Sequence-based prioritization of nonsynonymous single-nucleotide polymorphisms for the study of disease mutations (Q35946228)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

title

Sequence-based prioritization of nonsynonymous single-nucleotide polymorphisms for the study of disease mutations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

single-nucleotide polymorphism

2 January 2020

main subject

1 reference

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

author name string

Hua Yang

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Linqi Zhou

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

C-C Jay Kuo

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Fengzhu Sun

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Ting Chen

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

language of work or name

English

0 references

publication date

22 June 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

2 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

volume

81

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

page(s)

346-360

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

The Universal Protein Resource (UniProt).

2 January 2020

cites work

1 reference

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Non-DNA binding, dominant-negative, human PPARgamma mutations cause lipodystrophic insulin resistance

2 October 2017

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Searching for interpretable rules for disease mutations: a simulated annealing bump hunting strategy

2 October 2017

1 reference

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Gene prioritization through genomic data fusion

2 October 2017

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Microfabricated bioprocessor for integrated nanoliter-scale Sanger DNA sequencing

2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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A haplotype map of the human genome

2 October 2017

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Genome sequencing in microfabricated high-density picolitre reactors

2 October 2017

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Sequence variation in G-protein-coupled receptors: analysis of single nucleotide polymorphisms

2 October 2017

1 reference

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Coding single-nucleotide polymorphisms associated with complex vs. Mendelian disease: evolutionary evidence for differences in molecular effects.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Functional classification of proteins and protein variants.

2 October 2017

1 reference

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A comparative study of machine-learning methods to predict the effects of single nucleotide polymorphisms on protein function.

2 October 2017

1 reference

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PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification

2 October 2017

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Finding genes that underlie complex traits

2 October 2017

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Human non-synonymous SNPs: server and survey

2 October 2017

1 reference

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A comprehensive review of genetic association studies

2 October 2017

1 reference

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Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Variability of the CD36 gene in West Africa

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Predicting deleterious amino acid substitutions

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: structure-based assessment of amino acid variation

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Prediction of deleterious human alleles

2 October 2017

1 reference

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The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Dominant negative mutations in human PPARgamma associated with severe insulin resistance, diabetes mellitus and hypertension

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Genetic studies of the Lac repressor. XV: 4000 single amino acid substitutions and analysis of the resulting phenotypes on the basis of the protein structure

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Genetic dissection of complex traits

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

A simple method for displaying the hydropathic character of a protein

2 October 2017

1 reference

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Basic local alignment search tool

2 October 2017

1 reference

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Identification of the gene variations in human CD22.

2 October 2017

1 reference

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Hemoglobin La Desirade alpha A2 beta 2 129 (H7) Ala----Val: a new unstable hemoglobin

11 July 2018

1 reference

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Systematic mutation of bacteriophage T4 lysozyme.

11 July 2018

1 reference

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Conformational preferences of amino acids in globular proteins

11 July 2018

1 reference

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Prediction of the phenotypic effects of non-synonymous single nucleotide polymorphisms using structural and evolutionary information.

11 July 2018

1 reference

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PPARG F388L, a transactivation-deficient mutant, in familial partial lipodystrophy

24 September 2018

1 reference

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Evaluation of structural and evolutionary contributions to deleterious mutation prediction.

24 September 2018

1 reference

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A novel heterozygous mutation in peroxisome proliferator-activated receptor-gamma gene in a patient with familial partial lipodystrophy

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Genetic studies of the lac repressor. XIV. Analysis of 4000 altered Escherichia coli lac repressors reveals essential and non-essential residues, as well as "spacers" which do not require a specific sequence.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Hemoglobin connecticut (β21(b3) Asp→Gly): A hemoglobin variant with low oxygen affinity

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950793

Physiologic implications of a hemoglobin with decreased oxygen affinity (hemoglobin seattle)

24 September 2018

1 reference

12 December 2020

Hemoglobin-Seattle (alpha-2 beta-2 76-Glu): an unstable hemoglobin causing chronic hemolytic anemia

1 reference

12 December 2020

Hemoglobin saitama or beta 117 (G19) His leads to Pro, a new variant causing hemolytic disease

1 reference

12 December 2020

Hb Seattle [beta 70(E14)Ala- > Asp]: a report of a second kindred in a Ukrainian family

1 reference

12 December 2020

A novel mutation (E767K) in the second extracellular loop of the calcium sensing receptor in a family with autosomal dominant hypocalcemia

1 reference

12 December 2020

Sequence-based prediction of pathological mutations

1 reference

12 December 2020

Identifiers

DOI

10.1086/519747

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17668383%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

1 reference