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Publications by Mohammad Sarwar Jamal
Computing Disease-Linked SOD1 Mutations: Deciphering Protein Stability and Patient-Phenotype Relations
Scientific Reports
Multidisciplinary
Computational Analysis of Protein Structure Changes as a Result of Nondeletion Insertion Mutations in Human Β-Globin Gene Suggests Possible Cause of Β-Thalassemia
BioMed Research International
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
Related publications
Point Mutations in Ferroportin Disease: Genotype/Phenotype Correlation
Prediction of Protein Stability Upon Point Mutations
Biochemical Society Transactions
Biochemistry
Genotype-Phenotype Relations of the Von Hippel-Lindau Tumor Suppressor Inferred From a Large-Scale Analysis of Disease Mutations and Interactors
PLoS Computational Biology
Molecular Neuroscience
Evolution
Ecology
Genetics
Behavior
Molecular Biology
Systematics
Simulation
Cellular
Computational Theory
Mathematics
Modeling
Menkes X Linked Disease: Heterozygous Phenotype in Uncloned Fibroblast Cultures.
Journal of Medical Genetics
Genetics
Patient Mutations Linked to Arrhythmogenic Cardiomyopathy Enhance Calpain-Mediated Desmoplakin Degradation
JCI insight
Medicine
Gut Microbiota in Parkinson's Disease: Temporal Stability and Relations to Disease Progression
EBioMedicine
Biochemistry
Medicine
Genetics
Molecular Biology
X-Linked Carriers of Chronic Granulomatous Disease: Illness, Lyonization, and Stability
Journal of Allergy and Clinical Immunology
Allergy
Immunology
Combined Effects of Two Mutations in Von Willebrand Disease 2M Phenotype
Research and Practice in Thrombosis and Haemostasis
ACTH (Acthar Gel) Reduces Toxic SOD1 Protein Linked to Amyotrophic Lateral Sclerosis in Transgenic Mice: A Novel Observation
PLoS ONE
Multidisciplinary
