Multiple uses for BIST test latches von FERGUSON STEVEN ROSS, WHITE MICHAEL BRIAN, KOCH GARRETT STEPHEN, TAKAHASHI OSAMU

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Multiple uses for BIST test latches von FERGUSON STEVEN ROSS, WHITE MICHAEL BRIAN, KOCH GARRETT STEPHEN, TAKAHASHI OSAMU

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MULTIPLE USES FOR BIST TEST LATCHES von FERGUSON STEVEN ROSS, WHITE MICHAEL BRIAN, KOCH GARRETT STEPHEN, TAKAHASHI OSAMU

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Method and apparatus for real time two dimensional redundancy allocation von KOCH, GARRETT STEPHEN, HEDBERG, ERIK LEIGH

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Enhanced built-in self-test circuit and method von WISTORT, REID ALLEN, KOCH, GARRETT STEPHEN, OUELLETTE, MICHAEL RICHARD

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Memory array built-in self-test circuit having a programmable pattern generator for allowing unique read/write operations to adjacent memory cells, and method therefor von TERNULLO, JR., LUIGI, CONNOR, JOHN, KOCH, GARRETT STEPHEN, ADAMS, ROBERT DEAN

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Rapid compare of two binary numbers von TERNULLO, JR., LUIGI, CONNOR, JOHN, KOCH, GARRETT STEPHEN, ADAMS, ROBERT DEAN

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APPARATUS AND METHOD FOR REAL TIME DATA ERROR CAPTURE AND COMPRESSION FOR REDUNDANCY ANALYSIS OF A MEMORY von KOCH, GARRETT STEPHEN, GOMEZ, RICHARD SANTIAGO, WOYKE, JUSTIN ALDEN, BULA, OREST

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PRECISION TIMING CIRCUIT von KOCH, GARRETT STEPHEN, GOMEZ, RICHARD SANTIAGO, WOYKE, JUSTIN ALDEN, BULA, OREST

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Using one memory to supply addresses to an associated memory during testing von SOUSA, JOSE RORIZ, KOCH, GARRETT STEPHEN, COVINO, JAMES J, ADAMS, ROBERT DEAN, CONNOR, JOHN, ROBERTS, ALAN LEE, FLAKER, ROY CHILDS, TERNULLO JR., LUIGI

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Präzisionszeitschaltung von GOMEZ, RICHARD SANTIAGO, FOREST GROVE, OR 97116, US, WOYKE, JUSTIN ALDEN, ESSEX JUNCTION, VT 05452, US, BULA, OREST, SHELBURNE, VT 05482, US, KOCH, GARRETT STEPHEN, JEFFERSONVILLE, VT 05464, US

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Rare and de novo coding variants in chromodomain genes in Chiari I malformation von Sadler, Brooke, Wilborn, Jackson, Antunes, Lilian, Kuensting, Timothy, Hale, Andrew T., Gannon, Stephen R., McCall, Kevin, Cruchaga, Carlos, Harms, Matthew, Voisin, Norine, Reymond, Alexandre, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Tartaglia, Marco, Niceta, Marcello, Leoni, Chiara, Zampino, Giuseppe, Ashley-Koch, Allison, Urbizu, Aintzane, Garrett, Melanie E., Soldano, Karen, Macaya, Alfons, Conrad, Donald, Strahle, Jennifer, Dobbs, Matthew B., Turner, Tychele N., Shannon, Chevis N., Brockmeyer, Douglas, Limbrick, David D., Gurnett, Christina A., Haller, Gabe

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Genetic modifiers of the severity of sickle cell anemia identified through a genome‐wide association study von Sebastiani, Paola, Solovieff, Nadia, Hartley, Stephen W., Milton, Jacqueline N., Riva, Alberto, Dworkis, Daniel A., Melista, Efthymia, Klings, Elizabeth S., Garrett, Melanie E., Telen, Marilyn J., Ashley‐Koch, Allison, Baldwin, Clinton T., Steinberg, Martin H.

