries MM, Nguyen ATH, Gobbo OL, Tam LCS, Suzuki M, Hanrahan F, Ozaki E, Farrar G-J, Kiang A-S, Kenna PF, Humphries P. , Systemic low-molecular weight drug delivery to pre-selected neuronal regions, EMBO Molecular Medicine, 3, (4), 2011, p235-245

Bowne, S.J., Humphries, M.M., Sullivan, L.S., Kenna, P.F., Tam, L.C.S., Kiang, A.S., Campbell, M., (...), Humphries, P. , Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86), 2011, - 1109

Campbell M, Humphries P, Size-selective and in vitro assessment of inner blood retina barrier permeability., Methods in molecular biology (Clifton, N.J.), 763, 2011, p355-67

Seeliger, M.W., Brombas, A., Weiler, R., Humphries, P., Knop, G., Tanimoto, N., Müller, F., Modulation of rod photoreceptor output by HCN1 channels is essential for regular mesopic cone vision, Nature Communications, 2, (1), 2011, part. no. 532

Bowne, SJ, Humphries, MM, Sullivan, LS, Kenna, PF, Tam, LCS, Kiang, AS, Campbell, M, Weinstock, GM, Koboldt, DC, Ding, L, Fulton, RS, Sodergren, EJ, Allman, D, Millington-Ward, S, Palfi, A, McKee, A, Blanton, SH, Slifer, S, Konidari, I, Farrar, GJ, Daiger, SP, Humphries, P, A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement, EUROPEAN JOURNAL OF HUMAN GENETICS, 19, (10), 2011, p1074-1081

Keaney J, Campbell M, Humphries P, From RNA interference technology to effective therapy: how far have we come and how far to go?, Therapeutic delivery, 2, (11), 2011, p1395-406

Sophia Millington-Ward, Naomi Chadderton, Mary O'Reilly, Arpad Palfi, Tobias Goldmann, Claire Kilty, Marian Humphries, Uwe Wolfrum, Jean Bennett, Peter Humphries, Paul F Kenna and G Jane Farrar, Suppression and Replacement Gene Therapy for Autosomal Dominant Disease in a Murine Model of Dominant Retinitis Pigmentosa, Molecular Therapy, 2011

Hanrahan, F., Humphries, P., Campbell, M., RNAi-mediated barrier modulation: Synergies of the brain and eye, Therapeutic Delivery , 1, (4), 2010, p587-594

Tam LC, Kiang AS, Chadderton N, Kenna PF, Campbell M, Humphries MM, Farrar GJ, Humphries P, Protection of photoreceptors in a mouse model of RP10., Advances in Experimental Medicine and Biology, 664, (Part 5), 2010, p559-65

Campbell M, Nguyen AT, Kiang AS, Tam L, Kenna PF, Dhubhghaill SN, Humphries M, Farrar GJ, Humphries P, Reversible and size-selective opening of the inner Blood-Retina barrier: a novel therapeutic strategy., Advances in Experimental Medicine and Biology, 664, (Part 3), 2010, p301-8

McKee AG, Loscher JS, O'Sullivan NC, Chadderton N, Palfi A, Batti L, Sheridan GK, O'Shea S, Moran M, McCabe O, Fernández AB, Pangalos MN, O'Connor JJ, Regan CM, O'Connor WT, Humphries P, Farrar GJ, Murphy KJ., AAV-mediated chronic over-expression of SNAP-25 in adult rat dorsal hippocampus impairs memory-associated synaptic plasticity, Journal of Neurochemistry, 112, (4), 2010, p991-1004

Mansergh FC, Vawda R, Millington-Ward S, Kenna PF, Haas J, Gallagher C, Wilson J, Humphries P, Ader M, Farrar GJ., Loss of photoreceptor potential from retinal progenitor cell cultures, despite improvements in survival, Experimental Eye Research, 91, (4), 2010, p500 - 512

Busskamp, V., Duebel, J., Balya, D., Fradot, M., Viney, T.J., Siegert, S., Groner, A.C., (...), Roska, B., Genetic reactivation of cone photoreceptors restores visual responses in retinitis pigmentosa, Science, 329, (5990), 2010, 413-417

Ni Dhubhghaill SS, Cahill MT, Campbell M, Cassidy L, Humphries MM, Humphries P, The pathophysiology of cigarette smoking and age-related macular degeneration., Advances in Experimental Medicine and Biology, 664, (Part 4), 2010, p437-46

Jaissle, G.B., Albrecht May, C., Van De Pavert, S.A., Wenzel, A., Claes-May, E., Giel, A., Szurman, P., (...), Seeliger, M.W. , Erratum: Bone spicule pigment formation in retinitis pigmentosa: Insights from a mouse model (Graefe's Archive for Clinical and Experimental Ophthalmology DOI: 10.1007/s00417-009-1253-9), 2010, - 1365

