日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Recurrent Immunogenic Neoantigens and Their Cognate T-cell Receptors in Treatment-Resistant Metastatic Prostate Cancer.

治疗耐药性转移性前列腺癌中复发的免疫原性新抗原及其同源T细胞受体。

Gumpert Nofar, Sagie Shira, Arnedo-Pac Claudia, Babu Tomer, Weller Chen, Gonzalez-Perez Abel, Wang Yuan, Michel Todó Lucas, Levy Ronen, Chen Xi, Greenberg Polina, Dayan-Rubinov Maria, Yakubovich Elizabeta, Wasserman-Bartov Talya, Zerbib Mirie, Gong Jianhui, Rebernick Ryan J, Oliveira Tercero Anna, Agundez Muriel Laura, Benedek Gil, Kedmi Merav, Oren Roni, Ben-Dor Shifra, Levin Yishai, Troyanskaya Olga G, Munzur Aslı D, Wyatt Alexander W, Cieslik Marcin P, Quigley David A, Van Allen Eliezer M, Anandasabapathy Niroshana, Mateo Joaquin, Yang Xinbo, Martínez-Jiménez Francisco, Lopez-Bigas Nuria, Samuels Yardena

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies

对snRNA基因的系统分析揭示了显性和隐性发育性脑病和癫痫性脑病中常见的RNU2-2变异。

Leitão, Elsa; Santini, Amandine; Cogne, Benjamin; Essid, Miriam; Athanasiadou, Maria; LaFlamme, Christy W; Marijon, Pierre; Bernard, Virginie; Jousselin, Kevin; Chatron, Nicolas; Barcia, Giulia; Keren, Boris; Mignot, Cyril; Charles, Perrine; Besnard, Thomas; Paluch, Robin; de Sainte Agathe, Jean-Madeleine; Almanza Fuerte, Edith P; Sengupta, Soham; Milh, Mathieu; Ramond, Francis; Allan, Talia; An, Isabelle; Araujo, Camila; Arpin, Stéphanie; Austin-Tse, Christina; Auvin, Stéphane; Baer, Sarah; Bahi-Buisson, Nadia; Bak, Mads; Barth, Magalie; Baulac, Stéphanie; Bednarek-Weirauch, Nathalie; Begemann, Matthias; Bennett, Mark F; Bensabath, Uriel; Bézieau, Stéphane; Bhouri, Rakia; Biehler, Margaux; Hammer, Trine Bjørg; Bogoin, Julie; Bonanno, Emilie; Boussion, Simon; Bris, Céline; Brosseau-Beauvir, Adelaide; Bruel, Ange-Line; Briand-Suleau, Audrey; Buratti, Julien; Celse, Tristan; Chambon, Pascal; Chemaly, Nicole; Chesneau, Bertrand; Colin, Estelle; Colmard, Maxime; Colson, Cindy; Conrad, Solène; Courtin, Thomas; Creveaux, Isabelle; Cullier, Anne-Charlotte; Dang, Louis T; de Saint Martin, Anne; de Vanssay de Blavous Legendre, Caroline; Demeer, Bénédicte; Denommé-Pichon, Anne-Sophie; Diekhoff, Philine; DiTroia, Stephanie; Doco-Fenzy, Martine; Dubourg, Christèle; Dubucs, Charlotte; Ducreux, Stéphanie; Dufour, Louis; Duquet, Romain; Durand, Benjamin; El Chehadeh, Salima; Elbracht, Miriam; Faivre, Laurence; Faoucher, Marie; Faudet, Anne; Forlani, Sylvie; Fradin, Mélanie; Gaignard, Pauline; Ganne, Benjamin; Garde, Aurore; Géraud, Justine; Gill, Deepak; Goldenberg, Alice; Grabli, David; Grisel, Coraline; Gueden, Sophie; Gueguen, Paul; Guerrot, Anne-Marie; Guichet, Agnès; Haack, Tobias