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Number of Items: 22
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11.

Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy.

Volume 76 , No of Volumes: 2 (2005)
F Molinari , A Raas-Rothschild , M Rio , J
12.

Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans.

Volume 135 , No of Volumes: 1 (2016)
HE Shamseldin , LL Smith , A Kentab
13.

Expanding the phenotype of SLC25A42-associated mitochondrial encephalomyopathy.

Volume 93 , No of Volumes: 5 (2018)
M Almannai , A Alasmari , A Alqasmi
14.

Predicting the functional impact of protein mutations: application to cancer genomics.

Volume 39 , No of Volumes: 17 (2011)
B Reva , Y Antipin , C Sander
15.

Predicting the functional consequences of non-synonymous DNA sequence variants-evaluation of bioinformatics tools and development of a consensus strategy.

Volume 102 , No of Volumes: 4 (2013)
K Frousios , CS Iliopoulos , T Schlitt
16.

Functional annotations improve the predictive score of human disease-related mutations in proteins.

Human mutation , Volume 30 , Issue 8 (2009)
Remo Calabrese , Emidio Capriotti , Piero Fariselli , Pier Luigi Martelli , Rita Casadio
17.

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

Bioinformatics (Oxford, England) , Volume 22 , Issue 22 (2006)
E Capriotti , R Calabrese , R Casadio
18.

SNPs3D: candidate gene and SNP selection for association studies.

BMC bioinformatics , Volume 7 (2006)
Peng Yue , Eugene Melamud , John Moult
19.

An enhanced MITOMAP with a global mtDNA mutational phylogeny.

(2007)
E Ruiz-Pesini , MT Lott , V Procaccio
20.

The human mitochondrial transcriptome.

Volume 146 , No of Volumes: 4 (2011)
TR Mercer , S Neph , ME Dinger