Disease-related versus polymorphic mutations in human mitochondrial tRNAs: Where is the difference?

Por Florentz, Catherine, Sissler, Marie
Publicado em 2001

Mamit-tRNA, a database of mammalian mitochondrial tRNA primary and secondary structures

Por Pütz, Joern, Dupuis, Bruno, Sissler, Marie, Florentz, Catherine
Publicado em 2007

Pathology-related mutation A7526G (A9G) helps in the understanding of the 3D structural core of human mitochondrial tRNA(Asp)

Por Messmer, Marie, Gaudry, Agnès, Sissler, Marie, Florentz, Catherine
Publicado em 2009

Aminoacylation properties of pathology-related human mitochondrial tRNA(Lys) variants

Por SISSLER, MARIE, HELM, MARK, FRUGIER, MAGALI, GIEGÉ, RICHARD, FLORENTZ, CATHERINE
Publicado em 2004

An aminoacyl-tRNA synthetase paralog with a catalytic role in histidine biosynthesis

Por Sissler, Marie, Delorme, Christine, Bond, Jeff, Ehrlich, S. Dusko, Renault, Pierre, Francklyn, Christopher
Publicado em 1999

A yeast arginine specific tRNA is a remnant aspartate acceptor

Por Fender, Aurélie, Geslain, Renaud, Eriani, Gilbert, Giegé, Richard, Sissler, Marie, Florentz, Catherine
Publicado em 2004

Tertiary network in mammalian mitochondrial tRNA(Asp) revealed by solution probing and phylogeny

Por Messmer, Marie, Pütz, Joern, Suzuki, Takeo, Suzuki, Tsutomu, Sauter, Claude, Sissler, Marie, Catherine, Florentz
Publicado em 2009

Thermodynamic properties distinguish human mitochondrial aspartyl-tRNA synthetase from bacterial homolog with same 3D architecture

Por Neuenfeldt, Anne, Lorber, Bernard, Ennifar, Eric, Gaudry, Agnès, Sauter, Claude, Sissler, Marie, Florentz, Catherine
Publicado em 2013

Neurodegenerative disease-associated mutants of a human mitochondrial aminoacyl-tRNA synthetase present individual molecular signatures

Por Sauter, Claude, Lorber, Bernard, Gaudry, Agnès, Karim, Loukmane, Schwenzer, Hagen, Wien, Frank, Roblin, Pierre, Florentz, Catherine, Sissler, Marie
Publicado no Sci Rep (2015)

Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome

Por Simon, Mariella, Richard, Elodie M., Wang, Xinjian, Shahzad, Mohsin, Huang, Vincent H., Qaiser, Tanveer A., Potluri, Prasanth, Mahl, Sarah E., Davila, Antonio, Nazli, Sabiha, Hancock, Saege, Yu, Margret, Gargus, Jay, Chang, Richard, Al-sheqaih, Nada, Newman, William G., Abdenur, Jose, Starr, Arnold, Hegde, Rashmi, Dorn, Thomas, Busch, Anke, Park, Eddie, Wu, Jie, Schwenzer, Hagen, Flierl, Adrian, Florentz, Catherine, Sissler, Marie, Khan, Shaheen N., Li, Ronghua, Guan, Min-Xin, Friedman, Thomas B., Wu, Doris K., Procaccio, Vincent, Riazuddin, Sheikh, Wallace, Douglas C., Ahmed, Zubair M., Huang, Taosheng, Riazuddin, Saima
Publicado no PLoS Genet (2015)