(Q33517577)

27 July 2017

title

PhosSNP for systematic analysis of genetic polymorphisms that influence protein phosphorylation (English)

1 reference

27 July 2017

1 reference

Zexian Liu

4

0 references

Jian Ren

object named as

Jian Ren

1

0 references

Yu Xue

object named as

Yu Xue

9

0 references

Xinjiao Gao

3

object named as

Xinjiao Gao

1 reference

27 July 2017

6

Changjiang Jin

1 reference

27 July 2017

7

Longping Wen

1 reference

27 July 2017

10

Xuebiao Yao

1 reference

27 July 2017

Chunhui Jiang

2

1 reference

27 July 2017

Zineng Yuan

5

1 reference

27 July 2017

Zhaolei Zhang

8

1 reference

27 July 2017

publication date

8 December 2009

1 reference

Molecular & Cellular Proteomics

27 July 2017

published in

1 reference

27 July 2017

volume

9

1 reference

27 July 2017

issue

4

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27 July 2017

page(s)

623-634

1 reference

SysPTM: a systematic resource for proteomic research on post-translational modifications

27 July 2017

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1 reference

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14 July 2018

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Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases

14 July 2018

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14 July 2018

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The human ERG1 channel polymorphism, K897T, creates a phosphorylation site that inhibits channel activity

14 July 2018

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14 July 2018

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GPS 2.0, a tool to predict kinase-specific phosphorylation sites in hierarchy

14 July 2018

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14 July 2018

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A second generation human haplotype map of over 3.1 million SNPs

14 July 2018

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coliSNP database server mapping nsSNPs on protein structures.

14 July 2018

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Systematic Discovery of In Vivo Phosphorylation Networks

14 July 2018

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Structure SNP (StSNP): a web server for mapping and modeling nsSNPs on protein structures with linkage to metabolic pathways

14 July 2018

1 reference

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Regulation of cyclin-dependent kinase inhibitor p21WAF1/CIP1 by protein kinase Cdelta-mediated phosphorylation

14 July 2018

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PolyDoms: a whole genome database for the identification of non-synonymous coding SNPs with the potential to impact disease

14 July 2018

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NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

14 July 2018

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Global variation in copy number in the human genome

14 July 2018

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Phosphoproteomics toolbox: computational biology, protein chemistry and mass spectrometry

14 July 2018

1 reference

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Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

Cyclosporin and Timothy syndrome increase mode 2 gating of CaV1.2 calcium channels through aberrant phosphorylation of S6 helices

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

Substrate specificity of protein kinases and computational prediction of substrates

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

Phosphorylation states of cell cycle and DNA repair proteins can be altered by the nsSNPs

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

Dynamic relocalization of hOGG1 during the cell cycle is disrupted in cells harbouring the hOGG1-Cys326 polymorphic variant

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

Whole-genome patterns of common DNA variation in three human populations

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

topoSNP: a topographic database of non-synonymous single nucleotide polymorphisms with and without known disease association

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

The protein kinase complement of the human genome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

BLAT—The BLAST-Like Alignment Tool

14 July 2018

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14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

Sequence and structure-based prediction of eukaryotic protein phosphorylation sites

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

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

14 July 2018

1 reference

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A DNA polymorphism discovery resource for research on human genetic variation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

PhosphoBase, a database of phosphorylation sites: release 2.0.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

A rule for termination-codon position within intron-containing genes: when nonsense affects RNA abundance

14 July 2018

1 reference

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

14 July 2018

1 reference

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How do protein kinases recognize their substrates?

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

A structural basis for substrate specificities of protein Ser/Thr kinases: primary sequence preference of casein kinases I and II, NIMA, phosphorylase kinase, calmodulin-dependent kinase II, CDK5, and Erk1.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860229

Human Gene Mutation Database (HGMD): 2003 update

14 July 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

SNPeffect v2.0: a new step in investigating the molecular phenotypic effects of human non-synonymous SNPs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

Identification and analysis of deleterious human SNPs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

Phospho.ELM: a database of phosphorylation sites--update 2008.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

Comparative analysis reveals conserved protein phosphorylation networks implicated in multiple diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

The codon 47 polymorphism in p53 is functionally significant.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

SNP2NMD: a database of human single nucleotide polymorphisms causing nonsense-mediated mRNA decay.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

Statistical analysis of protein kinase specificity determinants

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

Identification of two serine residues essential for agonist-induced 5-HT2A receptor desensitization

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

RET Gly691Ser mutation is associated with primary vesicoureteral reflux in the French-Canadian population from Quebec.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

DOG 1.0: illustrator of protein domain structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M900273-MCP200

10.1074/MCP.M900273-MCP200

21 January 2018

Identifiers

DOI

1 reference

27 July 2017

1 reference

27 July 2017

1 reference