Fiber stabilization of optical path differences (OPD) over a wide bandwidth frequency range for extended periods of time von Portillo, Angel A, Cates, Michael C, Knowlton, Paul V

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Fiber stabilization of optical path differences (OPD) over a wide bandwidth frequency range for extended periods of time von PORTILLO ANGEL A, CATES MICHAEL C, KNOWLTON PAUL V

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FIBER STABILIZATION OF OPTICAL PATH DIFFERENCES (OPD) OVER WIDE BANDWIDTH FREQUENCY RANGE FOR EXTENDED PERIODS OF TIME von MICHAEL C CATES, ANGEL A PORTILLO, PAUL V KNOWLTON

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Fiber Stabilization of Optical Path Differences (OPD) Over a Wide Bandwidth Frequency Range for Extended Periods of Time von PORTILLO ANGEL A, CATES MICHAEL C, KNOWLTON PAUL V

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Fiber stabilization of optical path differences (OPD) over a wide bandwidth frequency range for extended periods of time von KNOWLTON, PAUL V, PORTILLO, ANGEL A, CATES, MICHAEL C

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Fiber Stabilization Of Optical Path Differences (opd) Over A Wide Bandwidth Frequency Range For Extended Periods Of Time von PAUL V. KNOWLTON, MICHAEL C. CATES, ANGEL A. PORTILLO

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Multiomics in the central Arctic Ocean for benchmarking biodiversity change von Mock, Thomas, Boulton, William, Balmonte, John-Paul, Barry, Kevin, Bertilsson, Stefan, Bowman, Jeff, Buck, Moritz, Bratbak, Gunnar, Chamberlain, Emelia J, Cunliffe, Michael, Creamean, Jessie, Ebenhöh, Oliver, Eggers, Sarah Lena, Fong, Allison A, Gardner, Jessie, Gradinger, Rolf, Granskog, Mats A, Havermans, Charlotte, Hill, Thomas, Hoppe, Clara J. M, Korte, Kerstin, Larsen, Aud, Müller, Oliver, Nicolaus, Anja, Oldenburg, Ellen, Popa, Ovidiu, Rogge, Swantje, Schäfer, Hendrik, Shoemaker, Katyanne, Snoeijs-Leijonmalm, Pauline, Torstensson, Anders, Valentin, Klaus, Vader, Anna, Barry, Kerrie, Chen, I.-M. A, Clum, Alicia, Copeland, Alex, Daum, Chris, Eloe-Fadrosh, Emiley, Foster, Brian, Foster, Bryce, Grigoriev, Igor V, Huntemann, Marcel, Ivanova, Natalia, Kuo, Alan, Kyrpides, Nikos C, Mukherjee, Supratim, Palaniappan, Krishnaveni, Reddy, T. B. K, Salamov, Asaf, Roux, Simon, Varghese, Neha, Woyke, Tanja, Wu, Dongying, Leggett, Richard M, Moulton, Vincent, Metfies, Katja

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Mouse Genome Informatics: an integrated knowledgebase system for the laboratory mouse von Baldarelli, Richard M, Smith, Cynthia L, Ringwald, Martin, Richardson, Joel E, Bult, Carol J

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Ultra-rare genetic variation in common epilepsies: a case-control sequencing study von Allen, Andrew S, Bellows, Susannah T, Berkovic, Samuel F, Bridgers, Joshua, Burgess, Rosemary, Cavalleri, Gianpiero, Chung, Seo-Kyung, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Heinzen, Erin L, Hildebrand, Michael S, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mayeux, Richard, Mebane, Caroline, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slavgé, Pickrell, William O, Poduri, Annapurna, Radtke, Rodney A, Rees, Mark I, Regan, Brigid M, Ren, Zhong, Scheffer, Ingrid E, Sills, Graeme J, Thomas, Rhys H, Wang, Quanli, Abou-Khalil, Bassel, Alldredge, Brian K, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Bautista, Jocelyn F., Bluvstein, Judith, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Geller, Eric B, Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R, Hayward, Jean, Helmers, Sandra L, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Sadleir, Lynette G, Shellhaas, Renée A., Sherr, Elliott H, Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

