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

Dysregulated Sheddase Signalling as a Molecular Driver of Plaque Instability Revealed by Integrative Transcriptomics

整合转录组学揭示失调的脱落酶信号传导是斑块不稳定性的分子驱动因素

Alahmadi, Alaa G; Alkhatabi, Hind A; Alotibi, Reem M; Albeshri, Wedad M; El-Mezgueldi, Mohammed; Al-Farga, Ammar; Pushparaj, Peter Natesan

Discovery of novel cardiac troponin activators using fluorescence polarization-based high throughput screening assays

使用基于荧光偏振的高通量筛选试验发现新型心脏肌钙蛋白激活剂

Priyanka Parijat, Saraswathi Ponnam, Seetharamaiah Attili, Kenneth S Campbell, Mohammed El-Mezgueldi, Mark Pfuhl, Thomas Kampourakis

Value of hematological parameters for predicting patients with severe coronavirus disease 2019: a real-world cohort from Morocco

血液学参数对预测2019冠状病毒病重症患者的价值:来自摩洛哥的真实世界队列研究

Azghar, Ali; Bensalah, Mohammed; Berhili, Abdelilah; Slaoui, Mounia; Mouhoub, Boutaina; El Mezgueldi, Imane; Nassiri, Oumaima; El Malki, Jalila; Maleb, Adil; Seddik, Rachid

Diagnostic Accuracy of Routinely Available Biomarkers to Predict Bacteremia in Children With Community-Acquired Pneumonia: A Secondary Analysis of the GPIP/ACTIV Pneumonia Study in France, 2009-2018

常规可用生物标志物预测社区获得性肺炎患儿菌血症的诊断准确性:法国 GPIP/ACTIV 肺炎研究(2009-2018 年)的二次分析

Dudognon, Danaé; Levy, Corinne; Chalumeau, Martin; Biscardi, Sandra; Dommergues, Marie-Aliette; Dubos, François; Levieux, Karine; Aurel, Marie; Minodier, Philippe; Zenkhri, Ferielle; Mezgueldi, Ellia; Craiu, Irina; Morin, Laurence; Béchet, Stéphane; Varon, Emmanuelle; Cohen, Robert; Cohen, Jérémie F

Visceral leishmaniasis associated with macrophage activation syndrome: Case report and literature review

内脏利什曼病合并巨噬细胞活化综合征:病例报告及文献综述

Mouhoub, Boutaina; Bensalah, Mohammed; Berhili, Abdelilah; Azghar, Ali; El Malki, Jalila; El Mezgueldi, Imane; Nassiri, Oumaima; Slaoui, Mounia; Miri, Achraf; Rochdi, Chaymae; Benajiba, Noufissa; Seddik, Rachid

Long-term Association of 13-Valent Pneumococcal Conjugate Vaccine Implementation With Rates of Community-Acquired Pneumonia in Children

13价肺炎球菌结合疫苗长期接种与儿童社区获得性肺炎发病率的关联

Ouldali, Naïm; Levy, Corinne; Minodier, Philippe; Morin, Laurence; Biscardi, Sandra; Aurel, Marie; Dubos, François; Dommergues, Marie Alliette; Mezgueldi, Ellia; Levieux, Karine; Madhi, Fouad; Hees, Laure; Craiu, Irina; Gras Le Guen, Chrystèle; Launay, Elise; Zenkhri, Ferielle; Lorrot, Mathie; Gillet, Yves; Béchet, Stéphane; Hau, Isabelle; Martinot, Alain; Varon, Emmanuelle; Angoulvant, François; Cohen, Robert

Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca(2+)-sensitivity and suppress the modulation of Ca(2+)-sensitivity by troponin I phosphorylation.

与肥厚型心肌病相关的肌钙蛋白 T 突变会增加 Ca(2+) 敏感性,并抑制肌钙蛋白 I 磷酸化对 Ca(2+) 敏感性的调节

Messer Andrew E, Bayliss Christopher R, El-Mezgueldi Mohammed, Redwood Charles S, Ward Douglas G, Leung Man-Ching, Papadaki Maria, Dos Remedios Cristobal, Marston Steven B

Molecular basis of sugar recognition by collectin-K1 and the effects of mutations associated with 3MC syndrome

凝集素-K1识别糖的分子基础及与3MC综合征相关的突变的影响

Venkatraman Girija, Umakhanth; Furze, Christopher M; Gingras, Alexandre R; Yoshizaki, Takayuki; Ohtani, Katsuki; Marshall, Jamie E; Wallis, A Katrine; Schwaeble, Wilhelm J; El-Mezgueldi, Mohammed; Mitchell, Daniel A; Moody, Peter C E; Wakamiya, Nobutaka; Wallis, Russell

Early-onset hypoparathyroidism and chronic keratitis revealing APECED

早发性甲状旁腺功能减退症和慢性角膜炎提示APECED

Mezgueldi, Ellia; Bertholet-Thomas, Aurélia; Milazzo, Solange; Morris, Michael; Bacchetta, Justine; Fabien, Nicole; Cochat, Pierre; Weetman, Anthony P; Kemp, Elizabeth Helen; Belot, Alexandre

Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients

原肌球蛋白重复结构基序的突变会导致骨骼肌肌病患者获得功能。

Marston, Steven; Memo, Massimiliano; Messer, Andrew; Papadaki, Maria; Nowak, Kristen; McNamara, Elyshia; Ong, Royston; El-Mezgueldi, Mohammed; Li, Xiaochuan; Lehman, William