B; Härting, Nina; Häusler, Martin Georg; Heide, Solveig; Herget, Theresia; Héron, Bénédicte; Héron, Delphine; Herwig, Johanna; Heulin, Mathilde; Holling, Tess; Houdayer, Clara; Isidor, Bertrand; Jacquette, Aurélia; Januel, Louis; Jean-Marçais, Nolwenn; Kaiser, Frank J; Kaya, Sabine; King, Chontelle; Konyukh, Marina; Kraft, Florian; Krause, Jeremias; Kirstetter, Rémi; Kuechler, Alma; Kurth, Ingo; Kutsche, Kerstin; Labalme, Audrey; Laloy, Jean-Serene; Laugel, Vincent; Le Bricquir, Floriane; Lèbre, Anne-Sophie; Lebrun, Marine; Leguern, Eric; Levy, Jonathan; Lieffering, Nico; Lyonnet, Stanislas; Lüthy, Kevin; Macdonald, Sian M W; Mansour-Hendili, Lamisse; Maraval, Julien; Marquardt, Iris; Mattausch, Carolin; Mercier, Sandra; Messaoud, Olfa; Morel, Godelieve; Mortreux, Jérémie; Munnich, Arnold; Nabbout, Rima; Nambot, Sophie; Navarro, Vincent; Neale, Ashana; Nguyen, Laetitia; Nizon, Mathilde; Nowak, Frédérique; O'Leary, Melanie C; Odent, Sylvie; Ojeda, Naomi Meave; Olin, Valérie; Olivieri, Simone; Õunap, Katrin; Pais, Lynn S; Panagiotakaki, Eleni; Patat, Olivier; Perrin-Sabourin, Laurence; Petit, Florence; Philippe, Christophe; Piton, Amélie; Planes, Marc; Poirsier, Céline; Pouzet, Antoine; Prouteau, Clément; Quéméner-Redon, Sylvia; Renaud, Mathilde; Richard, Anne-Claire; Rio, Marlène; Rivier, Clotilde; Robin-Renaldo, Florence; Rollier, Paul; Rossi, Massimiliano; Roubertie, Agathe; Ruault, Valentin; Rupin-Mas, Maïlys; Saugier-Veber, Pascale; Saunier, Aline; Saneto, Russell; Sarrazin, Elisabeth; Sarret, Catherine; Schaefer, Elise; Schluth-Bolard, Caroline; Schneider, Amy; Schumann, Isabell; Seplyarskiy, Vladimir B; Spranger, Stephanie; Smol, Thomas; Sturm, Marc; Sunyaev, Shamil R; Sperelakis-Beedham, Brian; Stenton, Sarah L; Stock, Friedrich; Tharreau, Mylène; Torun, Deniz; Toulouse, Joseph; Thiyagarajah, Harshini; Valence, Stéphanie; Valleix, Sophie; Van-Gils, Julien; Villard, Laurent; Ville, Dorothée; Villeneuve, Nathalie; Vitobello, Antonio; Waernessyckle, Aurélie; Wagner, Jan; Weber, Yvonne; Wieczorek, Dagmar; Witkowski, Tom; Yadavilli, Manya; Yammine, Tony; Zaafrane-Khachnaoui, Khaoula; Zaki, Maha S; Ziegler, Alban; Bramswig, Nuria C; Lermine, Alban; Nicolas, Gael; Gleeson, Joseph G; Sadleir, Lynette G; Hildebrand, Michael S; Scheffer, Ingrid E; Whiffin, Nicola; O'Donnell-Luria, Anne; Mefford, Heather C; Blanc, Pierre; Thevenon, Julien; Charbonnier, Camille; Charenton, Clément; Depienne, Christel; Lesca, Gaetan; Nava, Caroline

