Muhammad A. Latif

Medina, Saudi Arabia

Last Updated: 09/26/2026

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Found 47 publications

Iodine-catalyzed green and efficient synthesis of secondary and tert-esters of N-acetyl-protected amino acids.

Iodine-catalyzed green and efficient synthesis of secondary and tert-esters of N-acetyl-protected amino acids.

Journal: RSC advances

Published: April 21, 2026

Molecular Profiling of Soil-Derived Bacillus subtilis and Bacillus paralicheniformis: Evaluation of Anticancer and Antibacterial Efficacy Against Gastrointestinal Pathogens.

Molecular Profiling of Soil-Derived Bacillus subtilis and Bacillus paralicheniformis: Evaluation of Anticancer and Antibacterial Efficacy Against Gastrointestinal Pathogens.

Journal: Current issues in molecular biology

Published: April 08, 2026

Pharmacological investigation of a selected triazole derivative against acetic acid-induced ulcerative colitis in mouse model.

Pharmacological investigation of a selected triazole derivative against acetic acid-induced ulcerative colitis in mouse model.

Journal: Biochemical and biophysical research communications

Published: March 15, 2026

Mutation mapping and functional characterization of a missense mutation p.Arg228Cys in ALDH3A2 gene causing Sjögran-Larson syndrome.

Mutation mapping and functional characterization of a missense mutation p.Arg228Cys in ALDH3A2 gene causing Sjögran-Larson syndrome.

Journal: Molecular biology reports

Published: March 04, 2026

Recessive PPTC7 deficiency triggers excessive mitophagy to cause a severe inborn error of metabolism with hypomyelinating leukodystrophy.

Recessive PPTC7 deficiency triggers excessive mitophagy to cause a severe inborn error of metabolism with hypomyelinating leukodystrophy.

Journal: Research square

Published: February 27, 2026

Design, synthesis, and enzyme kinetic evaluation of oxadiazole derivatives as nucleoside triphosphate diphosphohydrolase (NTPDase) inhibitors: an integrated in vitro and in silico approach.

Design, synthesis, and enzyme kinetic evaluation of oxadiazole derivatives as nucleoside triphosphate diphosphohydrolase (NTPDase) inhibitors: an integrated in vitro and in silico approach.

Journal: RSC advances

Published: February 21, 2026

Potentially Deleterious Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in the Human MCPH1 Gene: Systematic In Silico Predictions and Implications for Structure and Function.

Potentially Deleterious Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in the Human MCPH1 Gene: Systematic In Silico Predictions and Implications for Structure and Function.

Journal: Human mutation

Published: October 07, 2025

Nephrotoxicity Evaluation of Green and Chemically Synthesized Copper Oxide Nanoparticles in Rats: A Biochemical and Genotoxic Approach.

Nephrotoxicity Evaluation of Green and Chemically Synthesized Copper Oxide Nanoparticles in Rats: A Biochemical and Genotoxic Approach.

Journal: Current pharmaceutical design

Published: March 29, 2025

Whole exome sequencing: Unlocking the molecular diagnostic odyssey in Pakhtun ethnic group of Pakistani population.

Whole exome sequencing: Unlocking the molecular diagnostic odyssey in Pakhtun ethnic group of Pakistani population.

Journal: Gene

Published: March 06, 2025

Correction: Novel pyrimidine linked acyl thiourea derivatives as potent α-amylase and proteinase K inhibitors: design, synthesis, molecular docking and ADME studies.

Correction: Novel pyrimidine linked acyl thiourea derivatives as potent α-amylase and proteinase K inhibitors: design, synthesis, molecular docking and ADME studies.

Journal: RSC advances

Published: January 13, 2025

Genetic Studies on Multiple Consanguineous Families Segregating Diverse Phenotypes of Microphthalmia Identified Novel and Recurrent Mutations.

Genetic Studies on Multiple Consanguineous Families Segregating Diverse Phenotypes of Microphthalmia Identified Novel and Recurrent Mutations.

Journal: Current medicinal chemistry

Published: November 10, 2024

Identification of a Protein-truncating Variant in SCAPER Gene Causing Syndromic form of Intellectual Disability.

Identification of a Protein-truncating Variant in SCAPER Gene Causing Syndromic form of Intellectual Disability.

Journal: Current medicinal chemistry

Published: November 08, 2024

Showing 1-12 of 47

Last Updated: 09/26/2026