A PIP5 Kinase Essential for Efficient Chemotactic Signaling von Fets, Louise, Nichols, John M.E., Kay, Robert R.

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Chemotaxis of a model organism: progress with Dictyostelium von Nichols, John ME, Veltman, Douwe, Kay, Robert R

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The Atypical MAP Kinase ErkB Transmits Distinct Chemotactic Signals through a Core Signaling Module von Nichols, John M.E., Paschke, Peggy, Peak-Chew, Sew, Williams, Thomas D., Tweedy, Luke, Skehel, Mark, Stephens, Elaine, Chubb, Jonathan R., Kay, Robert R.

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The fate of cells undergoing spontaneous DNA damage during development von Miermont, Agnes, Antolović, Vlatka, Lenn, Tchern, Nichols, John M E, Millward, Lindsey J, Chubb, Jonathan R

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Cell and molecular transitions during efficient dedifferentiation von Nichols, John M. E., Antolovic, Vlatka, Reich, Jacob D., Brameyer, Sophie, Paschke, Peggy, Chubb, Jonathan R.

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Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia von Meyer, Esther, Carss, Keren J, Rankin, Julia, Nichols, John M E, Grozeva, Detelina, Joseph, Agnel P, Mencacci, Niccolo E, Papandreou, Apostolos, Ng, Joanne, Barral, Serena, Ngoh, Adeline, Ben-Pazi, Hilla, Willemsen, Michel A, Arkadir, David, Barnicoat, Angela, Bergman, Hagai, Bhate, Sanjay, Boys, Amber, Darin, Niklas, Foulds, Nicola, Gutowski, Nicholas, Hills, Alison, Houlden, Henry, Hurst, Jane A, Israel, Zvi, Kaminska, Margaret, Limousin, Patricia, Lumsden, Daniel, McKee, Shane, Misra, Shibalik, Mohammed, Shekeeb S, Nakou, Vasiliki, Nicolai, Joost, Nilsson, Magnus, Pall, Hardev, Peall, Kathryn J, Peters, Gregory B, Prabhakar, Prab, Reuter, Miriam S, Rump, Patrick, Segel, Reeval, Sinnema, Margje, Smith, Martin, Turnpenny, Peter, White, Susan M, Wieczorek, Dagmar, Wiethoff, Sarah, Wilson, Brian T, Winter, Gidon, Wragg, Christopher, Pope, Simon, Heales, Simon J H, Morrogh, Deborah, Pittman, Alan, Carr, Lucinda J, Perez-Dueñas, Belen, Lin, Jean-Pierre, Reis, Andre, Gahl, William A, Toro, Camilo, Bhatia, Kailash P, Wood, Nicholas W, Kamsteeg, Erik-Jan, Chong, Wui K, Gissen, Paul, Topf, Maya, Dale, Russell C, Chubb, Jonathan R, Raymond, F Lucy, Kurian, Manju A

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Hysteroscopic Essure Inserts for Permanent Contraception: Extended Follow-Up Results of a Phase III Multicenter International Study von Chudnoff, Scott G., MD, MS, Nichols, John E., MD, Levie, Mark, MD

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Erratum: Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia von Meyer, Esther, Carss, Keren J, Rankin, Julia, Nichols, John M E, Grozeva, Detelina, Joseph, Agnel P, Mencacci, Niccolo E, Papandreou, Apostolos, Ng, Joanne, Barral, Serena, Ngoh, Adeline, Ben-Pazi, Hilla, Willemsen, Michel A, Arkadir, David, Barnicoat, Angela, Bergman, Hagai, Bhate, Sanjay, Boys, Amber, Darin, Niklas, Foulds, Nicola, Gutowski, Nicholas, Hills, Alison, Houlden, Henry, Hurst, Jane A, Israel, Zvi, Kaminska, Margaret, Limousin, Patricia, Lumsden, Daniel, McKee, Shane, Misra, Shibalik, Mohammed, Shekeeb S, Nakou, Vasiliki, Nicolai, Joost, Nilsson, Magnus, Pall, Hardev, Peall, Kathryn J, Peters, Gregory B, Prabhakar, Prab, Reuter, Miriam S, Rump, Patrick, Segel, Reeval, Sinnema, Margje, Smith, Martin, Turnpenny, Peter, White, Susan M, Wieczorek, Dagmar, Wiethoff, Sarah, Wilson, Brian T, Winter, Gidon, Wragg, Christopher, Pope, Simon, Heales, Simon J H, Morrogh, Deborah, Pittman, Alan, Carr, Lucinda J, Perez-Dueñas, Belen, Lin, Jean-Pierre, Reis, Andre, Gahl, William A, Toro, Camilo, Bhatia, Kailash P, Wood, Nicholas W, Kamsteeg, Erik-Jan, Chong, Wui K, Gissen, Paul, Topf, Maya, Dale, Russell C, Chubb, Jonathan R, Raymond, F Lucy, Kurian, Manju A