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

非编码RNA基因RNU4-2的双等位基因变异会导致一种隐性遗传的神经发育综合征,并伴有明显的白质改变。

Rius, Rocio; Blakes, Alexander J M; Chen, Yuyang; De Jonghe, Joachim; Lecoquierre, François; Dawes, Ruebena; Cogne, Benjamin; Kim, Hyung Chul; Alvi, Javeria R; Amblard, Florence; Ansari, Morad; Arlt, Annabelle; Austin-Tse, Christina; Baer, Sarah; Balasubramanian, Meena; Balton, Elsa V; Barcia, Giulia; Beleza-Meireles, Ana; Bernstein, Jonathan A; Beygo, Jasmin; Blanc, Pierre; Bramswig, Nuria C; Braun, Frederik; Buchzik, Daniel; Calame, Daniel G; Campbell, Jamie; Coutton, Charles; Cunningham, Chloe A; Dargie, Nitsuh; Depienne, Christel; Dipple, Katrina M; Dieux, Anne; Dixit, Abhijit; Dreyer, Lauren; Du, Haowei; El Chehadeh, Salima; Field, Michael; Ewans, Lisa J; Geiger, Vanessa; Gibbs, Richard A; Glass, Ian; Grunewald, Olivier; Gueguen, Paul; Haack, Tobias B; Hadj Abdallah, Hamza; Harbuz, Radu; Helbig, Ingo; Horvath, Judit; Hustinx, Alexander; Isidor, Bertrand; Jacquemont, Marie-Line; Jamie, Fraser; Jeanne, Médéric; Kessler, Riley; Klinkhammer, Hannah; Korenke, G Christoph; Kotzaeridou, Urania; Krawitz, Peter; Laurie, Steven; Leventer, Richard J; Levy, Rebecca J; Lupski, James R; Marijon, Pierre; McGinnis, Kaitlin E; Mendez, Rodrigo; Messaoud, Olfa; Nava, Caroline; Nizard, Mevyn; O'Donnell-Luria, Anne; O'Leary, Melanie C; Olivieri, Simone; Parida, Amitav; Pehlivan, Davut; Prentice, Anna Jenne; Posey, Jennifer E; Reuter, Chloe M; Satre, Véronique; Schluth-Bolard, Caroline; Smol, Thomas; Sultan, Tipu; Taylor, John; Thauvin-Robinetvin, Christel; Thevenon, Julien; Uebergang, Eloise; Ueberberg, Sandra; Vincent-Delorme, Catherine; Wassmer, Evangeline; Westwood, Emma; Wheeler, Matthew T; Gulec, Elif Yilmaz; Vanderver, Adeline; Vossough, Arastoo; Sanders, Stephan J; Banka, Siddharth; Findlay, Gregory M; MacArthur, Daniel G; Simons, Cas; Whiffin, Nicola

CPX-351 vs daunorubicin, cytarabine, and gemtuzumab ozogamicin in older adults with non-adverse-risk AML: the NCRI AML18 trial

CPX-351 与柔红霉素、阿糖胞苷和吉妥珠单抗治疗老年非不良风险 AML 患者的疗效比较:NCRI AML18 试验

Knapper, Steven; Dillon, Laura W; Babu, Malavika; Thomas, Abin; Thomas, Ian; Hourigan, Christopher S; Andrew, Georgia; Dillon, Richard; Gilkes, Amanda; Marquez Almuina, Nuria; King, Sophie; McCarthy, Nicholas; Bahr, Reem; Al-Ali, Rasha W; Stone, Louisa; Coats, Tom; Byrne, Jennifer; Green, Simone; Overgaard, Ulrik Malthe; Sellar, Rob S; Dennis, Mike; Mehta, Priyanka; Hills, Robert; Freeman, Sylvie D; Russell, Nigel H

Prenatal Exposure to Zika Virus and Risk of Epilepsy-Related Hospitalization During Early Childhood

产前接触寨卡病毒与幼儿期癫痫相关住院风险

Tedde, João Guilherme G; Cerqueira-Silva, Thiago; Carroll, Orlagh; Rodrigues, Laura C; Teixeira, Maria Gloria; Clemente, Nuria Sanchez; Barreto, Mauricio L; Paixão, Enny S

Prophylactic Treatment of Patent Ductus Arteriosus With Acetaminophen: A Randomized Clinical Trial

