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Abbreviation : nsSNPs
Long Form : non-synonymous single nucleotide polymorphisms
No. Year Title Co-occurring Abbreviation
2020 Assessing protein sequencing in human single hair shafts of decreasing lengths. SAPs
2020 Conformational Changes Induced by S34Y and R98C Variants in the Death Domain of Myd88. DD, MD, MyD88
2020 In silico analysis and high-risk pathogenic phenotype predictions of non-synonymous single nucleotide polymorphisms in human Crystallin beta A4 gene associated with congenital cataract. CRYBA4
2020 In silico analysis of non-synonymous single nucleotide polymorphisms (nsSNPs) in the human GJA3 gene associated with congenital cataract. GJA3
2020 In silico analysis of nonsynonymous single-nucleotide polymorphisms (nsSNPs) of the SMPX gene. ---
2020 In Silico Prediction of the Effects of Nonsynonymous Single Nucleotide Polymorphisms in the Human Catechol-O-Methyltransferase (COMT) Gene. COMT
2019 Assessment of structurally and functionally high-risk nsSNPs impacts on human bone morphogenetic protein receptor type IA (BMPR1A) by computational approach. ALK3, GDF5, TGF-beta
2019 Biochemical regulation and structural analysis of copper-transporting ATPase in a human hepatoma cell line for Wilson disease. MDS, MTT, ROS, WD
2019 Computational Screening and Analysis of Lung Cancer Related Non-Synonymous Single Nucleotide Polymorphisms on the Human Kirsten Rat Sarcoma Gene. KRAS
10  2019 Contribution of non-HLA incompatibility between donor and recipient to kidney allograft survival: genome-wide analysis in a prospective cohort. ---
11  2019 Cynomolgus macaque IL37 polymorphism and control of SIV infection. ---
12  2019 DAMpred: Recognizing Disease-Associated nsSNPs through Bayes-Guided Neural-Network Model Built on Low-Resolution Structure Prediction of Proteins and Protein-Protein Interactions. ---
13  2019 dbPTM in 2019: exploring disease association and cross-talk of post-translational modifications. PTMs
14  2019 Enriching Human Interactome with Functional Mutations to Detect High-Impact Network Modules Underlying Complex Diseases. DIMSUM, GWAS, PPI
15  2019 From genomic variation to protein aberration: Mutational analysis of single nucleotide polymorphism present in ULBP6 gene and implication in immune response. NKG2D, ULBP6
16  2019 Genome analysis of Yucatan miniature pigs to assess their potential as biomedical model animals. GO, KEGG, SIFT, YMPs
17  2019 Identification and structural characterization of deleterious non-synonymous single nucleotide polymorphisms in the human SKP2 gene. SCF, SKP2
18  2019 Investigation of deleterious effects of nsSNPs in the POT1 gene: a structural genomics-based approach to understand the mechanism of cancer development. POT1
19  2019 Investigation of hub genes and their nonsynonymous single nucleotide polymorphism analysis in Plasmodium falciparum for designing therapeutic methodologies using next-generation sequencing approach. PPI
20  2019 Molecular Modelling and Dynamics Study of nsSNP in STXBP1 Gene in Early Infantile Epileptic Encephalopathy Disease. ---
21  2019 Prediction and Structural Comparison of Deleterious Coding Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in Human LEP Gene Associated with Obesity. ---
22  2019 Shedding Light on the Interaction of Human Anti-Apoptotic Bcl-2 Protein with Ligands through Biophysical and in Silico Studies. FLD, HTVS, TSA
23  2019 SOD1 in amyotrophic lateral sclerosis development - in silico analysis and molecular dynamics of A4F and A4V variants. ALS, FALS
24  2019 Structural bioinformatics analysis of variants on GPCR function. CB1, CNS, GPCRs
25  2019 Systematic exploration of predicted destabilizing nonsynonymous single nucleotide polymorphisms (nsSNPs) of human aldehyde oxidase: A Bio-informatics study. XO
26  2019 The rs61742690 (S783N) single nucleotide polymorphism is a suitable target for disrupting BCL11A-mediated foetal-to-adult globin switching. BCL11A, SCD, UTR
27  2019 Understanding the structure-function relationship of HPRT1 missense mutations in association with Lesch-Nyhan disease and HPRT1-related gout by in silico mutational analysis. HGPRT1, HPRT1, MDS
28  2018 Characterization of gene expression and genetic variation of horse ERBB receptor feedback inhibitor 1 in Thoroughbreds. ERRFI1, TF
29  2018 Functional Polymorphisms in DNA Repair Genes Are Associated with Sporadic Colorectal Cancer Susceptibility and Clinical Outcome. CRC, TNM
30  2018 Impact of a non-synonymous Q281R polymorphism on structure of human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2 ). ED, LDL, Lp-PLA2, MD, ProSA, SVM, WT
