ADVANCED METER SECURITY SYSTEM von MCDONALD JEREMY, GOODING DAVID JEFFREY, BUBB JOHN H

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Regulatory characterisation of the schizophrenia-associated CACNA1C proximal promoter and the potential role for the transcription factor EZH2 in schizophrenia aetiology von Billingsley, Kimberley J., Manca, Maurizio, Gianfrancesco, Olympia, Collier, David A., Sharp, Helen, Bubb, Vivien J., Quinn, John P.

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A Dopamine Transporter Gene Functional Variant Associated with Cocaine Abuse in a Brazilian Sample von Guindalini, Camila, Howard, Mark, Haddley, Kate, Laranjeira, Ronaldo, Collier, David, Ammar, Nik, Craig, Ian, O'Gara, Colin, Bubb, Vivian J., Greenwood, Tiffany, Kelsoe, John, Asherson, Phil, Murray, Robin M., Castelo, Adauto, Quinn, John P., Vallada, Homero, Breen, Gerome

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Genetic interaction between two VNTRs in the MAOA gene is associated with the nicotine dependence von Kõks, Gea, Prans, Ele, Ho, Xuan D, Duy, Binh H, Tran, Ha DT, Ngo, Ngoc BT, Hoang, Linh NN, Tran, Hue MT, Bubb, Vivien J, Quinn, John P, Kõks, Sulev

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YB-1 and CTCF Differentially Regulate the 5-HTT Polymorphic Intron 2 Enhancer Which Predisposes to a Variety of Neurological Disorders von Klenova, Elena, Scott, Alison C, Roberts, Julian, Shamsuddin, Shaharum, Lovejoy, Elizabeth A, Bergmann, Stephan, Bubb, Vivien J, Royer, Hans-Dieter, Quinn, John P

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A regulatory domain spanning the repeat sequence RE1 from herpes simplex virus type 1 has cell specific differential functions in trigeminal neurons and fibroblasts von Stevens, Hannah C., Fiskerstrand, Carolyn, Bubb, Vivien J., Dalziel, Robert, Quinn, John P.

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The DNA sequence of human chromosome 7 von Hillier, LaDeana W., Fulton, Robert S., Fulton, Lucinda A., Graves, Tina A., Pepin, Kymberlie H., Wagner-McPherson, Caryn, Layman, Dan, Maas, Jason, Jaeger, Sara, Walker, Rebecca, Wylie, Kristine, Sekhon, Mandeep, Becker, Michael C., O'Laughlin, Michelle D., Schaller, Mark E., Fewell, Ginger A., Miner, Tracie L., Nash, William E., Cordes, Matt, Edwards, Jennifer, Bradshaw-Cordum, Holland, Ali, Johar, Andrews, Stephanie, Isak, Amber, VanBrunt, Andrew, Nguyen, Christine, Du, Feiyu, Lamar, Betty, Courtney, Laura, Kalicki, Joelle, Ozersky, Philip, Bielicki, Lauren, Scott, Kelsi, Holmes, Andrea, Harkins, Richard, Harris, Anthony, Strong, Cynthia Madsen, Hou, Shunfang, Tomlinson, Chad, Dauphin-Kohlberg, Sara, Kozlowicz-Reilly, Amy, Leonard, Shawn, Rohlfing, Theresa, Rock, Susan M., Tin-Wollam, Aye-Mon, Abbott, Amanda, Minx, Patrick, Maupin, Rachel, Strowmatt, Catrina, Latreille, Phil, Miller, Nancy, Johnson, Doug, Murray, Jennifer, Woessner, Jeffrey P., Wendl, Michael C., Yang, Shiaw-Pyng, Schultz, Brian R., Wallis, John W., Bieri, Tamberlyn A., Nelson, Joanne O., Berkowicz, Nicolas, Wohldmann, Patricia E., Cook, Lisa L., Hickenbotham, Matthew T., Eldred, James, Williams, Donald, Bedell, Joseph A., Mardis, Elaine R., Clifton, Sandra W., Marra, Marco A., Raymond, Christopher, Haugen, Eric, Gillett, Will, Zhou, Yang, James, Rose, Phelps, Karen, Iadanoto, Shawn, Bubb, Kerry, Simms, Elizabeth, Levy, Ruth, Clendenning, James, Kaul, Rajinder, Furey, Terrence S., Baertsch, Robert A., Brent, Michael R., Keibler, Evan, Flicek, Paul, Bork, Peer, Suyama, Mikita, Bailey, Jeffrey A., Portnoy, Matthew E., Torrents, David, Chinwalla, Asif T., Gish, Warren R., Eddy, Sean R., McPherson, John D., Eichler, Evan E., Green, Eric D., Waterston, Robert H., Wilson, Richard K.

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Abnormalities in brain biochemistry associated with lack of dystrophin: studies of the mdx mouse von Rae, Caroline, Griffin, Julian L, Blair, Duncan H, Bothwell, John H, Bubb, William A, Maitland, Annie, Head, Stewart

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