Pages that link to "Q33737049"

The following pages link to Sequence feature-based prediction of protein stability changes upon amino acid substitutions (Q33737049):

Displaying 36 items.

• Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia (Q24300321) (← links)
• Molecular mechanisms of disease-causing missense mutations (Q27021940) (← links)
• Predicting protein sumoylation sites from sequence features (Q28250129) (← links)
• Investigating regulatory signatures of human autophagy related gene 5 (ATG5) through functional in silico analysis (Q28828390) (← links)
• Deciphering the impact of somatic mutations in exon 20 and exon 9 of PIK3CA gene in breast tumors among Indian women through molecular dynamics approach. (Q30371703) (← links)
• Genetic diversity of tyrosine hydroxylase (TH) and dopamine β-hydroxylase (DBH) genes in cattle breeds. (Q30420305) (← links)
• Sequence-only evolutionary and predicted structural features for the prediction of stability changes in protein mutants (Q30426634) (← links)
• MAESTRO--multi agent stability prediction upon point mutations. (Q30641756) (← links)
• The role of balanced training and testing data sets for binary classifiers in bioinformatics (Q30656566) (← links)
• Towards sequence-based prediction of mutation-induced stability changes in unseen non-homologous proteins (Q33715655) (← links)
• Feature-based multiple models improve classification of mutation-induced stability changes (Q33851583) (← links)
• Computational and experimental approaches to reveal the effects of single nucleotide polymorphisms with respect to disease diagnostics (Q33907569) (← links)
• Pathological unfoldomics of uncontrolled chaos: intrinsically disordered proteins and human diseases (Q33909288) (← links)
• Computational analysis of missense mutations causing Snyder-Robinson syndrome (Q34101193) (← links)
• Variation Interpretation Predictors: Principles, Types, Performance, and Choice (Q34518645) (← links)
• Structural assessment of the effects of Amino Acid Substitutions on protein stability and protein protein interaction (Q35869151) (← links)
• Molecular findings of Colombian patients with type VI mucopolysaccharidosis (Maroteaux-Lamy syndrome). (Q36521405) (← links)
• Misfolding of galactose 1-phosphate uridylyltransferase can result in type I galactosemia. (Q36920205) (← links)
• Disparate thermostability profiles and HN gene domains of field isolates of Newcastle disease virus from live bird markets and waterfowl in Uganda (Q37024583) (← links)
• Potential entry inhibitors of the envelope protein (E2) of Chikungunya virus: in silico structural modeling, docking and molecular dynamic studies (Q38688307) (← links)
• A Computational Approach to Identify a Potential Alternative Drug With Its Positive Impact Toward PMP22. (Q38735331) (← links)
• SDM: a server for predicting effects of mutations on protein stability (Q38774417) (← links)
• In silico analysis of non-synonymous single nucleotide polymorphisms in human DAZL gene associated with male infertility. (Q38847871) (← links)
• Annotating Mutational Effects on Proteins and Protein Interactions: Designing Novel and Revisiting Existing Protocols (Q38966406) (← links)
• Multifactorial level of extremostability of proteins: can they be exploited for protein engineering? (Q39173556) (← links)
• Molecular Characterization of a Novel Germline VHL Mutation by Extensive In Silico Analysis in an Indian Family with Von Hippel-Lindau Disease (Q39649309) (← links)
• The Bioinformatics Report of Mutation Outcome on NADPH Flavin Oxidoreductase Protein Sequence in Clinical Isolates of H. pylori. (Q40048498) (← links)
• An In Silico Evaluation of Deleterious Nonsynonymous Single Nucleotide Polymorphisms in the ErbB3 Oncogene (Q41133462) (← links)
• Computational Analysis of High Risk Missense Variant in Human UTY Gene: A Candidate Gene of AZFa Sub-region (Q44579596) (← links)
• Structural and functional in silico analysis of LRRK2 missense substitutions (Q45143202) (← links)
• A profound computational study to prioritize the disease-causing mutations in PRPS1 gene (Q47631088) (← links)
• Computational insights of K1444N substitution in GAP-related domain of NF1 gene associated with neurofibromatosis type 1 disease: a molecular modeling and dynamics approach (Q57657552) (← links)
• Computer-Assisted Recombination (CompassR) Teaches us How to Recombine Beneficial Substitutions from Directed Evolution Campaigns (Q90274270) (← links)
• Survivin polymorphisms and susceptibility to prostate cancer: A genetic association study and an in silico analysis (Q90400839) (← links)
• Convolution Neural Network-Based Prediction of Protein Thermostability (Q90969189) (← links)
• Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome (Q92751178) (← links)