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Apolipoprotein E Polymorphism And It's Lifestyle Impact.
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- Journal of Advanced Zoology, 2024, v. 45, n. 1, p. 425
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Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach.
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- PLoS ONE, 2017, v. 12, n. 4, p. 1, doi. 10.1371/journal.pone.0174953
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Bioinformatics classification of mutations in patients with Mucopolysaccharidosis IIIA.
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- Metabolic Brain Disease, 2019, v. 34, n. 6, p. 1577, doi. 10.1007/s11011-019-00465-6
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Computational modelling approaches as a potential platform to understand the molecular genetics association between Parkinson’s and Gaucher diseases.
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- Metabolic Brain Disease, 2018, v. 33, n. 6, p. 1835, doi. 10.1007/s11011-018-0286-3
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Impact of missense mutations in survival motor neuron protein (SMN1) leading to Spinal Muscular Atrophy (SMA): A computational approach.
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- Metabolic Brain Disease, 2018, v. 33, n. 6, p. 1823, doi. 10.1007/s11011-018-0285-4
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- Article
Computational approach to unravel the impact of missense mutations of proteins (D2HGDH and IDH2) causing D-2-hydroxyglutaric aciduria 2.
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- Metabolic Brain Disease, 2018, v. 33, n. 5, p. 1699, doi. 10.1007/s11011-018-0278-3
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Determination of potential combination of non‐β‐lactam, β‐lactam, and β‐lactamase inhibitors/β‐lactam enhancer against class D oxacillinases producing Acinetobacter baumannii: Evidence from in‐vitro, molecular docking and dynamics simulation
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- Journal of Cellular Biochemistry, 2023, v. 124, n. 7, p. 974, doi. 10.1002/jcb.30424
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Comparison of potential inhibitors and targeting fat mass and obesity‐associated protein causing diabesity through docking and molecular dynamics strategies.
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- Journal of Cellular Biochemistry, 2021, v. 122, n. 11, p. 1625, doi. 10.1002/jcb.30109
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- Article
An integrative bioinformatics pipeline to demonstrate the alteration of the interaction between the ALDH2*2 allele with NAD<sup>+</sup> and Disulfiram.
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- Journal of Cellular Biochemistry, 2019, v. 120, n. 10, p. 17030, doi. 10.1002/jcb.28964
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A computational method to characterize the missense mutations in the catalytic domain of GAA protein causing Pompe disease.
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- Journal of Cellular Biochemistry, 2019, v. 120, n. 3, p. 3491, doi. 10.1002/jcb.27624
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Structural analysis of missense mutations in galactokinase 1 (GALK1) leading to galactosemia type‐2.
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- Journal of Cellular Biochemistry, 2018, v. 119, n. 9, p. 7585, doi. 10.1002/jcb.27097
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A Molecular Docking and Dynamics Approach to Screen Potent Inhibitors Against Fosfomycin Resistant Enzyme in Clinical Klebsiella pneumoniae.
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- Journal of Cellular Biochemistry, 2017, v. 118, n. 11, p. 4088, doi. 10.1002/jcb.26064
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Structural Analysis of G1691S Variant in the Human Filamin B Gene Responsible for Larsen Syndrome: A Comparative Computational Approach.
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- Journal of Cellular Biochemistry, 2017, v. 118, n. 7, p. 1900, doi. 10.1002/jcb.25920
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Designing, Synthesis, and Anti‐Breast Cancer Activity of a Series of New Quinazolin‐4(1H)‐one Derivatives.
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- Chemistry & Biodiversity, 2022, v. 19, n. 12, p. 1, doi. 10.1002/cbdv.202200662
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- Article
Deciphering the Role of Filamin B Calponin-Homology Domain in Causing the Larsen Syndrome, Boomerang Dysplasia, and Atelosteogenesis Type I Spectrum Disorders via a Computational Approach.
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- Molecules, 2020, v. 25, n. 23, p. 5543, doi. 10.3390/molecules25235543
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A COMPREHENSIVE INSILICO ANALYSIS OF MISSENSE MUTATIONS IN CDH7 PROTEIN CAUSING CHARGE SYNDROME.
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- Nitte University Journal of Health Science, 2018, p. 173
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- Article
Involvement of Essential Signaling Cascades and Analysis of Gene Networks in Diabesity.
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- Genes, 2020, v. 11, n. 11, p. 1256, doi. 10.3390/genes11111256
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Genotype--phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants.
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- Human Molecular Genetics, 2017, v. 26, n. 16, p. 3105, doi. 10.1093/hmg/ddx195
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Inhibition of MMP2-PEX by a novel ester of dihydroxy cinnamic and linoleic acid from the seagrass Cymodocea serrulata.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-90845-9
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Analysis of Differentially Expressed Genes and Molecular Pathways in Familial Hypercholesterolemia Involved in Atherosclerosis: A Systematic and Bioinformatics Approach.
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- Frontiers in Genetics, 2020, v. 11, p. 1, doi. 10.3389/fgene.2020.00734
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Mixed azo dyes degradation by an intracellular azoreductase enzyme from alkaliphilic Bacillus subtilis: a molecular docking study.
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- Archives of Microbiology, 2021, v. 203, n. 6, p. 3033, doi. 10.1007/s00203-021-02299-2
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In Silico Identification of Multi-target Anti-SARS-CoV-2 Peptides from Quinoa Seed Proteins.
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- International Journal of Peptide Research & Therapeutics, 2021, v. 27, n. 3, p. 1837, doi. 10.1007/s10989-021-10214-y
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Molecular dynamics, residue network analysis, and cross-correlation matrix to characterize the deleterious missense mutations in GALE causing galactosemia III.
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- Cell Biochemistry & Biophysics, 2021, v. 79, n. 2, p. 201, doi. 10.1007/s12013-020-00960-z
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Mechanism of artemisinin resistance for malaria PfATP6 L263 mutations and discovering potential antimalarials: An integrated computational approach.
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- Scientific Reports, 2016, p. 30106, doi. 10.1038/srep30106
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3-Hydroxypropane-1,2-Diyl Dipalmitoleate—A Natural Compound with Dual Roles (CB1 Agonist/FAAH1 Blocker) in Inhibiting Ovarian Cancer Cell Line.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 3, p. 255, doi. 10.3390/ph14030255
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DNA Repair Gene (XRCC1) Polymorphism (Arg399Gln) Associated with Schizophrenia in South Indian Population: A Genotypic and Molecular Dynamics Study.
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- PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0147348
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- Article