9
results
for author:"Fonknechten N."
in Literature Citations
| A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition. Tarrade A., Fassier C., Courageot S., Charvin D., Vitte J., Peris L., Thorel A., Mouisel E., Fonknechten N., Roblot N. et al. Hum. Mol. Genet. 15:3544-3558(2006) · UniProtKB (1) |
| Deciphering the evolution and metabolism of an anammox bacterium from a community genome. Strous M., Pelletier E., Mangenot S., Rattei T., Lehner A., Taylor M.W., Horn M., Daims H., Bartol-Mavel D., Wincker P. et al. Nature 440:790-794(2006) · UniProtKB (4,495) |
| Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A. Abel A., Fonknechten N., Hofer A., Durr A., Cruaud C., Voit T., Weissenbach J., Brice A., Klimpe S., Auburger G. et al. Neurogenetics 5:239-243(2004) · Mapped (5) |
| Unique features revealed by the genome sequence of Acinetobacter sp. ADP1, a versatile and naturally transformation competent bacterium. Barbe V., Vallenet D., Fonknechten N., Kreimeyer A., Oztas S., Labarre L., Cruveiller S., Robert C., Duprat S., Wincker P. et al. Nucleic Acids Res. 32:5766-5779(2004) · UniProtKB (3,293) |
| The DNA sequence and analysis of human chromosome 14. Heilig R., Eckenberg R., Petit J.-L., Fonknechten N., Da Silva C., Cattolico L., Levy M., Barbe V., De Berardinis V., Ureta-Vidal A. et al. Nature 421:601-607(2003) · UniProtKB (543) |
| Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus. Charvin D., Cifuentes-Diaz C., Fonknechten N., Joshi V., Hazan J., Melki J., Betuing S. Hum. Mol. Genet. 12:71-78(2003) · Mapped (3) |
| Hereditary spastic paraplegia caused by mutations in the SPG4 gene. Buerger J., Fonknechten N., Hoeltzenbein M., Neumann L., Bratanoff E., Hazan J., Reis A. Eur. J. Hum. Genet. 8:771-776(2000) · UniProtKB (1) |
| Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia. Fonknechten N., Mavel D., Byrne P., Davoine C.-S., Cruaud C., Bonsch D., Samson D., Coutinho P., Hutchinson M., McMonagle P. et al. Hum. Mol. Genet. 9:637-644(2000) · UniProtKB (1) |
| Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Hazan J., Fonknechten N., Mavel D., Paternotte C., Samson D., Artiguenave F., Davoine C.-S., Cruaud C., Durr A., Wincker P. et al. Nat. Genet. 23:296-303(1999) · UniProtKB (2) |
