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

Retraction Note: Antibodies against endogenous retroviruses promote lung cancer immunotherapy

撤稿声明:针对内源性逆转录病毒的抗体可促进肺癌免疫疗法

Ng, Kevin W; Boumelha, Jesse; Enfield, Katey S S; Almagro, Jorge; Cha, Hongui; Pich, Oriol; Karasaki, Takahiro; Moore, David A; Salgado, Roberto; Sivakumar, Monica; Young, George; Molina-Arcas, Miriam; de Carné Trécesson, Sophie; Anastasiou, Panayiotis; Fendler, Annika; Au, Lewis; Shepherd, Scott T C; Martínez-Ruiz, Carlos; Puttick, Clare; Black, James R M; Watkins, Thomas B K; Kim, Hyemin; Shim, Seohee; Faulkner, Nikhil; Attig, Jan; Veeriah, Selvaraju; Magno, Neil; Ward, Sophia; Frankell, Alexander M; Al Bakir, Maise; Lim, Emilia L; Hill, Mark S; Wilson, Gareth A; Cook, Daniel E; Birkbak, Nicolai J; Behrens, Axel; Yousaf, Nadia; Popat, Sanjay; Hackshaw, Allan; Hiley, Crispin T; Litchfield, Kevin; McGranahan, Nicholas; Jamal-Hanjani, Mariam; Larkin, James; Lee, Se-Hoon; Turajlic, Samra; Swanton, Charles; Downward, Julian; Kassiotis, George

IL-36γ armored CAR T cells reprogram neutrophils to induce endogenous antitumor immunity.

IL-36α 装甲 CAR T 细胞可重编程中性粒细胞,诱导内源性抗肿瘤免疫。

Zuo Yihan, Vohwinkel David J, Dong Bowen, McDowell James R, Guzman Brandon V, Manickavel Pandian Tharuna Sri, Chattopadhyay Saborni, McGray A J R, Olejniczak Scott H, Ohm Joyce, Wang Jianmin, Long Mark D, Gomez Eduardo Cortes, Purdon Terence J, Luo Wei, Mohammadpour Hemn, Hackett Christopher S, Cherkassky Leonid, Davila Marco, Abrams Scott I, Brentjens Renier J

FLIPI24: A Modern Prognostic Model and Clinical Trial Enrichment Tool for Newly Diagnosed Follicular Lymphoma

FLIPI24:一种用于新诊断滤泡性淋巴瘤的现代预后模型和临床试验富集工具

Maurer, Matthew J; Prochazka, Vit K; El-Galaly, Tarec Christoffer; Flowers, Christopher R; Villa, Diego; Bachy, Emmanuel; Cahn, Elliot J; Fournier, Marguerite; Larson, Melissa C; Dietrich, Caroline E; Jakobsen, Lasse Hjort; Ghesquières, Hervé; Kridel, Robert; Gandhi, Maher K; Cheah, Chan Y; Hawkes, Eliza A; Seymour, John F; Freeman, Ciara L; Clausen, Michael R; Wahlin, Björn E; Friedberg, Jonathan W; Casulo, Carla; Habermann, Thomas M; Wang, Yucai; Nastoupil, Loretta J; de Nully Brown, Peter; Belada, David; Janíková, Andrea; Mocikova, Heidi; Fürst, Tomáš; Feugier, Pierre; Tilly, Hervé; Haioun, Corinne; Davies, Andrew J; Cartron, Guillaume; Burack, Richard; Chihara, Dai; Martin, Peter; Cohen, Jonathon B; Lossos, Izidore S; Kahl, Brad S; Sehn, Laurie H; Smedby, Karin E; Salles, Gilles; Trneny, Marek; Link, Brian K; Morschhauser, Franck; Cerhan, James R

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

Epitope-focused discovery of SARS-CoV-2 antibodies that potently neutralize Omicron variants.

