Arif Mahmood - Hunan Key Lab Med Genet, Cent South Univ

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个人简介

Arif Mahmood currently works at the Department of Biochemistry, Quaid-i-Azam University. Arif does research in Human Molecular Genetics, Biochemistry and Cell Biology

研究兴趣

论文共 30 篇作者统计合作学者相似作者

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The Deleterious Variants of N-acetylgalactosamine-6-sulfatase (galn6s) Enzyme Trigger Morquio a Syndrome by Disrupting Protein Foldings

Jiuyi Li, Waqas Ahmad Khalid, Hina Imtiaz,Lingkun Huang,Yasir Ali,Rimsha Yousaf,Fouzia Gul,Arif Mahmood,Abid Ali Shah,Huiyin Deng,Saadullah Khattak

JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICSno. 7 (2024): 3700-3711

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A Novel CLRN2 Variant: Expanding the Mutation Spectrum and Its Critical Role in Isolated Hearing Impairment

Farooq Ahmad,Arif Mahmood, Ibrahim Abdullah Almazni, Afnan Mohammed Shakoori, Fatemah Alhakami,Qamre Alam, Muhammad Ismail, Muhammad Umair

Genes &amp Genomics（2024）

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Structural and Dynamics Insights into the GBA Variants Associated with Parkinson's Disease

Arif Mahmood,Abdus Samad,Shazia Bano,Muhammad Umair,Amar Ajmal,Iqra Ilyas,Abid Ali Shah, Ping Li,Junjian Hu

JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS（2024）

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Loss-of-function Variant in the LRR Domain of SLITRK2 Implicated in a Neurodevelopmental Disorder

Tayyaba Afsar, Hongxia Fu,Hammal Khan, Zain Ali,Zamrud Zehri,Gohar Zaman,Safdar Abbas,Arif Mahmood,Qamre Alam,Junjian Hu,Suhail Razak,Muhammad Umair

Frontiers in genetics (2024): 1308116-1308116

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Identification of Novel NLRP3 Inhibitors As Therapeutic Options for Epilepsy by Machine Learning-Based Virtual Screening, Molecular Docking and Biomolecular Simulation Studies

Maryam Zulfat,Mohammed Ageeli Hakami,Ali Hazazi,Arif Mahmood,Asaad Khalid, Roaya S. Alqurashi,Ashraf N. Abdalla,Junjian Hu,Abdul Wadood, Xiaoyun Huang

Heliyonno. 15 (2024): e34410-e34410

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Truncated DNM1 Variant Underlines Developmental Delay and Epileptic Encephalopathy

Tayyaba Afsar, Xiaoyun Huang,Abid Ali Shah,Safdar Abbas,Shazia Bano,Arif Mahmood,Junjian Hu,Suhail Razak,Muhammad Umair

Frontiers in pediatrics（2023）

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Uncovering the Genetic Basis of Hyperphosphatasia with Impaired Intellectual Development Syndrome Type 2: Identification of a Novel Biallelic Nonsense Mutation in PIGO Gene

Anam Nayab, Shagufta Andleeb,Shah Zeb, Hafiza Manzoor,Zamrud Zehri,Arif Mahmood,Hammal Khan,Muhammad Umair,Ahmed Waqas

Journal of Biochemical and Clinical Geneticspp.22-28, (2023)

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Microglia and Astrocytes Dysfunction and Key Neuroinflammation-Based Biomarkers in Parkinson’s Disease

Kun Chen, Haoyang Wang,Iqra Ilyas,Arif Mahmood,Lijun Hou

Brain Sciences（2023）

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A novel biallelic variant in the Popeye domain-containing protein 1 (POPDC1) underlies limb girdle muscle dystrophy type 25

Arif Mahmood,Abdus Samad,Abid Ali Shah,Abdul Wadood,Afnan Alkathiri,Mohammed Ali Alshehri,Mohammad Zubair Alam, Taimur Hussain,Pei He,Muhammad Umair

Clin Genet（2023）

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Identification of Novel STAT3 Inhibitors for Liver Fibrosis, Using Pharmacophore-Based Virtual Screening, Molecular Docking, and Biomolecular Dynamics Simulations

Huma Rafiq,Junjian Hu,Mohammed Ageeli Hakami,Ali Hazazi,Mubarak A. Alamri,Hind A. Alkhatabi,Arif Mahmood,Bader S. Alotaibi,Abdul Wadood,Xiaoyun Huang

Scientific Reportsno. 1 (2023)

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