23
results
for author:"Fletcher C.F."
in Literature Citations
| Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies. Miki T., Zwingman T.A., Wakamori M., Lutz C.M., Cook S.A., Hosford D.A., Herrup K., Fletcher C.F., Mori Y., Frankel W.N. et al. Neuroscience 155:31-44(2008) · Mapped (16) |
| Pain sensitivity in mice lacking the Ca(v)2.1alpha1 subunit of P/Q-type Ca2+ channels. Luvisetto S., Marinelli S., Panasiti M.S., D'Amato F.R., Fletcher C.F., Pavone F., Pietrobon D. Neuroscience 142:823-832(2006) · Mapped (8) |
| The transcriptional landscape of the mammalian genome. Carninci P., Kasukawa T., Katayama S., Gough J., Frith M.C., Maeda N., Oyama R., Ravasi T., Lenhard B., Wells C. et al. Science 309:1559-1563(2005) · UniProtKB (27,424) · Mapped (12,732) |
| Transposon mutagenesis of the mouse germline. Carlson C.M., Dupuy A.J., Fritz S., Roberg-Perez K.J., Fletcher C.F., Largaespada D.A. Genetics 165:243-256(2003) · Mapped (3) |
| Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Okazaki Y., Furuno M., Kasukawa T., Adachi J., Bono H., Kondo S., Nikaido I., Osato N., Saito R., Suzuki H. et al. Nature 420:563-573(2002) · UniProtKB (17,872) · Mapped (20,305) |
| Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease. Wilson S.M., Bhattacharyya B., Rachel R.A., Coppola V., Tessarollo L., Householder D.B., Fletcher C.F., Miller R.J., Copeland N.G., Jenkins N.A. Nat. Genet. 32:420-425(2002) · Mapped (11) |
| Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice. Matesic L.E., Yip R., Reuss A.E., Swing D.A., O'Sullivan T.N., Fletcher C.F., Copeland N.G., Jenkins N.A. Proc. Natl. Acad. Sci. U.S.A. 98:10238-10243(2001) · UniProtKB (1) · Mapped (1) |
| Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity. Fletcher C.F., Tottene A., Lennon V.A., Wilson S.M., Dubel S.J., Paylor R., Hosford D.A., Tessarollo L., McEnery M.W., Pietrobon D. et al. FASEB J. 15:1288-1290(2001) · Mapped (8) |
| The status of voltage-dependent calcium channels in alpha 1E knock-out mice. Wilson S.M., Toth P.T., Oh S.B., Gillard S.E., Volsen S., Ren D., Philipson L.H., Lee E.C., Fletcher C.F., Tessarollo L. et al. J. Neurosci. 20:8566-8571(2000) · Mapped (3) |
| Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol)). Mori Y., Wakamori M., Oda S., Fletcher C.F., Sekiguchi N., Mori E., Copeland N.G., Jenkins N.A., Matsushita K., Matsuyama Z. et al. J. Neurosci. 20:5654-5662(2000) · Mapped (8) |
| Ataxic mouse mutants and molecular mechanisms of absence epilepsy. Fletcher C.F., Frankel W.N. Hum. Mol. Genet. 8:1907-1912(1999) · Mapped (16) |
| Excitatory but not inhibitory synaptic transmission is reduced in lethargic (Cacnb4(lh)) and tottering (Cacna1atg) mouse thalami. Caddick S.J., Wang C., Fletcher C.F., Jenkins N.A., Copeland N.G., Hosford D.A. J. Neurophysiol. 81:2066-2074(1999) · Mapped (13) |
| Mrvi1, a common MRV integration site in BXH2 myeloid leukemias, encodes a protein with homology to a lymphoid-restricted membrane protein Jaw1. Shaughnessy J.D. Jr., Largaespada D.A., Tian E., Fletcher C.F., Cho B.C., Vyas P., Jenkins N.A., Copeland N.G. |
| Exon structure of the nuclear factor I DNA-binding domain from C. elegans to mammals. Fletcher C.F., Jenkins N.A., Copeland N.G., Chaudhry A.Z., Gronostajski R.M. |
| Assignment of the mouse Pde7A gene to the proximal region of chromosome 3 and of the human PDE7A gene to chromosome 8q13. Han P., Fletcher C.F., Copeland N.G., Jenkins N.A., Yaremko L.M., Michaeli T. Genomics 48:275-276(1998) · Mapped (9) |
| The cut-homeodomain transcriptional activator HNF-6 is coexpressed with its target gene HNF-3 beta in the developing murine liver and pancreas. Rausa F., Samadani U., Ye H., Lim L., Fletcher C.F., Jenkins N.A., Copeland N.G., Costa R.H. |
| Mouse chromosomal locations of nine genes encoding homologs of human paraneoplastic neurologic disorder antigens. Fletcher C.F., Okano H.J., Gilbert D.J., Yang Y., Yang C., Copeland N.G., Jenkins N.A., Darnell R.B. Genomics 45:313-319(1997) · Mapped (148) |
| Chromosomal mapping of five highly conserved murine homologues of the Drosophila RING finger gene seven-in-absentia. Holloway A.J., Della N.G., Fletcher C.F., Largespada D.A., Copeland N.G., Jenkins N.A., Bowtell D.D. Genomics 41:160-168(1997) · Mapped (42) |
| Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Fletcher C.F., Lutz C.M., O'Sullivan T.N., Shaughnessy J.D. Jr., Hawkes R., Frankel W.N., Copeland N.G., Jenkins N.A. |
| No title Fan C.-M., Kuwana E., Bulfone A., Fletcher C.F., Copeland N.G., Jenkins N.A., Crews S., Martinez S., Puelles L., Rubenstein J.L. et al. Mol. Cell. Neurosci. 7:519-519(1996) |
| Expression patterns of two murine homologs of Drosophila single-minded suggest possible roles in embryonic patterning and in the pathogenesis of Down syndrome. Fan C.-M., Kuwana E., Bulfone A., Fletcher C.F., Copeland N.G., Jenkins N.A., Crews S., Martinez S., Puelles L., Rubenstein J.L. et al. Mol. Cell. Neurosci. 7:1-16(1996) · UniProtKB (2) · Mapped (45) |
| Genesis, a winged helix transcriptional repressor with expression restricted to embryonic stem cells. Sutton J., Costa R., Klug M., Field L., Xu D., Largaespada D.A., Fletcher C.F., Jenkins N.A., Copeland N.G., Klemsz M. et al. J. Biol. Chem. 271:23126-23133(1996) · UniProtKB (1) · Mapped (17) |
| Genomic structure and mapping of precerebellin and a precerebellin-related gene. Kavety B., Jenkins N.A., Fletcher C.F., Copeland N.G., Morgan J.I. Brain Res. Mol. Brain Res. 27:152-156(1994) · UniProtKB (2) · Mapped (19) |
