Catherine Brunel‐Guitton

LRPPRC and SLIRP Interact in a Ribonucleoprotein Complex That Regulates Posttranscriptional Gene Expression in Mitochondria

Florin Sasarman, Catherine Brunel‐Guitton, Hana Antonická et al. · Molecular Biology of the Cell · 2010 · 279 citations · Full text

Genetics, Signal Recognition, Molecular Biology +16

De Novo Mutations in the Motor Domain of KIF1A Cause Cognitive Impairment, Spastic Paraparesis, Axonal Neuropathy, and Cerebellar Atrophy

Jae-Ran Lee, Myriam Srour, Doyoun Kim et al. · Human Mutation · 2014 · 151 citations

Neurological Disorder, Genetics, Spastic Paraparesis +20

The 3′ addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1

Florin Sasarman, Isabelle Thiffault, Woranontee Weraarpachai et al. · Human Molecular Genetics · 2015 · 70 citations · Full text

Combined malonic and methylmalonic aciduria due to <i>ACSF3</i> mutations: Benign clinical course in an unselected cohort

Alina Levtova, Paula J. Waters, Daniela Buhaş et al. · Journal of Inherited Metabolic Disease · 2019 · 33 citations

An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase

Reetta Hinttala, Florin Sasarman, Takashi Nishimura et al. · Human Molecular Genetics · 2015 · 28 citations · Full text

Mitophagy, Bioorganic Chemistry, Genetics +20