In Silico Analysis of the deleterious nsSNP's (missense) in the Homeobox domain of human HOXB13 gene responsible for hereditary prostate cancer. (Q30397277)

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Language	Label	Description	Also known as
English	In Silico Analysis of the deleterious nsSNP's (missense) in the Homeobox domain of human HOXB13 gene responsible for hereditary prostate cancer.	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

In Silico Analysis of the deleterious nsSNP's (missense) in the Homeobox domain of human HOXB13 gene responsible for hereditary prostate cancer. (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

author name string

Gopalakrishnan Chandrasekaran

1

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

Eu Chang Hwang

2

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

Taek Won Kang

3

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

Dongdeuk Kwon

4

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

Kwangsung Park

5

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

Je-Jung Lee

6

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

Vinoth-Kumar Lakshmanan

7

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

publication date

10 January 2017

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

Chemical Biology and Drug Design

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

Epidemiology of prostate cancer in South Korea

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

Rising prostate cancer rates in South Korea.

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

HOXB13 promotes androgen independent growth of LNCaP prostate cancer cells by the activation of E2F signaling

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

International variation in prostate cancer incidence and mortality rates.

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

Identification of Two Novel HOXB13 Germline Mutations in Portuguese Prostate Cancer Patients

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

The G84E mutation of HOXB13 is associated with increased risk for prostate cancer: results from the REDUCE trial

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

The HOXB13 G84E Mutation Is Associated with an Increased Risk for Prostate Cancer and Other Malignancies

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

Germline mutations in HOXB13 and prostate-cancer risk

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

An In Silico Evaluation of Deleterious Nonsynonymous Single Nucleotide Polymorphisms in the ErbB3 Oncogene

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

Prevalence of the HOXB13 G84E germline mutation in British men and correlation with prostate cancer risk, tumour characteristics and clinical outcomes

1 reference

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Identification of functional SNPs in BARD1 gene and in silico analysis of damaging SNPs: based on data procured from dbSNP database

1 reference

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21 January 2018

Confirmation of the HOXB13 G84E germline mutation in familial prostate cancer

1 reference

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Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes.

1 reference

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21 January 2018

Non-synonymous and synonymous coding SNPs show similar likelihood and effect size of human disease association

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

A structural bioinformatics approach to the analysis of nonsynonymous single nucleotide polymorphisms (nsSNPs) and their relation to disease.

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

A rapid screening method for a single nucleotide polymorphism (SNP) in the human MOR gene

1 reference

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21 January 2018

Identification, analysis, and prediction of protein ubiquitination sites

1 reference

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Screening and structural evaluation of deleterious Non-Synonymous SNPs of ePHA2 gene involved in susceptibility to cataract formation

1 reference

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In silico analysis of functional single nucleotide polymorphisms in the human TRIM22 gene

1 reference

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LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources.

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

Prostate cancer: germline prediction for a commonly variable malignancy.

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

A method and server for predicting damaging missense mutations

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

Prediction of deleterious human alleles

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

Human non-synonymous SNPs: server and survey

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

Prostate cancer epidemiology in the United States

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

A catalog of neutral and deleterious polymorphism in yeast

1 reference

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21 January 2018

Associations and interactions of genetic polymorphisms in innate immunity genes with early viral infections and susceptibility to asthma and asthma-related phenotypes.

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

1 reference

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21 January 2018

A prostate cancer susceptibility allele at 6q22 increases RFX6 expression by modulating HOXB13 chromatin binding.

1 reference

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21 January 2018

In silico analysis of Single Nucleotide Polymorphisms (SNPs) in human BRAF gene

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

dbSNP: the NCBI database of genetic variation

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

SIFT missense predictions for genomes

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

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

1 reference

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21 January 2018

Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutations

1 reference

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21 January 2018

PANTHER in 2013: modeling the evolution of gene function, and other gene attributes, in the context of phylogenetic trees

1 reference

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21 January 2018

Mining for SNPs and SSRs using SNPServer, dbSNP and SSR taxonomy tree

1 reference

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21 January 2018

SWISS‐MODEL and the Swiss‐Pdb Viewer: An environment for comparative protein modeling

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

Using quaternions to calculate RMSD

1 reference

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21 January 2018

Evaluation of the performance of 3D virtual screening protocols: RMSD comparisons, enrichment assessments, and decoy selection--what can we learn from earlier mistakes?

1 reference

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21 January 2018

Comment on "Using quaternions to calculate RMSD" [J. Comp. Chem. 25, 1849 (2004)]

1 reference

https://api.crossref.org/works/10.1111%2FCBDD.12938

21 January 2018

Ramachandran-type plots for glycosidic linkages: Examples from molecular dynamic simulations using the Glycam06 force field

1 reference

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21 January 2018

Large-scale gene function analysis with the PANTHER classification system

1 reference

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21 January 2018

ProTherm, version 4.0: thermodynamic database for proteins and mutants

1 reference

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NOMAD-Ref: visualization, deformation and refinement of macromolecular structures based on all-atom normal mode analysis

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In silico analysis of structural and functional consequences in p16INK4A by deleterious nsSNPs associated CDKN2A gene in malignant melanoma

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ProTherm and ProNIT: thermodynamic databases for proteins and protein-nucleic acid interactions

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Phi/psi-chology: Ramachandran revisited

1 reference

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21 January 2018

Identifiers

10.1111/CBDD.12938

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

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