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

Integrase anchors viral RNA to the HIV-1 capsid interior

整合酶将病毒RNA锚定到HIV-1衣壳内部

Singer, Matthew R; Li, Zhen; Rey, Juan S; Hope, Joshua; Chenavier, Florian; Cook, Nicola J; Punch, Emma; Smith, Jamie; Zhou, Zhiyu; Maslen, Sarah; Masino, Laura; Nans, Andrea; Skehel, Mark; Taylor, Ian A; Zanetti, Giulia; Zhang, Peijun; Perilla, Juan R; Engelman, Alan N; Cherepanov, Peter

Ancestry and somatic profile indicate acral melanoma origin and prognosis

祖先和体细胞特征提示肢端黑色素瘤的起源和预后

Basurto-Lozada, Patricia; Vázquez-Cruz, Martha Estefania; Molina-Aguilar, Christian; Jiang, Amanda; Deacon, Dekker C; Cerrato-Izaguirre, Dennis; Simonin-Wilmer, Irving; Arriaga-González, Fernanda G; Contreras-Ramírez, Kenya L; Ferro-Rodríguez, Emiliano; Billington, Jamie; Dawson, Eric T; Wong-Ramirez, J Rene C; Ramos-Galguera, Johana Itzel; Álvarez-Cano, Alethia; García-Ortega, Dorian Y; García-Salinas, O Isaac; Hidalgo-Miranda, Alfredo; Cisneros-Villanueva, Mireya; Johansson, Peter A; Martínez-Said, Héctor; Gallego-García, Pilar; Arends, Mark J; Ferreira, Ingrid; Tullett, Mark; Olvera-León, Rebeca; van der Weyden, Louise; Del Castillo Velasco-Herrera, Martín; Roldán-Marín, Rodrigo; Vidaurri de la Cruz, Helena; Tavares-de-la-Paz, Luis Alberto; Hinojosa-Ugarte, Diego; Belote, Rachel L; Bishop, D Timothy; Díaz-Gay, Marcos; Alexandrov, Ludmil B; Sánchez-Pérez, Yesennia; In, Gino K; White, Richard M; Possik, Patrícia A; Judson-Torres, Robert L; Adams, David J; Robles-Espinoza, Carla Daniela

The oncogenome of the domestic cat

家猫的癌基因组

Francis, Bailey A; Ludwig, Latasha; He, Chang; Dobromylskyj, Melanie; Bertram, Christof A; Aupperle-Lellbach, Heike; Wong, Hannah; Foster, Aiden P; Arends, Mark J; Suárez-Bonnet, Alejandro; Priestnall, Simon L; Tatiersky, Laetitia; Castillo-Alcala, Fernanda; Rupp, Angie; Khachadoorian, Arlene; Parlak, Eda; Inglebert, Marine; Umamaheswaran, Shevaniee; Cheema, Saamin; Del Castillo Velasco-Herrera, Martin; Wong, Kim; Vermes, Ian C; Billington, Jamie; Rottenberg, Sven; Wood, Geoffrey A; Adams, David J; van der Weyden, Louise

Reply to: "NeoADAURA: Can We Afford to Overlook Objective Response Rates?" and "Is Major Pathologic Response the Best Surrogate End Point for Neoadjuvant Trials?"

回复:“NeoADAURA:我们能否忽视客观缓解率?”以及“主要病理缓解是新辅助治疗试验的最佳替代终点吗?”

