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

Factor XI Deficiency in apoE/FXI Double-Knockout Mice Decreases Atherosclerosis by Lowering MSR1 mRNA Expression Within the Plaque

apoE/FXI双敲除小鼠中因子XI缺乏通过降低斑块内MSR1 mRNA表达来减轻动脉粥样硬化

Shnerb Ganor, Reut; Paraboschi, Elvezia M; Stefano, Duga; Harats, Dror; Asselta, Rosanna; Schiby, Ginette; Leichner, Gil S; Anekstein Spigel, Mika; Tamarin, Ilia; Kandel Kfir, Michal; Steinberg, David M; Shaish, Aviv; Salomon, Ophira

In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear

透光相关 formin 2 (DIAPH2) 的深入遗传和分子表征及其在内耳中的作用

Chiara Chiereghin, Michela Robusto, Morag A Lewis, Susana Caetano, Valentina Massa, Pierangela Castorina, Umberto Ambrosetti, Karen P Steel, Stefano Duga, Rosanna Asselta, Giulia Soldà

β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration

β-葡萄糖脑苷脂酶缺乏症会激活异常的溶酶体-质膜轴,从而引发神经退行性疾病

Giulia Lunghi, Emma Veronica Carsana, Nicoletta Loberto, Laura Cioccarelli, Simona Prioni, Laura Mauri, Rosaria Bassi, Stefano Duga, Letizia Straniero, Rosanna Asselta, Giulia Soldà, Alessio Di Fonzo, Emanuele Frattini, Manuela Magni, Nara Liessi, Andrea Armirotti, Elena Ferrari, Maura Samarani, Mas

Massive Accumulation of Sphingomyelin Affects the Lysosomal and Mitochondria Compartments and Promotes Apoptosis in Niemann-Pick Disease Type A

鞘磷脂大量积累影响溶酶体和线粒体区室并促进 A 型尼曼匹克病细胞凋亡

Emma Veronica Carsana, Giulia Lunghi, Simona Prioni, Laura Mauri, Nicoletta Loberto, Alessandro Prinetti, Fabio Andrea Zucca, Rosaria Bassi, Sandro Sonnino, Elena Chiricozzi, Stefano Duga, Letizia Straniero, Rosanna Asselta, Giulia Soldà, Maura Samarani, Massimo Aureli

Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer

放射组学和基因表达谱用于表征肺癌患者的疾病并预测其预后

Margarita Kirienko, Martina Sollini, Marinella Corbetta, Emanuele Voulaz, Noemi Gozzi, Matteo Interlenghi, Francesca Gallivanone, Isabella Castiglioni, Rosanna Asselta, Stefano Duga, Giulia Soldà, Arturo Chiti

A Novel Homozygous VPS11 Variant May Cause Generalized Dystonia

一种新型纯合 VPS11 变异可能导致全身性肌张力障碍

Edoardo Monfrini, Filippo Cogiamanian, Sabrina Salani, Letizia Straniero, Gigliola Fagiolari, Manuela Garbellini, Emma Carsana, Linda Borellini, Fabio Biella, Maurizio Moggio, Nereo Bresolin, Stefania Corti, Stefano Duga, Giacomo P Comi, Massimo Aureli, Alessio Di Fonzo

Post-Biopsy Cell-Free DNA From Blood: An Open Window on Primary Prostate Cancer Genetics and Biology

血液活检后游离 DNA:了解前列腺原发性癌遗传学和生物学的窗口

Marinella Corbetta, Chiara Chiereghin, Ilaria De Simone, Giulia Soldà, Monica Zuradelli, Michele Giunta, Giovanni Lughezzani, Nicolò Maria Buffi, Rodolfo Hurle, Alberto Saita, Paolo Casale, Rosanna Asselta, Massimo Lazzeri, Giorgio Guazzoni, Stefano Duga

Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations

患有 EARS2 隐性突变的患者的晚发型白质脑病

Edoardo Monfrini, Dario Ronchi, Giulia Franco, Manuela Garbellini, Letizia Straniero, Elisa Scola, Federica Arienti, Stefano Duga, Giacomo Pietro Comi, Nereo Bresolin, Alessio Di Fonzo

Chromosome Transplantation: A Possible Approach to Treat Human X-linked Disorders

染色体移植:治疗人类 X 连锁疾病的一种可能方法

Marianna Paulis, Lucia Susani, Alessandra Castelli, Teruhiko Suzuki, Takahiko Hara, Letizia Straniero, Stefano Duga, Dario Strina, Stefano Mantero, Elena Caldana, Lucia Sergi Sergi, Anna Villa, Paolo Vezzoni

Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency

了解凝血因子 V 缺乏症中异常剪接的影响

Elvezia Maria Paraboschi, Marzia Menegatti, Flora Peyvandi, Stefano Duga, Rosanna Asselta