Palfi A, Millington-Ward S, Chadderton N, O'Reilly M, Goldmann T, Humphries MM, Li T, Wolfrum U, Humphries P, Kenna PF, Farrar GJ., Adeno-associated virus-mediated rhodopsin replacement provides therapeutic benefit in mice with a targeted disruption of the rhodopsin gene, Human Gene Therapy, 21, (3), 2010, p311-323

Campbell M, Ozaki E, Humphries P, Systemic delivery of therapeutics to neuronal tissues: a barrier modulation approach., Expert Opinion on Drug Delivery, 7, (7), 2010, p859-69

Lawrence C. S. Tam, Anna-Sophia Kiang, Matthew Campbell, James Keaney, G. Jane Farrar, Marian M. Humphries, Paul F. Kenna and Pete Humphries, Prevention of autosomal dominant retinitis pigmentosa by systemic drug therapy targeting heat shock protein 90 (Hsp90), Human Molecular Genetics, 19, (22), 2010, p4421-4436

Matthew Campbell, Anh T. H. Nguyen, Anna-Sophia Kiang, Lawrence C. S. Tam, Oliviero L. Gobbo, Christian Kerskens, Sorcha Ni Dhubhghaill, Marian M. Humphries, G.-Jane Farrar, Paul F. Kenna and Peter Humphries, An experimental platform for systemic drug delivery to the retina, Proceedings of the National Academy of Sciences of the United States, 106, (42), 2009, p17817 - 17822

Bujakowska KM, Maubaret C, Chakarova CF, Tanimoto N, Beck SC, Fahl E, Humphries MM, Kenna P, Makarov E, Makarova O, Paquet-Durand F, Ekström P, van Veen T, Leveillard T, Humphries P, Seeliger M, Bhattacharya SS, Study of gene targeted mouse models of splicing factor gene Prpf31 implicated in human autosomal dominant retinitis pigmentosa (RP), Investigative Ophthalmology & Visual Science, 50, (12), 2009

Tanimoto, N, Muehlfriedel, RL, Fischer, MD, Fahl, E, Humphries, P, Biel, M, Seeliger, MW, Vision tests in the mouse: Functional phenotyping with electroretinography., Frontiers in Bioscience : A Journal and Virtual Library, 14, 2009, p2730 - 2737

Chadderton, N, Millington-Ward, S, Palfi, A, O'Reilly, M, Tuohy, G, Humphries, MM, Li, T, Humphries, P, Kenna, PF, Farrar, GJ, Improved retinal function in a mouse model of dominant retinitis pigmentosa following AAV-delivered gene therapy., Molecular Therapy : The Journal of the American Society of Gene Therapy, 17, (4), 2009, p593-599

Huber G, Beck SC, Grimm C, Sahaboglu-Tekgoz A, Paquet-Durand F, Wenzel A, Humphries P, Redmond TM, Seeliger MW, Fischer MD, Spectral domain optical coherence tomography in mouse models of retinal degeneration., Investigative Ophthalmology & Visual Science, 50, (12), 2009, p5888-5895

Balan G, Bauman J, Bhattacharya S, Castrodad M, Healy DR, Herr M, Humphries P, Jennings S, Kalgutkar AS, Kapinos B, Khot V, Lazarra K, Li M, Li Y, Neagu C, Oliver R, Piotrowski DW, Price D, Qi H, Simmons HA, Southers J, Wei L, Zhang Y, Paralkar VM, The discovery of novel calcium sensing receptor negative allosteric modulators., Bioorganic & Medicinal Chemistry Letters, 19, (12), 2009, p3328-32

Humphries PS, Lafontaine JA, Agree CS, Alexander D, Chen P, Do QQ, Li LY, Lunney EA, Rajapakse RJ, Siegel K, Timofeevski SL, Wang T, Wilhite DM, Synthesis and SAR of 4-substituted-2-aminopyrimidines as novel c-Jun N-terminal kinase (JNK) inhibitors., Bioorganic and Medicinal Chemistry Letters, 19, (8), 2009, p2099-102

Jaissle GB, May CA, van de Pavert SA, Wenzel A, Claes-May E, Gießl A, Szurman P, Wolfrum U, Wijnholds J, Fisher MD, Humphries P, Seeliger MW, Bone spicule pigment formation in retinitis pigmentosa: insights from a mouse model., Graefe's Archive for Clinical and Experimental Ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2009

Tam, LC, Kiang, AS, Kennan, A, Kenna, PF, Chadderton, N, Ader, M, Palfi, A, Aherne, A, Ayuso, C, Campbell, M, Reynolds, A, McKee, A, Humphries, MM, Farrar, GJ, Humphries, P, Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10)., Human Molecular Genetics, 17, (14), 2008, p2084-2100

Trümpler, J, Dedek, K, Schubert, T, de Sevilla Müller, LP, Seeliger, M, Humphries, P, Biel, M, Weiler, R, Rod and cone contributions to horizontal cell light responses in the mouse retina., The Journal of Neuroscience, 28, (27), 2008, p6818-6825

O'Reilly, M, Millington-Ward, S, Palfi, A, Chadderton, N, Cronin, T, McNally, N, Humphries, MM, Humphries, P, Kenna, PF, Farrar, GJ, A transgenic mouse model for gene therapy of rhodopsin-linked Retinitis Pigmentosa., Vision Research, 48, (3), 2008, p386-391

