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

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

Antigen-specific activation of gut immune cells drives autoimmune neuroinflammation

肠道免疫细胞的抗原特异性激活驱动自身免疫性神经炎症

Siewert, Lena K; Berve, Kristina; Pössnecker, Elisabeth; Dyckow, Julia; Zulji, Amel; Baumann, Ryan; Munoz-Blazquez, Aida; Krishnamoorthy, Gurumoorthy; Schreiner, David; Sagan, Sharon; Nelson, Charlotte; Sabatino, Joseph J Jr; Nagashima, Kazuki; Diard, Médéric; J Macpherson, Andrew; Ganal-Vonarburg, Stephanie C; Fischbach, Michael A; Zamvil, Scott S; Schirmer, Lucas; Baranzini, Sergio E; Pröbstel, Anne-Katrin

Missense variants in DPYSL5 associated with neurodevelopmental disorders and brain malformations cause impaired neuronal maturation in vitro

DPYSL5基因中的错义变异与神经发育障碍和脑畸形相关,会导致体外神经元成熟受损。

Desprez, Florence; Remize, Solène; François-Moutal, Liberty; Ung, Dévina C; Dangoumau, Audrey; Marouillat, Sylviane; Kennedy, Joanna; Low, Karen J; Kumps, Camille; Unger, Sheila; Keren, Boris; de Sainte Agathe, Jean-Madeleine; Poirsier, Céline; Mirzaa, Ghayda M; Aldinger, Kimberly A; Lesca, Gaetan; Ruault, Valentin; Finnila, Candice R; Kelley, Whitley V; Latner, Donald R; Guptha, Sushma N; Tuttle, Annabelle; Glass, Ian; Chung, Wendy K; Hayek, Jennifer Cassady; Boute, Odile; Moutal, Aubin; Jeanne, Médéric; Laumonnier, Frédéric

Feasibility of Very High Cumulative Equivalent Dose in 2 Gy Fraction in Locally Advanced Central/Ultracentral Nonsmall Cell Lung Cancer Treated With Conventional Chemoradiation Therapy and a Stereotactic Boost

在采用常规放化疗联合立体定向增强治疗的局部晚期中央型/超中央型非小细胞肺癌中,2 Gy分割剂量下极高累积等效剂量的可行性研究

Gueiderikh, Anna; Lhomel, Baptiste; Schiappa, Renaud; Barret, Médéric; Ferrari, Victoria; Naghavi, Arash O; Chanoux, Bastien; Bondiau, Pierre-Yves; Doyen, Jérôme

Democratizing high-Q plasmonic optical fiber biosensing with low-resolution interrogation and Fourier demodulation

利用低分辨率检测和傅里叶解调技术普及高品质因子等离子体光纤生物传感技术

Fasseaux, Hadrien; Loyez, Médéric; Caucheteur, Christophe

Dual-Mode Comb Plasmonic Optical Fiber Sensing

双模梳状等离子体光纤传感

Villatoro, Efraín; Loyez, Médéric; Villatoro, Joel; Caucheteur, Christophe; Albert, Jacques

Detection of NT-proBNP Using Optical Fiber Back-Reflection Plasmonic Biosensors

利用光纤背反射等离子体生物传感器检测NT-proBNP

Assunção, Ana Sofia; Vidal, Miguel; Martins, Maria João; Girão, Ana Violeta; Loyez, Médéric; Caucheteur, Christophe; Mesquita-Bastos, José; Costa, Florinda M; Pereira, Sónia O; Leitão, Cátia

Machine learning unveils surface refractive index dynamics in comb-like plasmonic optical fiber biosensors

机器学习揭示梳状等离子体光纤生物传感器的表面折射率动态变化

Chernyadiev, Alexander V; But, Dmytro B; Ivonyak, Yurii; Ikamas, Kęstutis; Lisauskas, Alvydas; Fasseaux, Hadrien; Loyez, Médéric; Caucheteur, Christophe

Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism

ATP1A1基因的复发性变异Gly903Arg会导致发育迟缓、智力障碍和自闭症。

Dohrn, Maike F; Bademci, Guney; Rebelo, Adriana P; Jeanne, Médéric; Borja, Nicholas A; Beijer, Danique; Danzi, Matt C; Bivona, Stephanie A; Gueguen, Paul; Zafeer, Mohammad F; Tekin, Mustafa; Züchner, Stephan

A Child with a Congenital Aplasia of the Scalp: A Quiz

患有先天性头皮发育不全的儿童:小测验

Dours, Louis; Jeanne, Médéric; Srour, Maya; Leducq, Sophie