对乙酰氨基酚预防动脉导管未闭:一项随机临床试验

Rozé, Jean-Christophe; Cambonie, Gilles; Flamant, Cyril; Patkaï, Juliana; Mühlbacher, Tobias; Gascoin, Geraldine; Rideau Batista Novais, Aline; Tauzin, Manon; Le Duc, Kevin; Beuchée, Alain; Joye, Sebastien; Babacheva, Evgeniya; Bouissou, Antoine; Ligi, Isabelle; Tammela, Outi; Plourde, Marion; Dempsey, Eugene; Tosello, Barthelemy; Nguyen, Kim; Vincent, Marine; Andresson, Pille; Binder, Christoph; Kruse, Charlotte; Barcos Munoz, Francisca; Kuhn, Pierre; Proença, Elisa; Bartocci, Marco; Kermorvant-Duchemin, Elsa; Nellis, Georgi; Lumia, Mirka; Giapros, Vasileios; Rigo, Vincent; Sankilampi, Ulla; Mendes da Graça, André; Rønnestad, Arild; Soukka, Hanna; Mondì, Vito; Aikio, Outi; Torre-Monmany, Nuria; Rüegger, Christoph; Baud, Olivier; Zeitlin, Jennifer; Morgan, Andrei Scott; Baruteau, Alban-Elouen; Ancel, Pierre-Yves; Carbajal, Ricardo; Bouazza, Naim; Diallo, Alpha; Levoyer, Lea; Kemper, Ruth; Hallman, Mikko; Alberti, Corinne; Ursino, Moreno

Voltage-Driven Generation of Ferromagnetism in a Magneto-Ionically Active Antiferromagnet Enabling Room-Temperature Exchange Bias

电压驱动在磁离子活性反铁磁体中产生铁磁性,从而实现室温交换偏置

Privitera, Simone; Ma, Zheng; Gómez-Torres, Hugo; Arredondo-López, Aitor; Liedke, Maciej Oskar; Hirschmann, Eric; Wagner, Andreas; Tan, Huan; Solsona, Pau; Quintana, Alberto; Dias, Thiago; Gouéré, Diane; Monteblanco, Elmer; Ravelosona, Dafiné; Del-Valle, Nuria; Navau, Carles; Lopeandia, Aitor; Sort, Jordi; Menéndez, Enric

Succinate receptor 1 restricts hematopoiesis and prevents acute myeloid leukemia progression

琥珀酸受体1限制造血作用并阻止急性髓系白血病进展

Cuminetti, Vincent; Boet, Emeline; Heugel, Marcel; Konieczny, Joanna; Bernal, Aurora; Gomez, Manuel J; Grimolizzi, Franco; Vilaplana-Lopera, Nuria; Ferré, Marc; Villatoro, Alicia; Pandey, Deo P; Torroja, Carlos; Taman, Hagar; Paulssen, Ruth H; Vogl, Thomas; Heckman, Caroline A; Vik, Anders; Giovinazzo, Giovanna; van Gastel, Nick; García, Paloma; Sánchez-Cabo, Fátima; Sarry, Jean-Emmanuel; Arranz, Lorena

Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humans

CELSR1基因的双等位基因变异会导致人类脑畸形、神经发育障碍和癫痫。

Bonardi, Claudia M; Møller, Rikke S; Ruiz-Reig, Nuria; Chai, Guoliang; Madsen, Camilla G; Bayat, Allan; Hammer, Trine B; Fenger, Christina D; Gardella, Elena; Gawlinski, Pawel; Dawidziuk, Mateusz; Wiszniewski, Wojciech; Bekiesinska-Figatowska, Monika; Cabet, Sara; Rossi, Massimiliano; Lesca, Gaetan; Gouy, Evan; Jepsen, Birgit; Mieszczanek, Tomasz S; Sanchez Russo, Rossana; Barr, Eileen E; Õunap, Katrin; Ilves, Pilvi; Wojcik, Monica H; Aittaleb, Mohamed; Brusgaard, Klaus; Tissir, Fadel; Rubboli, Guido

Versican expression from lung fibroblasts suppresses pulmonary fibrosis.

肺成纤维细胞中 Versican 的表达抑制肺纤维化。

Kanellopoulou Paraskevi, Barbayianni Ilianna, Fanidis Dionysios, Samiotaki Martina, Katsiouli Eleni, Nastos Dimitris, Smyrniotis Stefanos, Shira Maria, Galaris Apostolos, Rinotas Vagelis, Grammenoudi Sofia, Magkrioti Christiana, Tomos Ioannis, Martinez Blanco Africa, Tremi Ioanna, Vamvakaris Ioannis, Gavara Nuria, Havaki Sophia, Gorgoulis Vassilis, Watanabe Hideto, Aidinis Vassilis