以表位为导向发现能有效中和 Omicron 变体的 SARS-CoV-2 抗体。

Zost Seth J, Suryadevara Naveenchandra, Williamson Lauren E, Scheaffer Suzanne M, Binshtein Elad, Buchman Cameron D, Johnson Nicole V, Catanzaro Nicholas J, Ravera Silvia, Chapman Nathaniel S, Myers Luke, Ramamohan Ajit R, Handal Laura S, Nguyen Doan C, Trivette Andrew, Martinez James R, Villalobos Eduardo, Rutherford Stacey A, Eun-Hyung Lee F, Schäfer Alexandra, Baric Ralph S, McLellan Jason S, Diamond Michael S, Carnahan Robert H, Crowe James E Jr

National and State Societal Costs of Schizophrenia in the US in 2024

2024年美国精神分裂症的国家和州社会成本

Krasa, Holly B; Baumgardner, James R; Brewer, Iris P; Chou, Jacquelyn W; Flottemesch, Thomas; Markowitz, Jessica T; Williams, Cory; Nagendra, Arundati

Balancing land use for conservation, agriculture, and renewable energy

平衡土地利用,兼顾保护、农业和可再生能源

Brock, Cameryn; Roehrdanz, Patrick R; Beringer, Tim; Chaplin-Kramer, Rebecca; Enquist, Brian J; Frazier, Amy E; Johnson, Justin A; Kennedy, Christina M; Kiesecker, Joseph; Larsen, Ashley E; Loyola, Rafael; Marquet, Pablo A; Neugarten, Rachel A; Oakleaf, James R; Roopsind, Anand; Schuster, Richard; Williams, David R; Wu, Grace C; Zvoleff, Alex; Hannah, Lee

Design-driven optimization of low-cost reagent formulations for reproducible and high-yielding cell-free gene expression

以设计为导向,优化低成本试剂配方,实现可重复且高产的无细胞基因表达

Olsen, Meagan L; Copeland, Caroline E; Sundberg, Chad A; Aw, Rochelle; Shaver, Zachary M; Rao, Govind; Swartz, James R; Karim, Ashty S; Jewett, Michael C

De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders

剪接因子基因SF3B1的新生变异与神经发育障碍相关。

Uguen, Kevin; Bergot, Tiffany; Scott-Boyer, Marie-Pier; Chapalain, Solène; Desdouets, Camille; Commet, Séverine; Zhu, Changlian; Xu, Yiran; Wang, Yangong; Roscioli, Tony; Tran-Mau-Them, Frederic; Faivre, Laurence; Maraval, Julien; Delanne, Julian; Denommé-Pichon, Anne-Sophie; Vitobello, Antonio; Jost, Céline; Planes, Marc; Hiatt, Susan; Wheeler, Patricia; Gonzaga-Jauregui, Claudia; Wang, Heng; Xin, Baozhong; Sency, Valerie; Kruer, Michael C; Bakhtiari, Somayeh; Sulem, Patrick; Curry, Cynthia; Prescott, Trine; Strobl-Wildemann, Gertrud; Brunet, Theresa; Doco Fenzy, Martine; Courtin, Thomas; Poirsier, Céline; Bjørg Hammer, Trine; Fenger, Christina D; MacPherson, Melissa; Izumi, Kosuke; Leonard, Jacqueline; Li, Dong; Zackai, Elaine H; Glass, Ian A; Ward, Scott; Campeau, Philippe M; Borroto, Maria Carla Hermida; Le Moigno, Laurence; Van Esch, Hilde; De Waele, Liesbeth; Calame, Daniel G; Lupski, James R; Barcia, Giulia; Peduto, Cristina; Planté-Bordeneuve, Pauline; Dupuis, Lucie; Mendoza-Londono, Roberto; Stavropoulos, Dimitri J; Gillibert-Duplantier, Jennifer; Besnard, Thomas; Do Souto Ferreira, Laura; Cogné, Benjamin; Bézieau, Stéphane; Droit, Arnaud; Corcos, Laurent; Lippert, Eric; Férec, Claude; Küry, Sebastien; Bernard, Delphine G

Sequential transcriptional waves and NF-κB-driven chromatin remodeling direct drug-induced dedifferentiation in cancer.

连续的转录波和 NF-κB 驱动的染色质重塑直接导致药物诱导的癌症去分化。

Su Yapeng, Liu Chunmei, Lu Xiang, Chuang Hui-Yu, Li Guideng, Shao Shiqun, Kong Yan, Lee Jihoon W, Ng Rachel H, Wong Stephanie, Robert Lidia, Warden Charles, Liu Victoria, Chen Jie, Wang Zhuo, Qin Guangrong, Tang Yin, Cheng Hanjun, Ng Alphonsus H C, Chen Daniel, Peng Songming, Xue Min, Johnson Dazy, Xu Yu, Wang Jinhui, Wu Xiwei, Shmulevich Ilya, Shi Qihui, Levine Raphael, Ribas Antoni, Baltimore David, Guo Jun, Heath James R, Wei Wei