Pages that link to "Q34101193"
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The following pages link to Computational analysis of missense mutations causing Snyder-Robinson syndrome (Q34101193):
Displaying 50 items.
- DelPhi: a comprehensive suite for DelPhi software and associated resources (Q21195848) (← links)
- Analyzing effects of naturally occurring missense mutations (Q21284966) (← links)
- Structural and physico-chemical effects of disease and non-disease nsSNPs on proteins (Q26865027) (← links)
- Molecular mechanisms of disease-causing missense mutations (Q27021940) (← links)
- Chronic Beryllium Disease: revealing the role of beryllium ion and small peptides binding to HLA-DP2 (Q28397104) (← links)
- Cancer missense mutations alter binding properties of proteins and their interaction networks (Q28533927) (← links)
- Rational design of small-molecule stabilizers of spermine synthase dimer by virtual screening and free energy-based approach (Q28544065) (← links)
- In silico and in vitro investigations of the mutability of disease-causing missense mutation sites in spermine synthase (Q28744180) (← links)
- Computational identification of pathogenic associated nsSNPs and its structural impact in UROD gene: a molecular dynamics approach. (Q30361884) (← links)
- An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity. (Q30448340) (← links)
- ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons. (Q30660227) (← links)
- Integrating in silico prediction methods, molecular docking, and molecular dynamics simulation to predict the impact of ALK missense mutations in structural perspective (Q33903573) (← links)
- Investigating the structural impacts of I64T and P311S mutations in APE1-DNA complex: a molecular dynamics approach (Q34181867) (← links)
- Oncogenic potential is related to activating effect of cancer single and double somatic mutations in receptor tyrosine kinases (Q34323807) (← links)
- Protein Nano-Object Integrator (ProNOI) for generating atomic style objects for molecular modeling (Q34503059) (← links)
- Enhancing human spermine synthase activity by engineered mutations (Q34611078) (← links)
- P.Arg82Leu von Hippel-Lindau (VHL) gene mutation among three members of a family with familial bilateral pheochromocytoma in India: molecular analysis and in silico characterization (Q34692517) (← links)
- A missense mutation in CLIC2 associated with intellectual disability is predicted by in silico modeling to affect protein stability and dynamics (Q35093751) (← links)
- On the role of electrostatics in protein–protein interactions (Q35107618) (← links)
- Predicting the Impact of Missense Mutations on Protein-Protein Binding Affinity. (Q35164244) (← links)
- Predicting folding free energy changes upon single point mutations (Q35789039) (← links)
- Structural assessment of the effects of Amino Acid Substitutions on protein stability and protein protein interaction (Q35869151) (← links)
- Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease (Q36324695) (← links)
- Birt-Hogg-Dubé syndrome: a large single family cohort (Q36628829) (← links)
- SAAMBE: Webserver to Predict the Charge of Binding Free Energy Caused by Amino Acids Mutations (Q36847179) (← links)
- Extrapolating the effect of deleterious nsSNPs in the binding adaptability of flavopiridol with CDK7 protein: a molecular dynamics approach (Q37053442) (← links)
- A mutation in a ganglioside biosynthetic enzyme, ST3GAL5, results in salt & pepper syndrome, a neurocutaneous disorder with altered glycolipid and glycoprotein glycosylation (Q37406440) (← links)
- Utilizing multiple in silico analyses to identify putative causal SCN5A variants in Brugada syndrome (Q37517198) (← links)
- Using DelPhi capabilities to mimic protein's conformational reorganization with amino acid specific dielectric constants (Q37664351) (← links)
- SAAFEC: Predicting the Effect of Single Point Mutations on Protein Folding Free Energy Using a Knowledge-Modified MM/PBSA Approach (Q39857355) (← links)
- On human disease-causing amino acid variants: statistical study of sequence and structural patterns (Q39951577) (← links)
- The Bioinformatics Report of Mutation Outcome on NADPH Flavin Oxidoreductase Protein Sequence in Clinical Isolates of H. pylori. (Q40048498) (← links)
- Revealing the Effects of Missense Mutations Causing Snyder-Robinson Syndrome on the Stability and Dimerization of Spermine Synthase (Q40114114) (← links)
- Prediction of phenotypes of missense mutations in human proteins from biological assemblies (Q41955954) (← links)
- A rational free energy-based approach to understanding and targeting disease-causing missense mutations (Q42250997) (← links)
- Investigating the linkage between disease-causing amino acid variants and their effect on protein stability and binding (Q42409589) (← links)
- A Y328C missense mutation in spermine synthase causes a mild form of Snyder-Robinson syndrome (Q42563242) (← links)
- Computational analysis of prolyl hydroxylase domain-containing protein 2 (PHD2) mutations promoting polycythemia insurgence in humans. (Q43093361) (← links)
- In silico profiling and structural insights of missense mutations in RET protein kinase domain by molecular dynamics and docking approach (Q44076075) (← links)
- An Integrated Computational Framework to Assess the Mutational Landscape of α-L-Iduronidase IDUA Gene (Q48285312) (← links)
- Protein-protein interaction sites are hot spots for disease-associated nonsynonymous SNPs. (Q52618147) (← links)
- The impact of active site protonation on substrate ring conformation in Melanocarpus albomyces cellobiohydrolase Cel7B. (Q53211915) (← links)
- Improvement of catalytic efficiency and thermostability of recombinant Streptomyces griseus trypsin by introducing artificial peptide. (Q53633728) (← links)
- Advances in Human Biology: Combining Genetics and Molecular Biophysics to Pave the Way for Personalized Diagnostics and Medicine (Q59042601) (← links)
- Myosin Va and spermine synthase: partners in exosome transport (Q64077575) (← links)
- DFMD: Fast and Effective DelPhiForce Steered Molecular Dynamics Approach to Model Ligand Approach Toward a Receptor: Application to Spermine Synthase Enzyme (Q90267542) (← links)
- Computational Approaches to Prioritize Cancer Driver Missense Mutations (Q90419543) (← links)
- A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations (Q92195237) (← links)
- Bioinformatics classification of mutations in patients with Mucopolysaccharidosis IIIA (Q92440413) (← links)
- In silico analysis predicting effects of deleterious SNPs of human RASSF5 gene on its structure and functions (Q98944936) (← links)