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

Influence of a Two-Fold Ligation Pattern on Iron-Mediated Aryl-Heteroaryl Cross-Electrophile Couplings

双重配位模式对铁介导的芳基-杂芳基交叉亲电偶联反应的影响

Djebbar, Faycel; Chamoreau, Lise-Marie; Lefèvre, Guillaume

The age at onset of LRRK2 p.Gly2019Ser Parkinson's disease across ancestries and countries of origin

LRRK2 p.Gly2019Ser 帕金森病在不同种族和原籍国的发病年龄

Lüth, Theresa; Laabs, Björn-Hergen; Sendel, Sebastian; König, Inke R; Caliebe, Amke; Noyce, Alastair J; Screven, Laurel A; Bardien, Soraya; Farrer, Matthew; Hentati, Faycel; Klein, Christine; Ben Sassi, Samia; Trinh, Joanne

RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses

RAB32 Ser71Arg 与常染色体显性帕金森病:连锁、关联和功能分析

Gustavsson, Emil K; Follett, Jordan; Trinh, Joanne; Barodia, Sandeep K; Real, Raquel; Liu, Zhiyong; Grant-Peters, Melissa; Fox, Jesse D; Appel-Cresswell, Silke; Stoessl, A Jon; Rajput, Alex; Rajput, Ali H; Auer, Roland; Tilney, Russel; Sturm, Marc; Haack, Tobias B; Lesage, Suzanne; Tesson, Christelle; Brice, Alexis; Vilariño-Güell, Carles; Ryten, Mina; Goldberg, Matthew S; West, Andrew B; Hu, Michele T; Morris, Huw R; Sharma, Manu; Gan-Or, Ziv; Samanci, Bedia; Lis, Pawel; Periñan, Maria Teresa; Amouri, Rim; Ben Sassi, Samia; Hentati, Faycel; Tonelli, Francesca; Alessi, Dario R; Farrer, Matthew J

A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase

RAB32基因的致病变异会导致常染色体显性遗传帕金森病,并激活LRRK2激酶。

Gustavsson, Emil K; Follett, Jordan; Trinh, Joanne; Barodia, Sandeep K; Real, Raquel; Liu, Zhiyong; Grant-Peters, Melissa; Fox, Jesse D; Appel-Cresswell, Silke; Stoessl, A Jon; Rajput, Alex; Rajput, Ali H; Auer, Roland; Tilney, Russel; Sturm, Marc; Haack, Tobias B; Lesage, Suzanne; Tesson, Christelle; Brice, Alexis; Vilariño-Güell, Carles; Ryten, Mina; Goldberg, Matthew S; West, Andrew B; Hu, Michele T; Morris, Huw R; Sharma, Manu; Gan-Or, Ziv; Samanci, Bedia; Lis, Pawel; Tocino, Teresa; Amouri, Rim; Sassi, Samia Ben; Hentati, Faycel; Tonelli, Francesca; Alessi, Dario R; Farrer, Matthew J

Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson's disease

线粒体 DNA 异质体可区分 PINK1/PRKN 相关帕金森病的疾病表现

Joanne Trinh, Andrew A Hicks, Inke R König, Sylvie Delcambre, Theresa Lüth, Susen Schaake, Kobi Wasner, Jenny Ghelfi, Max Borsche, Carles Vilariño-Güell, Faycel Hentati, Elisabeth L Germer, Peter Bauer, Masashi Takanashi, Vladimir Kostić, Anthony E Lang, Norbert Brüggemann, Peter P Pramstaller, Iren

Novel variable neighborhood search heuristics for truck management in distribution warehouses problem

针对配送仓库卡车管理问题,提出了一种新的可变邻域搜索启发式算法

Sarhan, Akram Y; B Melhim, Loai Kayed; Jemmali, Mahdi; El Ayeb, Faycel; Alharbi, Hadeel; Banjar, Ameen

Spinal mesenchymal chondrosarcoma: A case report of a rare malignant tumor

脊髓间叶软骨肉瘤:一例罕见恶性肿瘤病例报告

Dehneh, Younes; Aldabbas, Mohannad; Elfarissi, Mohammed Alamine; Khoulali, Mohamed; Oulali, Noureddine; Moufid, Faycel

Double-interpenetrating nanostructured networks of marine polysaccharides possessing properties comparable to synthetic polymers

具有与合成聚合物相当的性能的海洋多糖双重互穿纳米结构网络

Ghrissi, Faycel; Gu, Yawei; Shastri, V Prasad

Genital abnormalities associated to lack of uterine adenogenesis or endometrial gland dysgenesis of female dromedary camels (Camelus dromedarius)

与雌性单峰骆驼(Camelus dromedarius)子宫腺发育不全或子宫内膜腺体发育不良相关的生殖器异常

Gherissi, Djallel Eddine; Lamraoui, Ramzi; Chacha, Faycel; Bouzebda, Zoubir; Bouzebda, Farida Afri; Hanzen, Christian

Taenia saginata: an unusual cause of post-appendectomy faecal fistula

牛带绦虫:阑尾切除术后粪瘘的一种罕见病因

Najih, Mohammed; Laraqui, Hicham; Njoumi, Nouredine; Mouhafid, Faycel; Moujahid, Mountassir; Ehirchiou, Abdelkader; Zentar, Aziz