ENGINE SHAFT INTEGRATED MOTOR von DUCE, JEFFREY LYNN, KARNOFSKI, KENT E, OEHLER, STEPHEN D

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Engine shaft integrated motor von Duce, Jeffrey Lynn, Karnofski, Kent E, Oehler, Stephen D

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Fluid flow control device von Calkins, Frederick T, Duce, Jeffrey L, Oehler, Stephen D

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Deforming shape memory alloy using self-regulating thermal elements von Calkins, Frederick T, Duce, Jeffrey L, Oehler, Stephen D

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ENGINE SHAFT INTEGRATED MOTOR von Duce, Jeffrey Lynn, Karnofski, Kent E, Oehler, Stephen D

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POWER GENERATION DEVICE AND CORRESPONDING AIRCRAFT von OEHLER, Stephen D, KARNOFSKI, Kent E, DUCE, Jeffrey Lynn

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ENGINE SHAFT INTEGRATED MOTOR von DUCE, JEFFREY LYNN, KARNOFSKI, KENT E, OEHLER, STEPHEN D

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FLUID FLOW CONTROL DEVICE von Calkins, Frederick T, Duce, Jeffrey L, Oehler, Stephen D

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DEFORMING SHAPE MEMORY ALLOY USING SELF-REGULATING THERMAL ELEMENTS von Calkins, Frederick T, Duce, Jeffrey L, Oehler, Stephen D

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SANDWICH COMPOSITE WITH SHAPE MEMORY ALLOY CORE AND METHOD OF MAKING SAME von OEHLER STEPHEN D, CALKINS FREDERICK T

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ENGINE SHAFT INTEGRATED MOTOR von OEHLER STEPHEN D, KARNOFSKI KENT E, DUCE JEFFREY LYNN

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Electrophysiologic Substrate and Risk of Mortality in Incident Hemodialysis von Tereshchenko, Larisa G, Kim, Esther D, Oehler, Andrew, Meoni, Lucy A, Ghafoori, Elyar, Rami, Tejal, Maly, Maggie, Kabir, Muammar, Hawkins, Lauren, Tomaselli, Gordon F, Lima, Joao A, Jaar, Bernard G, Sozio, Stephen M, Estrella, Michelle, Kao, W H Linda, Parekh, Rulan S

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Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutation von Watts, Joel C., Giles, Kurt, Serban, Ana, Patel, Smita, Oehler, Abby, Bhardwaj, Sumita, Guan, Shenheng, Greicius, Michael D., Miller, Bruce L., DeArmond, Stephen J., Geschwind, Michael D., Prusiner, Stanley B.

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Refined cut-off for TP53 immunohistochemistry improves prediction of TP53 mutation status in ovarian mucinous tumors: implications for outcome analyses von Cheasley, Dane, da Cunha Torres, Michelle, Salazar, Carolina, Xing, Zhongyue, Mes-Masson, Anne-Marie, Provencher, Diane M., Rahimi, Kurosh, Fasching, Peter A., Goodman, Marc T., Deen, Suha, Sieh, Weiva, Mateoiu, Constantina, Cook, Linda S., Le, Nhu D., Anglesio, Michael S., Chenevix-Trench, G., Traficante, N., Harrap, K., Sadkowsky, T., Mellon, A., Jones, M., Green, L., Ranieri, B., White, J., Bowes, L., Galletta, L., Giles, D., Hendley, J., Alsop, K., Young, C., Viduka, S., Glavinas, Lydia, Rutovitz, J., Glasgow, A., Bonaventura, T., Begbie, S., Baron-Hay, S., Nevell, D., Valmadre, S., Marsden, D., Beale, P., Beith, J., Carter, J., Dalrymple, C., Brand, A., Byth, K., Jaworski, R., Papadimos, D., Crandon, A., Cummings, M., Horwood, K., Perrin, L., Wyld, D., Davy, M., Oehler, M.K., Hall, C., Henderson, D., Miller, J., Blomfield, P., Rome, R., Grant, P., Laurie, R., Robbie, M., Manolitsas, T., McNealage, J., Susil, B., Sumithran, E., Phillips, K., Rischin, D., Fox, S., Loughrey, M., Billson, V., Neesham, D., Quinn, M., Blum, R., Leung, Y., Buck, M., Purdie, D., Ramus, Susan J., Scott, Clare L., Köbel, Martin, Gorringe, Kylie L., Allan, Prue E., Böhm, Maret, Christie, Michael, DeFazio, Anna, Fairweather, Nicole, Hadley, Alison M., Hendley, Joy, Ho, Gwo-Yaw, Huntsman, David G., Jobling, Tom W., Kennedy, Catherine J., Le Page, Cecile, Pyman, Jan, Rahimi, Kurosh, Samimi, Goli, Sharma, Ragwha, Antill, Yoland C., Gorringe, Kylie L.

