1 - 25 of
43
results
for author:"Sullivan L."
in Literature Citations
| Essential and synergistic roles of RP1 and RP1L1 in rod photoreceptor axoneme and retinitis pigmentosa. Yamashita T., Liu J., Gao J., LeNoue S., Wang C., Kaminoh J., Bowne S.J., Sullivan L.S., Daiger S.P., Zhang K. et al. J. Neurosci. 29:9748-9760(2009) · Mapped (10) |
| Differential recognition of CD1d-alpha-galactosyl ceramide by the V beta 8.2 and V beta 7 semi-invariant NKT T cell receptors. Pellicci D.G., Patel O., Kjer-Nielsen L., Pang S.S., Sullivan L.C., Kyparissoudis K., Brooks A.G., Reid H.H., Gras S., Lucet I.S. et al. Immunity 31:47-59(2009) · Mapped (2) |
| Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa. Friedman J.S., Ray J.W., Waseem N., Johnson K., Brooks M.J., Hugosson T., Breuer D., Branham K.E., Krauth D.S., Bowne S.J. et al. Am. J. Hum. Genet. 84:792-800(2009) · UniProtKB (1) · Mapped (7) |
| Nigrostriatal rAAV-mediated GDNF overexpression induces robust weight loss in a rat model of age-related obesity. Manfredsson F.P., Tumer N., Erdos B., Landa T., Broxson C.S., Sullivan L.F., Rising A.C., Foust K.D., Zhang Y., Muzyczka N. et al. Mol. Ther. 17:980-991(2009) · Mapped (1) |
| Vascular endothelial growth factor, its soluble receptor, and hepatocyte growth factor: clinical and genetic correlates and association with vascular function. Lieb W., Safa R., Benjamin E.J., Xanthakis V., Yin X., Sullivan L.M., Larson M.G., Smith H.M., Vita J.A., Mitchell G.F. et al. Eur. Heart J. 30:1121-1127(2009) · Mapped (10) |
| The shaping of T cell receptor recognition by self-tolerance. Gras S., Burrows S.R., Kjer-Nielsen L., Clements C.S., Liu Y.C., Sullivan L.C., Bell M.J., Brooks A.G., Purcell A.W., McCluskey J. et al. Immunity 30:193-203(2009) · Mapped (1) |
| PAX immunoreactivity identifies alveolar rhabdomyosarcoma. Sullivan L.M., Atkins K.A., LeGallo R.D. Am. J. Surg. Pathol. 33:775-780(2009) · Mapped (23) |
| Genotype score in addition to common risk factors for prediction of type 2 diabetes. Meigs J.B., Shrader P., Sullivan L.M., McAteer J.B., Fox C.S., Dupuis J., Manning A.K., Florez J.C., Wilson P.W., D'Agostino R.B. Sr. et al. N. Engl. J. Med. 359:2208-2219(2008) · Mapped (105) |
| Comprehensive evaluation of CDX2 in invasive cervical adenocarcinomas: immunopositivity in the absence of overt colorectal morphology. Sullivan L.M., Smolkin M.E., Frierson H.F. Jr., Galgano M.T. Am. J. Surg. Pathol. 32:1608-1612(2008) · Mapped (1) |
| Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa. Bowne S.J., Sullivan L.S., Gire A.I., Birch D.G., Hughbanks-Wheaton D., Heckenlively J.R., Daiger S.P. Mol. Vis. 14:922-927(2008) · Mapped (2) |
| Subtle changes in peptide conformation profoundly affect recognition of the non-classical MHC class I molecule HLA-E by the CD94-NKG2 natural killer cell receptors. Hoare H.L., Sullivan L.C., Clements C.S., Ely L.K., Beddoe T., Henderson K.N., Lin J., Reid H.H., Brooks A.G., Rossjohn J. J. Mol. Biol. 377:1297-1303(2008) · Mapped (3) |
| CD94-NKG2A recognition of human leukocyte antigen (HLA)-E bound to an HLA class I leader sequence. Petrie E.J., Clements C.S., Lin J., Sullivan L.C., Johnson D., Huyton T., Heroux A., Hoare H.L., Beddoe T., Reid H.H. et al. J. Exp. Med. 205:725-735(2008) · Mapped (30) |
