Description of Larval Instars To Fill a Gap in Forensic Entomology: The Larvae of Paralucilia pseudolyrcea (Diptera: Calliphoridae) by Silva, S. M. Da, Vairo, K. P., Moura, M. O.

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Maple syrup urine disease: mechanisms and management by Blackburn, Patrick R, Gass, Jennifer M, Vairo, Filippo Pinto E, Farnham, Kristen M, Atwal, Herjot K, Macklin, Sarah, Klee, Eric W, Atwal, Paldeep S

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Butyrophilin 2A1 is essential for phosphoantigen reactivity by γδ T cells by Rigau, Marc, Ostrouska, Simone, Fulford, Thomas S, Johnson, Darryl N, Woods, Katherine, Ruan, Zheng, McWilliam, Hamish E G, Hudson, Christopher, Tutuka, Candani, Wheatley, Adam K, Kent, Stephen J, Villadangos, Jose A, Pal, Bhupinder, Kurts, Christian, Simmonds, Jason, Pelzing, Matthias, Nash, Andrew D, Hammet, Andrew, Verhagen, Anne M, Vairo, Gino, Maraskovsky, Eugene, Panousis, Con, Gherardin, Nicholas A, Cebon, Jonathan, Godfrey, Dale I, Behren, Andreas, Uldrich, Adam P

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Heavy quarkonium: progress, puzzles, and opportunities by Brambilla, N., Eidelman, S., Heltsley, B. K., Vogt, R., Bodwin, G. T., Eichten, E., Frawley, A. D., Meyer, A. B., Mitchell, R. E., Papadimitriou, V., Petreczky, P., Petrov, A. A., Robbe, P., Vairo, A., Andronic, A., Arnaldi, R., Artoisenet, P., Bali, G., Bertolin, A., Bettoni, D., Brodzicka, J., Bruno, G. E., Caldwell, A., Catmore, J., Chang, C.-H., Chao, K.-T., Chudakov, E., Cortese, P., Crochet, P., Drutskoy, A., Ellwanger, U., Faccioli, P., Gabareen Mokhtar, A., Garcia i Tormo, X., Hanhart, C., Harris, F. A., Kaplan, D. M., Klein, S. R., Kowalski, H., Lansberg, J.-P., Levichev, E., Lombardo, V., Lourenço, C., Maltoni, F., Mocsy, A., Mussa, R., Navarra, F. S., Negrini, M., Nielsen, M., Olsen, S. L., Pakhlov, P., Pakhlova, G., Peters, K., Polosa, A. D., Qian, W., Qiu, J.-W., Rong, G., Sanchis-Lozano, M. A., Scomparin, E., Senger, P., Simon, F., Stracka, S., Sumino, Y., Voloshin, M., Weiss, C., Wöhri, H. K., Yuan, C.-Z.

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QCD and strongly coupled gauge theories: challenges and perspectives by Brambilla, N., Eidelman, S., Foka, P., Gardner, S., Kronfeld, A. S., Alford, M. G., Alkofer, R., Butenschoen, M., Cohen, T. D., Erdmenger, J., Fabbietti, L., Faber, M., Goity, J. L., Ketzer, B., Lin, H. W., Llanes-Estrada, F. J., Meyer, H. B., Pakhlov, P., Pallante, E., Polikarpov, M. I., Sazdjian, H., Schmitt, A., Snow, W. M., Vairo, A., Vogt, R., Vuorinen, A., Wittig, H., Arnold, P., Christakoglou, P., Di Nezza, P., Fodor, Z., Garcia i Tormo, X., Höllwieser, R., Janik, M. A., Kalweit, A., Keane, D., Kiritsis, E., Mischke, A., Mizuk, R., Odyniec, G., Papadodimas, K., Pich, A., Pittau, R., Qiu, J.-W., Ricciardi, G., Salgado, C. A., Schwenzer, K., Stefanis, N. G., von Hippel, G. M., Zakharov, V. I.

