Loss of Neutrophil Homing to the Periodontal Tissues Modulates the Composition and Disease Potential of the Oral Microbiota von Hashim, A., Alsam, A., Payne, M. A., Aduse-Opoku, J., Curtis, M. A., Joseph, S.

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Horizontal and Vertical Transfer of Oral Microbial Dysbiosis and Periodontal Disease von Payne, M.A., Hashim, A., Alsam, A., Joseph, S., Aduse-Opoku, J., Wade, W.G., Curtis, M.A.

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Mutations in the Retinal Guanylate Cyclase (RETGC-1) Gene in Dominant Cone-Rod Dystrophy von Kelsell, Rosemary E., Gregory-Evans, Kevin, Payne, Annette M., Perrault, Isabelle, Kaplan, Josseline, Yang, Ruey-Bing, Garbers, David L., Bird, Alan C., Moore, Anthony T., Hunt, David M.

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Halothane genotype, pre-slaughter handling and stunning method all influence pork quality von Channon, H.A, Payne, A.M, Warner, R.D

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis von Daiger, Stephen P, Sohocki, Melanie M, Bowne, Sara J, Sullivan, Lori S, Blackshaw, Seth, Cepko, Constance L, Payne, Annette M, Bhattacharya, Shomi S, Khaliq, Shagufta, Qasim Mehdi, S, Birch, David G, Harrison, Wilbur R, Elder, Frederick F.B, Heckenlively, John R

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Coccidia-induced mucogenesis promotes the onset of necrotic enteritis by supporting Clostridium perfringens growth von Collier, C.T., Hofacre, C.L., Payne, A.M., Anderson, D.B., Kaiser, P., Mackie, R.I., Gaskins, H.R.

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A Mutation in Guanylate Cyclase Activator 1A (GUCA1A) in an Autosomal Dominant Cone Dystrophy Pedigree Mapping to a New Locus on Chromosome 6p21.1 von Payne, Annette M., Downes, Susan M., Bessant, David A.R., Taylor, Rachel, Holder, Graham E., Warren, Martin J., Bird, Alan C., Bhattacharya, Shomi S.

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Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies von Payne, Annette M, Morris, Alex G, Downes, Susan M, Johnson, Samantha, Bird, Alan C, Moore, Anthony T, Bhattacharya, Shomi S, Hunt, David M

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Comparison of CO2 stunning with manual electrical stunning (50 Hz) of pigs on carcass and meat quality von CHANNON, H. A, PAYNE, A. M, WARNER, R. D

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The use of an e-learning constructivist solution in workplace learning von Payne, A.M., Stephenson, J.E., Morris, W.B., Tempest, H.G., Mileham, A., Griffin, D.K.

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A Novel Locus for Leber Congenital Amaurosis (LCA4) with Anterior Keratoconus Mapping to Chromosome 17p13 von Hameed, Abdul, Khaliq, Shagufta, Ismail, Muhammed, Anwar, Khalid, Ebenezer, Neil D, Jordan, Tim, Mehdi, S. Qasim, Payne, Annette M, Bhattacharya, Shomi S

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Ligand-Specific Opening of a Gated-Porin Channel in the Outer Membrane of Living Bacteria von Jiang, Xunqing, Payne, Marvin A., Cao, Zhenghua, Foster, Samuel B., Feix, Jimmy B., Salete M. C. Newton, Klebba, Phillip E.

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Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12) von Cremers, Frans P.M, den Hollander, Anneke I, ten Brink, Jacoline B, de Kok, Yvette J.M, van Soest, Simone, van den Born, L. Ingeborgh, van Driel, Marc A, van de Pol, Dorien J.R, Payne, Annette M, Bhattacharya, Shomi S, Kellner, Ulrich, Hoyng, Carel B, Westerveld, Andries, Brunner, Han G, Bleeker-Wagemakers, Elisabeth M, Deutman, August F, Heckenlively, John R, Bergen, Arthur A.B

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Spectroscopic diagnostics of chemical processes: applications of tunable optical parametric oscillators von Baxter, G.W., Payne, M.A., Austin, B.D.W., Halloway, C.A., Haub, J.G., He, Y., Milce, A.P., Nibler, J.F., Orr, B.J.

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Neurogenesis of excitation-contraction uncoupling in aging skeletal muscle von Payne, Anthony Michael, Delbono, Osvaldo

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Founder Effect, Seen in the British Population, of the 172 Peripherin/RDS Mutation—and Further Refinement of Genetic Positioning of the Peripherin/RDS Gene von Payne, Annette M., Downes, Susan M., Bessant, David A.R., Bird, Alan C., Bhattacharya, Shomi S.

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A Locus for Autosomal Recessive Congenital Microphthalmia Maps to Chromosome 14q32 von Bessant, David A.R., Khaliq, Shagufta, Hameed, Abdul, Anwar, Khalid, Mehdi, S. Qasim, Payne, Annette M., Bhattacharya, Shomi S.

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Halifax, Nova Scotia one of Canada's Atlantic gateways / [by A.M. Payne] von Payne, A. M. 1839-1922

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Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies von Payne, Annette M, Downes, Susan M, Bessant, David A R, Plant, Catherine, Moore, Tony, Bird, Alan C, Bhattacharya, Shomi S

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Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32 von Bessant, David A R, Anwar, Khalid, Khaliq, Shagufta, Hameed, Abdul, Ismail, M, Payne, Annette M, Mehdi, S Qasim, Bhattacharya, Shomi S

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