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

Identification of Candidate Genes for Pigmentation in Camels Using Genotyping-by-Sequencing

利用基因分型测序技术鉴定骆驼色素沉着候选基因

Bitaraf Sani, Morteza; Zare Harofte, Javad; Banabazi, Mohammad Hossein; Faraz, Asim; Esmaeilkhanian, Saeid; Naderi, Ali Shafei; Salim, Nader; Teimoori, Abbas; Bitaraf, Ahmad; Zadehrahmani, Mohammad; Burger, Pamela Anna; Asadzadeh, Nader; Silawi, Mohammad; Taghipour Sheshdeh, Afsaneh; Mohammad Nazari, Behrouz; Faghihi, Mohammad Ali; Roudbari, Zahra

Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran

针对表现为脑瘫的各种神经发育障碍的基因检测:来自伊朗的案例研究

Nejabat, Marzieh; Inaloo, Soroor; Sheshdeh, Afsaneh Taghipour; Bahramjahan, Shima; Sarvestani, Fatima Masoomi; Katibeh, Pegah; Nemati, Hamid; Tabei, Seyed Mohammad Bagher; Faghihi, Mohammad Ali

Cytokine Gene Expression Alterations in Human Macrophages Infected by Leishmania major

利什曼原虫感染的人类巨噬细胞中细胞因子基因表达的改变

Kalavi, Khodaberdi; Jorjani, Ogholniaz; Faghihi, Mohammad Ali; Mowla, Seyed Javad

Pre-Implantation Genetic Testing for Monogenic Disorders (PGT-M) in A Family with A Novel Mutation in DPAGT1 Gene.

对携带 DPAGT1 基因新突变的家庭进行单基因疾病植入前遗传学检测 (PGT-M)

Tabatabaei Zahra, Karbalaie K Hadijeh, Habibzadeh Parham, Farazi Fard Mohammad Ali, Faghihi Mohammad Ali, Nasr Esfahani Mohammad Hossein

Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia

明确衔接蛋白复合物 4 相关遗传性痉挛性截瘫的临床、分子和影像学特征

Ebrahimi-Fakhari, Darius; Teinert, Julian; Behne, Robert; Wimmer, Miriam; D'Amore, Angelica; Eberhardt, Kathrin; Brechmann, Barbara; Ziegler, Marvin; Jensen, Dana M; Nagabhyrava, Premsai; Geisel, Gregory; Carmody, Erin; Shamshad, Uzma; Dies, Kira A; Yuskaitis, Christopher J; Salussolia, Catherine L; Ebrahimi-Fakhari, Daniel; Pearson, Toni S; Saffari, Afshin; Ziegler, Andreas; Kölker, Stefan; Volkmann, Jens; Wiesener, Antje; Bearden, David R; Lakhani, Shenela; Segal, Devorah; Udwadia-Hegde, Anaita; Martinuzzi, Andrea; Hirst, Jennifer; Perlman, Seth; Takiyama, Yoshihisa; Xiromerisiou, Georgia; Vill, Katharina; Walker, William O; Shukla, Anju; Dubey Gupta, Rachana; Dahl, Niklas; Aksoy, Ayse; Verhelst, Helene; Delgado, Mauricio R; Kremlikova Pourova, Radka; Sadek, Abdelrahim A; Elkhateeb, Nour M; Blumkin, Lubov; Brea-Fernández, Alejandro J; Dacruz-Álvarez, David; Smol, Thomas; Ghoumid, Jamal; Miguel, Diego; Heine, Constanze; Schlump, Jan-Ulrich; Langen, Hendrik; Baets, Jonathan; Bulk, Saskia; Darvish, Hossein; Bakhtiari, Somayeh; Kruer, Michael C; Lim-Melia, Elizabeth; Aydinli, Nur; Alanay, Yasemin; El-Rashidy, Omnia; Nampoothiri, Sheela; Patel, Chirag; Beetz, Christian; Bauer, Peter; Yoon, Grace; Guillot, Mireille; Miller, Steven P; Bourinaris, Thomas; Houlden, Henry; Robelin, Laura; Anheim, Mathieu; Alamri, Abdullah S; Mahmoud, Adel A H; Inaloo, Soroor; Habibzadeh, Parham; Faghihi, Mohammad Ali; Jansen, Anna C; Brock, Stefanie; Roubertie, Agathe; Darras, Basil T; Agrawal, Pankaj B; Santorelli, Filippo M; Gleeson, Joseph; Zaki, Maha S; Sheikh, Sarah I; Bennett, James T; Sahin, Mustafa

Molecular mechanisms of long non-coding RNAs in anaplastic thyroid cancer: a systematic review

长链非编码RNA在间变性甲状腺癌中的分子机制:系统综述

Samimi, Hilda; Sajjadi-Jazi, Sayed Mahmoud; Seifirad, Soroush; Atlasi, Rasha; Mahmoodzadeh, Habibollah; Faghihi, Mohammad Ali; Haghpanah, Vahid

Viral metagenomic analysis of fecal samples reveals an enteric virome signature in irritable bowel syndrome

对粪便样本进行病毒宏基因组分析揭示了肠易激综合征中的肠道病毒组特征

Ansari, Mina Hojat; Ebrahimi, Mehregan; Fattahi, Mohammad Reza; Gardner, Michael G; Safarpour, Ali Reza; Faghihi, Mohammad Ali; Lankarani, Kamran Bagheri

Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

病例报告:扩展夏洛瓦-萨格奈常染色体隐性痉挛性共济失调的遗传和表型谱

Habibzadeh, Parham; Tabatabaei, Zahra; Inaloo, Soroor; Nashatizadeh, Muhammad Mahdi; Synofzik, Matthis; Ostovan, Vahid Reza; Faghihi, Mohammad Ali

Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal Encephalomyopathy

线粒体神经胃肠脑肌病患者的临床和分子特征分析

Habibzadeh, Parham; Silawi, Mohammad; Dastsooz, Hassan; Bahramjahan, Shima; Ezzatzadegan Jahromi, Shahrokh; Ostovan, Vahid Reza; Yavarian, Majid; Mofatteh, Mohammad; Faghihi, Mohammad Ali

Reporting one very rare pathogenic variation c.1106G>A in POMT2 gene

报告POMT2基因中一种非常罕见的致病性变异c.1106G>A

Mahjoub, Ghazale; Faghihi, Mohammad Ali; Taghdiri, Maryam