Chaft, Jamie E; Tsuboi, Masahiro; Weder, Walter

Targeted delivery of genome editors in vivo

体内靶向递送基因组编辑工具

Ngo, Wayne; Wu, Jamie L Y; Wasko, Kevin M; Doudna, Jennifer A

Negative Selection Maintains Grossly Altered but Broadly Stable Karyotypes in Metastatic Colorectal Cancer

负选择维持转移性结直肠癌中显著改变但总体稳定的核型

Cross, William C H; Nowinski, Salpie; Cresswell, George D; Mossner, Maximilian; Banerjee, Abhirup; Lu, Bingxin; Williams, Marc J; Vlachogiannis, Georgios; Gay, Laura J; Baker, Ann-Marie; Kimberley, Christopher; Whiting, Frederick J H; Belnoue-Davis, Hayley L; Martinez, Pierre; Traki, Maria; Walther, Viola; Smith, Kane; Fernandez-Mateos, Javier; Yara-Romero, Erika; Oliveira, Erica A; Milite, Salvatore; Caravagna, Giulio; James, Chela T; Elia, George; Berner, Alison; Ryan Choi, Chang-Ho; Ramagiri, Pradeep; Chauhan, Ritika; Matthews, Nik; Murphy, Jamie; Antoniou, Anthony; Clark, Susan K; Mitchison, Miriam; Chin Aleong, Jo-Anne; Domingo, Enric; Spiteri, Inmaculada; McDonald, Stuart A C; Shibata, Darryl; Laclé, Miangela M; Wang, Lai Mun; Moorghen, Morgan; Tomlinson, Ian P M; Novelli, Marco; Jansen, Marnix; Watson, Alan; Valeri, Nicola; Wright, Nicholas A; Bridgewater, John A; Rodriguez-Justo, Manuel; Barnes, Chris P; Kocher, Hemant M; Leedham, Simon J; Sottoriva, Andrea; Graham, Trevor A