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A Neutralizing Monoclonal Antibody for Hospitalized Patients with Covid-19 von Lundgren, Jens D, Grund, Birgit, Barkauskas, Christina E, Holland, Thomas L, Gottlieb, Robert L, Sandkovsky, Uriel, Brown, Samuel M, Knowlton, Kirk U, Self, Wesley H, Files, D Clark, Jain, Mamta K, Benfield, Thomas, Bowdish, Michael E, Leshnower, Bradley G, Baker, Jason V, Jensen, Jens-Ulrik, Gardner, Edward M, Ginde, Adit A, Harris, Estelle S, Johansen, Isik S, Markowitz, Norman, Matthay, Michael A, Østergaard, Lars, Chang, Christina C, Davey, Victoria J, Goodman, Anna, Higgs, Elizabeth S, Murray, Daniel D, Murray, Thomas A, Paredes, Roger, Parmar, Mahesh K B, Phillips, Andrew N, Reilly, Cavan, Sharma, Shweta, Dewar, Robin L, Teitelbaum, Marc, Wentworth, Deborah, Cao, Huyen, Klekotka, Paul, Babiker, Abdel G, Gelijns, Annetine C, Kan, Virginia L, Polizzotto, Mark N, Thompson, B Taylor, Lane, H Clifford, Neaton, James D

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Positive Relationships between Association Strength and Phenotypic Similarity Characterize the Assembly of Mixed-Species Bird Flocks Worldwide von Sridhar, Hari, Srinivasan, Umesh, Askins, Robert A., Canales-Delgadillo, Julio Cesar, Chen, Chao-Chieh, Ewert, David N., Gale, George A., Goodale, Eben, Gram, Wendy K., Hart, Patrick J., Hobson, Keith A., Hutto, Richard L., Kotagama, Sarath W., Knowlton, Jessie L., Lee, Tien Ming, Munn, Charles A., Nimnuan, Somchai, Nizam, B. Z., Péron, Guillaume, Robin, V. V., Rodewald, Amanda D., Rodewald, Paul G., Thomson, Robert L., Trivedi, Pranav, Van Wilgenburg, Steven L., Shanker, Kartik

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A map of human genome variation from population-scale sequencing von Abecasis, Gonçalo R, Altshuler, David, Auton, Adam, Brooks, Lisa D, Durbin, Richard M, Gibbs, Richard A, Hurles, Matt E, McVean, Gil A

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Demographic history and rare allele sharing among human populations von Gravel, Simon, Henn, Brenna M, Gutenkunst, Ryan N, Indap, Amit R, Marth, Gabor T, Clark, Andrew G, Yu, Fuli, Gibbs, Richard A, Bustamante, Carlos D

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Variation in genome-wide mutation rates within and between human families von CONRAD, Donald F, KEEBLER, Jonathan E. M, ZILVERSMIT, Martine, CARTWRIGHT, Reed, ROULEAU, Guy A, DALY, Mark, STONE, Eric A, HURLES, Matthew E, AWADALLA, Philip, DEPRISTO, Mark A, LINDSAY, Sarah J, YUJUN ZHANG, CASALS, Ferran, IDAGHDOUR, Youssef, HARTL, Chris L, TORROJA, Carlos, GARIMELLA, Kiran V

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Mapping copy number variation by population-scale genome sequencing von Mills, Ryan E., Walter, Klaudia, Stewart, Chip, Handsaker, Robert E., Chen, Ken, Alkan, Can, Abyzov, Alexej, Yoon, Seungtai Chris, Ye, Kai, Cheetham, R. Keira, Chinwalla, Asif, Conrad, Donald F., Fu, Yutao, Grubert, Fabian, Hajirasouliha, Iman, Hormozdiari, Fereydoun, Iakoucheva, Lilia M., Iqbal, Zamin, Kang, Shuli, Kidd, Jeffrey M., Konkel, Miriam K., Korn, Joshua, Khurana, Ekta, Kural, Deniz, Lam, Hugo Y. K., Leng, Jing, Li, Ruiqiang, Li, Yingrui, Lin, Chang-Yun, Luo, Ruibang, Mu, Xinmeng Jasmine, Nemesh, James, Peckham, Heather E., Rausch, Tobias, Scally, Aylwyn, Shi, Xinghua, Stromberg, Michael P., Stütz, Adrian M., Urban, Alexander Eckehart, Walker, Jerilyn A., Wu, Jiantao, Zhang, Yujun, Zhang, Zhengdong D., Batzer, Mark A., Ding, Li, Marth, Gabor T., McVean, Gil, Sebat, Jonathan, Snyder, Michael, Wang, Jun, Ye, Kenny, Eichler, Evan E., Gerstein, Mark B., Hurles, Matthew E., Lee, Charles, McCarroll, Steven A., Korbel, Jan O.

