A null mutation in the Bacillus subtilis aconitase gene causes a block in Spo0A-phosphate-dependent gene expression by Craig, J E, Ford, M J, Blaydon, D C, Sonenshein, A L

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The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UK by Blaydon, DC, Mueller, RF, Hutchin, TP, Leroy, BP, Bhattacharya, SS, Bird, AC, Malcolm, S, Bitner-Glindzicz, M

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RHBDF2 Mutations Are Associated with Tylosis, a Familial Esophageal Cancer Syndrome by Blaydon, Diana C., Etheridge, Sarah L., Risk, Janet M., Hennies, Hans-Christian, Gay, Laura J., Carroll, Rebecca, Plagnol, Vincent, McRonald, Fiona E., Stevens, Howard P., Spurr, Nigel K., Bishop, D. Timothy, Ellis, Anthony, Jankowski, Janusz, Field, John K., Leigh, Irene M., South, Andrew P., Kelsell, David P.

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A null mutation in the Bacillus subtilis aconitase gene causes a block in SpoOA-phosphate-dependent gene expression by Craig, JE, d, MJ, Blaydon, D C, Sonenshein, AL

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Mutations in AQP5, Encoding a Water-Channel Protein, Cause Autosomal-Dominant Diffuse Nonepidermolytic Palmoplantar Keratoderma by Blaydon, Diana C., Lind, Lisbet K., Plagnol, Vincent, Linton, Kenneth J., Smith, Francis J.D., Wilson, Neil J., McLean, W.H. Irwin, Munro, Colin S., South, Andrew P., Leigh, Irene M., O’Toole, Edel A., Lundström, Anita, Kelsell, David P.

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Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event by TEH, Muy-Teck, BLAYDON, Diana, KELSELL, David P, CHAPLIN, Tracy, FOOT, Nicola J, SKOULAKIS, Spyros, RAGHAVAN, Manoj, HARWOOD, Catherine A, PROBY, Charlotte M, PHILPOTT, Michael P, YOUNG, Bryan D

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A Phenome-Wide Association Study (PheWAS) of Late Onset Alzheimer Disease Genetic Risk in Children of European Ancestry at Middle Childhood: Results from the ABCD Study by Gorelik, Aaron J., Paul, Sarah E., Karcher, Nicole R., Johnson, Emma C., Nagella, Isha, Blaydon, Lauren, Modi, Hailey, Hansen, Isabella S., Colbert, Sarah M. C., Baranger, David A. A., Norton, Sara A., Spears, Isaiah, Gordon, Brian, Zhang, Wei, Hill, Patrick L., Oltmanns, Thomas F., Bijsterbosch, Janine D., Agrawal, Arpana, Hatoum, Alexander S., Bogdan, Ryan

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Combination 5-Fluorouracil and Microneedling Therapy for Wound Modification: A Histological Murine Study by Watson, Alison H., O’Mary, Hannah L., Cui, Zhengrong, Baer, Susan C., Somogyi, Marie B., Homer, Natalie, Blaydon, Sean M., Huggins, Jonathan, Shore, John W., Durairaj, Vikram D., Nakra, Tanuj

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Primary, Nonsyndromic Vesicoureteric Reflux and Its Nephropathy Is Genetically Heterogeneous, with a Locus on Chromosome 1 by Feather, Sally A., Malcolm, Sue, Woolf, Adrian S., Wright, Victoria, Blaydon, Diana, Reid, Christopher J.D., Flinter, Frances A., Proesmans, Willem, Devriendt, Koen, Carter, Joan, Warwicker, Paul, Goodship, Timothy H.J., Goodship, Judith A.

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