31  2018 In Silico Analysis of nsSNPs of Carp TLR22 Gene Affecting its Binding Ability with Poly I:C. LRR, TLR22
32  2018 In silico approaches to discover the functional impact of non-synonymous single nucleotide polymorphisms in selective sweep regions of the Landrace genome. ---
33  2018 In silico approaches to identify the functional and structural effects of non-synonymous SNPs in selective sweeps of the Berkshire pig genome. ---
34  2018 Non-Synonymous Single-Nucleotide Polymorphisms and Physical Activity Interactions on Adiposity Parameters in Malaysian Adolescents. GRS, PA, PAQ-C
35  2018 Nonsynonymous Polymorphism in Guanine Monophosphate Synthetase Is a Risk Factor for Unfavorable Thiopurine Metabolite Ratios in Patients With Inflammatory Bowel Disease. 6-MMP, 6-TGN, GMPS, IBD
36  2018 Novel polymorphisms associated with hyperalphalipoproteinemia and apparent cardioprotection. CHD, HALP, HDL-C
37  2018 Simulation Based Investigation of Deleterious nsSNPs in ATXN2 Gene and Its Structural Consequence Toward Spinocerebellar Ataxia. HAT, NH bonds
38  2018 Vitamin D receptor (VDR) non-synonymous single nucleotide polymorphisms (nsSNPs) affect the calcitriol drug response - A theoretical insight. MD, SNPs, VDR
39  2017 A Comprehensive Functional Assessment of Carboxylesterase 1 Nonsynonymous Polymorphisms. CES1
40  2017 Computational study of putative functional variants in human kisspeptin. SIFT
41  2017 Effects of ADAMTS14 genetic polymorphism and cigarette smoking on the clinicopathologic development of hepatocellular carcinoma. HCC
42  2017 In silico approach to identify non-synonymous SNPs in human obesity related gene, MC3R (melanocortin-3-receptor). MC3R, RMSD
43  2017 Predicting nsSNPs that Disrupt Protein-Protein Interactions Using Docking. ---
44  2017 Prediction of functionally significant single nucleotide polymorphisms in PTEN tumor suppressor gene: An in silico approach. MD, PTEN
45  2017 Single-Nucleotide Polymorphism of PPARgamma, a Protein at the Crossroads of Physiological and Pathological Processes. ---
46  2017 The Possible Influence of Non-synonymous Point Mutations within the FimA Adhesin of Non-typhoidal Salmonella (NTS) Isolates in the Process of Host Adaptation. NTS
47  2016 A Comprehensive In Silico Analysis on the Structural and Functional Impact of SNPs in the Congenital Heart Defects Associated with NKX2-5 Gene-A Molecular Dynamic Simulation Approach. ASD, AVB, CHD, MDS, SNPs
48  2016 Amyotrophic Lateral Sclerosis Type 20 - In Silico Analysis and Molecular Dynamics Simulation of hnRNPA1. ALS
49  2016 Deciphering the recent phylogenetic expansion of the originally deeply rooted Mycobacterium tuberculosis lineage 7. M. tuberculosis
50  2016 In silico Analysis Revealed High-risk Single Nucleotide Polymorphisms in Human Pentraxin-3 Gene and their Impact on Innate Immune Response against Microbial Pathogens. PTX-3
51  2016 Investigating the impact of missense mutations in hCES1 by in silico structure-based approaches. CESs, hCES1
52  2016 Loss and Gain of Human Acidic Mammalian Chitinase Activity by Nonsynonymous SNPs. AMCase
53  2016 Structural insights and functional implications of inter-individual variability in beta2-adrenergic receptor. beta2AR, GPCR
54  2015 Allelic variation contributes to bacterial host specificity. ---
55  2015 Association of the I264T variant in the sulfide quinone reductase-like (SQRDL) gene with osteoporosis in Korean postmenopausal women. SQRDL
56  2015 Germ line variants of human N-methylpurine DNA glycosylase show impaired DNA repair activity and facilitate 1,N6-ethenoadenine-induced mutations. hMPG
57  2015 GESPA: classifying nsSNPs to predict disease association. GESPA
58  2015 Homo- and hetero-dimerization of human UDP-glucuronosyltransferase 2B7 (UGT2B7) wild type and its allelic variants affect zidovudine glucuronidation activity. A71S, FRET, UGT, UGT2B7, WT
59  2015 Performance of In Silico Tools for the Evaluation of UGT1A1 Missense Variants. SIFT, UGT1A1
60  2015 Phenotype Prediction of Pathogenic Nonsynonymous Single Nucleotide Polymorphisms in WFS1. WFS1, WS
61  2015 Prediction of the damage-associated non-synonymous single nucleotide polymorphisms in the human MC1R gene. MC1R, RHC
62  2015 Significance of 5,10-methylenetetrahydrofolate reductase gene variants in acute lymphoblastic leukemia in Indian population: an experimental, computational and meta-analysis. ALL, MTHFR, UTR
63  2015 SNP2Structure: A Public and Versatile Resource for Mapping and Three-Dimensional Modeling of Missense SNPs on Human Protein Structures. ---
