1 - 25 of
43
results
for author:"Francis F."
in Literature Citations
| The location of DCX mutations predicts malformation severity in X-linked lissencephaly. Leger P.L., Souville I., Boddaert N., Elie C., Pinard J.M., Plouin P., Moutard M.L., des Portes V., Van Esch H., Joriot S. et al. Neurogenetics 9:277-285(2008) · Mapped (3) |
| Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A. Fallet-Bianco C., Loeuillet L., Poirier K., Loget P., Chapon F., Pasquier L., Saillour Y., Beldjord C., Chelly J., Francis F. Brain 131:2304-2320(2008) · Mapped (5) |
| Epilepsy in Dcx knockout mice associated with discrete lamination defects and enhanced excitability in the hippocampus. Nosten-Bertrand M., Kappeler C., Dinocourt C., Denis C., Germain J., Phan Dinh Tuy F., Verstraeten S., Alvarez C., Metin C., Chelly J. et al. PLoS ONE 3:e2473-e2473(2008) · Mapped (6) |
| Characterization of a novel aphid prenyltransferase displaying dual geranyl/farnesyl diphosphate synthase activity. Vandermoten S., Charloteaux B., Santini S., Sen S.E., Beliveau C., Vandenbol M., Francis F., Brasseur R., Cusson M., Haubruge E. FEBS Lett. 582:1928-1934(2008) · UniProtKB (5) |
| Alternative transcripts of Dclk1 and Dclk2 and their expression in doublecortin knockout mice. Tuy F.P., Saillour Y., Kappeler C., Chelly J., Francis F. Dev. Neurosci. 30:171-186(2008) · Mapped (21) |
| Solution-state molecular structure of apo and oleate-liganded liver fatty acid-binding protein. He Y., Yang X., Wang H., Estephan R., Francis F., Kodukula S., Storch J., Stark R.E. Biochemistry 46:12543-12556(2007) · UniProtKB (1) |
| Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A). Poirier K., Keays D.A., Francis F., Saillour Y., Bahi N., Manouvrier S., Fallet-Bianco C., Pasquier L., Toutain A., Tuy F.P. et al. |
| Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency. Kappeler C., Dhenain M., Phan Dinh Tuy F., Saillour Y., Marty S., Fallet-Bianco C., Souville I., Souil E., Pinard J.M., Meyer G. et al. J. Comp. Neurol. 500:239-254(2007) · Mapped (3) |
| Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice. Kappeler C., Saillour Y., Baudoin J.P., Tuy F.P., Alvarez C., Houbron C., Gaspar P., Hamard G., Chelly J., Metin C. et al. Hum. Mol. Genet. 15:1387-1400(2006) · Mapped (29) |
| The DNA sequence of the human X chromosome. Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P. et al. Nature 434:325-337(2005) · UniProtKB (1,194) |
| Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes. Friocourt G., Kappeler C., Saillour Y., Fauchereau F., Rodriguez M.S., Bahi N., Vinet M.C., Chafey P., Poirier K., Taya S. et al. Mol. Cell. Neurosci. 28:153-164(2005) · Mapped (10) |
| Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neurons. Poirier K., Van Esch H., Friocourt G., Saillour Y., Bahi N., Backer S., Souil E., Castelnau-Ptakhine L., Beldjord C., Francis F. et al. Brain Res. Mol. Brain Res. 122:35-46(2004) · Mapped (5) |
| Cre-mediated germline mosaicism: a new transgenic mouse for the selective removal of residual markers from tri-lox conditional alleles. Leneuve P., Colnot S., Hamard G., Francis F., Niwa-Kawakita M., Giovannini M., Holzenberger M. Nucleic Acids Res. 31:e21-e21(2003) · Mapped (11) |
| So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation. des Portes V., Abaoub L., Joannard A., Souville I., Francis F., Pinard J.-M., Chelly J., Beldjord C., Jouk P.S. Seizure 11:273-277(2002) · UniProtKB (1) |
| ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation. Bienvenu T., Poirier K., Friocourt G., Bahi N., Beaumont D., Fauchereau F., Ben-Jeema L., Zemni R., Vinet M.-C., Francis F. et al. Hum. Mol. Genet. 11:981-991(2002) · UniProtKB (1) · Mapped (1) |
| Doublecortin interacts with mu subunits of clathrin adaptor complexes in the developing nervous system. Friocourt G., Chafey P., Billuart P., Koulakoff A., Vinet M.C., Schaar B.T., McConnell S.K., Francis F., Chelly J. Mol. Cell. Neurosci. 18:307-319(2001) · Mapped (24) |
| Deletion of the cell-division inhibitor MinC results in lysis of Neisseria gonorrhoeae. Ramirez-Arcos S., Szeto J., Beveridge T., Victor C., Francis F., Dillon J. Microbiology 147:225-237(2001) · UniProtKB (4) |
| The DNA sequence of human chromosome 21. Hattori M., Fujiyama A., Taylor T.D., Watanabe H., Yada T., Park H.-S., Toyoda A., Ishii K., Totoki Y., Choi D.-K. et al. Nature 405:311-319(2000) · UniProtKB (506) |
| Genomic, transcriptional and phenotypic analysis of ftsE and ftsX of Neisseria gonorrhoeae. Bernatchez S., Francis F.M., Salimnia H., Beveridge T.J., Li H., Dillon J.-A.R. DNA Res. 7:75-81(2000) · UniProtKB (6) |
| Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia. McDonell N., Ramser J., Francis F., Vinet M.-C., Rider S., Sudbrak R., Riesselman L., Yaspo M.-L., Reinhardt R., Monaco A.P. et al. Genomics 64:221-229(2000) · UniProtKB (1) |
| A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation. Zemni R., Bienvenu T., Vinet M.C., Sefiani A., Carrie A., Billuart P., McDonell N., Couvert P., Francis F., Chafey P. et al. |
| Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues. Filisetti D., Ostermann G., von Bredow M., Strom T.M., Filler G., Ehrich J., Pannetier S., Garnier J.-M., Rowe P.S.N., Francis F. et al. Eur. J. Hum. Genet. 7:615-619(1999) · UniProtKB (1) |
| Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons. Francis F., Koulakoff A., Boucher D., Chafey P., Schaar B., Vinet M.C., Friocourt G., McDonnell N., Reiner O., Kahn A. et al. Neuron 23:247-256(1999) · Mapped (3) |
| Analysis of the spermine synthase gene region in Fugu rubripes, Tetraodon fluviatilis, and Danio rerio. Boeddrich A., Burgtorf C., Roest Crollius H., Hennig S., Bernot A., Clark M., Reinhardt R., Lehrach H., Francis F. Genomics 57:164-168(1999) · UniProtKB (3) |
| Genomic organization of a 225-kb region in Xq28 containing the gene for X-linked myotubular myopathy (MTM1) and a related gene (MTMR1). Kioschis P., Wiemann S., Heiss N.S., Francis F., Goetz C., Poustka A., Taudien S., Platzer M., Wiehe T., Beckmann G. et al. Genomics 54:256-266(1998) · UniProtKB (1) |