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Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer von Shen, Hui, Fridley, Brooke L., Song, Honglin, Lawrenson, Kate, Cicek, Mine S., Tyrer, Jonathan, Zheng, Wei, Yang, Hannah P., Wozniak, Eva L., Ling Woo, Yin, Winterhoff, Boris, Wentzensen, Nicolas, Palmieri Weber, Rachel, Vitonis, Allison F., Vincent, Daniel, Vierkant, Robert A., Vergote, Ignace, Van Den Berg, David, Van Altena, Anne M., Thompson, Pamela J., Tessier, Daniel C., Terry, Kathryn L., Templeman, Claire, Siddiqui, Nadeem, Shu, Xiao-Ou, Severi, Gianluca, Schwaab, Ira, Salvesen, Helga B., Anne Rossing, Mary, Risch, Harvey A., Renner, Stefan P., Poole, Elizabeth M., Pike, Malcolm C., Phelan, Catherine M., Pelttari, Liisa M., Pejovic, Tanja, Ness, Roberta B., Moysich, Kirsten B., Monteiro, Alvaro N.A., Menon, Usha, Matsuo, Keitaro, Mat Adenan, Noor Azmi, Massuger, Leon F.A.G, Lurie, Galina, Lundvall, Lene, Lubiński, Jan, Lissowska, Jolanta, Levine, Douglas A., Lambrechts, Diether, Kupryjanczyk, Jolanta, Kiemeney, Lambertus A., Karlan, Beth Y., Karevan, Rod, Kalli, Kimberly R., Ji, Bu-Tian, Jakubowska, Anna, Iversen, Edwin, Høgdall, Claus K., Hoatlin, Maureen, Hillemanns, Peter, Halle, Mari K., Hall, Per, Gronwald, Jacek, Gore, Martin, Giles, Graham G., Gentry-Maharaj, Aleksandra, Fasching, Peter A., Ekici, Arif B., Edwards, Robert, Eccles, Diana, Easton, Douglas F., Doherty, Jennifer A., Despierre, Evelyn, Dansonka-Mieszkowska, Agnieszka, Cybulski, Cezary, Cramer, Daniel W., Cook, Linda S., Chen, Xiaoqing, Charbonneau, Bridget, Campbell, Ian, Butzow, Ralf, Bunker, Clareann H., Brueggmann, Doerthe, Brown, Robert, Brooks-Wilson, Angela, Brinton, Louise A., Bogdanova, Natalia, Block, Matthew S., Benjamin, Elizabeth, Beesley, Jonathan, Beckmann, Matthias W., Bandera, Elisa V., Baglietto, Laura, Armasu, Sebastian M., Liang, Dong, Lu, Karen, Hildebrandt, Michelle A.T., Sellers, Thomas A., Laird, Peter W., Leigh Pearce, Celeste

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White matter involvement in sporadic Creutzfeldt-Jakob disease von CAVERZASI, Eduardo, MANDELLI, Maria Luisa, GESCHWIND, Michael D, HENRY, Roland G, DEARMOND, Stephen J, HESS, Christopher P, VITALI, Paolo, PAPINUTTO, Nico, OEHLER, Abby, MILLER, Bruce L, LOBACH, Irina V, BASTIANELLO, Stefano

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Health Innovation Networks to Help Developing Countries Address Neglected Diseases von Morel, Carlos M, Acharya, Tara, Broun, Denis, Dangi, Ajit, Elias, Christopher, Ganguly, N. K, Gardner, Charles A, Gupta, R. K, Haycock, Jane, Heher, Anthony D, Hotez, Peter J, Kettler, Hannah E, Keusch, Gerald T, Krattiger, Anatole F, Kreutz, Fernando T, Lall, Sanjaya, Lee, Keun, Mahoney, Richard, Martinez-Palomo, Adolfo, Mashelkar, R. A, Matlin, Stephen A, Mzimba, Mandi, Oehler, Joachim, Ridley, Robert G, Senanayake, Pramilla, Singer, Peter, Yun, Mikyung

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New Irreversible α‐l‐Iduronidase Inhibitors and Activity‐Based Probes von Artola, Marta, Kuo, Chi‐Lin, McMahon, Stephen A., Oehler, Verena, Hansen, Thomas, van der Lienden, Martijn, He, Xu, van den Elst, Hans, Florea, Bogdan I., Kermode, Allison R., van der Marel, Gijsbert A., Gloster, Tracey M., Codée, Jeroen D. C., Overkleeft, Herman S., Aerts, Johannes M. F. G.

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Prognostic implications of the IDH1 synonymous SNP rs11554137 in pediatric and adult AML: a report from the Children's Oncology Group and SWOG von Ho, Phoenix A., Kopecky, Kenneth J., Alonzo, Todd A., Gerbing, Robert B., Miller, Kristen L., Kuhn, Julia, Zeng, Rong, Ries, Rhonda E., Raimondi, Susana C., Hirsch, Betsy A., Oehler, Vivian, Hurwitz, Craig A., Franklin, Janet L., Gamis, Alan S., Petersdorf, Stephen H., Anderson, Jeanne E., Godwin, John E., Reaman, Gregory H., Willman, Cheryl L., Bernstein, Irwin D., Radich, Jerald P., Appelbaum, Frederick R., Stirewalt, Derek L., Meshinchi, Soheil

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Modulation of C reutzfeldt‐ J akob disease prion propagation by the A 224 V mutation von Watts, Joel C., Giles, Kurt, Serban, Ana, Patel, Smita, Oehler, Abby, Bhardwaj, Sumita, Guan, Shenheng, Greicius, Michael D., Miller, Bruce L., DeArmond, Stephen J., Geschwind, Michael D., Prusiner, Stanley B.

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