MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease. - Wikidata - wikimedia - TriplyDB

MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease.

MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease.

http://www.wikidata.org/entity/Q33503932

about

Resources, challenges and way forward in rare mitochondrial diseases research Between proteins and phenotypes: annotation and interpretation of mutations.Phylomedicine: an evolutionary telescope to explore and diagnose the universe of disease mutations.MitoLSDB: a comprehensive resource to study genotype to phenotype correlations in human mitochondrial DNA variations.PON-mt-tRNA: a multifactorial probability-based method for classification of mitochondrial tRNA variations Human genomic disease variants: a neutral evolutionary explanation.A multi-parametric workflow for the prioritization of mitochondrial DNA variants of clinical interest Mitochondrial ATP 6 and 8 polymorphisms in irritable bowel syndrome with diarrhea Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution.Comprehensive analysis of common and rare mitochondrial DNA variants in elite Japanese athletes: a case-control study.

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P2860

MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease.

http://www.wikidata.org/entity/Q33503932

description

2009 nî lūn-bûn

@nan

2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2009年の論文

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2009年論文

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2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

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2009年論文

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2009年论文

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name

MtSNPscore: a combined evidenc ...... ondrial variations in disease.

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MtSNPscore: a combined evidenc ...... ondrial variations in disease.

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type

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MtSNPscore: a combined evidenc ...... ondrial variations in disease.

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MtSNPscore: a combined evidenc ...... ondrial variations in disease.

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MtSNPscore: a combined evidenc ...... ondrial variations in disease.

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MtSNPscore: a combined evidenc ...... ondrial variations in disease.

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BMC Bioinformatics

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MtSNPscore: a combined evidenc ...... ondrial variations in disease.

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Achal K Srivastava

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Anshu Bhardwaj

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Shipra Sharma

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Shrish Tiwari

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P2860

The mitochondrial RNA polymerase contributes critically to promoter specificity in mammalian cells

The mitochondrial transcription termination factor mTERF modulates replication pausing in human mitochondrial DNA

mtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences

Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients.

De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency

A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine

Human non-synonymous SNPs: server and survey

Mitochondrial diseases in man and mouse

tRNA punctuation model of RNA processing in human mitochondria

Experimentally determined hydrophobicity scale for proteins at membrane interfaces

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1471-2105-10-s8-s7

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10 Suppl 8

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Chaitanya S. Gokhale

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