Long-range chromosomal interactions regulate the timing of the transition between poised and active gene expression von Vernimmen, Douglas, Gobbi, Marco De, Sloane-Stanley, Jacqueline A, Wood, William G, Higgs, Douglas R

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Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease von Higgs, Douglas R, Tufarelli, Cristina, Stanley, Jackie A Sloane, Garrick, David, Sharpe, Jackie A, Ayyub, Helena, Wood, William G

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Regulatory SNP Causes a Human Genetic Disease by Creating a New Transcriptional Promoter von De Gobbi, Marco, Viprakasit, Vip, Hughes, Jim R, Fisher, Chris, Buckle, Veronica J, Ayyub, Helena, Gibbons, Richard J, Vernimmen, Douglas, Yoshinaga, Yuko, de Jong, Pieter, Cheng, Jan-Fang, Rubin, Edward M, Wood, William G, Bowden, Don, Higgs, Douglas R

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Coregulated human globin genes are frequently in spatial proximity when active von Brown, Jill M, Leach, Joanne, Reittie, Joyce E, Atzberger, Ann, Lee-Prudhoe, Jane, Wood, William G, Higgs, Douglas R, Iborra, Francisco J, Buckle, Veronica J

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Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues von Garrick, David, Sharpe, Jackie A, Arkell, Ruth, Dobbie, Lorraine, Smith, Andrew J H, Wood, William G, Higgs, Douglas R, Gibbons, Richard J

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Genetic dissection of the α-globin super-enhancer in vivo von Hay, Deborah, Hughes, Jim R, Babbs, Christian, Davies, James O J, Graham, Bryony J, Hanssen, Lars L P, Kassouf, Mira T, Oudelaar, A Marieke, Sharpe, Jacqueline A, Suciu, Maria C, Telenius, Jelena, Williams, Ruth, Rode, Christina, Li, Pik-Shan, Pennacchio, Len A, Sloane-Stanley, Jacqueline A, Ayyub, Helena, Butler, Sue, Sauka-Spengler, Tatjana, Gibbons, Richard J, Smith, Andrew J H, Wood, William G, Higgs, Douglas R

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Advances in the understanding of the congenital dyserythropoietic anaemias von Wickramasinghe, Sunitha N., Wood, William G.

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Posterior Glenohumeral Joint Dislocation: A Rare Complication of Central Venous Cannulation in a Patient Undergoing Coronary Artery Surgery von Wood, William G., MD, MS, Guy, T. Sloane, MD, MBA, Arora, Karishma, MD, Firoozabadi, Reza, MD, Kim, Hubert, MD, Kukreja, Jasleen, MD, MPH, Pagel, Paul S., MD, PhD, Brzezinski, Marek, MD, PhD

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Long-range regulation of α globin gene expression during erythropoiesis von Higgs, Douglas R, Wood, William G

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Chromosome looping at the human α-globin locus is mediated via the major upstream regulatory element (HS −40) von Vernimmen, Douglas, Marques-Kranc, Fatima, Sharpe, Jacqueline A., Sloane-Stanley, Jacqueline A., Wood, William G., Wallace, Helen A.C., Smith, Andrew J.H., Higgs, Douglas R.

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Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1α localization in erythroblasts von Renella, Raffaele, Roberts, Nigel A., Brown, Jill M., De Gobbi, Marco, Bird, Louise E., Hassanali, Tasneem, Sharpe, Jacqueline A., Sloane-Stanley, Jacqueline, Ferguson, David J.P., Cordell, Jacqueline, Buckle, Veronica J., Higgs, Douglas R., Wood, William G.

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Tissue-specific histone modification and transcription factor binding in α globin gene expression von De Gobbi, Marco, Anguita, Eduardo, Hughes, Jim, Sloane-Stanley, Jacqueline A., Sharpe, Jacqueline A., Koch, Christoph M., Dunham, Ian, Gibbons, Richard J., Wood, William G., Higgs, Douglas R.

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Nprl3 is required for normal development of the cardiovascular system von Kowalczyk, Monika S, Hughes, Jim R, Babbs, Christian, Sanchez-Pulido, Luis, Szumska, Dorota, Sharpe, Jacqueline A, Sloane-Stanley, Jacqueline A, Morriss-Kay, Gillian M, Smoot, Leslie B, Roberts, Amy E, Watkins, Hugh, Bhattacharya, Shoumo, Gibbons, Richard J, Ponting, Chris P, Wood, William G, Higgs, Douglas R

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A human PKD1 transgene generates functional polycystin-1 in mice and is associated with a cystic phenotype von PRITCHARD, Lynn, SLOANE-STANLEY, Jackie A, JING ZHOU, WOOD, William G, HARRIS, Peter C, SHARPE, Jackie A, ASPINWALL, Richard, WEINING LU, BUCKLE, Veronica, STRMECKI, Lana, WALKER, Denise, WARD, Christopher J, ALPERS, Charles E

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A novel molecular basis for β thalassemia intermedia poses new questions about its pathophysiology von Premawardhena, Anuja, Fisher, Christopher A., Olivieri, Nancy F., de Silva, Shanthimala, Sloane-Stanley, Jackie, Wood, William G., Weatherall, David J.

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A novel deletion causing α thalassemia clarifies the importance of the major human alpha globin regulatory element von Viprakasit, Vip, Harteveld, Cornelis L., Ayyub, Helena, Stanley, Jackie S., Giordano, Piero C., Wood, William G., Higgs, Douglas R.

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Severe intrauterine anemia: a new form of ɛγγδβ thalassemia presenting in utero in a Norwegian family von Brantberg, Anne, Eik-Nes, Sturla H., Roberts, Nigel, Fisher, Chris, Wood, William G.

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Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I von Ahmed, Momin R., Chehal, Aref, Zahed, Laila, Taher, Ali, Haidar, Joud, Shamseddine, Ali, O'Hea, Anne-Marie, Bienz, Nicola, Dgany, Orly, Avidan, Nili, Beckmann, Jacqui S., Tamary, Hannah, Higgs, Douglas, Vyas, Paresh, Wood, William G., Wickramasinghe, Sunitha N.

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Asymptomatic Carotid Atherosclerosis Is Associated With Circulating Chlamydia pneumoniae DNA in Younger Normotensive Subjects in a General Population Survey von Mitusch, Rolf, Luedemann, Jan, Wood, William G, Berger, Klaus, Schminke, Ulf, Suter, Matthias, Kessler, Christof, John, Ulrich, Rupp, Jan, Kentsch, Michael, Maass, Matthias

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Skeletal analysis of the Fgfr3P244R mouse, a genetic model for the Muenke craniosynostosis syndrome von Twigg, Stephen R. F., Healy, Chris, Babbs, Christian, Sharpe, Jacqueline A., Wood, William G., Sharpe, Paul T., Morriss‐Kay, Gillian M., Wilkie, Andrew O. M.

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