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

Robust cytoplasmic partitioning by solving a cytoskeletal instability.

通过解决细胞骨架不稳定性问题,实现稳健的细胞质分配。

Rinaldin Melissa, Kickuth Alison, Lamson Adam, Dalton Benjamin, Xu Yitong, Mejstřík Pavel, Di Talia Stefano, Brugués Jan

Rapid directed evolution guided by protein language models and epistatic interactions

蛋白质语言模型和上位性相互作用指导下的快速定向进化

Tran, Vincent Q; Nemeth, Matthew; Bartie, Liam J; Chandrasekaran, Sita S; Fanton, Alison; Moon, Hyungseok C; Hie, Brian L; Konermann, Silvana; Hsu, Patrick D

Vitamin B2 and B3 nutrigenomics reveals a therapy for NAXD disease.

维生素 B2 和 B3 营养基因组学揭示了 NAXD 疾病的治疗方法。

Garg Ankur, Blume Skyler Y, Huynh Helen, Barrios Alec M, Karabulut Onurkan O, Zhao Qian, Midha Ayush D, Turner Adam W, Resnick B Vittorio, Chen Xuewen, Agrawal Ayushi, Kim JaeYeon, Chen Liuji, Ran Qitao, Ryan Alison M, Larson Reece C, Negahban Mina, Nelson Sophia C K, Yang Andrew C, Traglia Michela, Thomas Reuben, Sun Ramon, Paredes Mercedes, Corces M Ryan, Lin Hening, Jain Isha H

CD47 blockade-driven necroptosis complements BCL-2 inhibition-driven apoptosis in lymphoid malignancies.

CD47阻断驱动的坏死性凋亡可与BCL-2抑制驱动的淋巴恶性肿瘤细胞凋亡相辅相成。

Chong Stephen J F, Valentin Rebecca, Wang Jing, Zhu Fen, Gokhale Prafulla C, Eschle Benjamin K, Garbicz Filip, Iskandar Kartini, Sewastianik Tomasz, Toh Brienne C Y, Penailillo Johany, Peluso Marisa O, Zhang Jeremy, Hackett Liam, Collins Mary C, Lehmberg Timothy Z, Adam Ammar, Zhang Li, Armet Caroline M, Rausch Matthew, Lee Benjamin H, Holland Pamela M, Palombella Vito J, Paterson Alison M, Kong Li Ren, Ten Hacken Elisa, Guerriero Jennifer L, Herbaux Charles, Wu Catherine J, Chng Wee Joo, Pervaiz Shazib, Niemann Carsten U, Carrasco Ruben D, Davids Matthew S

Exercise blood pressure relative to fitness and cardiovascular outcomes: the EXERTION study

运动血压与体能和心血管结局的关系:EXERTION 研究

Schultz, Martin G; Otahal, Petr; Roberts-Thomson, Philip; Stanton, Tony; Hamilton-Craig, Christian; Wahi, Sudhir; La Gerche, Andre; Hare, James L; Selvanayagam, Joseph; Maiorana, Andrew; Venn, Alison J; Marwick, Thomas H; Sharman, James E

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

Glutamate indicators with increased sensitivity and tailored deactivation rates

具有更高灵敏度和定制失活速率的谷氨酸指示剂

Aggarwal, Abhi; Negrean, Adrian; Chen, Yang; Iyer, Rishyashring; Reep, Daniel; Liu, Anyi; Palutla, Anirudh; Xie, Michael E; MacLennan, Bryan J; Hagihara, Kenta M; Kinsey, Lucas W; Sun, Julianna L; Yao, Pantong; Zheng, Jihong; Tsang, Arthur; Tsegaye, Getahun; Zhang, Yonghai; Patel, Ronak H; Arthur, Benjamin J; Hiblot, Julien; Leippe, Philipp; Tarnawski, Miroslaw; Marvin, Jonathan S; Vevea, Jason D; Turaga, Srinivas C; Tebo, Alison G; Carandini, Matteo; Rossi, L Federico; Kleinfeld, David; Konnerth, Arthur; Svoboda, Karel; Turner, Glenn C; Hasseman, Jeremy P; Podgorski, Kaspar

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

Mutational scanning reveals oncogenic CTNNB1 mutations have diverse effects on signaling

突变扫描揭示致癌性CTNNB1突变对信号传导具有多种影响

Krishna, Anagha; Meynert, Alison; Dolt, Karamjit Singh; Kelder, Martijn; Mesropian, Agavni; Ewing, Ailith; Brouwers, Conny; Claassens, Jill Wc; Linssen, Margot M; Sheraz, Shahida; Taylor, Gillian Ca; Gautier, Philippe; Ferrer-Vaquer, Anna; Grimes, Graeme; Becher, Hannes; Silk, Ryan; Gris-Oliver, Albert; Pinyol, Roser; Semple, Colin A; Kendall, Timothy J; Bird, Thomas Graham; Hadjantonakis, Anna-Katerina; Marsh, Joseph A; Llovet, Josep M; Hohenstein, Peter; Wood, Andrew J; Ozdemir, Derya D

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