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

U4 和 U6 snRNA 基因的新生突变和遗传性显性突变会导致视网膜色素变性。

Quinodoz, Mathieu; Rodenburg, Kim; Cvackova, Zuzana; Kaminska, Karolina; de Bruijn, Suzanne E; Iglesias-Romero, Ana Belén; Boonen, Erica G M; Ullah, Mukhtar; Zomer, Nick; Folcher, Marc; Bijon, Jacques; Holtes, Lara K; Tsang, Stephen H; Corradi, Zelia; Freund, K Bailey; Shliaga, Stefanida; Panneman, Daan M; Hitti-Malin, Rebekkah J; Ali, Manir; AlTalbishi, Ala'a; Andréasson, Sten; Ansari, Georg; Arno, Gavin; Astuti, Galuh D N; Ayuso, Carmen; Ayyagari, Radha; Banfi, Sandro; Banin, Eyal; Barakat, Tahsin Stefan; Barboni, Mirella T S; Bauwens, Miriam; Ben-Yosef, Tamar; Bernard, Virginie; Birch, David G; Biswas, Pooja; Blanco-Kelly, Fiona; Bocquet, Beatrice; Boon, Camiel J F; Branham, Kari; Bremond-Gignac, Dominique; Britten-Jones, Alexis Ceecee; Bujakowska, Kinga M; Burin des Roziers, Cyril; Cadena, Elizabeth L; Calzetti, Giacomo; Cancellieri, Francesca; Cattaneo, Luca; Chadderton, Naomi; Charbel Issa, Peter; Coutinho-Santos, Luísa; Daiger, Stephen P; De Baere, Elfride; De Bruyne, Marieke; de la Cerda, Berta; De Roach, John N; De Zaeytijd, Julie; Derks, Ronny; Dhaenens, Claire-Marie; Dudakova, Lubica; Duncan, Jacque L; Farrar, G Jane; Feltgen, Nicolas; Fenner, Beau J; Fernández-Caballero, Lidia; Ferraz Sallum, Juliana M; Gana, Simone; Garanto, Alejandro; Gardner, Jessica C; Gilissen, Christian; Gonzàlez-Duarte, Roser; Goto, Kensuke; Griffiths-Jones, Sam; Haack, Tobias B; Haer-Wigman, Lonneke; Hardcastle, Alison J; Hayashi, Takaaki; Héon, Elise; Hoefsloot, Lies H; Hoischen, Alexander; Holtan, Josephine P; Hoyng, Carel B; Ibanez, Manuel Benjamin B 4th; Inglehearn, Chris F; Iwata, Takeshi; Jensson, Brynjar O; Jones, Kaylie; Kalatzis, Vasiliki; Kamakari, Smaragda; Karali, Marianthi; Kellner, Ulrich; Klaver, Caroline C W; Knézy, Krisztina; Koenekoop, Robert K; Kohl, Susanne; Kominami, Taro; Kühlewein, Laura; Lamey, Tina M; Leibu, Rina; Leroy, Bart P; Liskova, Petra; Lopez, Irma; López-Rodríguez, Victor R de J; Mahieu, Quinten; Mahroo, Omar A; Manes, Gaël; Mansard, Luke; Martín-Gutiérrez, M Pilar; Martins, Nelson; Mauring, Laura; McKibbin, Martin; McLaren, Terri L; Meunier, Isabelle; Michaelides, Michel; Millán, José M; Mizobuchi, Kei; Mukherjee, Rajarshi; Nagy, Zoltán Zsolt; Neveling, Kornelia; Ołdak, Monika; Oorsprong, Michiel; Pan, Yang; Papachristou, Anastasia; Percesepe, Antonio; Pfau, Maximilian; Pierce, Eric A; Place, Emily; Ramesar, Raj; Ramond, Francis; Rasquin, Florence Andrée; Rice, Gillian I; Roberts, Lisa; Rodríguez-Hidalgo, María; Ruiz-Ederra, Javier; Sabir, Ataf H; Sajiki, Ai Fujita; Sánchez-Barbero, Ana Isabel; Sarma, Asodu Sandeep; Sangermano, Riccardo; Santos, Cristina M; Scarpato, Margherita; Scholl, Hendrik P N; Sharon, Dror; Signorini, Sabrina G; Simonelli, Francesca; Sousa, Ana Berta; Stefaniotou, Maria; Stefansson, Kari; Stingl, Katarina; Suga, Akiko; Sulem, Patrick; Sullivan, Lori S; Szabó, Viktória; Szaflik, Jacek P; Taurina, Gita; Thiadens, Alberta A H J; Toomes, Carmel; Tran, Viet H; Tsilimbaris, Miltiadis K; Tsoka, Pavlina; Vaclavik, Veronika; Vajter, Marie; Valeina, Sandra; Valente, Enza Maria; Valentine, Casey; Valero, Rebeca; Valleix, Sophie; van Aerschot, Joseph; van den Born, L Ingeborgh; Van Heetvelde, Mattias; Verhoeven, Virginie J M; Vincent, Andrea L; Webster, Andrew R; Whelan, Laura; Wissinger, Bernd; Yioti, Georgia G; Yoshitake, Kazutoshi; Zenteno, Juan C; Zeuli, Roberta; Zuleger, Theresia; Landau, Chaim; Jacob, Allan I; Lin, Siying; Cremers, Frans P M; Lee, Winston; Ellingford, Jamie M; Stanek, David; Roosing, Susanne; Rivolta, Carlo

Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy

RNU2-2基因的双等位基因变异会导致一种非常常见的发育性和癫痫性脑病。

Jackson, Adam; Blakes, Alexander J M; Alhaddad, Bader; Henry, Olivia J; Delgado-Vega, Angelica M; Wall, Elizabeth; Abdelhadi, Ola; Agrawal, Shakti; Bakur, Khadijah; Blair, Edward; Brady, Angela F; Brittain, Helen; Chandler, Kate E; Clarke, Natasha; Danelli, Miriana; Drinkall, Nicholas; Duba, Irene; Elmslie, Frances; Ellingford, Jamie; Ewans, Lisa J; Fennell, Andrew P; Gazdagh, Gabriella; Heller, Simon P; Hammarsjö, Anna; Karrman, Kristina; Kini, Usha; Lesko, Nicole; Lindstrand, Anna; Macintosh, Rebecca; Mansour, Sahar; Menzies, Lara; Metcalfe, Kay; Milhench, Alison; Nashef, Lina; O'Keefe, Raymond T; Pacheco, Nadja Pekkola; Palmer, Elizabeth E; Parida, Amitav; Prescott, Katrina; Redman, Melody; Renieri, Alessandra; Fallerini, Chiara; Rizzo, Caterina Lo; Sachdev, Rani; Simons, Cas; Sisodiya, Sanjay M; Stewart, Helen; Stödberg, Tommy; Banos-Pinero, Benito; Taylan, Fulya; Thomas, Huw B; Tinella, Flavia; Wiafe, Samuel; Wedell, Anna; Whiffin, Nicola; Walker, Susan; Rius, Rocio; Chae, Jong Hee; Nordgren, Ann; Alkuraya, Fowzan; Lord, Jenny; Banka, Siddharth

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

Red Blood Cell Exchange Transfusion for Severe Babesiosis

重症巴贝虫病的红细胞置换输血

Leaf, David E; Monson, Audrey E; Dias, Julie-Alexia; Marcos, Luis A; Wu, Ulysses; Rossi, Michael; Ng, Jia H; Patell, Rushad; Hundert, Joshua; El Khoury, Marc Y; Higgs, James; Smith, Robert P; Ramsaroop, Vishali; Green, Adam; Abdul Azim, Ahmed; Weisenberg, Scott; Kirkman, Laura A; Ingram, David; Hsu, Caroline M; Dieckhaus, Kevin; Hyson, Peter; Burger, Zoe; Chengsupanimit, Tayoot; Stalmack, Tammy; Aber, Rachel; Golden, Marjorie; Koshy, Maria; Wright, Kendall; Cortezzo, Grace; McLeod, Gavin; Wenzel-Rideout, Rebecca; Baigorri, Julio Javier; Bagchi, Aranya; Jaser, Ahmad; Socorro Matos, Guillermo; Sanchez-Almanzar, Daniel; Hoge, Steven T; Shenoy, Tushar; Krishnamurthy, Shobana; Kaunfer, Sarah A; Blau, Jack A; Woolley, Ann; Zamor, Rudline; Maczaj, Brigitte; Kenison, David; Totten, Arthur; Bateman, Victoria; Mohsin, Sabrina; Lee, Eun Sun; Garner, Joseph; Rath, Payal; Wu, Quinlan; Guermazi, Dorra; London, Abby; Arvanitis, Panos; Yune, Philip S; Abdullah, Mahie; Kim, Angela; Roy, Juby; George, Reshma; Kashfi, Simon; Hong, Susana; Upadrista, Pratap; Hirsch, Jamie S; Bulteel, Alexander; Sharma, Riya; Guo, Tina; Garcia, Daniela; Shaefi, Shahzad; Yeb, Joseph; Williams, George; Verma, Eesha; Gouda, Nourelhoda; Rosenthal, Hannah R; Chan, Angelica; Zainah, Hadeel; Heithaus, Seth; Saldivar, Miguel A; Wood, Emily; DiPalazzo, John; Elias, Susan; McAuliffe, Matthew; Abbas, Ramsha; Orenstein, Abigail; Tidswell, Mark A; Galiano, Peter; Spencer, Sanjae; Srinivasan, Sidharth; Xu, Joyce; Alla, Sivani; Alidoost, Leila; Jacobson, Eliana; Menghani, Sanjay V; Kannabran, Priyanka; Ogunribido, Deborah B; Ssentongo, Paddy; Powell, Debra; Meyer, Leah; Prabhune, Kshitij; Griffiths, Bianca; Gonzalez Aponte, Daphne; Dixon, Graham; Vannier, Edouard; Roberts, Scott C; Farmakiotis, Dimitrios; Krause, Peter J