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

av Florentz, Catherine, Sissler, Marie
Publicerad 2001

Pathology-related substitutions in human mitochondrial tRNA(Ile) reduce precursor 3′ end processing efficiency in vitro

av Levinger, Louis, Giegé, Richard, Florentz, Catherine
Publicerad 2003

Mitochondrial tRNA 3′ end metabolism and human disease

av Levinger, Louis, Mörl, Mario, Florentz, Catherine
Publicerad 2004

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

av Pütz, Joern, Dupuis, Bruno, Sissler, Marie, Florentz, Catherine
Publicerad 2007

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

av Messmer, Marie, Gaudry, Agnès, Sissler, Marie, Florentz, Catherine
Publicerad 2009

Decreased aminoacylation in pathology-related mutants of mitochondrial tRNA(Tyr) is associated with structural perturbations in tRNA architecture

av Bonnefond, Luc, Florentz, Catherine, Giegé, Richard, Rudinger-Thirion, Joëlle
Publicerad 2008

Armless mitochondrial tRNAs in Enoplea (Nematoda)

av Jühling, Frank, Pütz, Joern, Florentz, Catherine, Stadler, Peter F.
Publicerad 2012

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

av SISSLER, MARIE, HELM, MARK, FRUGIER, MAGALI, GIEGÉ, RICHARD, FLORENTZ, CATHERINE
Publicerad 2004

A yeast arginine specific tRNA is a remnant aspartate acceptor

av Fender, Aurélie, Geslain, Renaud, Eriani, Gilbert, Giegé, Richard, Sissler, Marie, Florentz, Catherine
Publicerad 2004

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

av Neuenfeldt, Anne, Lorber, Bernard, Ennifar, Eric, Gaudry, Agnès, Sauter, Claude, Sissler, Marie, Florentz, Catherine
Publicerad 2013

tRNA-Like Structure Regulates Translation of Brome Mosaic Virus RNA

av Barends, Sharief, Rudinger-Thirion, Joëlle, Florentz, Catherine, Giegé, Richard, Pleij, Cornelis W. A., Kraal, Barend
Publicerad 2004

Improved systematic tRNA gene annotation allows new insights into the evolution of mitochondrial tRNA structures and into the mechanisms of mitochondrial genome rearrangements

av Jühling, Frank, Pütz, Joern, Bernt, Matthias, Donath, Alexander, Middendorf, Martin, Florentz, Catherine, Stadler, Peter F.
Publicerad 2012

Tyrosyl-tRNA synthetase: the first crystallization of a human mitochondrial aminoacyl-tRNA synthetase

av Bonnefond, Luc, Frugier, Magali, Touzé, Elodie, Lorber, Bernard, Florentz, Catherine, Giegé, Richard, Rudinger-Thirion, Joëlle, Sauter, Claude
Publicerad 2007

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

av Sauter, Claude, Lorber, Bernard, Gaudry, Agnès, Karim, Loukmane, Schwenzer, Hagen, Wien, Frank, Roblin, Pierre, Florentz, Catherine, Sissler, Marie
I publikationen Sci Rep (2015)

Small but large enough: structural properties of armless mitochondrial tRNAs from the nematode Romanomermis culicivorax

av Jühling, Tina, Duchardt-Ferner, Elke, Bonin, Sonja, Wöhnert, Jens, Pütz, Joern, Florentz, Catherine, Betat, Heike, Sauter, Claude, Mörl, Mario
I publikationen Nucleic Acids Res (2018)

Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders

av Bannwarth, Sylvie, Procaccio, Vincent, Lebre, Anne Sophie, Jardel, Claude, Chaussenot, Annabelle, Hoarau, Claire, Maoulida, Hassani, Charrier, Nathanaël, Gai, Xiaowu, Xie, Hongbo M, Ferre, Marc, Fragaki, Konstantina, Hardy, Gaëlle, Mousson de Camaret, Bénédicte, Marlin, Sandrine, Dhaenens, Claire Marie, Slama, Abdelhamid, Rocher, Christophe, Paul Bonnefont, Jean, Rötig, Agnès, Aoutil, Nadia, Gilleron, Mylène, Desquiret-Dumas, Valérie, Reynier, Pascal, Ceresuela, Jennifer, Jonard, Laurence, Devos, Aurore, Espil-Taris, Caroline, Martinez, Delphine, Gaignard, Pauline, Le Quan Sang, Kim-Hanh, Amati-Bonneau, Patrizia, Falk, Marni J, Florentz, Catherine, Chabrol, Brigitte, Durand-Zaleski, Isabelle, Paquis-Flucklinger, Véronique
Publicerad 2013

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

av 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
I publikationen PLoS Genet (2015)