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A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome von Aung, Tin, Ozaki, Mineo, Li, Zheng, Uebe, Steffen, Harder, Jeffrey M, Chan, Anita S Y, Lee, Mei Chin, Burdon, Kathryn P, Pakravan, Mohammad, Wang, Ya Xing, Williams, Susan, Huang, Lulin, Foo, Jia Nee, Kumar, Rajesh S, Ueno, Morio, Manabe, Shin-ichi, Hayashi, Ken, Ideta, Ryuichi, Mori, Yosai, Miyata, Kazunori, Sugiyama, Kazuhisa, Higashide, Tomomi, Chihara, Etsuo, Inoue, Kenji, Yoshida, Akitoshi, Yanagi, Masahide, Aihara, Makoto, Ohashi, Tsutomu, Sakurai, Toshiya, Sugimoto, Takako, Chuman, Hideki, Yamashiro, Kenji, Gotoh, Norimoto, Osman, Essam A, Al-Obeidan, Saleh A, Al-Jasim, Leyla, Shahwan, Sami Al, Leo, Paul, Yetkin, Yaz, Oğuz, Çilingir, Kanavi, Mozhgan Rezaei, Yazdani, Shahin, Akopov, Evgeny L, Howell, Gareth R, Goh, Yufen, Meah, Wee Yang, Peh, Su Qin, Lukasik, Urszula, Krumbiegel, Mandy, Vithana, Eranga N, Wong, Tien Yin, Liu, Yutao, Challa, Pratap, Hewitt, Alex W, Mitchell, Paul, Ziskind, Ari, Venkatesh, Rangaraj, Vijayan, Saravanan, Zhao, Peiquan, Guadarrama-Vallejo, Dalia, Perera, Shamira A, Husain, Rahat, Ho, Su-Ling, Welge-Luessen, Ulrich-Christoph, Schloetzer-Schrehardt, Ursula, Herms, Stefan, Nöthen, Markus M, Weisschuh, Nicole, Ghosh, Arkasubhra, Teo, Yik Ying, Brown, Matthew A, Lischinsky, Ignacio, Crowston, Jonathan G, Sang, Jinghong, Zhang, Nihong, You, Qisheng, Founti, Panayiota, Lambropoulos, Alexandros, Anastasopoulos, Eleftherios, Rhee, Douglas J, May-Bolchakova, Inna, Heegaard, Steffen, Alward, Wallace L M, Jonas, Jost B, Xu, Liang, Chowbay, Balram, Schaeffeler, Elke, Lerner, Fabian, Yang, Zhenglin, Frezzotti, Paolo, Kinoshita, Shigeru, Inatani, Masaru, Tashiro, Kei, Reis, André, Edward, Deepak P, Pasquale, Louis R, Wiggs, Janey L, Yoshimura, Nagahisa, Ritch, Robert, Khor, Chiea-Chuen

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The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects von Rizzi, Thais S., Arias-Vasquez, Alejandro, Rommelse, Nanda, Kuntsi, Jonna, Anney, Richard, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Ruano, Dina, Van der Sluis, Sophie, Markunas, Christina A., Garrett, Melanie E., Ashley-Koch, Allison E., Kollins, Scott H., Anastopoulos, Arthur D., Hansell, Narelle K., Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G., Harris, Sarah E., Davies, Gail, Tenesa, Albert, Porteous, David J., Starr, John M., Deary, Ian J., St. Pourcain, Beate, Smith, George Davey, Timpson, Nicholas J., Evans, David M., Gill, Michael, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund, Steinhausen, Hans Christoph, Taylor, Eric, Faraone, Stephen V., Franke, Barbara, Posthuma, Danielle

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Demographic characteristics and epigenetic biological aging among post-9/11 veterans: Associations of DunedinPACE with sex, race, and age von Bourassa, Kyle J., Halverson, Tate F., Garrett, Melanie E., Hair, Lauren, Dennis, Michelle, Ashley-Koch, Allison E., Beckham, Jean C., Kimbrel, Nathan A.

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Epigenome‐wide association of PTSD from heterogeneous cohorts with a common multi‐site analysis pipeline von Ratanatharathorn, Andrew, Boks, Marco P., Maihofer, Adam X., Aiello, Allison E., Amstadter, Ananda B., Ashley‐Koch, Allison E., Baker, Dewleen G., Beckham, Jean C., Bromet, Evelyn, Dennis, Michelle, Garrett, Melanie E., Geuze, Elbert, Guffanti, Guia, Hauser, Michael A., Kilaru, Varun, Kimbrel, Nathan A., Koenen, Karestan C., Kuan, Pei‐Fen, Logue, Mark W., Luft, Benjamin J., Miller, Mark W., Mitchell, Colter, Nugent, Nicole R., Ressler, Kerry J., Rutten, Bart P. F., Stein, Murray B., Vermetten, Eric, Vinkers, Christiaan H., Youssef, Nagy A., Uddin, Monica, Nievergelt, Caroline M., Smith, Alicia K.

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A Multicenter Randomized Trial of Atorvastatin Therapy in Intensive Care Patients with Severe Sepsis von KRUGER, Peter, BAILEY, Michael, MCNEIL, John, NICHOL, Alistair, ROBERTS, Michael S, SYRES, Gillian, VENKATESH, Bala, BELLOMO, Rinaldo, COOPER, David James, HARWARD, Meg, HIGGINS, Alisa, HOWE, Belinda, JONES, Darryl, JOYCE, Chris, KOSTNER, Karam

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Genome-wide association study identifies four pan-ancestry loci for suicidal ideation in the Million Veteran Program von Ashley-Koch, Allison E, Kimbrel, Nathan A, Qin, Xue J, Lindquist, Jennifer H, Garrett, Melanie E, Dennis, Michelle F, Hair, Lauren P, Huffman, Jennifer E, Jacobson, Daniel A, Madduri, Ravi K, Coon, Hilary, Docherty, Anna R, Kang, Jooeun, Mullins, Niamh, Ruderfer, Douglas M, Harvey, Philip D, McMahon, Benjamin H, Oslin, David W, Hauser, Elizabeth R, Hauser, Michael A, Beckham, Jean C

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Sex and Menopause Modify the Effect of Single Nucleotide Polymorphism Genotypes on Fibrosis in NAFLD von Wegermann, Kara, Garrett, Melanie E., Zheng, Jiayin, Coviello, Andrea, Moylan, Cynthia A., Abdelmalek, Manal F., Chow, Shein‐Chung, Guy, Cynthia D., Diehl, Anna Mae, Ashley‐Koch, Allison, Suzuki, Ayako

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