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Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings by Wilson, Matthew P., Garanto, Alejandro, Pinto e Vairo, Filippo, Ng, Bobby G., Ranatunga, Wasantha K., Ventouratou, Marina, Baerenfaenger, Melissa, Huijben, Karin, Thiel, Christian, Ashikov, Angel, Keldermans, Liesbeth, Souche, Erika, Vuillaumier-Barrot, Sandrine, Dupré, Thierry, Michelakakis, Helen, Fiumara, Agata, Pitt, James, White, Susan M., Lim, Sze Chern, Gallacher, Lyndon, Peters, Heidi, Rymen, Daisy, Witters, Peter, Ribes, Antonia, Morales-Romero, Blai, Rodríguez-Palmero, Agustí, Ballhausen, Diana, de Lonlay, Pascale, Barone, Rita, Janssen, Mirian C.H., Jaeken, Jaak, Freeze, Hudson H., Matthijs, Gert, Morava, Eva, Lefeber, Dirk J.

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TGF-α and IL-6 plasma levels selectively identify CML patients who fail to achieve an early molecular response or progress in the first year of therapy by Nievergall, E, Reynolds, J, Kok, C H, Watkins, D B, Biondo, M, Busfield, S J, Vairo, G, Fuller, K, Erber, W N, Sadras, T, Grose, R, Yeung, D T, Lopez, A F, Hiwase, D K, Hughes, T P, White, D L

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Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients by Santiago, K.M., Castro, L.P., Neto, J.P.D., Nóbrega, A.F., Pinto, C.A.L., Ashton‐Prolla, P., Pinto e Vairo, F., Medeiros, P.F.V., Ribeiro, E.M., Ribeiro, B.F.R., Valle, F.F., Doriqui, M.J.R., Leite, C.H.B., Rocha, R.M., Moura, L.M.S., Munford, V., Galante, P.A.F., Menck, C.F.M., Rogatto, S.R., Achatz, M.I.

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De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias by Helbig, Katherine L., Lauerer, Robert J., Bahr, Jacqueline C., Souza, Ivana A., Uysal, Betül, Gandini, Maria A., Huang, Sun, Keren, Boris, Mignot, Cyril, Billette de Villemeur, Thierry, Nava, Caroline, Valence, Stéphanie, Buratti, Julien, Fagerberg, Christina R., Soerensen, Kristina P., Kamsteeg, Erik-Jan, Koolen, David A., Gunning, Boudewijn, Schelhaas, H. Jurgen, Fox, Jordana, Bakhtiari, Somayeh, Jarrar, Randa, Lindstrom, Kristin, Jin, Sheng Chih, Zeng, Xue, Bilguvar, Kaya, Papavasileiou, Antigone, Xing, Qinghe, Zhu, Changlian, Boysen, Katja, Vairo, Filippo, Klee, Eric W., Tillema, Jan-Mendelt, Payne, Eric T., Cousin, Margot A., Kruisselbrink, Teresa M., Wick, Myra J., Baker, Joshua, Smith, Nicholas, Angrist, Misha, Ashley, Patricia, Bidegain, Margarita, Chambers, Eileen, Cope, Heidi, Cotten, C. Michael, Curington, Theresa, Davis, Erica E., Fisher, Kimberley, French, Amanda, Gallentine, William, Hill, Kevin, Kansagra, Sujay, Katsanis, Sara, Kurtzberg, Joanne, Marcus, Jeffrey, McDonald, Marie, Mikati, Mohammed, Miller, Stephen, Murtha, Amy, Perilla, Yezmin, Pizoli, Carolyn, Ross, Sherry, Sadeghpour, Azita, Smith, Edward, Wiener, John, Corbett, Mark A., Goldmann, Eva, Kichula, Elizabeth, Segal, Eric, Jackson, Kelly E., Asamoah, Alexander, McCarrier, Julie, Botto, Lorenzo D., Tvrdik, Tatiana, Cascino, Gregory D., Klingerman, Sherry, Neumann, Catherine, Nolan, Melinda A., Snell, Russell G., Lehnert, Klaus, Sadleir, Lynette G., Kvarnung, Malin, Guerrini, Renzo, Friez, Michael J., Lyons, Michael J., Leonhard, Jennifer, Kringlen, Gabriel, El Achkar, Christelle M., Smith, Lacey A., Carss, Keren J., Rankin, Julia, Zeman, Adam, Blyth, Moira, Kerr, Bronwyn, Ruiz, Karla, Urquhart, Jill, Banka, Siddharth, Scheffer, Ingrid E., Zamponi, Gerald W., Mefford, Heather C.