| Mutations in known genes account for 58% of autosomal dominant retinitis pigmentosa (adRP). Daiger S.P., Sullivan L.S., Gire A.I., Birch D.G., Heckenlively J.R., Bowne S.J. Adv. Exp. Med. Biol. 613:203-209(2008) · Mapped (7) |
| The phosphorylation state of Ser-129 in human alpha-synuclein determines neurodegeneration in a rat model of Parkinson disease. Gorbatyuk O.S., Li S., Sullivan L.F., Chen W., Kondrikova G., Manfredsson F.P., Mandel R.J., Muzyczka N. Proc. Natl. Acad. Sci. U.S.A. 105:763-768(2008) · Mapped (4) |
| The heterodimeric assembly of the CD94-NKG2 receptor family and implications for human leukocyte antigen-E recognition. Sullivan L.C., Clements C.S., Beddoe T., Johnson D., Hoare H.L., Lin J., Huyton T., Hopkins E.J., Reid H.H., Wilce M.C. et al. Immunity 27:900-911(2007) · Mapped (29) |
| Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer. Rikova K., Guo A., Zeng Q., Possemato A., Yu J., Haack H., Nardone J., Lee K., Reeves C., Li Y. et al. Cell 131:1190-1203(2007) · UniProtKB (487) |
| The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa. Gire A.I., Sullivan L.S., Bowne S.J., Birch D.G., Hughbanks-Wheaton D., Heckenlively J.R., Daiger S.P. Mol. Vis. 13:1970-1975(2007) · Mapped (4) |
| A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy. Sullivan L.S., Baylin E.B., Font R., Daiger S.P., Pepose J.S., Clinch T.E., Nakamura H., Zhao X.C., Yee R.W. Mol. Vis. 13:975-980(2007) · Mapped (1) |
| Murine CXCR1 is a functional receptor for GCP-2/CXCL6 and interleukin-8/CXCL8. Fan X., Patera A.C., Pong-Kennedy A., Deno G., Gonsiorek W., Manfra D.J., Vassileva G., Zeng M., Jackson C., Sullivan L. et al. J. Biol. Chem. 282:11658-11666(2007) · Mapped (6) |
| Genomic rearrangements of the PRPF31 gene account for 2.5% of autosomal dominant retinitis pigmentosa. Sullivan L.S., Bowne S.J., Seaman C.R., Blanton S.H., Lewis R.A., Heckenlively J.R., Birch D.G., Hughbanks-Wheaton D., Daiger S.P. Invest. Ophthalmol. Vis. Sci. 47:4579-4588(2006) · Mapped (3) |
| Why do mutations in the ubiquitously expressed housekeeping gene IMPDH1 cause retina-specific photoreceptor degeneration? Bowne S.J., Liu Q., Sullivan L.S., Zhu J., Spellicy C.J., Rickman C.B., Pierce E.A., Daiger S.P. Invest. Ophthalmol. Vis. Sci. 47:3754-3765(2006) · Mapped (11) |
| Coregulation of estrogen receptor by ERBB4/HER4 establishes a growth-promoting autocrine signal in breast tumor cells. Zhu Y., Sullivan L.L., Nair S.S., Williams C.C., Pandey A.K., Marrero L., Vadlamudi R.K., Jones F.E. Cancer Res. 66:7991-7998(2006) · Mapped (61) |
| Structural basis for a major histocompatibility complex class Ib-restricted T cell response. Hoare H.L., Sullivan L.C., Pietra G., Clements C.S., Lee E.J., Ely L.K., Beddoe T., Falco M., Kjer-Nielsen L., Reid H.H. et al. Nat. Immunol. 7:256-264(2006) · Mapped (3) |
| Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis. Bowne S.J., Sullivan L.S., Mortimer S.E., Hedstrom L., Zhu J., Spellicy C.J., Gire A.I., Hughbanks-Wheaton D., Birch D.G., Lewis R.A. et al. Invest. Ophthalmol. Vis. Sci. 47:34-42(2006) · Mapped (9) |
| Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 gene. Kozma P., Hughbanks-Wheaton D.K., Locke K.G., Fish G.E., Gire A.I., Spellicy C.J., Sullivan L.S., Bowne S.J., Daiger S.P., Birch D.G. Am. J. Ophthalmol. 140:858-867(2005) · Mapped (9) |
