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

Multivalent Exosome Based Protein Vaccine: A "Mix and Match" Approach to Epidemic Viruses' Challenges.

基于多价外泌体的蛋白质疫苗:应对流行病毒挑战的“混合搭配”方法

Cacciottolo Mafalda, Hsieh Li-En, Li Yujia, LeClaire Michael J, Mora Ciana L, Lau Christy, Dwyer Charles, Elliott Kristi, Sun Minghao

Chimpanzee and human ApoE isoforms differ in the stimulation of neurite differentiation consistent with structural predictions with relevance to brain development and aging

黑猩猩和人类的ApoE同种型在刺激神经突分化方面存在差异,这与结构预测相符,并涉及大脑发育和衰老。

Thorwald, Max A; Cacciottolo, Mafalda; Hou, Xiaogang; Morgan, Todd E; Finch, Caleb E

Age, sex, and cerebral microbleeds in EFAD Alzheimer disease mice

EFAD阿尔茨海默病小鼠的年龄、性别和脑微出血

Cacciottolo, Mafalda; Morgan, Todd E; Finch, Caleb E

Corrigendum to "Traffic-related air pollutants (TRAP-PM) promote neuronal amyloidogenesis through oxidative damage to lipid rafts" [FRBM 147C (2019) 242-251]

对“交通相关空气污染物(TRAP-PM)通过氧化损伤脂筏促进神经元淀粉样变性”的更正[FRBM 147C (2019) 242-251]

Cacciottolo, Mafalda; Morgan, Todd E; Saffari, Arian A; Shirmohammadi, Farimah; Forman, Henry Jay; Sioutas, Costantinos; Finch, Caleb E

Traffic-related air pollutants (TRAP-PM) promote neuronal amyloidogenesis through oxidative damage to lipid rafts

交通相关空气污染物(TRAP-PM)通过对脂筏的氧化损伤促进神经元淀粉样蛋白生成

Cacciottolo, Mafalda; Morgan, Todd E; Saffari, Arian A; Shirmohammadi, Farimah; Forman, Henry Jay; Sioutas, Costantinos; Finch, Caleb E

The APOE4 allele shows opposite sex bias in microbleeds and Alzheimer's disease of humans and mice

APOE4等位基因在人类和小鼠的微出血和阿尔茨海默病中表现出相反的性别偏向性。

Cacciottolo, Mafalda; Christensen, Amy; Moser, Alexandra; Liu, Jiahui; Pike, Christian J; Smith, Conor; LaDu, Mary Jo; Sullivan, Patrick M; Morgan, Todd E; Dolzhenko, Egor; Charidimou, Andreas; Wahlund, Lars-Olof; Wiberg, Maria Kristofferson; Shams, Sara; Chiang, Gloria Chia-Yi; Finch, Caleb E

Activation of the Unfolded Protein Response in Sporadic Inclusion-Body Myositis but Not in Hereditary GNE Inclusion-Body Myopathy

散发性包涵体肌炎中未折叠蛋白反应被激活,而遗传性GNE包涵体肌病中则未激活。

Nogalska, Anna; D'Agostino, Carla; Engel, W King; Cacciottolo, Mafalda; Asada, Shinichi; Mori, Kazutoshi; Askanas, Valerie

Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations

肌营养不良症伴有明显的肌营养不良蛋白缺乏症,通常是由原发性肌营养不良蛋白基因突变引起的。

Cacciottolo, Mafalda; Numitone, Gelsomina; Aurino, Stefania; Caserta, Imma Rosaria; Fanin, Marina; Politano, Luisa; Minetti, Carlo; Ricci, Enzo; Piluso, Giulio; Angelini, Corrado; Nigro, Vincenzo

Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complex

α和ε肌聚糖的联合缺乏会破坏心肌肌营养不良蛋白复合物。

Lancioni, Alessio; Rotundo, Ida Luisa; Kobayashi, Yvonne Monique; D'Orsi, Luca; Aurino, Stefania; Nigro, Gerardo; Piluso, Giulio; Acampora, Dario; Cacciottolo, Mafalda; Campbell, Kevin P; Nigro, Vincenzo