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Mitochondrial parts, pathways, and pathogenesis.
Mitochondial parts, pathways, and pathogenesisFree accessDSpace@MIT | 2009| -
Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans
Free accessDSpace@MIT | 2009| -
MitoCarta2.0: An updated protein inventory of the mammalian mitochondrion
British Library Online Contents | 2015| -
CLYBL is a polymorphic human enzyme with malate synthase and {beta}-methylmalate synthase activity
Oxford University Press | 2014| -
Bayesian hidden Markov tree models for clustering genes with shared evolutionary history
Project Euclid | 2019| -
Bayesian Hidden Markov Tree Models for Clustering Genes with Shared Evolutionary History
Free accessArXiv | 2018| -
Systematic identification of human mitochondrial disease genes through integrative genomics
National licenceNature Publishing Group | 2006| -
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome
British Library Online Contents | 2017| -
The molecular basis of human complex I deficiency
Online Contents | 2011|Contributors: Calvo, Sarah E. -
MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion
National licenceNature Publishing Group | 2006| -
Mutations in MTFMT Underlie a Human Disorder of Formylation Causing Impaired Mitochondrial Translation
Free accessDSpace@MIT | 2011| -
Expansion of Biological Pathways Based on Evolutionary Inference
Online Contents | 2014|Contributors: Calvo, Sarah E. -
Research - The Complete Genome and Proteome of Mycoplasma mobile
Online Contents | 2004|Contributors: Calvo, Sarah
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