Abdul Aziz
Karak, KP, Pakistan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications
Network pharmacology and molecular simulations reveal multi-target neuroprotective potential of Rhamnolipid and Surfactin against Alzheimer's disease.
Journal: Brain research bulletin
Published: August 25, 2025
Inflammatory cell death and leukemia treatment.
Journal: Critical reviews in oncology/hematology
Published: August 01, 2025
Evaluation of fluorinated phospholipid analogs: A study on ADMET profiles, molecular docking and dynamics simulation in anticancer therapy.
Journal: Heliyon
Published: August 05, 2024
In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis.
Journal: Pharmaceuticals (Basel, Switzerland)
Published: April 09, 2023
Structural Evaluation and Conformational Dynamics of ZNF141T474I Mutation Provoking Postaxial Polydactyly Type A.
Journal: Bioengineering (Basel, Switzerland)
Published: October 20, 2022
Identification and In Silico Analysis of a Homozygous Nonsense Variant in TGM1 Gene Segregating with Congenital Ichthyosis in a Consanguineous Family.
Journal: Medicina (Kaunas, Lithuania)
Published: October 18, 2022
A detailed comparative analysis of codon usage bias in Alongshan virus.
Journal: Virus research
Published: August 06, 2021
Novel Frameshift Mutations in XPC Gene Underlie Xeroderma Pigmentosum in Pakistani Families.
Journal: Indian journal of dermatology
Published: June 30, 2021
Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly.
Journal: Human genetics
Published: January 29, 2019
FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: April 30, 2018
A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family.
Journal: BMC medical genetics
Published: August 22, 2016
Last Updated: 09/26/2026