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Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia von Meyer, Esther, Carss, Keren J, Rankin, Julia, Nichols, John M E, Grozeva, Detelina, Joseph, Agnel P, Mencacci, Niccolo E, Papandreou, Apostolos, Ng, Joanne, Barral, Serena, Ngoh, Adeline, Ben-Pazi, Hilla, Willemsen, Michel A, Arkadir, David, Barnicoat, Angela, Bergman, Hagai, Bhate, Sanjay, Boys, Amber, Darin, Niklas, Foulds, Nicola, Gutowski, Nicholas, Hills, Alison, Houlden, Henry, Hurst, Jane A, Israel, Zvi, Kaminska, Margaret, Limousin, Patricia, Lumsden, Daniel, McKee, Shane, Misra, Shibalik, Mohammed, Shekeeb S, Nakou, Vasiliki, Nicolai, Joost, Nilsson, Magnus, Pall, Hardev, Peall, Kathryn J, Peters, Gregory B, Prabhakar, Prab, Reuter, Miriam S, Rump, Patrick, Segel, Reeval, Sinnema, Margje, Smith, Martin, Turnpenny, Peter, White, Susan M, Wieczorek, Dagmar, Wiethoff, Sarah, Wilson, Brian T, Winter, Gidon, Wragg, Christopher, Pope, Simon, Heales, Simon J H, Morrogh, Deborah, Pittman, Alan, Carr, Lucinda J, Perez-Dueñas, Belen, Lin, Jean-Pierre, Reis, Andre, Gahl, William A, Toro, Camilo, Bhatia, Kailash P, Wood, Nicholas W, Kamsteeg, Erik-Jan, Chong, Wui K, Gissen, Paul, Topf, Maya, Dale, Russell C, Chubb, Jonathan R, Raymond, F Lucy, Kurian, Manju A

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Correction: Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia von Meyer, Esther, Carss, Keren J, Rankin, Julia, Nichols, John M E, Grozeva, Detelina, Joseph, Agnel P, Mencacci, Niccolo E, Papandreou, Apostolos, Ng, Joanne, Barral, Serena, Ngoh, Adeline, Ben-Pazi, Hilla, Willemsen, Michel A, Arkadir, David, Barnicoat, Angela, Bergman, Hagai, Bhate, Sanjay, Boys, Amber, Darin, Niklas, Foulds, Nicola, Gutowski, Nicholas, Hills, Alison, Houlden, Henry, Hurst, Jane A, Israel, Zvi, Kaminska, Margaret, Limousin, Patricia, Lumsden, Daniel, McKee, Shane, Misra, Shibalik, Mohammed, Shekeeb S, Nakou, Vasiliki, Nicolai, Joost, Nilsson, Magnus, Pall, Hardev, Peall, Kathryn J, Peters, Gregory B, Prabhakar, Prab, Reuter, Miriam S, Rump, Patrick, Segel, Reeval, Sinnema, Margje, Smith, Martin, Turnpenny, Peter, White, Susan M, Wieczorek, Dagmar, Wiethoff, Sarah, Wilson, Brian T, Winter, Gidon, Wragg, Christopher, Pope, Simon, Heales, Simon J H, Morrogh, Deborah, Pittman, Alan, Carr, Lucinda J, Perez-Dueñas, Belen, Lin, Jean-Pierre, Reis, Andre, Gahl, William A, Toro, Camilo, Bhatia, Kailash P, Wood, Nicholas W, Kamsteeg, Erik-Jan, Chong, Wui K, Gissen, Paul, Topf, Maya, Dale, Russell C, Chubb, Jonathan R, Raymond, F Lucy, Kurian, Manju A

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Cell and molecular transitions during efficient dedifferentiation von Nichols, John M. E, Antolovic, Vlatka, Reich, Jacob D, Brameyer, Sophie, Paschke, Peggy, Chubb, Jonathan R

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Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA–DTI working group von Jahanshad, Neda, Kochunov, Peter V., Sprooten, Emma, Mandl, René C., Nichols, Thomas E., Almasy, Laura, Blangero, John, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Martin, Nicholas G., McMahon, Katie L., Medland, Sarah E., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Hulshoff Pol, Hilleke E., Bastin, Mark E., McIntosh, Andrew M., Deary, Ian J., Thompson, Paul M., Glahn, David C.