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Monoclonal antibody targeting of IL-3 receptor α with CSL362 effectively depletes CML progenitor and stem cells by Nievergall, Eva, Ramshaw, Hayley S., Yong, Agnes S.M., Biondo, Mark, Busfield, Samantha J., Vairo, Gino, Lopez, Angel F., Hughes, Timothy P., White, Deborah L., Hiwase, Devendra K.

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The strong coupling constant: state of the art and the decade ahead by d’Enterria, D, Kluth, S, Zanderighi, G, Ayala, C, Benitez-Rathgeb, M A, Blümlein, J, Boito, D, Brambilla, N, Britzger, D, Camarda, S, Cooper-Sarkar, A M, Cridge, T, Cvetič, G, d’Enterria, D, Dalla Brida, M, Deur, A, Giuli, F, Golterman, M, Hoang, A H, Huston, J, Jamin, M, Kluth, S, Kotikov, A V, Krivokhizhin, V G, Kronfeld, A S, Leino, V, Lipka, K, Mäkelä, T, Malaescu, B, Maltman, K, Marzani, S, Mateu, V, Moch, S, Monni, P F, Nadolsky, P, Nason, P, Nesterenko, A V, Pérez-Ramos, R, Peris, S, Petreczky, P, Pich, A, Rabbertz, K, Ramos, A, Reichelt, D, Rodríguez-Sánchez, A, Rojo, J, Saragnese, M, Sawyer, L, Schott, M, Schumann, S, Shaikhatdenov, B G, Sint, S, Soyez, G, Teca, D, Vairo, A, Vos, M, Waits, C, Weber, J H, Wobisch, M, Xie, K, Zanderighi, G

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Robotic Ubiquitous Cognitive Ecology for Smart Homes by Amato, G., Bacciu, D., Broxvall, M., Chessa, S., Coleman, S., Di Rocco, M., Dragone, M., Gallicchio, C., Gennaro, C., Lozano, H., McGinnity, T. M., Micheli, A., Ray, A. K., Renteria, A., Saffiotti, A., Swords, D., Vairo, C., Vance, P.

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Evidences for the involvement of cell surface glycans in stem cell pluripotency and differentiation by Alisson-Silva, Frederico, de Carvalho Rodrigues, Deivid, Vairo, Leandro, Asensi, Karina Dutra, Vasconcelos-dos-Santos, Andréia, Mantuano, Natalia Rodrigues, Dias, Wagner Barbosa, Rondinelli, Edson, Goldenberg, Regina Coeli dos Santos, Urmenyi, Turán Peter, Todeschini, Adriane R

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Influence of mesoscale properties on the mechanisms of plastic strain accommodation in plane strain dynamic deformation of concentric Ni-Al laminates by Olney, K. L., Chiu, P.-H., Ribero Vairo, M. S., Higgins, A., Serge, M., Benson, D. J., Nesterenko, V. F.

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Telehealth Is Effective in the Evaluation of Individuals With Undiagnosed Rare Disorders: An Undiagnosed Diseases Network Study by Tan, Queenie K-G, McConkie-Rosell, Allyn, Mahoney, Rachel, Spillmann, Rebecca C, Schoch, Kelly, Chanprasert, Sirisak, Acosta, Maria T, Toro, Camilo, Rosenfeld, Jill A, Orengo, James P, Scott, Daryl A, Granadillo, Jorge L, Sisco, Kathleen, Wegner, Daniel J, Tekin, Mustafa, Bivona, Stephanie, Peart, LéShon, Rodan, Lance, Bonner, Devon, Wheeler, Matthew T, Bernstein, Jonathan A, Ruzhnikov, Maura, Adams, David R, Hisama, Fuki M, Shashi, Vandana

