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

A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions

GOLGA8A基因的重复扩增是伴有泛素阳性包涵体的非典型额颞叶变性的主要风险因素。

De Coster, Wouter; Van den Broeck, Marleen; Baker, Matt; Ghayal, Nikhil B; Wynants, Sarah; Batzler, Anthony; Pottier, Cyril; Alidadiani, Sara; Küçükali, Fahri; Jenkins, Gregory D; Policarpo, Rafaela; van Blitterswijk, Marka; DeJesus-Hernandez, Mariely; Soto-Beasley, Alexandra I; Faura, Júlia; Coopman, Elise; Hutten, Saskia; Mol, Merel O; Wallon, David; Sieben, Anne; Finger, Elizabeth C; Murray, Melissa E; Forrest, Shelley L; Tartaglia, Maria C; Troakes, Claire; van Rooij, Jeroen G J; Nguyen, Aivi T; Reichard, R Ross; Woodman, Natalie L; Nana, Alissa L; Weintraub, Sandra; Gefen, Tamar; De Vil, Bart; Bodi, Istvan; Lopez, Oscar L; Boluda, Susana; Belliard, Serge; Lebert, Florence; Marguet, Florent; Mao, Qinwen; Mesulam, Marsel M; Boxer, Adam L; Vandenbulcke, Mathieu; Suh, EunRan; Schaeverbeke, Jolien; Lambert, Jean-Charles; Scholz, Sonja W; Dalgard, Clifton L; Traynor, Bryan J; Gibbs, Raphael J; Schellenberg, Gerard D; Dormann, Dorothee; Joris, Geert; De Pooter, Tim; De Rijk, Peter; D'Hert, Svenn; Van Dongen, Jasper; van der Zee, Julie; Strazisar, Mojca; Gearing, Marla; Kukar, Thomas; Flanagan, Margaret; Engelborghs, Sebastiaan; Ghetti, Bernardino; Newell, Kathy L; King, Andrew; Roeber, Sigrun; Rosen, Howard J; Spina, Salvatore; Cras, Patrick; Ertekin-Taner, Nilüfer; Wszolek, Zbigniew K; Uitti, Ryan J; Cheshire, William P; Singer, Wolfgang; Herms, Jochen; Josephs, Keith A; Whitwell, Jennifer L; Petersen, Ronald C; Pasquier, Florence; Nicolas, Gaël; Castellani, Rudolph; Glass, Jonathan; Miller, Bruce L; Kovacs, Gabor G; Rissman, Robert A; Hiniker, Annie; Deramecourt, Vincent; Ang, Lee-Cyn; Lee-Way, Jin; Van Deerlin, Vivianna M; Dugger, Brittany N; Thal, Dietmar R; Grinberg, Lea T; Cruchaga, Carlos; Arzberger, Thomas; Munoz, David G; Keith, Julia; Zinman, Lorne; Rogaeva, Ekaterina; Lee, Edward B; Haggarty, Stephen J; Ansorge, Olaf; Husain, Masud; Halliday, Glenda M; Al-Sarraj, Safa; Ross, Owen A; Sleegers, Kristel; Vandenberghe, Rik; Boeve, Bradley F; Graff-Radford, Neill R; Kofler, Julia; White, Charles L 3rd; Lashley, Tammaryn; Neumann, Manuela; Biernacka, Joanna M; Seeley, William W; Seelaar, Harro; van Swieten, John C; Rohrer, Jonathan D; Dickson, Dennis W; Mackenzie, Ian R A; Rademakers, Rosa

Five-year outcomes of the early-generation Intrepid transapical transcatheter mitral valve replacement system

早期Intrepid经心尖导管二尖瓣置换系统的五年疗效

Tang, Gilbert H L; Rajagopal, Vivek; Sorajja, Paul; Bajwa, Tanvir; Gooley, Robert; Walton, Antony; Modine, Thomas; Ng, Martin K; Williams, Mathew R; Zajarias, Alan; Hildick-Smith, David; Tchétché, Didier; Spargias, Konstantinos; Rajani, Ronak; Bapat, Vinayak N; De Backer, Ole; Blackman, Daniel; McCarthy, Patrick; Laine, Mika; Jain, Renuka; Martin, Randolph; Thaden, Jeremy J; Marka, Nicholas A; Mack, Michael; Adams, David H; Leon, Martin B; Reardon, Michael J