U. Bartsch, W. Oriyakhel, P. Kenna, S. Linke, G. Richard, B. Petrowitz, P. Humphries, J. Farrar, M. Ader, Retinal cells integrate into the outer nuclear layer and differentiate into mature photoreceptors after sub-retinal transplantation into adult mice, Experimental Eye Research, 86, (4), 2008, p691 - 700

N. Chadderton, S. Millington-Ward, S. Palfi, M, O'Reilly, G. Touhy, M. Humphries, P. Kenna, J. Farrar, Improved retinal function in a mouse model of dominant retinitis pigmentosa following AAV-delivered gene therapy, Molecular Therapy, 17, (4), 2008, p593 - 599

D. Allen, E. Winters, P. Kenna, P. Humphries, J. Farrar, Reference gene selection for real-time rtPCR in human epidermal keratinocytes, Journal of Dermatological Science, 49, (3), 2008, p217 - 225

Reynolds, AL, Danciger, M, Farrar, GJ, Humphries, P, Kenna, PF, Influence of a quantitative trait locus on mouse chromosome 19 to the light-adapted electroretinogram., Investigative ophthalmology & visual science, 49, (9), 2008

Campbell, M, Kiang, AS, Kenna, PF, Kerskens, C, Blau, C, O'Dwyer, L, Tivnan, A, Kelly, JA, Brankin, B, Farrar, GJ, Humphries, P, RNAi-mediated reversible opening of the blood-brain barrier., The Journal of Gene Medicine, 10, (8), 2008, p930 - 947

Loscher, CJ, Hokamp, K, Wilson, JH, Li, T, Humphries, P, Farrar, GJ, Palfi, A, A common microRNA signature in mouse models of retinal degeneration., Experimental eye research, 87, (6), 2008, p529 - 534

A. Reynolds, G.J. Farrar, P. Humphries, P. Kenna, Variation in the electroretinogram of C57BL/6J sub-strains of mouse, Advances in Experimental Medical Biology, 613, 2008, p383 - 391

Campbell, M, Humphries, M, Kenna, P, Humphries, P, Brankin, B, Altered expression and interaction of adherens junction proteins in the developing OLM of the Rho(-/-) mouse., Experimental Eye Research, 85, (5), 2007, p714-720

D. Allen, P.F. Kenna, A. Palfi, H.P. McMahon, S. Millington-Ward, M. O'Reilly, P. Humphries and G.J. Farrar, Development of strategies for conditional RNA interference, Journal of Gene Medicine, 9, (4), 2007, p287 - 98

O'Reilly, M, Palfi, A, Chadderton, N, Millington-Ward, S, Ader, M, Cronin, T, Tuohy, T, Auricchio, A, Hildinger, M, Tivnan, A, McNally, N, Humphries, MM, Kiang, AS, Humphries, P, Kenna, PF, Farrar, GJ, RNA interference-mediated suppression and replacement of human rhodopsin in vivo., American Journal of Human Genetics, 81, (1), 2007, p127-135

Loscher, CJ, Hokamp, K, Kenna, PF, Ivens, AC, Humphries, P, Palfi, A, Farrar, GJ, Altered retinal microRNA expression profile in a mouse model of retinitis pigmentosa., Genome biology, 8, (11), 2007

Haverkamp S, Michalakis S, Claes E, Seeliger MW, Humphries P, Biel M and Feigenspan A., Synaptic plasticity in GNGA3-/- mice: Cone bipolar cells react up0onthe missing cone input and form ectopic synapses with rods, Journal of Neuroscience, 26, (19), 2006, p5248 - 5255

De Goover TE, Stevenson KA, Humphries P, Simpson DA, Curtis TM, Gardiner TA and Stitt AW., Rod photoreceptor loss in Rho-/- mice reduces retinal hypoxia and hypoxia-regulated gene expression, Invest Ophthalmol Vis Sci, 47, (12), 2006, p5553 - 5560

De Goover TE, Stevenson KA, Humphries P, Simpson DA, Gardiner TA and Stitt AW, Retinopathy is reduced during experimental diabetes in a mouse model of outer retinal degeneration, Invest Ophthalmol Vis Sci., 47, (12), 2006, p5561 - 5568

Aherne A, Kennan A, Kenna PE, McNally N, Farrar GJ, Humphries P, Molecular mechanisms of photoreceptor degeneration in RP caused by IMPDH1 mutations, RETINAL DEGENERATIVE DISEASES ADVANCES IN EXPERIMENTAL MEDICINE AND BIOLOGY, 572, 2006, p81 - 87

Campbell M, Humphries MM, Kennan A, Kenna PF, Humphries P and Brankin B., Aberrant Retinal Tight Junction and Adherens junction protein expression in an animal model of autosomal recessive retinitis pigmentosa: The Rho (-/-) mouse, Exp. Eye Res, 83, (3), 2006, p484 - 492