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Crystal Structure of an LSD-Bound Human Serotonin Receptor von Wacker, Daniel, Wang, Sheng, McCorvy, John D., Betz, Robin M., Venkatakrishnan, A.J., Levit, Anat, Lansu, Katherine, Schools, Zachary L., Che, Tao, Nichols, David E., Shoichet, Brian K., Dror, Ron O., Roth, Bryan L.

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Janus kinase inhibition lessens inflammation and ameliorates disease in murine models of hemophagocytic lymphohistiocytosis von Das, Rupali, Guan, Peng, Sprague, Leslee, Verbist, Katherine, Tedrick, Paige, An, Qi Angel, Cheng, Cheng, Kurachi, Makoto, Levine, Ross, Wherry, E. John, Canna, Scott W., Behrens, Edward M., Nichols, Kim E.

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Functional Adult Outcomes 16 Years After Childhood Diagnosis of Attention-Deficit/Hyperactivity Disorder: MTA Results von Hechtman, Lily, Dr, Swanson, James M., Dr, Sibley, Margaret H., Dr, Stehli, Annamarie, Ms, Owens, Elizabeth B., Dr, Mitchell, John T., Dr, Arnold, L. Eugene, Dr, Molina, Brooke S.G., Dr, Hinshaw, Stephen P., Dr, Jensen, Peter S., Dr, Abikoff, Howard, Dr, Algorta, Guillermo Perez, Dr, Howard, Andrea L., Dr, Hoza, Betsy, Dr, Etcovitch, Joy, Mss, Houssais, Sylviane, MA, Lakes, Kimberly D., Dr, Nichols, J. Quyen, Mr

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The genomic landscape of pediatric myelodysplastic syndromes von Schwartz, Jason R., Ma, Jing, Lamprecht, Tamara, Walsh, Michael, Wang, Shuoguo, Bryant, Victoria, Song, Guangchun, Wu, Gang, Easton, John, Kesserwan, Chimene, Nichols, Kim E., Mullighan, Charles G., Ribeiro, Raul C., Klco, Jeffery M.

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A long-term study of AAV gene therapy in dogs with hemophilia A identifies clonal expansions of transduced liver cells von Nguyen, Giang N., Everett, John K., Kafle, Samita, Roche, Aoife M., Raymond, Hayley E., Leiby, Jacob, Wood, Christian, Assenmacher, Charles-Antoine, Merricks, Elizabeth P., Long, C. Tyler, Kazazian, Haig H., Nichols, Timothy C., Bushman, Frederic D., Sabatino, Denise E.

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How Is Physician Work Valued? von Jacobs, Jeffrey P., MD, Lahey, Stephen J., MD, Nichols, Francis C., MD, Levett, James M., MD, Johnston, George Gilbert, MD, Freeman, Richard K., MD, MBA, St. Louis, James D., MD, Painter, Julie, MBA, CCVTC, Yohe, Courtney, MPP, Wright, Cameron D., MD, Kanter, Kirk R., MD, Mayer, John E., MD, Naunheim, Keith S., MD, Rich, Jeffrey B., MD, Bavaria, Joseph E., MD

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Clinical Effectiveness of Elexacaftor/Tezacaftor/Ivacaftor in People with Cystic Fibrosis: A Clinical Trial von Nichols, David P, Paynter, Alex C, Heltshe, Sonya L, Donaldson, Scott H, Frederick, Carla A, Freedman, Steven D, Gelfond, Daniel, Hoffman, Lucas R, Kelly, Andrea, Narkewicz, Michael R, Pittman, Jessica E, Ratjen, Felix, Rosenfeld, Margaret, Sagel, Scott D, Schwarzenberg, Sarah Jane, Singh, Pradeep K, Solomon, George M, Stalvey, Michael S, Clancy, John P, Kirby, Shannon, Van Dalfsen, Jill M, Kloster, Margaret H, Rowe, Steven M

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Chemical Characterization of Exopolysaccharides from Antarctic Marine Bacteria von Nichols, Carol Mancuso, Lardière, Sandrine Garon, Bowman, John P., Nichols, Peter D., Gibson, John A. E., Guézennec, Jean

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