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

Correction: Vol. 32, No. 1

更正:第32卷,第1期

Uraki, Ryuta; Halfmann, Peter J; Iida, Shun; Yamayoshi, Seiya; Furusawa, Yuri; Kiso, Maki; Ito, Mutsumi; Iwatsuki-Horimoto, Kiyoko; Mine, Sohtaro; Kuroda, Makoto; Maemura, Tadashi; Sakai-Tagawa, Yuko; Ueki, Hiroshi; Li, Rong; Liu, Yanan; Larson, Deanna; Fukushi, Shuetsu; Watanabe, Shinji; Maeda, Ken; Pekosz, Andrew; Kandeil, Ahmed; Webby, Richard J; Wang, Zhongde; Imai, Masaki; Suzuki, Tadaki; Kawaoka, Yoshihiro; Mohan, Shaan; Khan, Ahmad; Chorba, Terence

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

Childhood brain tumors instruct cranial hematopoiesis and immunotolerance.

儿童脑肿瘤会影响颅内造血和免疫耐受。

Cooper Elizabeth, Posner David A, Lee Colin Y C, Hu Linda, Bonner Sigourney, Taylor Jessica T, Baldwin Oscar, Jimenez-Guerrero Rocio, Masih Katherine E, Rahrmann Katherine Wickham, Eigenbrood Jason, Ngo Gina, Franklin Valar Nila Roamio, D'Santos Clive S, Mair Richard, Santarius Thomas, Craven Claudia, Jalloh Ibrahim, Moreno Vicente Julia, Halim Timotheus Y F, Wang Li, Kreigstien Arnold R, Wainwright Brandon, Swartling Fredrik J, Khan Javed, Clatworthy Menna R, Gilbertson Richard J

Investigation of a global mouse methylome atlas reveals subtype-specific copy number alterations in pediatric cancer models.

对全球小鼠甲基化组图谱的研究揭示了儿童癌症模型中亚型特异性拷贝数改变。

Schoof Melanie, Zheng Tuyu, Sill Martin, Imle Roland, Cais Alessia, Altendorf Lea, Fürst Alicia, Hofmann Nina, Ernst Kati, Vonficht Dominik, Chan Kenneth Chun-Ho, Holland-Letz Tim, Postlmayr Andreas, Shiraishi Ryo, Wang Wanchen, Morcavallo Alaide, Spohn Michael, Göbel Carolin, Niesen Judith, Peter Levke-Sophie, Bourdeaut Franck, Han Zhi-Yan, Pei Yanxin, Murad Najiba, Swartling Fredrik J, Taylor Jessica, Yadav Monika, Gibson Garrett R, Gilbertson Richard J, Dottermusch Matthias, Roy Rajanya, Kerl Kornelius, Glass Rainer, Cheng Jiying, Horstmann Martin A, Wolters-Eisfeld Gerrit, Zhao Haotian, Sturm Dominik, Yadav Viveka Nand, Chesler Louis, Haas Simon, Weiss William A, Northcott Paul A, Kutscher Lena M, Guerreiro Stucklin Ana, Ayrault Olivier, Neumann Julia E, Kawauchi Daisuke, Jones David T W, Pajtler Kristian, Banito Ana, Pfister Stefan M, Schüller Ulrich, Zuckermann Marc

Brain Volumes After Hypertensive Pregnancy and Postpartum Blood Pressure Management: A POP-HT Randomized Clinical Trial Imaging Substudy

妊娠期高血压及产后血压管理后脑容量的变化:一项 POP-HT 随机临床试验影像学子研究

Lapidaire, Winok; Kitt, Jamie; Krasner, Samuel; Bateman, Paul A; Cutler, Hannah R; Barr, Logan; Frost, Annabelle; Tucker, Katherine; Suriano, Katie; Kenworthy, Yvonne; Milner, George; Lacharie, Miriam; Mills, Rebecca; Roman, Cristian; Mackillop, Lucy; Aye, Christina; Cairns, Alexandra; Thilaganathan, Basky; Chappell, Lucy C; Lewandowski, Adam J; McManus, Richard J; Leeson, Paul

Organ Preservation for Nasal Cavity Cancers Using Definitive Radiotherapy for Avoiding Rhinectomy

利用根治性放射疗法治疗鼻腔癌,避免鼻切除术,实现器官保留

Mankuzhy, Nikhil P; Yang, Fan; Boe, Lillian A; Gui, Chengcheng; Wu, Yingzhi; Riaz, Nadeem; Yu, Yao; McBride, Sean M; Shamseddine, Achraf; Shim, Andy; Mah, Dennis; Dunn, Lara A; Michel, Loren S; Pfister, David G; Sherman, Eric J; Ganly, Ian; Cracchiolo, Jennifer R; Patel, Snehal G; Wong, Richard J; Cohen, Marc A; Lee, Nancy Y

Adaptor-mediated recruitment of three dyneins to dynactin enhances force generation.

衔接蛋白介导的三种动力蛋白向动力蛋白激活蛋白的募集增强了力的产生。

Rao Lu, Liu Xinglei, Arnold Mirjam, Okada Kyoko, McKenney Richard J, Stengel Kristy, Sidoli Simone, Berger Florian, Gennerich Arne

C5aR1 Inhibition Alleviates Cranial Radiation-Induced Cognitive Decline.

C5aR1抑制可缓解颅脑放射引起的认知能力下降。

Krattli Robert P Jr, Do An H, El-Khatib Sanad M, Alikhani Leila, Markarian Mineh, Vagadia Arya R, Usmani Manal T, Madan Shreya, Baulch Janet E, Clark Richard J, Woodruff Trent M, Tenner Andrea J, Acharya Munjal M

Rational design and in vivo validation of capsid inhibitors for enterovirus D68.

肠道病毒D68衣壳抑制剂的合理设计及体内验证。

Li Kan, Rudy Michael J, Klose Thomas, Tan Haozhou, Wu Xiangmeng, Demssie Hiwot A, Anderson Jacqueline S, Jadhav Prakash, Zhang Qing-Yu, Clarke Penny, Kuhn Richard J, Tyler Kenneth L, Wang Jun

ATRX loss couples genome instability at a G-rich repeat to dysregulation of human alpha-globin expression.

ATRX 的缺失导致富含 G 的重复序列处的基因组不稳定性与人类 α-珠蛋白表达失调有关。

Shen Yuqi, Gupta Kinam, Tan-Wong Sue Mei, Wen Sean, Fisher Christopher A, Tamon Liezel, Proudfoot Nicholas J, Gibbons Richard J, Higgs Douglas R