Palfi A, Kiang A-S, O'Reilly M, Millington-Ward S, Kenna P, Humphries P and Farrar GJ, RNAi-based suppression and replacement of RDS-Peripherin in retinal organotypic culture, Human Mutation, 27, (3), 2006, p260 - 268

Schmucker C, Seeliger M, Humphries P, Biel M and Schaeffel F, Grating acuity at different luminances in wild-type mice and in mice lacking rod or cone function, Invest Ophthalmol Vis Sci, 46, (1), 2005, p398 - 407

Kiang A-S, Palfi A, Ader M, Kenna PF, Millington-Ward, Clark G, Kennan A, O'Reilly M, Tam LCT, Aherne A, McNally N, Humphries P and Farrar GJ, Toward a gene therapy for dominant disease: validation of an RNA interference-based mutation-independent approach, Molecular Therapy, 12, (3), 2005, p555 - 561

Rohrer B, Lohr HR, Humphries P, Redmond MT, Seeliger MW and Crouch RK, Cone opsin mislocalization in Rpe65-/- mice: A defect that can be corrected by 11-cis retinal, Investigative Ophthalmology and Visual Science, 46, (10), 2005, p3876 - 3881

Molecular mechanisms of photoreceptor degeneration in RP caused by IMPDH1 mutations in, editor(s)Joe G. Hollyfield, Robert E. Anderson, and Matthew M. LaVail , Retinal Degenerative Diseases, New York, NY, Springer, 2005, [Aherne. A., Kennan. A., Kenna, P.F, McNally, N., Farrar, G.J, Humphries, P.]

Kennan A, Aherne and Humphries P, Light in retinitis pigmentosa, Trends in Genetics, 21, (2), 2005, p103 - 110

Millington-Ward SM, McMahon HP, Allen D, Tuohy G, Kiang A-S, Palfi A, Kenna PF, Humphries P and GJ Farrar, RNAi of COL1A1 in mesenchymal progenitor cells, European Journal of Human Genetics, 12, (10), 2004, p864 - 866

Claes E, Seeliger M, Michalakis S, Biel M, Humphries P and Haverkamp S, Morphological characterization of the retina of the CNGA3(-/-)Rho(-/-) mutant mouse lacking functional cones and rods, Investigative Ophthalmology and Visual Science., 45, (6), 2004, p2039 - 2048

Aherne A, Kennan A, Kenna PF, McNally N, Lloyd DG, Alberts IL, Kaing A-S, Humphries MM, Ayuso C, Engel PC, Gu JJ, Mitchell BS, Farrar GJ and Humphries P., On the molecular pathology of neurodegeneration in IMPDH1-based retinitis pigmentosa, HUMAN MOLECULAR GENETICS, 13, (6), 2004, p641 - 650

Barnard AR, Appleford JM, Sekaran S, Chinthapalli K, Jenkens A, Seeliger M, Biel M, Humphries P, Douglas RH, Wenzel A, Foster RG, Hankins MW and Lucas RJ, Residual photosensitivity in mice lacking both rod opsin and cone photoreceptor cyclic nucleotide gated channel 3 alpha subunit, Visual Neuroscience, 21, 2004, p675 - 683

Aherne A, Kennan A, Kenna PF, McNally N, Lloyd DG, Alberts IL, Kaing A-S, Humphries MM, Ayuso C, Engel PC, Gu JJ, Mitchell BS, Farrar GJ and Humphries P., On the molecular pathology of neurodegeneration in IMPDH1-based retinitis pigmentosa, Hum Mol Genet, 13, (6), 2004, p641 - 650

Bowne SJ, Daiger SP, Malone KA, Heckenlively JR, Kennan A, Humphries P, Hughbanks-Wheaton D, Birch DG, Liu Q, Pierce EA, Zuo J, Huang Q, Donovan DD, and Sullivan LS, Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosxa 1 (RP1) gene, Molecular Vision, 24, (9), 2003, p129 - 137

Kerman A, Aherne A, Bowne SJ, Daiger SP, Farrar GJ, Kenna PF, Humphries P, On the role of IMPDH1 in retinal degeneration, RETINAL DEGENERATIONS: MECHANISMS AND EXPERIMENTAL THERAPY ADVANCES IN EXPERIMENTAL MEDICINE AND BIOLOGY, 533, 2003, p13 - 18

Keegan D, Kenna PF, Humphries MM, Humphries P, Flitcroft DI, Coffey PJ, Lund RD and Lawrence JM, Transplantation of syngeneic schwann cells to the retina of the rhodopsin knockout (Rho-/-) mouse, Investigative Ophthalmology and Visual Science, 44, (8), 2003, p3526 - 3532

Daiger SP, Sullivan LS, Bowne SJ, Kennan A, Humphries P, Birch DG, Heckenlively JR, RP1 Consortium. Identification of the RP1 and RP10 (IMPDH1) genes causing autosomal dominant RP, Advances in Experimental Medicine and Biology , 533, 2003, p1 - 11

