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

Leukemic Cells Hijack Stromal Bioelectricity to Reprogram the Bone Marrow Niche via CaV1.2-Dependent Mechanisms

白血病细胞通过CaV1.2依赖性机制劫持基质生物电,重编程骨髓微环境

Da Ros, Ambra; Benetton, Maddalena; Borella, Giulia; Longo, Giorgia; Borile, Giulia; Cani, Alice; Lopez-Pigozzi, Diego; Bortolozzi, Mario; Bresolin, Silvia; Tregnago, Claudia; Locatelli, Franco; Pigazzi, Martina

Lewy pathology formation in patient-derived GBA1 Parkinson's disease midbrain organoids.

患者来源的GBA1帕金森病中脑类器官中路易病理的形成

Frattini Emanuele, Faustini Gaia, Lopez Gianluca, Carsana Emma Veronica, Tosi Mattia, Trezzi Ilaria, Magni Manuela, Soldà Giulia, Straniero Letizia, Facchi Daniele, Samarani Maura, Martá-Ariza Mitchell, De Luca Chiara Maria Giulia, Vezzoli Elena, Pittaro Alessandra, Stepanyan Astghik, Silipigni Rosamaria, Rosety Isabel, Schwamborn Jens C, Sardi Sergio Pablo, Moda Fabio, Corti Stefania, Comi Giacomo P, Blandini Fabio, Tritsch Nicolas X, Bortolozzi Mario, Ferrero Stefano, Cribiù Fulvia Milena, Wisniewski Thomas, Asselta Rosanna, Aureli Massimo, Bellucci Arianna, Di Fonzo Alessio

Special Issue "Gap Junction Channels and Hemichannels in Health and Disease"

特刊“健康与疾病中的缝隙连接通道和半通道”

Rijtano, Barbara; Bortolozzi, Mario

Calcium Regulation of Connexin Hemichannels

钙离子对连接蛋白半通道的调控

Bayraktar, Erva; Lopez-Pigozzi, Diego; Bortolozzi, Mario

New perspectives for gene therapy of the X-linked form of Charcot-Marie-Tooth disease

夏科-马里-图斯病X连锁基因治疗的新视角

Caballé, Rafael Balada; Bortolozzi, Mario

Molecular dynamics simulations highlight structural and functional alterations in deafness-related M34T mutation of connexin 26

分子动力学模拟突显了与耳聋相关的连接蛋白26 M34T突变的结构和功能改变

Zonta, Francesco; Buratto, Damiano; Cassini, Chiara; Bortolozzi, Mario; Mammano, Fabio

The 3.5 ångström X-ray structure of the human connexin26 gap junction channel is unlikely that of a fully open channel

人类连接蛋白26间隙连接通道的3.5埃X射线晶体结构不太可能是完全开放通道的结构。

Zonta, Francesco; Polles, Guido; Sanasi, Maria Federica; Bortolozzi, Mario; Mammano, Fabio

BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice.

BAAV介导的GJB2基因转移恢复了来自耳聋Cx26Sox10Cre小鼠的耳蜗器官型培养物的间隙连接耦合

Crispino Giulia, Di Pasquale Giovanni, Scimemi Pietro, Rodriguez Laura, Galindo Ramirez Fabian, De Siati Romolo Daniele, Santarelli Rosa Maria, Arslan Edoardo, Bortolozzi Mario, Chiorini John A, Mammano Fabio

The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.

人类耳聋相关的连接蛋白 30 T5M 突变会导致轻度听力损失,并降低敲入小鼠耳蜗非感觉细胞之间的生化耦合

Schütz Melanie, Scimemi Pietro, Majumder Paromita, De Siati Romolo Daniele, Crispino Giulia, Rodriguez Laura, Bortolozzi Mario, Santarelli Rosamaria, Seydel Anke, Sonntag Stephan, Ingham Neil, Steel Karen P, Willecke Klaus, Mammano Fabio

ATP-mediated cell-cell signaling in the organ of Corti: the role of connexin channels.

科尔蒂氏器中 ATP 介导的细胞间信号传导:连接蛋白通道的作用

Majumder Paromita, Crispino Giulia, Rodriguez Laura, Ciubotaru Catalin Dacian, Anselmi Fabio, Piazza Valeria, Bortolozzi Mario, Mammano Fabio