On human disease-causing amino acid variants: statistical study of sequence and structural patterns.
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Induced Structural Disorder as a Molecular Mechanism for Enzyme Dysfunction in Phosphoglucomutase 1 DeficiencyInfluence of V54M mutation in giant muscle protein titin: a computational screening and molecular dynamics approach.Large scale analysis of protein stability in OMIM disease related human protein variantsIn silico Mapping of Protein Unfolding Mutations for Inherited DiseaseA Structural View of Negative Regulation of the Toll-like Receptor-Mediated Inflammatory Pathway.Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease.SAAMBE: Webserver to Predict the Charge of Binding Free Energy Caused by Amino Acids Mutations.Genetic Epidemiology of Glucose-6-Dehydrogenase Deficiency in the Arab World.Asp263 missense variants perturb the active site of human phosphoglucomutase 1.SAAFEC: Predicting the Effect of Single Point Mutations on Protein Folding Free Energy Using a Knowledge-Modified MM/PBSA Approach.mutation3D: Cancer Gene Prediction Through Atomic Clustering of Coding Variants in the Structural Proteome.The Contribution of Missense Mutations in Core and Rim Residues of Protein-Protein Interfaces to Human Disease.Forces and Disease: Electrostatic force differences caused by mutations in kinesin motor domains can distinguish between disease-causing and non-disease-causing mutations.Decoding disease-causing mechanisms of missense mutations from supramolecular structures.Spatial distribution of disease-associated variants in three-dimensional structures of protein complexes.Investigating the linkage between disease-causing amino acid variants and their effect on protein stability and binding.Computational Investigation of the Missense Mutations in DHCR7 Gene Associated with Smith-Lemli-Opitz Syndrome.Predicting protein-DNA binding free energy change upon missense mutations using modified MM/PBSA approach: SAMPDI webserver.Identification and in silico analysis of functional SNPs of human TAGAP protein: A comprehensive study.Blocking protein quality control to counter hereditary cancers.An Integrated Computational Framework to Assess the Mutational Landscape of α-L-Iduronidase IDUA Gene.Large differences in proportions of harmful and benign amino acid substitutions between proteins and diseasesOncogenic activation of the STAT3 pathway drives PD-L1 expression in natural killer/T-cell lymphoma
P2860
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P2860
On human disease-causing amino acid variants: statistical study of sequence and structural patterns.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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name
On human disease-causing amino ...... uence and structural patterns.
@en
On human disease-causing amino ...... uence and structural patterns.
@nl
type
label
On human disease-causing amino ...... uence and structural patterns.
@en
On human disease-causing amino ...... uence and structural patterns.
@nl
prefLabel
On human disease-causing amino ...... uence and structural patterns.
@en
On human disease-causing amino ...... uence and structural patterns.
@nl
P2093
P2860
P356
P1433
P1476
On human disease-causing amino ...... uence and structural patterns.
@en
P2093
Emil Alexov
Marharyta Petukh
Tugba G Kucukkal
P2860
P304
P356
10.1002/HUMU.22770
P577
2015-04-06T00:00:00Z