Kennan, A, Aherne A, Bowne SJ, Daiger SP, Farrar GJ, Kenna PF and Humphries P., On the role of IMPDH1 in retinal degeneration. Retinal Degenerations: Mechanisms and Experimental Therapy, Kluwer Academic, Plenum Publishers, 2003

Tuohy, G, Kenna P, Humphries P and Farrar GJ., Baculoviral p35 inhibition of apoptosis in 661W cone photoreceptor cells, Invest Ophthalmol Vis Sci, 43, (11), 2002, p3583 - 3589

McNally N, Kenna P, Rancourt D, Ahmed T, Stitt A, Colledge W, Llyod D, O'Neill B, Humphries MM, Humphries P and Farrar GJ, Dominant retinopathy induced in mice by targeted single base deletion at codon 307 of the rds-pheripherin gene, Hum Mol Genet, 11, (9), 2002, p1005 - 1016

McNally N, Kenna PF, Rancourt D, Ahmed T, Stitt A, Colledge WH, Lloyd DG, Palfi A, O'Neill B, Humphries MM, Humphries P, Farrar GJ, Murine model of autosomal dominant retinitis pigmentosa generated by targeted deletion at codon 307 of the rds-peripherin gene, Human Molecular Genetics , 11, (9), 2002, p1005 - 1016

Sophia Millington-Ward, Carolina Allers, Gearóid Tuohy, Paulette Conget, Danny Allen, Helena P. McMahon, Paul F. Kenna, Peter Humphries and G. Jane Farrar , Validation in mesenchymal progenitor cells of a mutation-independent ex vivo approach to gene therapy for osteogenesis imperfecta , Human Molecular Genetics, 11, (19), 2002, p2201 - 2206

Kennan A, Aherne A, Palfi A, Humphries MM, Stitt A, Simpson D, Demtroder K, Orntoft T. Ayuso C, Kenna PF, Farrar GJ and Humphries P. , Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-\- mice, Human Mol Genet, 11, (5), 2002, p547 - 558

Farrar GJ, Kenna PF, Humphries P., On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention, by Kenna, P. F. , EMBO Journal, 21, 2002

KENNAN, A, AHERNE, A, PALFI, A, HUMPHRIES, M, MCKEE, A, STITT, A, SIMPSON, DAC, DEMTRODER, K, ORNTOFT, T, AYUSO, C, KENNA, PF, FARRAR, GJ, HUMPHRIES, P, IDENTIFICATION OF AN IMPDH1 MUTATION IN AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA (RP10) REVEALED FOLLOWING COMPARATIVE MICROARRAY ANALYSIS OF TRANSCRIPTS DERIVED FROM RETINAS OF WILD-TYPE AND RHO(-/-) MICE, HUMAN MOLECULAR GENETICS, 11, 2002, p547 - 557

Farrar GJ, Kenna P and Humphries P., Molecular genetics of Retinitis Pigmentosa: mutation independent approaches to therapy, EMBO, 21, (5), 2002, p857 - 864

Millington-Ward S, Allers C, Tuohy G, Conget P, Allen D, McMahon HP, Kenna PF, Humphries P and Farrar GJ, Validation in human mesenchymal progenitor cells of a mutation-independent ex vivo approach to gene therapy for Osteogenesis Imperfecta, Hum Mol Genet, 11, (19), 2002, p2201 - 2206

Gearo"id Tuohy, Sophia Millington-Ward, Paul F. Kenna, Peter Humphries, and G. Jane Farrar, Sensitivity of Photoreceptor-Derived Cell Line (661W) to Baculoviral p35, Z-VAD.FMK, and Fas-Associated Death Domain , Investigative Ophthalmology and Visual Science, 43, 2002, p3583 - 3589

SEELIGER, MW, GRIMM, C, STAHLBERG, F, FRIEDBURG, C, JAISSLE, G, ZRENNER, E, GUO, H, REME, CE, HUMPHRIES, P, HOFMANN, F, BIEL, M, FARISS, RN, REDMOND, TM, WENZEL, A, NEW VIEWS ON RPE65 DEFICIENCY: THE ROD SYSTEM IS THE SOURCE OF VISION IN A MOUSE MODEL OF LEBER CONGENITAL AMAUROSIS, NATURE GENETICS, 29, 2001, p70 - 74

HUMPHRIES, MM, KIANG, S, MCNALLY, N, DONOVAN, MA, SIEVING, P, BUSH, RA, MACHIDA, S, COTTER, T, HOBSON, A, FARRAR, J, HUMPHRIES, P, KENNA, P, COMPARATIVE STRUCTURAL AND FUNCTIONAL ANALYSIS OF PHOTORECEPTOR NEURONS OF RHO-/- MICE REVEAL INCREASED SURVIVAL ON C57BL/6J IN COMPARISON TO 129SV GENETIC BACKGROUND, VISUAL NEUROSCIENCE, 18, 2001, p437 - 443

TUOHY, G, INHIBITION OF CASPASE ACTIVITY AND PREVENTION OF APOPTOSIS IN 661W CONE PHOTORECEPTOR CELLS., unknown, 2001, 69, ISI Web of Science, 2001, pp678 - 678

