Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm (Q29547194)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

protein function prediction

23 April 2017

main subject

0 references

Kumar P

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

23 April 2017

Henikoff S

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

23 April 2017

Ng PC

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

23 April 2017

language of work or name

1 reference

23 April 2017

publication date

2009

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

23 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

23 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

23 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

23 April 2017

page(s)

1073-81

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

Predicting deleterious amino acid substitutions

23 April 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

25 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

SIFT: Predicting amino acid changes that affect protein function

25 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Characterization of single-nucleotide polymorphisms in coding regions of human genes

25 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Predicting the effects of amino acid substitutions on protein function

25 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Human non-synonymous SNPs: server and survey

25 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Computational approaches for predicting the biological effect of p53 missense mutations: a comparison of three sequence analysis based methods

25 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

PANTHER: a library of protein families and subfamilies indexed by function

25 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Human Gene Mutation Database?A biomedical information and research resource

25 April 2017

2 references

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

31 March 2020

https://pubmed.ncbi.nlm.nih.gov/19561590

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Single-nucleotide mutations for plant functional genomics

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

In silico prediction of the deleterious effect of a mutation: proceed with caution in clinical genetics

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Accounting for human polymorphisms predicted to affect protein function

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Evaluation of structural and evolutionary contributions to deleterious mutation prediction.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

PMUT: a web-based tool for the annotation of pathological mutations on proteins.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Physicochemical constraint violation by missense substitutions mediates impairment of protein function and disease severity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Skin Type, Melanoma, and Melanocortin 1 Receptor Variants

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in Marfan syndrome and related connective tissue disorders

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

SNPs3D: candidate gene and SNP selection for association studies.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2009.86

31 March 2020

Identifiers

DOI

10.1038/NPROT.2009.86

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

23 April 2017

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1015642657

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=19561590

PubMed publication ID

2 references

23 April 2017

Consolidated OpenCitations Corpus – April 2017