10
results
for author:"Howell G.R."
in Literature Citations
| Axons of retinal ganglion cells are insulted in the optic nerve early in DBA/2J glaucoma. Howell G.R., Libby R.T., Jakobs T.C., Smith R.S., Phalan F.C., Barter J.W., Barbay J.M., Marchant J.K., Mahesh N., Porciatti V. et al. J. Cell Biol. 179:1523-1537(2007) · Mapped (15) |
| Inducible nitric oxide synthase, Nos2, does not mediate optic neuropathy and retinopathy in the DBA/2J glaucoma model. Libby R.T., Howell G.R., Pang I.H., Savinova O.V., Mehalow A.K., Barter J.W., Smith R.S., Clark A.F., John S.W. BMC Neurosci 8:108-108(2007) · Mapped (1) |
| The classical complement cascade mediates CNS synapse elimination. Stevens B., Allen N.J., Vazquez L.E., Howell G.R., Christopherson K.S., Nouri N., Micheva K.D., Mehalow A.K., Huberman A.D., Stafford B. et al. Cell 131:1164-1178(2007) · Mapped (8) |
| Absence of glaucoma in DBA/2J mice homozygous for wild-type versions of Gpnmb and Tyrp1. Howell G.R., Libby R.T., Marchant J.K., Wilson L.A., Cosma I.M., Smith R.S., Anderson M.G., John S.W. BMC Genet. 8:45-45(2007) · Mapped (13) |
| Mutation of a ubiquitously expressed mouse transmembrane protein (Tapt1) causes specific skeletal homeotic transformations. Howell G.R., Shindo M., Murray S., Gridley T., Wilson L.A., Schimenti J.C. |
| 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 (1,199) |
| The DNA sequence and analysis of human chromosome 6. Mungall A.J., Palmer S.A., Sims S.K., Edwards C.A., Ashurst J.L., Wilming L., Jones M.C., Horton R., Hunt S.E., Scott C.E. et al. Nature 425:805-811(2003) · UniProtKB (1,570) |
| A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation. McMullan T.W., Crolla J.A., Gregory S.G., Carter N.P., Cooper R.A., Howell G.R., Robinson D.O. |
| A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation. Carrie A., Jun L., Bienvenu T., Vinet M.-C., McDonell N., Couvert P., Zemni R., Cardona A., Van Buggenhout G., Frints S. et al. |
| Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene. Coffey A.J., Brooksbank R.A., Brandau O., Oohashi T., Howell G.R., Bye J.M., Cahn A.P., Durham J., Heath P., Wray P. et al. |
