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

Myotilin gene duplication causing late-onset myotilinopathy.

肌动蛋白基因重复导致迟发性肌动蛋白病

Spinazzi Marco, Savarese Marco, Letournel Franck, Sagath Lydia, Manero Florence, Guichet Agnès, Hoischen Alexander, Metay Corinne, Gouju Julien, Udd Bjarne

Correction: Mitochondrial defects caused by PARL deficiency lead to arrested spermatogenesis and ferroptosis

更正:PARL 缺乏引起的线粒体缺陷会导致精子发生停滞和铁死亡。

Radaelli, Enrico; Assenmacher, Charles-Antoine; Verrelle, Jillian; Banerjee, Esha; Manero, Florence; Khiati, Salim; Girona, Anais; Lopez-Lluch, Guillermo; Navas, Placido; Spinazzi, Marco

Opa1 and MT-Nd6 mutations induce early mitochondrial changes in the retina and prelaminar optic nerve of hereditary optic neuropathy mouse models

Opa1 和 MT-Nd6 突变可诱导遗传性视神经病变小鼠模型视网膜和视神经前层早期线粒体改变。

Bureau, Jacques; Manero, Florence; Baris, Olivier; Bodin, Alexia; Verny, Christophe; Chevrollier, Arnaud; Lenaers, Guy; Codron, Philippe

Role of membrane compartment occupied by Can1 (MCC) and eisosome subdomains in plant pathogenicity of the necrotrophic fungus Alternaria brassicicola

Can1 (MCC) 占据的膜区室和内体亚结构域在坏死性真菌芸苔链格孢菌植物致病性中的作用

Colou, Justine; N'Guyen, Guillaume Quang; Dubreu, Ophélie; Fontaine, Kévin; Kwasiborski, Anthony; Bastide, Franck; Manero, Florence; Hamon, Bruno; Aligon, Sophie; Simoneau, Philippe; Guillemette, Thomas