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

Rare STAT1 variants in Moroccan tuberculosis patients: insights into host genetic susceptibility

摩洛哥结核病患者中罕见的STAT1变异:对宿主遗传易感性的启示

Zaidi, Sanae; Rafik, Aniss; Skhoun, Hanaa; Elkarhat, Zouhair; Guennoun, Aya; Tabehout, Fatima; Errami, Abderrahmane; Abid, Ahmed; Abderrhamani Ghorfi, Ismail; El Ouazzani, Hanane; Souhi, Hicham; Zegmout, Adil; El Hassani, Amal; Ailal, Fatima; Abilkassem, Rachid; Ouzzif, Zohra; Benhsaien, Ibtihal; Bousfiha, Ahmed Aziz; El Baghdadi, Jamila

First identification of ORF virus causing contagious ecthyma in Morocco (MOR20): Genomic, phylogenetic, and sequence variants analyses for vaccine design

首次鉴定出摩洛哥传染性脓疱病病原体ORF病毒(MOR20):用于疫苗设计的基因组、系统发育和序列变异分析

Elkarhat, Zouhair; Tifrouin, Ikram; Bamouh, Zahra; Tadlaoui, Khalid Omari; Elharrak, Mehdi

Dominant ACO2 mutations are a frequent cause of isolated optic atrophy

显性 ACO2 突变是孤立性视神经萎缩的常见原因

Majida Charif, Naïg Gueguen, Marc Ferré, Zouhair Elkarhat, Salim Khiati, Morgane LeMao, Arnaud Chevrollier, Valerie Desquiret-Dumas, David Goudenège, Céline Bris, Selma Kane, Jennifer Alban, Stéphanie Chupin, Céline Wetterwald, Leonardo Caporali, Francesca Tagliavini, Chiara LaMorgia, Michele Carbon

Identification of p.Met215Ile mutation of the MC4R gene in a Moroccan woman with obesity

在一名患有肥胖症的摩洛哥女性中鉴定出MC4R基因的p.Met215Ile突变。

El Fessikh, Meriem; Belghiti, Hakim; Elkarhat, Zouhair; Guerinech, Hassania; Dakka, Nadia; El Baghdadi, Jamila

Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study

预测有害非同义单核苷酸多态性对人类RRM2B基因的影响:一项分子建模研究

Ait El Cadi, Chaimaa; Krami, Al Mehdi; Charoute, Hicham; Elkarhat, Zouhair; Sifeddine, Najat; Lakhiari, Hamid; Rouba, Hassan; Barakat, Abdelhamid; Nahili, Halima

Computational Analysis of nsSNPs of ADA Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation

利用分子建模和动力学模拟对重症联合免疫缺陷中ADA基因的非同义单核苷酸多态性进行计算分析

Essadssi, Soukaina; Krami, Al Mehdi; Elkhattabi, Lamiae; Elkarhat, Zouhair; Amalou, Ghita; Abdelghaffar, Houria; Rouba, Hassan; Barakat, Abdelhamid

In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure

利用计算机模拟分析人类RETN基因的编码/非编码SNP,并表征其对抵抗素稳定性和结构的影响

Elkhattabi, Lamiae; Morjane, Imane; Charoute, Hicham; Amghar, Soumaya; Bouafi, Hind; Elkarhat, Zouhair; Saile, Rachid; Rouba, Hassan; Barakat, Abdelhamid

Molecular Modelling and Dynamics Study of nsSNP in STXBP1 Gene in Early Infantile Epileptic Encephalopathy Disease

早期婴儿癫痫性脑病中STXBP1基因非同义单核苷酸多态性(nsSNP)的分子建模和动力学研究

Al Mehdi, Krami; Fouad, Benhnini; Zouhair, Elkarhat; Boutaina, Belkady; Yassine, Naasse; Chaimaa, Ait El Cadi; Najat, Sifeddine; Hassan, Rouba; Rachida, Roky; Abdelhamid, Barakat; Halima, Nahili