Pages that link to "Q21284966"

The following pages link to Analyzing effects of naturally occurring missense mutations (Q21284966):

Displaying 38 items.

• Structural and physico-chemical effects of disease and non-disease nsSNPs on proteins (Q26865027) (← links)
• Molecular mechanisms of disease-causing missense mutations (Q27021940) (← links)
• Direct evidence on the contribution of a missense mutation in GDF9 to variation in ovulation rate of Finnsheep (Q27337317) (← links)
• Chronic Beryllium Disease: revealing the role of beryllium ion and small peptides binding to HLA-DP2 (Q28397104) (← links)
• Combining structural modeling with ensemble machine learning to accurately predict protein fold stability and binding affinity effects upon mutation (Q28543126) (← links)
• Rational design of small-molecule stabilizers of spermine synthase dimer by virtual screening and free energy-based approach (Q28544065) (← links)
• A multiparametric computational algorithm for comprehensive assessment of genetic mutations in mucopolysaccharidosis type IIIA (Sanfilippo syndrome) (Q28544979) (← links)
• CoagVDb: a comprehensive database for coagulation factors and their associated SAPs (Q30376859) (← links)
• Computational and experimental approaches to reveal the effects of single nucleotide polymorphisms with respect to disease diagnostics (Q33907569) (← links)
• Contrasting patterns of polymorphism and selection in bacterial-sensing toll-like receptor 4 in two house mouse subspecies (Q34034719) (← links)
• Protein Nano-Object Integrator (ProNOI) for generating atomic style objects for molecular modeling (Q34503059) (← links)
• Variation Interpretation Predictors: Principles, Types, Performance, and Choice (Q34518645) (← links)
• Enhancing human spermine synthase activity by engineered mutations (Q34611078) (← links)
• Effect of single amino acid substitution observed in cancer on Pim-1 kinase thermodynamic stability and structure (Q34765874) (← links)
• MutaCYP: Classification of missense mutations in human cytochromes P450 (Q35215197) (← links)
• Types and effects of protein variations (Q35548241) (← links)
• Natural variability of minimotifs in 1092 people indicates that minimotifs are targets of evolution (Q35885933) (← links)
• SAAMBE: Webserver to Predict the Charge of Binding Free Energy Caused by Amino Acids Mutations (Q36847179) (← links)
• Association of epidermal growth factor and epidermal growth factor receptor polymorphisms with the risk of hepatitis B virus-related hepatocellular carcinoma in the population of North China (Q37067080) (← links)
• Single-Nucleotide Polymorphism of PPARγ, a Protein at the Crossroads of Physiological and Pathological Processes. (Q37690874) (← links)
• TopologyNet: Topology based deep convolutional and multi-task neural networks for biomolecular property predictions. (Q38657547) (← links)
• Computing disease-linked SOD1 mutations: deciphering protein stability and patient-phenotype relations (Q38692174) (← links)
• In silico analyses of deleterious missense SNPs of human apolipoprotein E3. (Q38755492) (← 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)
• Forces and Disease: Electrostatic force differences caused by mutations in kinesin motor domains can distinguish between disease-causing and non-disease-causing mutations. (Q41422778) (← links)
• A Y328C missense mutation in spermine synthase causes a mild form of Snyder-Robinson syndrome (Q42563242) (← links)
• Prediction of a highly deleterious mutation E17K in AKT-1 gene: An in silico approach (Q43297858) (← links)
• Structure-function studies on non-synonymous SNPs of chemokine receptor gene implicated in cardiovascular disease: a computational approach (Q45405994) (← links)
• Proteins linked to autosomal dominant and autosomal recessive disorders harbor characteristic rare missense mutation distribution patterns. (Q51820008) (← links)
• Advances in Human Biology: Combining Genetics and Molecular Biophysics to Pave the Way for Personalized Diagnostics and Medicine (Q59042601) (← links)
• GANAB and PKD1 Variations in a 12 Years Old Female Patient With Early Onset of Autosomal Dominant Polycystic Kidney Disease (Q64242779) (← links)
• In Silico Identification of QTL-Based Polymorphic Genes as Salt-Responsive Potential Candidates through Mapping with Two Reference Genomes in Rice (Q89698079) (← links)
• In silico mutational analysis and identification of stability centers in human interleukin-4 (Q90479878) (← links)
• The pharmacological chaperone N-n-butyl-deoxygalactonojirimycin enhances β-galactosidase processing and activity in fibroblasts of a patient with infantile GM1-gangliosidosis (Q90702742) (← links)
• A functional assay to classify ZBTB24 missense variants of unknown significance (Q91842548) (← links)
• 15 years of PhosphoSitePlus®: integrating post-translationally modified sites, disease variants and isoforms (Q93176511) (← links)