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

Unraveling the molecular mechanisms in severe Alzheimer's disease based on transcriptomic data using next generation knowledge discovery methods

利用新一代知识发现方法,基于转录组数据揭示重度阿尔茨海默病分子机制

Alkhatabi, Hind A; Alahmadi, Alaa G; Naseer, Muhammad Imran; Pushparaj, Peter Natesan

A narrative review of research advancements in pharmacogenetics of cardiovascular disease and impact on clinical implications

对心血管疾病药物遗传学研究进展及其对临床影响的叙述性综述

Shorbaji, Ayat; Pushparaj, Peter Natesan; Al-Ghafari, Ayat B; Mira, Loubna Siraj; Basabrain, Mohammad Abdullah; Naseer, Muhammad Imran; Ahmed, Farid; Abu-Elmagd, Muhammad; Rasool, Mahmood; Bakhashab, Sherin

Characterization of Desertihabitans sp. FB5, a halophyte associated Actinomycetes producing phytohormones

对Desertihabitans sp. FB5(一种与盐生植物相关的、产生植物激素的放线菌)进行表征

Bibi, Fehmida; Naseer, Muhammad Imran; Pushparaj, Peter Natesan; Haque, Absarul; Azhar, Esam Ibraheem

Short-term effectiveness and side effects of ketogenic diet for drug-resistant epilepsy in children with genetic epilepsy syndromes

生酮饮食治疗遗传性癫痫综合征患儿难治性癫痫的短期疗效及副作用

Muthaffar, Osama Y; Alyazidi, Anas S; Alsowat, Daad; Alasiri, Abdulaziz A; Albaradie, Raidah; Jad, Lamyaa A; Kayyali, Husam; Jan, Mohammed M S; Bamaga, Ahmed K; Alsubaie, Mohammed A; Daghistani, Rawan; Baeesa, Saleh S; Alaifan, Meshari A; Makraz, Abdelhakim; Alsharief, Abrar N; Naseer, Muhammad Imran

Whole exome sequencing of a novel homozygous missense variant in PALB2 gene leading to Fanconi anaemia complementation group

对PALB2基因中一种导致范可尼贫血互补群的新型纯合错义变异进行全外显子组测序

Abdulkareem, Angham Abdulrhman; Shirah, Bader H; Bagabir, Hala Abubaker; Haque, Absarul; Naseer, Muhammad Imran

A missense variant in the PACS2 gene cause Epileptic Encephalopathy and seizures in Saudi family

沙特阿拉伯一个家族中,PACS2基因的错义变异导致癫痫性脑病和癫痫发作。

Haque, Absarul; Naseer, Muhammad Imran

Clinical whole Exome Sequencing Reveals Novel Homozygous Missense Variant in the PMPCA Gene causing Autosomal Recessive Spinocerebellar Ataxia

临床全外显子组测序揭示PMPCA基因中一种新的纯合错义变异,该变异导致常染色体隐性脊髓小脑性共济失调。

Bagabir, Hala Abubaker; Abdulkareem, Angham Abdulrhman; Muthaffar, Osama Yousef; Shirah, Bader H; Naseer, Muhammad Imran

Current genetic models for studying congenital heart diseases: Advantages and disadvantages

目前用于研究先天性心脏病的遗传模型:优势和劣势

Shorbaji, Ayat; Pushparaj, Peter Natesan; Bakhashab, Sherin; Al-Ghafari, Ayat B; Al-Rasheed, Rana R; Siraj Mira, Loubna; Basabrain, Mohammad Abdullah; Alsulami, Majed; Abu Zeid, Isam M; Naseer, Muhammad Imran; Rasool, Mahmood

Effect of novel IL-8 gene mutation on its protein structure and stability among ovarian cancer patients in Saudi Arabia.

沙特阿拉伯卵巢癌患者中新型IL-8基因突变对其蛋白质结构和稳定性的影响

Haque Absarul, Baig Ghazanfar Ali, Alshawli Abdulelah Saleh, Wali Sait Khalid Hussain, Mohammed Ali Hani S H, Hussain Sait Hesham Khalid, Bibi Fehmida, Pushparaj Peter Natesan, Rasool Mahmood, Naseer Muhammad Imran

Combinatorial Therapeutic Potential of Stem Cells and Benzimidazol Derivatives for the Reduction of Liver Fibrosis

干细胞与苯并咪唑衍生物联合治疗在减少肝纤维化方面的潜力

Iqbal, Maryam; Shams, Sulaiman; Rafiq, Huma; Khan, Momin; Khan, Shahid; Sadique Khattak, Umer; Afridi, Sahib Gul; Bibi, Fehmida; Abdulkareem, Angham Abdulrhman; Naseer, Muhammad Imran