64  2015 [Phenotype predictions of the pathogenic nonsynonymous single nucleotide polymorphisms in deafness-causing gene COCH]. COCH
65  2014 A Comprehensive In Silico Analysis of the Functional and Structural Impact of Nonsynonymous SNPs in the ABCA1 Transporter Gene. ---
66  2014 A computational prospect to aspirin side effects: aspirin and COX-1 interaction analysis based on non-synonymous SNPs. COX, NSAID
67  2014 AUTO-MUTE 2.0: A Portable Framework with Enhanced Capabilities for Predicting Protein Functional Consequences upon Mutation. PDB
68  2014 Combined genetic and nutritional risk models of triple negative breast cancer. TNBC
69  2014 Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium. CI, GWASs
70  2014 Computational identification of pathogenic associated nsSNPs and its structural impact in UROD gene: a molecular dynamics approach. MD
71  2014 Computational SNP analysis: current approaches and future prospects. ---
72  2014 DEFLATE compression algorithm corrects for overestimation of phylogenetic diversity by Grantham approach to single-nucleotide polymorphism classification. MSAs
73  2014 DUET: a server for predicting effects of mutations on protein stability using an integrated computational approach. SVM
74  2014 EFIN: predicting the functional impact of nonsynonymous single nucleotide polymorphisms in human genome. AAS
75  2014 Inferring non-synonymous single-nucleotide polymorphisms-disease associations via integration of multiple similarity networks. ---
76  2014 Nucleotide excision repair gene polymorphisms, meat intake and colon cancer risk. CI, HCA, NER, OR, PAH
77  2014 Quantitative resistance in potato leaves to late blight associated with induced hydroxycinnamic acid amides. qRT-PCR, RR, THT, TyDC
78  2014 Ranking non-synonymous single nucleotide polymorphisms based on disease concepts. FATHMM
79  2014 Study of five novel non-synonymous polymorphisms in human brain-expressed genes in a Colombian sample. ---
80  2013 An association-adjusted consensus deleterious scheme to classify homozygous Mis-sense mutations for personal genome interpretation. AACDS
81  2013 Analysis of non-synonymous single-nucleotide polymorphisms and population variability of PLD2 gene associated with hypertension. MAF
82  2013 Computational study of ADD1 gene polymorphism associated with hypertension. ADD1
83  2013 Exploration of deleterious single nucleotide polymorphisms in late-onset Alzheimer disease susceptibility genes. AD
84  2013 Extrapolating the effect of deleterious nsSNPs in the binding adaptability of flavopiridol with CDK7 protein: a molecular dynamics approach. CDK7, MD, SNAP
85  2013 Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing. HCM, HTS
86  2013 Insights into the Molecular Mechanisms Underlying Mammalian P2X7 Receptor Functions and Contributions in Diseases, Revealed by Structural Modeling and Single Nucleotide Polymorphisms. P2X7Rs
87  2013 Multiscale modeling of the causal functional roles of nsSNPs in a genome-wide association study: application to hypoxia. ---
88  2013 PASE: a novel method for functional prediction of amino acid substitutions based on physicochemical properties. AASs, PASE
89  2013 Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models. FATHMM
90  2013 Prediction of deleterious nonsynonymous single-nucleotide polymorphism for human diseases. ---
91  2013 Proteins and domains vary in their tolerance of non-synonymous single nucleotide polymorphisms (nsSNPs). ---
92  2013 Roadmap to determine the point mutations involved in cardiomyopathy disorder: a Bayesian approach. ---
93  2013 SNPs altering ammonium transport activity of human Rhesus factors characterized by a yeast-based functional assay. OHSt
94  2013 Structural and functional analysis of human SOD1 in amyotrophic lateral sclerosis. ALS, SOD1
95  2013 Structural investigation of deleterious non-synonymous SNPs of EGFR gene. EGFR, MD, TKD
96  2013 The effects of non-synonymous single nucleotide polymorphisms (nsSNPs) on protein-protein interactions. ---
97  2013 Two polymorphic variants of ABCC1 selectively alter drug resistance and inhibitor sensitivity of the multidrug and organic anion transporter multidrug resistance protein 1. HEK, MRP1
98  2012 A structural systems biology approach for quantifying the systemic consequences of missense mutations in proteins. MAPK
99  2012 Analysis of candidate colitis genes in the Gdac1 locus of mice deficient in glutathione peroxidase-1 and -2. Gdac1
100  2012 Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia. SNPs