Spectrum of disease-causing mutations in protein secondary structures
about
Monoclonal antibodies specific for disease-associated point-mutants: lamin A/C R453W and R482WCoagVDb: a comprehensive database for coagulation factors and their associated SAPsSixty-five years of the long march in protein secondary structure prediction: the final stretch?Multiple in silico tools predict phenotypic manifestations in congenital thrombotic thrombocytopenic purpura.Prediction of disease-related mutations affecting protein localization.Feature-based multiple models improve classification of mutation-induced stability changes.Computational biophysical, biochemical, and evolutionary signature of human R-spondin family proteins, the member of canonical Wnt/β-catenin signaling pathwayVariSNP, a benchmark database for variations from dbSNP.Types and effects of protein variations.PaPI: pseudo amino acid composition to score human protein-coding variants.Mutational Spectrum Analysis of Neurodegenerative Diseases and Its Pathogenic ImplicationMolecular genetic characteristics of X-linked retinoschisis in KoreansPrivileged Electrophile Sensors: A Resource for Covalent Drug Development.Subcellular Redox Targeting: Bridging in Vitro and in Vivo Chemical Biology.Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q10 Deficiency in a Female Sib-Pair.Protein secondary structure analysis of dried blood serum using infrared spectroscopy to identify markers for colitis screening.Novel KRT9 missense mutation in a Japanese case of epidermolytic palmoplantar keratoderma.Leucine to proline substitution by SNP at position 197 in Caspase-9 gene expression leads to neuroblastoma: a bioinformatics analysis.NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.Mutation in angiotensin II type 1 receptor disrupts its binding to angiotensin II leading to hypotension: An insight into hydrogen bonding patternsSequence variant analysis of RNA sequences in severe equine asthmaClassification of mismatch repair gene missense variants with PON-MMRPerformance of mutation pathogenicity prediction methods on missense variants
P2860
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P2860
Spectrum of disease-causing mutations in protein secondary structures
description
2007 nî lūn-bûn
@nan
2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Spectrum of disease-causing mutations in protein secondary structures
@ast
Spectrum of disease-causing mutations in protein secondary structures
@en
type
label
Spectrum of disease-causing mutations in protein secondary structures
@ast
Spectrum of disease-causing mutations in protein secondary structures
@en
prefLabel
Spectrum of disease-causing mutations in protein secondary structures
@ast
Spectrum of disease-causing mutations in protein secondary structures
@en
P2860
P356
P1476
Spectrum of disease-causing mutations in protein secondary structures
@en
P2093
Sofia Khan
P2860
P2888
P356
10.1186/1472-6807-7-56
P577
2007-08-29T00:00:00Z
P5875
P6179
1046274733