(Q51517975)

6 April 2018

title

Non-neutral nonsynonymous single nucleotide polymorphisms in human ABC transporters: the first comparison of six prediction methods. (English)

1 reference

6 April 2018

single-nucleotide polymorphism

main subject

1 reference

Da Cheng Hao

1

1 reference

6 April 2018

Yao Feng

series ordinal

2

1 reference

6 April 2018

Rongrong Xiao

series ordinal

3

1 reference

6 April 2018

Pei Gen Xiao

series ordinal

4

1 reference

6 April 2018

publication date

1 January 2011

1 reference

6 April 2018

published in

Pharmacological Reports

1 reference

6 April 2018

volume

63

1 reference

6 April 2018

issue

4

1 reference

6 April 2018

page(s)

924-934

1 reference

6 April 2018

In silico mutagenesis: a case study of the melanocortin 4 receptor

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

SNAP: predict effect of non-synonymous polymorphisms on function

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Accurate prediction of the functional significance of single nucleotide polymorphisms and mutations in the ABCA1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Missense mutations and single nucleotide polymorphisms in ABCB11 impair bile salt export pump processing and function or disrupt pre-messenger RNA splicing

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Destabilization of the transmembrane domain induces misfolding in a phenotypic mutant of cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Sequence-based prediction of pathological mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

N-terminal CFTR missense variants severely affect the behavior of the CFTR chloride channel

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Phenotype prediction of nonsynonymous single nucleotide polymorphisms in human phase II drug/xenobiotic metabolizing enzymes: perspectives on molecular evolution

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Influence of ABCB1 gene polymorphisms on the pharmacokinetics of azithromycin among healthy Chinese Han ethnic subjects

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Host genetic influences on highly active antiretroviral therapy efficacy and AIDS-free survival.

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

The ABC transporter structure and mechanism: perspectives on recent research.

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Positional conservation and amino acids shape the correct diagnosis and population frequencies of benign and damaging personal amino acid mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Prediction of the deleterious nsSNPs in ABCB transporters

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Proportionally more deleterious genetic variation in European than in African populations.

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Accounting for human polymorphisms predicted to affect protein function

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

SIFT: Predicting amino acid changes that affect protein function

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Predicting the effects of amino acid substitutions on protein function

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Asians with chronic pulmonary disease: A pilot study

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Two novel missense mutations causing adrenoleukodystrophy in Italian patients

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Human non-synonymous SNPs: server and survey

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Sitosterolaemia in Switzerland: molecular genetics links the US Amish-Mennonites to their European roots.

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

PSIC: profile extraction from sequence alignments with position-specific counts of independent observations.

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Prediction of deleterious human alleles

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Adrenoleukodystrophy: subcellular localization and degradation of adrenoleukodystrophy protein (ALDP/ABCD1) with naturally occurring missense mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

The proportion of mutations predicted to have a deleterious effect differs between gain and loss of function genes in neurodegenerative disease

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

A bioinformatics approach for the phenotype prediction of nonsynonymous single nucleotide polymorphisms in human cytochromes P450.

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Phenotype prediction of non-synonymous single-nucleotide polymorphisms in human ATP-binding cassette transporter genes.

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

A kinetic study of Rhodamine123 pumping by P-glycoprotein

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function

1 reference

https://api.crossref.org/works/10.1016%2FS1734-1140%2811%2970608-9

7 January 2021

10.1016/S1734-1140(11)70608-9

Identifiers

DOI

1 reference

6 April 2018

1 reference

6 April 2018