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Specimen collection: An essential tool von Rocha, L. A., Aleixo, A., Allen, G., Barclay, M. V. L., Bates, J. M., Bauer, A. M., Benzoni, F., Berns, C. M., Blackburn, D. C., Blum, S., Bowie, R. C. K., Britz, R., Brown, R. M., Cadena, C. D., Carpenter, K., Ceríaco, L. M., Chakrabarty, P., Chaves, G., Choat, J. H., Clements, K. D., Collette, B. B., Coyne, J., Cracraft, J., Daniel, T., de Carvalho, M. R., de Queiroz, K., Drewes, R., Dumbacher, J. P., Engilis, A., Eschmeyer, W., Feldman, C. R., Fisher, B. L., Fritsch, P. W., Getahun, A., Gill, A., Gomon, M., Graves, G. R., Guralnick, R., Hartel, K., Helgen, K. M., Ho, H., Iskandar, D. T., Iwamoto, T., Jaafar, Z., James, H. F., Johnson, D., Knowlton, N., Lacey, E., Larson, H. K., Last, P., Leis, J. M., Liebherr, J., Lowman, M., Mahler, D. L., Mamonekene, V., Matsuura, K., Mays, H., McCosker, J., McGuire, J., Miller, M. J., Mooi, R., Mooi, R. D., Moritz, C., Myers, P., Nachman, M. W., Nussbaum, R. A., Foighil, D. Ó, Parenti, L. R., Parham, J. F., Pérez-Emán, J., Pérez-Matus, A., Poe, S., Randall, J. E., Reimer, J. D., Robertson, D. R., Rodrigues, M. T., Rüber, L., Ryan, M. J., Shinohara, G., Short, A., Simison, W. B., Smith-Vaniz, W. F., Springer, V. G., Stiassny, M., Tello, J. G., Thompson, C. W., Trnski, T., Tucker, P., Vecchione, M., Verheyen, E., Wainwright, P. C., Wheeler, T. A., White, W. T., Will, K., Williams, J. T., Williams, G., Wilson, E. O., Winker, K., Winterbottom, R., Witt, C. C.

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The 1000 Genomes Project: data management and community access von Clarke, Laura, Zheng-Bradley, Xiangqun, Smith, Richard, Kulesha, Eugene, Xiao, Chunlin, Toneva, Iliana, Vaughan, Brendan, Preuss, Don, Leinonen, Rasko, Shumway, Martin, Sherry, Stephen, Flicek, Paul

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Diversity of Human Copy Number Variation and Multicopy Genes von Sudmant, Peter H., Kitzman, Jacob O., Antonacci, Francesca, Alkan, Can, Malig, Maika, Tsalenko, Anya, Sampas, Nick, Bruhn, Laurakay, Shendure, Jay, Eichler, Evan E.