Biodiversity and Biotechnological Potential of Dunaliella sp. Isolates from Kalloni Solar Saltworks (Lesvos, Greece)

来自卡洛尼太阳能盐场(希腊莱斯沃斯岛)的杜氏藻分离株的生物多样性和生物技术潜力

Petridi, Athina; Koletti, Aikaterini; Marka, Sofia; Zografaki, Maria-Eleftheria; Fouskari, Ioanna; Karavidas, Ioannis; Ntzouvaras, Alexandros; Tzovenis, Ioannis; Efrose, Rodica C; Flemetakis, Emmanouil; Tsirtsis, George; Kalloniati, Chrysanthi

Fluorescence tracking Treg movement identifies anti-CCR8 and radiation as a therapeutic combination.

荧光追踪 Treg 的运动表明抗 CCR8 和放射疗法是一种有效的联合治疗方案。

Friedman David J, Ramin Sina, Blair Tiffany, Kramer Gwen, Bambina Shelly, Alice Alejandro F, Baird Jason, Medler Terry, Young Kristina H, Crittenden Marka R, Gough Michael J

Proprotein convertase subtilisin/kexin type 9-CC-motif chemokine ligand 2 interactions link lipoprotein(a) composition to intermediate monocyte inflammation in coronary artery disease

前蛋白转化酶枯草杆菌蛋白酶/kexin 9型-CC基序趋化因子配体2相互作用将脂蛋白(a)组成与冠状动脉疾病中的中间单核细胞炎症联系起来

Ugovšek, Sabina; Rehberger Likozar, Andreja; Levstek, Tina; Trebušak Podkrajšek, Katarina; Zupan, Janja; Marka, Frieda; Trimmel, Tamara; Brekalo, Mira; Speidl, Walter; Hohensinner, Philipp; Haider, Patrick; Šebeštjen, Miran

Amyotrophic lateral sclerosis caused by hexanucleotide repeat expansions in C9orf72: from genetics to therapeutics

由C9orf72基因六核苷酸重复序列扩增引起的肌萎缩侧索硬化症:从遗传学到治疗学

Mizielinska, Sarah; Hautbergue, Guillaume M; Gendron, Tania F; van Blitterswijk, Marka; Hardiman, Orla; Ravits, John; Isaacs, Adrian M; Rademakers, Rosa

Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypes.

对具有 TDP-43 病理的 FTLD 患者进行甲基化组分析,可识别出病理亚型特有的表观遗传特征

Vicente Cristina T, Niranjan Tejasvi, Coopman Elise, Faura Júlia, Alidadiani Sara, Schrauwen Claudia, Matchett Billie J, Heeman Bavo, Van den Broeck Marleen, De Coster Wouter, Nguyen Thuy, Lau Julie S, Baheti Saurabh, de Pooter Tim, De Rijk Peter, Strazisar Mojca, Baker Matt, DeJesus-Hernandez Mariely, Finch NiCole A, Pottier Cyril, van Blitterswijk Marka, Asmann Yan, Murray Melissa E, Petrucelli Leonard, King Andrew, Troakes Claire, Al-Sarraj Safa, Rissman Robert A, Hiniker Annie, Flanagan Margaret, Evers Bret M, White Charles L 3rd, Cruchaga Carlos, Castellani Rudolph, van Rooij Jeroen G J, Mol Merel O, Seelaar Harro, van Swieten John C, Oskarsson Björn, Reichard Robert Ross, Nguyen Aivi T, Josephs Keith A, Petersen Ronald C, Ertekin-Taner Nilüfer, Boeve Bradley F, Graff-Radford Neill R, Weckhuysen Sarah, Dickson Dennis W, Rademakers Rosa

Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing

通过全基因组测序解析FTLD-TDP病理亚型的不同遗传风险因素

Pottier, Cyril; Küçükali, Fahri; Baker, Matt; Batzler, Anthony; Jenkins, Gregory D; van Blitterswijk, Marka; Vicente, Cristina T; De Coster, Wouter; Wynants, Sarah; Van de Walle, Pieter; Ross, Owen A; Murray, Melissa E; Faura, Júlia; Haggarty, Stephen J; van Rooij, Jeroen Gj; Mol, Merel O; Hsiung, Ging-Yuek R; Graff, Caroline; Öijerstedt, Linn; Neumann, Manuela; Asmann, Yan; McDonnell, Shannon K; Baheti, Saurabh; Josephs, Keith A; Whitwell, Jennifer L; Bieniek, Kevin F; Forsberg, Leah; Heuer, Hilary; Lago, Argentina Lario; Geier, Ethan G; Yokoyama, Jennifer S; Oddi, Alexis P; Flanagan, Margaret; Mao, Qinwen; Hodges, John R; Kwok, John B; Domoto-Reilly, Kimiko; Synofzik, Matthis; Wilke, Carlo; Onyike, Chiadi; Dickerson, Bradford C; Evers, Bret M; Dugger, Brittany N; Munoz, David G; Keith, Julia; Zinman, Lorne; Rogaeva, Ekaterina; Suh, EunRan; Gefen, Tamar; Geula, Changiz; Weintraub, Sandra; Diehl-Schmid, Janine; Farlow, Martin R; Edbauer, Dieter; Woodruff, Bryan K; Caselli, Richard J; Donker Kaat, Laura L; Huey, Edward D; Reiman, Eric M; Mead, Simon; King, Andrew; Roeber, Sigrun; Nana, Alissa L; Ertekin-Taner, Nilufer; Knopman, David S; Petersen, Ronald C; Petrucelli, Leonard; Uitti, Ryan J; Wszolek, Zbigniew K; Ramos, Eliana Marisa; Grinberg, Lea T; Tempini, Maria Luisa Gorno; Rosen, Howard J; Spina, Salvatore; Piguet, Olivier; Grossman, Murray; Trojanowski, John Q; Keene, C Dirk; Jin, Lee-Way; Prudlo, Johannes; Geschwind, Daniel H; Rissman, Robert A; Cruchaga, Carlos; Ghetti, Bernardino; Halliday, Glenda M; Beach, Thomas G; Serrano, Geidy E; Arzberger, Thomas; Herms, Jochen; Boxer, Adam L; Honig, Lawrence S; Vonsattel, Jean P; Lopez, Oscar L; Kofler, Julia; White, Charles L 3rd; Gearing, Marla; Glass, Jonathan; Rohrer, Jonathan D; Irwin, David J; Lee, Edward B; Van Deerlin, Vivianna; Castellani, Rudolph; Mesulam, Marsel M; Tartaglia, Maria C; Finger, Elizabeth C; Troakes, Claire; Al-Sarraj, Safa; Dalgard, Clifton L; Miller, Bruce L; Seelaar, Harro; Graff-Radford, Neill R; Boeve, Bradley F; Mackenzie, Ian Ra; van Swieten, John C; Seeley, William W; Sleegers, Kristel; Dickson, Dennis W; Biernacka, Joanna M; Rademakers, Rosa

Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases

多种运动神经元疾病中超罕见基因变异的共同负担

Wu, Gang; Chen, Wenan; Wuu, Joanne; Jain, Angita; Myers, Jason; Cordts, Isabell; Rampersaud, Evadnie; Heckmann, Jeannine M; Nel, Melissa; Granit, Volkan; Statland, Jeffrey; Swenson, Andrea; Ravits, John; McMillan, Corey T; Elman, Lauren; Caress, James; Burns, Ted M; Pioro, Erik P; Trivedi, Jaya; Katz, Jonathan; Jackson, Carlayne; Maiser, Samuel; Walk, David; So, Yuen; McCauley, Jacob L; Baker, Matthew C; Taylor, J Paul; Zuchner, Stephan; Rademakers, Rosa; van Blitterswijk, Marka; Benatar, Michael

The Mayo MGRS Prediction Tool calculates the risk of finding monoclonal gammopathy of renal significance in a kidney biopsy in patients with monoclonal gammopathy

Mayo MGRS预测工具用于计算单克隆丙种球蛋白病患者在肾活检中发现肾脏意义的单克隆丙种球蛋白病的风险。

Klomjit, Nattawat; Evans, Michael D; Vargas, Maria; Marka, Nicholas; Fervenza, Fernando C; Sethi, Sanjeev; Zand, Ladan