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Arif Mahmood
Arif Mahmood
Central South University, China
在 sklmg.edu.cn 的电子邮件经过验证
标题
引用次数
引用次数
年份
Identification of novel inhibitors for SARS-CoV-2 as therapeutic options using machine learning-based virtual screening, molecular docking and MD simulation
A Samad, A Ajmal, A Mahmood, B Khurshid, P Li, SM Jan, AU Rehman, ...
Frontiers in Molecular Biosciences 10, 1060076, 2023
272023
Microglia and astrocytes dysfunction and key neuroinflammation-based biomarkers in Parkinson’s disease
K Chen, H Wang, I Ilyas, A Mahmood, L Hou
Brain Sciences 13 (4), 634, 2023
162023
The comparison of mutational progression in SARS-CoV-2: A short updated overview
A Asif, I Ilyas, M Abdullah, S Sarfraz, M Mustafa, A Mahmood
Journal of Molecular Pathology 3 (4), 201-218, 2022
152022
Molecular Insights into the Role of Pathogenic nsSNPs in GRIN2B Gene Provoking Neurodevelopmental Disorders
AA Shah, M Amjad, JU Hassan, A Ullah, A Mahmood, H Deng, Y Ali, F Gul, ...
Genes 13 (8), 1332, 2022
152022
Computer-assisted drug repurposing for thymidylate kinase drug target in monkeypox virus
A Ajmal, A Mahmood, C Hayat, MA Hakami, BS Alotaibi, M Umair, ...
Frontiers in Cellular and Infection Microbiology 13, 1159389, 2023
132023
Recalling the pathology of Parkinson's disease; lacking exact figure of prevalence and genetic evidence in Asia with an alarming outcome: A time to step‐up
A Mahmood, AA Shah, M Umair, Y Wu, A Khan
Clinical Genetics 100 (6), 659-677, 2021
132021
New drug target identification in Vibrio vulnificus by subtractive genome analysis and their inhibitors through molecular docking and molecular dynamics simulations
BS Alotaibi, A Ajmal, MA Hakami, A Mahmood, A Wadood, J Hu
Heliyon 9 (7), 2023
122023
A novel biallelic variant in the Popeye domain‐containing protein 1 (POPDC1) underlies limb girdle muscle dystrophy type 25
A Mahmood, A Samad, AA Shah, A Wadood, A Alkathiri, MA Alshehri, ...
Clinical Genetics 103 (2), 219-225, 2023
122023
Homozygous missense variant in POPDC3 causes recessive limb‐girdle muscular dystrophy type 26
A Ullah, Z Lin, M Younus, S Shafiq, S Khan, M Rasheed, A Mahmood, ...
The Journal of Gene Medicine 24 (4), e3412, 2022
112022
Assessment of antimicrobial, antioxidant and cytotoxicity properties of Camellia sinensis L.
SB Shah, Z Parveen, M Bilal, L Sartaj, S Bibi, A Nasir, A Mahmood
Pakistan Journal of Pharmaceutical Sciences 31 (4), 2018
92018
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia
A Ullah, AA Shah, F Syed, A Mahmood, H Ur Rehman, B Khurshid, ...
Medicina 59 (2), 379, 2023
72023
Identification of novel peptide inhibitors for oncogenic KRAS G12D as therapeutic options using mutagenesis-based remodeling and MD simulations
A Samad, B Khurshid, A Mahmood, AU Rehman, A Khalid, AN Abdalla, ...
Journal of Biomolecular Structure and Dynamics 41 (22), 13425-13437, 2023
62023
Genetic advances in skeletal disorders: an overview
S Abbas, H Khan, Q Alam, A Mahmood, M Umair
J Biochem Clin Genet 6 (1), 0, 2023
52023
Structural and dynamics insights into the GBA variants associated with Parkinson’s disease
A Mahmood, A Samad, S Bano, M Umair, A Ajmal, I Ilyas, AA Shah, P Li, ...
Journal of Biomolecular Structure and Dynamics 42 (12), 6256-6268, 2024
42024
Biallelic variants in seven different genes Associated with clinically suspected Bardet–Biedl Syndrome
H Nawaz, Mujahid, SA Khan, F Bibi, A Waqas, A Bari, Fardous, N Khan, ...
Genes 14 (5), 1113, 2023
42023
In Silico Analysis of nsSNPs of Human KRAS Gene and Protein Modeling Using Bioinformatic Tools
D Xu, Q Shao, C Zhou, A Mahmood, J Zhang
ACS omega 8 (14), 13362-13370, 2023
42023
Integrative Genomic Analysis of m6a-SNPs Identifies Potential Functional Variants Associated with Alzheimer’s Disease
SM Jan, A Fahira, Y Shi, MI Khan, A Jamal, A Mahmood, S Shams, ...
ACS omega 8 (14), 13332-13341, 2023
32023
Identification of novel STAT3 inhibitors for liver fibrosis, using pharmacophore-based virtual screening, molecular docking, and biomolecular dynamics simulations
H Rafiq, J Hu, MA Hakami, A Hazazi, MA Alamri, HA Alkhatabi, ...
Scientific Reports 13 (1), 20147, 2023
22023
A biallelic variant in IQCE predisposed to cause non-syndromic post-axial polydactyly type A
M Bilal, M Raheel, G Hassan, S Zeb, A Mahmood, Z Zehri, HY Manzoor, ...
J Biochem Clin Genet 6 (1), 29-35, 2023
22023
Next-generation sequencing to genetically diagnose a diverse range of inherited eye disorders in 15 consanguineous families from Pakistan.
R Basharat, SE de Bruijn, M Zahid, K Rodenburg, RJ Hitti-Malin, ...
Experimental Eye Research, 109945, 2024
2024
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