Humphries MM, Kiang S, McNally N, Donovan M, Sieving PA, Bush RA, Machida S, Cotter T, Hobson A, Farrar GJ, Humphries P and Kenna P., Comparative structural and functional analysis of photoreceptor neurones of Rho-/- mouse reveal increased survival on C57BL/6J in comparison to 129Sv genetic background, Vis Neurosci, 18, 2001, p437 - 443

OREILLY, M, IN VIVO SELECTION FROM A PHAGE DISPLAY LIBRARY OF PEPTIDES CAPABLE OF TARGETING THE RETINA., unknown, 2001, 69, ISI Web of Science, 2001, pp677

FARRAR, GJ, MUTATION-INDEPENDENT THERAPEUTIC STRATEGIES FOR OSTEOGENESIS IMPERFECTA., unknown, 2001, 69, ISI Web of Science, 2001, pp675 - 675

Seeliger M, Grimm C, Stahlberg F, Frieburg C, Jassle G, Zrenner E, Gue H, Reme C, Humphries P, Hofman F, Biel M, Fariss R, Redmond T and Wenzel A., New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis, Nature Genet, 29, (1), 2001, p70 - 74

ONEILL, BG, MUTATION-INDEPENDENT RIBOZYME-BASED THERAPIES FOR RETINITIS PIGMENTOSA., unknown, 2001, 69, ISI Web of Science, 2001, pp677 - 677

BOWNE, SJ, SULLIVAN, LS, DING, L, TRAER, E, PRESCOTT, SM, BIRCH, DG, KENNAN, A, HUMPHRIES, P, DAIGER, SP, EVALUATION OF HUMAN DIACYLGLYCEROL KINASE, DGKI, A HOMOLOG OF DROSOPHILA RDGA, IN INHERITED RETINOPATHY MAPPING TO 7Q, MOLECULAR VISION, 6, 2000, p6 - 9

HOBSON, AH, DONOVAN, M, HUMPHRIES, MM, TUOHY, G, MCNALLY, N, CARMODY, R, COTTER, T, FARRAR, GJ, KENNA, PF, HUMPHRIES, P, APOPTOTIC PHOTORECEPTOR DEATH IN THE RHODOPSIN KNOCKOUT MOUSE IN THE PRESENCE AND ABSENCE OF C-FOS, EXPERIMENTAL EYE RESEARCH, 71, 2000, p247 - 254

Browne, SJ, Sullivan LS, Ding L, Traer E, Prescott SM, Birch DG, Kennan A, Humphries P and Daiger SP, Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7q, Mol Vis, 22, (6), 2000, p6 - 9

O'Neill B, Millington-Ward S, O'Reilly M, Tuohy G, Kiang A-S, Kenna P, Humphries P and Farrar GJ., Ribozyme based therapeutic approaches for autosomal dominant Retinitis Pigmentosa, Invest Ophthalmol Vis Sci, 41, 2000, p2863 - 2869

MILLINGTON-WARD, S, ONEILL, B, KIANG, AS, HUMPHRIES, P, KENNA, PF, FARRAR, GJ, A MUTATION-INDEPENDENT THERAPEUTIC STRATEGEM FOR OSTEOGENESIS IMPERFECTA, ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 9, 2000, p537 - 542

ONEILL, B, MILLINGTON-WARD, S, OREILLY, M, TUOHY, G, KIANG, AS, KENNA, PF, HUMPHRIES, P, FARRAR, GJ, RIBOZYME-BASED THERAPEUTIC APPROACHES FOR AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA, INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 41, 2000, p2863 - 2869

BOWNE, SJ, SEARCHING FOR THE RP10 GENE: A MODEL FOR POSITIONAL CANDIDATE CLONING IN THE POST GENOME ERA., unknown, 2000, 67, ISI Web of Science, 2000, pp255 - 255

TUOHY, GP, IN VIVO ANALYSIS OF PHOTORECEPTOR DEGENERATION IN LIGHT-INDUCECD LACA MICE AND IN VITRO RIBOZYME CLEAVAGE OF KEY MRNA TARGETS INVOLVED IN APOPTOTIC MEDIATED CELL DEATH. IN VIVOLN VITRO., unknown, 1999, 65, ISI Web of Science, 1999, ppA503 - A503

TODA, K, BUSH, RA, HUMPHRIES, P, SIEVING, PA, THE ELECTRORETINOGRAM OF THE RHODOPSIN KNOCKOUT MOUSE, VISUAL NEUROSCIENCE, 16, 1999, p391 - 398

MCNALLY, N, KENNA, P, HUMPHRIES, MM, HOBSON, AH, KHAN, NW, BUSH, RA, SIEVING, PA, HUMPHRIES, P, FARRAR, GJ, STRUCTURAL AND FUNCTIONAL RESCUE OF MURINE ROD PHOTORECEPTORS BY HUMAN RHODOPSIN TRANSGENE, HUMAN MOLECULAR GENETICS, 8, 1999, p1309 - 1312