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Correction: Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD) by Pinto E Vairo, Filippo, Kemppainen, Jennifer L, Vitek, Carolyn R Rohrer, Whalen, Denise A, Kolbert, Kayla J, Sikkink, Kaitlin J, Kroc, Sarah A, Kruisselbrink, Teresa, Shupe, Gabrielle F, Knudson, Alyssa K, Burke, Elizabeth M, Loftus, Elle C, Bandel, Lorelei A, Prochnow, Carri A, Mulvihill, Lindsay A, Thomas, Brittany, Gable, Dale M, Graddy, Courtney B, Garzon, Giovanna G Moreno, Ekpoh, Idara U, Porquera, Eva M Carmona, Fervenza, Fernando C, Hogan, Marie C, El Ters, Mireille, Warrington, Kenneth J, Davis, 3rd, John M, Koster, Matthew J, Orandi, Amir B, Basiaga, Matthew L, Vella, Adrian, Kumar, Seema, Creo, Ana L, Lteif, Aida N, Pittock, Siobhan T, Tebben, Peter J, Abate, Ejigayehu G, Joshi, Avni Y, Ristagno, Elizabeth H, Patnaik, Mrinal S, Schimmenti, Lisa A, Dhamija, Radhika, Sabrowsky, Sonia M, Wierenga, Klaas J, Keddis, Mira T, Samadder, Niloy Jewel J, Presutti, Richard J, Robinson, Steven I, Stephens, Michael C, Roberts, Lewis R, Faubion, Jr, William A, Driscoll, Sherilyn W, Wong-Kisiel, Lily C, Selcen, Duygu, Flanagan, Eoin P, Ramanan, Vijay K, Jackson, Lauren M, Mauermann, Michelle L, Ortega, Victor E, Anderson, Sarah A, Aoudia, Stacy L, Klee, Eric W, McAllister, Tammy M, Lazaridis, Konstantinos N

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Immunological and hematological findings as major features in a patient with a new germline pathogenic CBL variant by Stellacci, Emilia, Stevenson, David, Moslehi, Dorsa, Adams, David R., Afzali, Ben, Allworth, Aimee, Alvey, Justin, Ashley, Euan A., Bacino, Carlos A., Baldwin, Erin, Bale, Jim, Beggs, Alan H., Behrens, Edward, Bejerano, Gill, Bernstein, Jonathan A., Blue, Elizabeth, Burke, Elizabeth A., Burrage, Lindsay C., Byrd, William E., Carey, John, Cassini, Thomas, Coakley, Terra R., Cobban, Laurel A., Cogan, Joy D., Coggins, Matthew, Corona, Rosario I., Cuddapah, Vishnu, D'Souza, Precilla, Dasari, Surendra, Dell'Angelica, Esteban C., Dipple, Katrina, Doherty, Daniel, Dorrani, Naghmeh, Earl, Dawn, Esteves, Cecilia, Ezell, Kimberly, Fieg, Elizabeth L., Fisher, Paul G., Gahl, William A., Gonzalez, Joanna M., Gropman, Andrea, Hamid, Rizwan, Hassey, Kelly, Holm, Ingrid A., Hom, Jason, Horike‐Pyne, Martha, Hurst, Anna, Jean‐Marie, Orpa, Jobanputra, Vaidehi, Kanca, Oguz, Kiley, Dana, Korf, Bruce, Krakow, Deborah, Lam, Christina, Lee, Brendan H., Leppig, Kathleen A., Longo, Nicola, Macnamara, Ellen F., Mao, Rong, Marth, Gabor, Martínez‐Agosto, Julian A., McConkie‐Rosell, Allyn, McMinn, Ashley, Mikati, Mohamad, Mitchell, Breanna, Morimoto, Marie, Mulvihill, John J., Orengo, James P., Petcharet, Leoyklang, Phillips, John A., Swerdzewski, Barbara N. Pusey, Quinlan, Aaron, Rajagopalan, Ramakrishnan, Rao, Deepak A., Raper, Anna, Rebelo, Adriana, Reuter, Chloe M., Rives, Lynette, Rosenthal, Elizabeth, Sampson, Jacinda B., Schedl, Timothy, Schoch, Kelly, Seto, Elaine, Shashi, Vandana, Sheppeard, Sam, Sirugo, Giorgio, Smith, Carson A., Solomon, Ben, Sullivan, Kathleen, Sybert, Virginia, Taylor, Herman, Tekin, Mustafa, Toro, Camilo, Ungar, Rachel A., Wahl, Colleen E., Walker, Melissa, Wegner, Daniel, Hubshman, Monika Weisz, Wheeler, Matthew T., Bernstein, Jonathan A.