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The role of copy number variants in the genetic architecture of common familial epilepsies von Almanza Fuerte, Edith P., Nguyen, John, Mehaffey, Michelle, Sulovari, Arvis, Wang, Tianyun, Galey, Miranda, Miller, Danny E., Eichler, Evan E., Mefford, Heather C., Abou‐Khalil, Bassel, Afawi, Zaid Afawi, Allen, Andrew S., Amrom, Dina, Andermann, Eva, Bautista, Jocelyn F., Bellows, Susannah T., Berkovic, Samuel F., Bluvstein, Judith, Boro, Alexis, Burgess, Rosemary, Cascino, Gregory D., Chung, Seo‐Kyung, Consalvo, Damian, Cossette, Patrick, Crompton, Douglas E., Crumrine, Patricia, Curtis, Sarah W., Delanty, Norman, Devinsky, Orrin, Dlugos, Dennis, Ellis, Colin A., Epstein, Michael P., Fiol, Miguel, Fountain, Nathan B., Freyer, Catharine, Friedman, Dan, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gravel, Micheline, Haas, Kevin, Harris, Rebekah V., Haut, Sheryl, Heinzen, Erin L., Helmers, Sandra, Henry, Olivia J., Joshi, Sucheta, Kirsch, Heidi E., Kivity, Sara, Knowlton, Robert C., Kossoff, Eric, Kuzniecky, Ruben, Loeb, Rebecca, Lowenstein, Daniel H., Marson, Anthony G., McCormack, Mark, McGuire, Shannon M., McKenna, Kevin, Motika, Paul V., Mullen, Saul A., Novotny, Edward J., O’Brien, Terence J., Oliver, Karen L., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack M., Park, Kristen L., Paterson, Sarah J., Petrovski, Slave, Pickrell, William O., Poduri, Annapurna, Rees, Mark I., Sadleir, Lynette G., Scheffer, Ingrid E., Shellhaas, Renee A., Sherr, Elliott H., Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K., Sirven, Joseph, Smith, Michael C., Smith, Philip E. M., Sperling, Michael R., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Vining, Eileen P. G., Von Allmen, Gretchen K., Weisenberg, Judith, Widdess‐Walsh, Peter, Winawer, Melodie R.

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Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study von Stanley, Kate E., Bobbili, Dheeraj R., Dhindsa, Ryan S., May, Patrick, Alldredge, Brian K., Allen, Andrew S., Altmüller, Janine, Amrom, Dina, Andermann, Eva, Auce, Pauls, Avbersek, Andreja, Bautista, Jocelyn F., Becker, Felicitas, Bellows, Susannah T., Berghuis, Bianca, Bluvstein, Judith, Boro, Alex, Burgess, Rosemary, Caglayan, Hande, Cascino, Gregory D., Chung, Seo‐Kyung, Cieuta‐Walti, Cécile, Consalvo, Damian, Cossette, Patrick, Crumrine, Patricia, Delanty, Norman, Depondt, Chantal, Desbiens, Richard, Dlugos, Dennis, Epstein, Michael P., Everett, Kate, Fountain, Nathan B., Francis, Ben, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Girard, Simon, Glauser, Tracy, Glynn, Simon, Gravel, Micheline, Haas, Kevin, Haut, Sheryl R., Heinzen, Erin L., Helbig, Ingo, Hildebrand, Michael S., Jorgensen, Andrea, Joshi, Sucheta, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Kossoff, Eric H., Krause, Roland, Kunz, Wolfram S., Langley, Sarah R., LeGuern, Eric, Lerche, Holger, Leu, Costin, Lortie, Anne, Marson, Anthony G., Mebane, Caroline, Mefford, Heather C., Meloche, Caroline, Motika, Paul V., Muhle, Hiltrud, Nabbout, Rima, Nguyen, Dang K., Nikanorova, Marina, Novotny, Edward J., Ottman, Ruth, O’Brien, Terence J., Paolicchi, Juliann M., Parent, Jack M., Peter, Sarah, Petrou, Steven, Pickrell, William O., Poduri, Annapurna, Radtke, Rodney A., Rees, Mark I., Regan, Brigid M., Sadleir, Lynette G., Sander, Josemir W., Sander, Thomas, Scheffer, Ingrid E., Singh, Rani K., Sirven, Joseph, Sisodiya, Sanjay M., Smith, Michael C., Sonsma, Anja C. M., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Von Allmen, Gretchen K., Wang, Quanli, Weber, Yvonne G., Weckhuysen, Sarah, Widdess‐Walsh, Peter, Winawer, Melodie R., Wolking, Stefan, Zimprich, Fritz

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