McNally N, Kenna P, Humphries MM, Hobson AH, Khan NN, Bush RA, Sieving PA, Humphries P and Farrar GJ., Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgene, Human Mol Genet, 8, 1999, p1309 - 1312

Mansergh FC, Millington-Ward S, Kennan A, Kiang A-S, Humphries MM, Farrar GJ, Humphries P and Kenna PF., Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene, Am J of Hum Genet, 64, 1999, p971 - 985

AL-JANDAL, N, FARRAR, GJ, KIANG, AS, HUMPHRIES, MM, BANNON, N, FINDLAY, JBC, HUMPHRIES, P, KENNA, PF, A NOVEL MUTATION WITHOUT THE RHODOPSIN GENE (THR-94-ILE) CAUSING AUTOSOMAL DOMINANT CONGENITAL STATIONARY NIGHT BLINDNESS, HUMAN MUTATION, 13, 1999, p75 - 81

Millington-Ward S, O'Neill B, Kiang A-S, Humphries P, Kenna PF and Farrar GJ. , A mutation-independent therapeutic stratagem for osteogenesis imperfecta, Antisense Nucleic Acids Drug Dev, 9, (6), 1999, p537 - 542

MANSERGH, FC, MILLINGTON-WARD, S, KENNAN, A, KIANG, AS, HUMPHRIES, M, FARRAR, GJ, HUMPHRIES, P, KENNA, PF, RETINITIS PIGMENTOSA AND PROGRESSIVE SENSORINEURAL HEARING LOSS CAUSED BY A C12258A MUTATION IN THE MITOCHONDRIAL MTTS2 GENE, AMERICAN JOURNAL OF HUMAN GENETICS, 64, 1999, p971 - 985

KENNAN, AM, MANSERGH, FC, FINGERT, JH, CLARK, T, AYUSO, C, KENNA, PF, HUMPHRIES, P, FARRAR, GJ, A NOVEL ASP380ALA MUTATION IN THE GLC1A/MYOCILIN GENE IN A FAMILY WITH JUVENILE ONSET PRIMARY OPEN ANGLE GLAUCOMA, JOURNAL OF MEDICAL GENETICS, 35, 1998, p957 - 960

MANSERGH, FC, TWO NOVEL MUTATIONS IN THE TIGR GENE IN PRIMARY OPEN ANGLE GLAUCOMA., unknown, 1997, 61, ISI Web of Science, 1998, ppA339 - A339

MANSERGH, FC, KENNA, PF, AYUSO, C, KIANG, AS, HUMPHRIES, P, FARRAR, GJ, NOVEL MUTATIONS IN THE TIGR GENE IN EARLY AND LATE ONSET OPEN ANGLE GLAUCOMA, HUMAN MUTATION, 11, 1998, p244 - 251

Mansergh F, Meitinger T, Rodolph G, Humphries P, Farrar GJ, Lack of evidence for genetic heterogeneity in Best vitelliform macular dystrophy, JOURNAL OF MEDICAL GENETICS , 35 (1), (JAN), 1998, p85 - 86

MILLINGTON-WARD, S, THREE STRATEGIES EXPLORED IN VITRO FOR GENE THERAPY OF DOMINANT AND POLYGENIC DISEASES., unknown, 1997, 61, ISI Web of Science, 1998, ppA357 - A357

HUMPHRIES, MM, RETINOPATHY INDUCED IN MICE BY TARGETED DISRUPTION OF THE RHODOPSIN GENE, NATURE GENETICS, 15, 1997, p216 - 219

BUSH, RA HUMPHRIES, P HUMPHRIES, MM FARRAR, GJ KENNA, P SIEVING, PA , PHOTORECEPTOR MORPHOLOGY IN RHODOPSIN KNOCKOUT MICE, INVESTIGATIVE OPHTHALMOLOGY AND VISUAL SCIENCE, 38, 1997, p3247

Humphries MM, Rancourt D, Farrar GJ, Kenna P, Hazel M, Bush RA, Sieving PA, Sheils DM, McNally N, Creighton P, Erven A, Boros A, Gulya K, Capecchi MR and Humphries P., Retinopathy induced in mice by targeted disruption of the rhodopsin gene, Nature Genetics, 15, 1997, p216 - 219

KENNA, P, MANSERGH, F, MILLINGTONWARD, S, ERVEN, A, KUMARSINGH, R, BRENNAN, R, FARRAR, GJ, HUMPHRIES, P, CLINICAL AND MOLECULAR GENETIC CHARACTERISATION OF A FAMILY SEGREGATING AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA AND SENSORINEURAL DEAFNESS, BRITISH JOURNAL OF OPHTHALMOLOGY, 81, 1997, p207 - 213

MILLINGTONWARD, S, ONEILL, B, TUOHY, G, ALJANDAL, N, KIANG, AS, KENNA, PF, PALFI, A, HAYDEN, P, MANSERGH, F, KENNAN, A, HUMPHRIES, P, FARRAR, GJ, STRATEGEMS IN VITRO FOR GENE THERAPIES DIRECTED TO DOMINANT MUTATIONS, HUMAN MOLECULAR GENETICS, 6, 1997, p1415 - 1426

