Detection of mRNA by reverse transcription-PCR as an indicator of viability in Escherichia coli cells von Sheridan, G.E.C. (Institute of Food Research, Reading, UK.), Masters, C.I, Shallcross, J.A, Mackey, B.M

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Effect of post-treatment holding conditions on detection of tufA mRNA in ethanol-treated Escherichia coli: implications for RT-PCR-based indirect viability tests von Sheridan, G.E.C, Szabo, E.A, Mackey, B.M

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Simple Detection of Germline Microsatellite Instability for Diagnosis of Constitutional Mismatch Repair Cancer Syndrome von Ingham, Danielle, Diggle, Christine P., Berry, Ian, Bristow, Claire A., Hayward, Bruce E., Rahman, Nazneen, Markham, Alexander F., Sheridan, Eamonn G., Bonthron, David T., Carr, Ian M.

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Gene symbol: VHL. Disease: von Hippel-Lindau syndrome. Accession #Hd0512 von Mavrogiannis, L A, Sheridan, E G, Burnell, L D, Taylor, G R

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Endocervical carcinoma and precursor lesions: c-myc expression and the demonstration of field changes von Polacarz, S V, Darne, J, Sheridan, E G, Ginsberg, R, Sharp, F

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GeneScreen: a program for high-throughput mutation detection in DNA sequence electropherograms von Carr, Ian M, Camm, Nick, Taylor, Graham R, Charlton, Ruth, Ellard, Sian, Sheridan, Eamonn G, Markham, Alexander F, Bonthron, David T

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Rapid and overnight microdilution antibiotic susceptibility testing with the Sensititre Breakpoint Autoreader system von NOLTE, F. S, KRISHER, K. K, BELTRAN, L. A, CHRISTIANSON, N. P, SHERIDAN, G. E

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Genetic diversity within commercial populations of watercress (Rorippa nasturtium-aquaticum), and between allied Brassicaceae inferred from RAPD-PCR von SHERIDAN, G. E. C, CLAXTON, J. R, CLARKSON, J. M, BLAKESLEY, D

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Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease von Elpidorou, M, Poulter, JA, Szymanska, K, Baron, W, Junger, K, Boldt, K, Ueffing, M, Green, L, Livingston, JH, Sheridan, EG, Johnson, CA

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Detection of mRNA by Reverse Transcription-PCR as an Indicator of Viability in Escherichia coliCells von G. E. C. Sheridan, C. I. Masters, J. A. Shallcross, B. M. Mackey

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Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality Defects von Bonnefoy, S, Watson, CM, Kernohan, KD, Lemos, M, Hutchinson, S, Poulter, JA, Crinnion, LA, Berry, I, Simmonds, J, Vasudevan, P, O'Callaghan, C, Hirst, RA, Rutman, A, Huang, L, Hartley, T, Grynspan, D, Moya, E, Li, C, Carr, IM, Bonthron, DT, Leroux, M, Consortium, CC, Boycott, KM, Bastin, P, Sheridan, EG

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De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome von Mirzaa, GM, Parry, DA, Fry, AE, Giamanco, KA, Schwartzentruber, J, Vanstone, M, Logan, CV, Roberts, N, Johnson, CA, Singh, S, Kholmanskikh, SS, Adams, C, Hodge, RD, Hevner, RF, Bonthron, DT, Braun, KPJ, Faivre, L, Rivière, J-B, St-Onge, J, Gripp, KW, Mancini, GMS, Pang, K, Sweeney, E, Van Esch, H, Verbeek, N, Wieczorek, D, Steinraths, M, Majewski, J, FORGE Canada Consortium, Boycott, KM, Pilz, DT, Ross, ME, Dobyns, WB, Sheridan, EG

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Obesity is associated with impaired immune response to influenza vaccination in humans von Sheridan, P A, Paich, H A, Handy, J, Karlsson, E A, Hudgens, M G, Sammon, A B, Holland, L A, Weir, S, Noah, T L, Beck, M A

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Cell-Type-Specific Interleukin 1 Receptor 1 Signaling in the Brain Regulates Distinct Neuroimmune Activities von Liu, Xiaoyu, Nemeth, Daniel P., McKim, Daniel B., Zhu, Ling, DiSabato, Damon J., Berdysz, Olimpia, Gorantla, Gowthami, Oliver, Braedan, Witcher, Kristina G., Wang, Yufen, Negray, Christina E., Vegesna, Rekha S., Sheridan, John F., Godbout, Jonathan P., Robson, Matthew J., Blakely, Randy D., Popovich, Phillip G., Bilbo, Staci D., Quan, Ning

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Epidemiology of Escherichia coli bacteraemia in England: Results of an enhanced sentinel surveillance programme von Abernethy, Julia, Guy, Rebecca, Sheridan, Elizabeth A, Hopkins, Susan, Kiernan, Martin, Wilcox, Mark H, Johnson, Alan P, Hope, Russell

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Rivaroxaban for Stroke Prevention after Embolic Stroke of Undetermined Source von Hart, Robert G, Sharma, Mukul, Mundl, Hardi, Kasner, Scott E, Bangdiwala, Shrikant I, Berkowitz, Scott D, Swaminathan, Balakumar, Lavados, Pablo, Wang, Yongjun, Wang, Yilong, Davalos, Antonio, Shamalov, Nikolay, Mikulik, Robert, Cunha, Luis, Lindgren, Arne, Arauz, Antonio, Lang, Wilfried, Czlonkowska, Anna, Eckstein, Jens, Gagliardi, Rubens J, Amarenco, Pierre, Ameriso, Sebastian F, Tatlisumak, Turgut, Veltkamp, Roland, Hankey, Graeme J, Toni, Danilo, Bereczki, Daniel, Uchiyama, Shinichiro, Ntaios, George, Yoon, Byung-Woo, Brouns, Raf, Endres, Matthias, Muir, Keith W, Bornstein, Natan, Ozturk, Serefnur, O’Donnell, Martin J, De Vries Basson, Matthys M, Pare, Guillaume, Pater, Calin, Kirsch, Bodo, Sheridan, Patrick, Peters, Gary, Weitz, Jeffrey I, Peacock, W. Frank, Shoamanesh, Ashkan, Benavente, Oscar R, Joyner, Campbell, Themeles, Ellison, Connolly, Stuart J

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Translational Research on Trichoderma: From 'Omics to the Field von Lorito, Matteo, Woo, Sheridan L, Harman, Gary E, Monte, Enrique

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Social stress up-regulates inflammatory gene expression in the leukocyte transcriptome via β-adrenergic induction of myelopoiesis von Powell, Nicole D., Sloan, Erica K., Bailey, Michael T., Arevalo, Jesusa M. G., Miller, Gregory E., Chen, Edith, Kobor, Michael S., Reader, Brenda F., Sheridan, John F., Cole, Steven W.

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Chronic COVID-19 infection in an immunosuppressed patient shows changes in lineage over time: a case report von Baker, Sheridan J C, Nfonsam, Landry E, Leto, Daniela, Rutherford, Candy, Smieja, Marek, McArthur, Andrew G

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Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte von Parry, David A., Logan, Clare V., Hayward, Bruce E., Shires, Michael, Landolsi, Hanène, Diggle, Christine, Carr, Ian, Rittore, Cécile, Touitou, Isabelle, Philibert, Laurent, Fisher, Rosemary A., Fallahian, Masoumeh, Huntriss, John D., Picton, Helen M., Malik, Saghira, Taylor, Graham R., Johnson, Colin A., Bonthron, David T., Sheridan, Eamonn G.

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