Muneeba Aslam
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View article: Core-genome-mediated promising alternative drug and multi-epitope vaccine targets prioritization against infectious Clostridium difficile
Core-genome-mediated promising alternative drug and multi-epitope vaccine targets prioritization against infectious Clostridium difficile Open
Prevention of Clostridium difficile infection is challenging worldwide owing to its high morbidity and mortality rates. C . difficile is currently being classified as an urgent threat by the CDC. Devising a new therapeutic strategy become …
View article: An Immunoinformatics Approach to Design Novel and Potent Multi-Epitope-Based Vaccine to Target Lumpy Skin Disease
An Immunoinformatics Approach to Design Novel and Potent Multi-Epitope-Based Vaccine to Target Lumpy Skin Disease Open
The lumpy skin disease (LSD) virus of the Poxviridae family is a serious threat that mostly affects cattle and causes significant economic loss. LSD has the potential to spread widely and its rapidly across borders. Despite the availabilit…
View article: Core genome mediated potential vaccine targets prioritization against Clostridium difficile via reverse vaccinology - an immuno-informatics approach
Core genome mediated potential vaccine targets prioritization against Clostridium difficile via reverse vaccinology - an immuno-informatics approach Open
The emergence of multi-drug resistance in clostridium difficile is an urgent bio-threat associated with high morbidity and mortality. The availability of core genome sequences for pathogen strains provides the opportunity to rationally app…
View article: Analyzing the Essential Proteins Set of Plasmodium Falciparum PF3D7 for Novel Drug Targets Identification Against Malaria
Analyzing the Essential Proteins Set of Plasmodium Falciparum PF3D7 for Novel Drug Targets Identification Against Malaria Open
Background: Plasmodium falciparum is an obligate intracellular parasite of humans that causes malaria. P. falciparum is a major public health threat to human life responsible for high mortality. Currently, the risk of multi-drug resistance…
View article: Additional file 2 of Analysing the essential proteins set of Plasmodium falciparum PF3D7 for novel drug targets identification against malaria
Additional file 2 of Analysing the essential proteins set of Plasmodium falciparum PF3D7 for novel drug targets identification against malaria Open
Additional file 2 : Plasmodium falciparum strain 3D7 proteins, non-homologous to human as well as human’s gut flora proteins.
View article: Additional file 1 of Analysing the essential proteins set of Plasmodium falciparum PF3D7 for novel drug targets identification against malaria
Additional file 1 of Analysing the essential proteins set of Plasmodium falciparum PF3D7 for novel drug targets identification against malaria Open
Additional file 1: Plasmodium falciparum strain 3D7 non paralogous essential proteins.
View article: Additional file 3 of Analysing the essential proteins set of Plasmodium falciparum PF3D7 for novel drug targets identification against malaria
Additional file 3 of Analysing the essential proteins set of Plasmodium falciparum PF3D7 for novel drug targets identification against malaria Open
Additional file 3 : Plasmodium falciparum 3D7 essential proteins homologs to human gut microbiome proteome.
View article: The In Silico Characterization of a Salicylic Acid Analogue Coding Gene Clusters in Selected <i>Pseudomonas fluorescens</i> Strains.
The In Silico Characterization of a Salicylic Acid Analogue Coding Gene Clusters in Selected <i>Pseudomonas fluorescens</i> Strains. Open
The computational biology and drug discovery analyses identified different gene clusters in P. fluorescens genomes coding for salicylic acid-like chemotypes biosynthesis. These gene clusters may worthy to target through metabolic engineeri…