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Proposed antimatter gravity measurement with an antihydrogen beam by Kellerbauer, A., Amoretti, M., Belov, A.S., Bonomi, G., Boscolo, I., Brusa, R.S., Büchner, M., Byakov, V.M., Cabaret, L., Canali, C., Carraro, C., Castelli, F., Cialdi, S., de Combarieu, M., Comparat, D., Consolati, G., Djourelov, N., Doser, M., Drobychev, G., Dupasquier, A., Ferrari, G., Forget, P., Formaro, L., Gervasini, A., Giammarchi, M.G., Gninenko, S.N., Gribakin, G., Hogan, S.D., Jacquey, M., Lagomarsino, V., Manuzio, G., Mariazzi, S., Matveev, V.A., Meier, J.O., Merkt, F., Nedelec, P., Oberthaler, M.K., Pari, P., Prevedelli, M., Quasso, F., Rotondi, A., Sillou, D., Stepanov, S.V., Stroke, H.H., Testera, G., Tino, G.M., Trénec, G., Vairo, A., Vigué, J., Walters, H., Warring, U., Zavatarelli, S., Zvezhinskij, D.S.

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De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias by Lauerer, Robert J., Bahr, Jacqueline C., Souza, Ivana A., Myers, Candace T., Schwarz, Niklas, Gandini, Maria A., Keren, Boris, Mignot, Cyril, Afenjar, Alexandra, Billette de Villemeur, Thierry, Héron, Delphine, Nava, Caroline, Buratti, Julien, Fagerberg, Christina R., Soerensen, Kristina P., Kibaek, Maria, Kamsteeg, Erik-Jan, Schelhaas, H. Jurgen, Fox, Jordana, Bakhtiari, Somayeh, Jarrar, Randa, Padilla-Lopez, Sergio, Lindstrom, Kristin, Bilguvar, Kaya, Papavasileiou, Antigone, Xing, Qinghe, Boysen, Katja, Vairo, Filippo, Lanpher, Brendan C., Klee, Eric W., Tillema, Jan-Mendelt, Cousin, Margot A., Baker, Joshua, Haan, Eric, Smith, Nicholas, Davis, Erica E., Katsanis, Nicholas, Angrist, Misha, Ashley, Patricia, Bidegain, Margarita, Chambers, Eileen, Cope, Heidi, Cotten, C. Michael, Curington, Theresa, Fisher, Kimberley, French, Amanda, Gallentine, William, Hill, Kevin, Kansagra, Sujay, Katsanis, Sara, Kurtzberg, Joanne, Marcus, Jeffrey, McDonald, Marie, Mikati, Mohammed, Miller, Stephen, Murtha, Amy, Perilla, Yezmin, Pizoli, Carolyn, Ross, Sherry, Smith, Edward, Wiener, John, Corbett, Mark A., MacLennan, Alastair H., Biskup, Saskia, Rodan, Lance H., Segal, Eric, Dimmock, David, McCarrier, Julie, Botto, Lorenzo D., Filloux, Francis, Klingerman, Sherry, Neumann, Catherine, Wang, Raymond, Jacobsen, Jessie C., Snell, Russell G., Lehnert, Klaus, Anderlid, Britt-Marie, Kvarnung, Malin, Guerrini, Renzo, Lyons, Michael J., Leonhard, Jennifer, Kringlen, Gabriel, Smith, Lacey A., Rotenberg, Alexander, Poduri, Annapurna, Sanchis-Juan, Alba, Carss, Keren J., Rankin, Julia, Zeman, Adam, Raymond, F. Lucy, Blyth, Moira, Kerr, Bronwyn, Urquhart, Jill, Hughes, Imelda, Banka, Siddharth, Hedrich, Ulrike B.S., Scheffer, Ingrid E., Zamponi, Gerald W., Lerche, Holger, Mefford, Heather C.

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TGF-[alpha] and IL-6 plasma levels selectively identify CML patients who fail to achieve an early molecular response or progress in the first year of therapy by Nievergall, E, Reynolds, J, Kok, C H, Watkins, D B, Biondo, M, Busfield, S J, Vairo, G, Fuller, K, Erber, W N, Sadras, T, Grose, R, Yeung, D T, Lopez, A F, Hiwase, D K, Hughes, T P, White, D L

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