TODA, K BUSH, RA HUMPHRIES, MM FARRER, GJ KENNA, P HUMPHRIES, P, SIEVING, PA, ERG OF THE RHODOPSIN KNOCKOUT MOUSE, INVESTIGATIVE OPHTHALMOLOGY AND VISUAL SCIENCE, 38, 1997, p4135

MARTIN, M, TREATMENT OF RETINOBLASTOMA ARISING IN TRANSGENIC MICE WITH A HSV-1 DELETION MUTANT VIRUS., unknown, 1996, 3, ISI Web of Science, 1997, ppP42 - P42

BUSH, RA, PHOTORECEPTOR MORPHOLOGY IN RHODOPSIN KNOCKOUT MICE, unknown, 1997, 38, ISI Web of Science, 1997, pp3247 - 3247

GARDINER, N, LAWLER, M, ORIORDAN, J, DEARCE, M, HUMPHRIES, P, MCCANN, SR, PERSISTENT DONOR CHIMAERISM IS CONSISTENT WITH DISEASE-FREE SURVIVAL FOLLOWING BMT FOR CHRONIC MYELOID LEUKAEMIA, BONE MARROW TRANSPLANTATION, 20, 1997, p235 - 241

TODA, K, ERG OF THE RHODOPSIN KNOCKOUT MOUSE., unknown, 1997, 38, ISI Web of Science, 1997, pp4135 - 4135

MANSERGH, F, HUMPHRIES, P, FARRAR, J, STILL NO EVIDENCE FOR HETEROGENEITY IN BEST'S VITELLIFORM MACULAR DYSTROPHY - REPLY, JOURNAL OF MEDICAL GENETICS, 33, 1996, 630 - 630

HUMPHRIES, MM, MANSERGH, FC, KIANG, AS, JORDAN, SA, SHEILS, DM, MARTIN, MJ, FARRAR, GJ, KENNA, PF, YOUNG, MM, HUMPHRIES, P, THREE KERATIN GENE MUTATIONS ACCOUNT FOR THE MAJORITY OF DOMINANT SIMPLEX EPIDERMOLYSIS BULLOSA CASES WITHIN THE POPULATION OF IRELAND, HUMAN MUTATION, 8, 1996, p57 - 63

MCGUIRE, RE, JORDAN, SA, BRADEN, VV, BOUFFARD, GG, HUMPHRIES, P, GREEN, ED, DAIGER, SP, MAPPING THE RP10 LOCUS FOR AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA ON 7Q: REFINED GENETIC POSITIONING AND LOCALIZATION WITHIN A WELL-DEFINED YAC CONTIG, GENOME RESEARCH, 6, 1996, p255 - 266

MOLLOY, K, GOULDEN, N, LAWLER, M, CORNISH, J, OAKHILL, A, PAMPHILON, D, POTTER, M, STEWARD, C, LANGLANDS, K, HUMPHRIES, P, MCCANN, SR, PATTERNS OF HEMATOPOIETIC CHIMERISM FOLLOWING BONE MARROW TRANSPLANTATION FOR CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA FROM VOLUNTEER UNRELATED DONORS, BLOOD, 87, 1996, p3027 - 3031

MANSERGH, FC, KENNA, PF, RUDOLPH, G, MEITINGER, T, FARRAR, GJ, KUMARSINGH, R, SCORER, J, HALLY, AM, MYNETTJOHNSON, L, HUMPHRIES, MM, KIANG, S, HUMPHRIES, P, EVIDENCE FOR GENETIC-HETEROGENEITY IN BESTS VITELLIFORM MACULAR DYSTROPHY, JOURNAL OF MEDICAL GENETICS, 32, 1995, p855 - 858

FARRAR, GJ, PROGRESS IN GENETIC-LINKAGE FOR RETINITIS-PIGMENTOSA AND GENE DELIVERY TO OCULAR-TISSUES, unknown, 1995, 36, ISI Web of Science, 1995, ppS1045 - S1045

MCCANN, S, LAWLER, M, GARDINER, N, HUMPHRIES, P, PROGNOSTIC-SIGNIFICANCE OF MIXED HEMATOPOIETIC CHIMERISM FOLLOWING ALLOGENEIC BONE-MARROW TRANSPLANTATION, CHINESE MEDICAL JOURNAL, 107, 1995, p729 - 730

KENNA, PF, AN IRISH PEDIGREE SEGREGATING RETINITIS-PIGMENTOSA AND DEAFNESS, unknown, 1995, 36, ISI Web of Science, 1995, ppS1044 - S1044

Вглядевшись, она как в тумане увидела еще одну панель с буквами алфавита от А до Z и тут же вспомнила, что нужно ввести шифр. Клубы дыма начали вытекать из треснувших оконных рам. Сьюзан в отчаянии колотила в дверную панель, но все было бесполезно.

One thought on “Tara S 2nd Assignment To Bcp

Leave a Reply

Your email address will not be published. Required fields are marked *