1 - 25 of
87
results
for author:"West S."
in Literature Citations
| beta-Defensin 1 haplotype associated with postoperative endophthalmitis. Carter J.G., West S.K., Painter S., Haynes R.J., Churchill A.J. Acta Ophthalmol 0:0-0(2009) · Mapped (2) |
| Poly(ADP-ribose)-dependent regulation of DNA repair by the chromatin remodeling enzyme ALC1. Ahel D., Horejsi Z., Wiechens N., Polo S.E., Garcia-Wilson E., Ahel I., Flynn H., Skehel M., West S.C., Jackson S.P. et al. |
| The DRD3 rs6280 polymorphism and prevalence of tardive dyskinesia: A meta-analysis. Tsai H.T., North K.E., West S.L., Poole C. Am. J. Med. Genet. B Neuropsychiatr. Genet. 0:0-0(2009) · Mapped (6) |
| Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer. van Haaften G., Dalgliesh G.L., Davies H., Chen L., Bignell G., Greenman C., Edkins S., Hardy C., O'Meara S., Teague J. et al. Nat. Genet. 41:521-523(2009) · Mapped (12) |
| IGF-I and IGFBP-3 polymorphisms in relation to circulating levels among African American and Caucasian women. D'Aloisio A.A., Schroeder J.C., North K.E., Poole C., West S.L., Travlos G.S., Baird D.D. Cancer Epidemiol. Biomarkers Prev. 18:954-966(2009) · Mapped (25) |
| Overexpression of myocilin in the Drosophila eye activates the unfolded protein response: implications for glaucoma. Carbone M.A., Ayroles J.F., Yamamoto A., Morozova T.V., West S.A., Magwire M.M., Mackay T.F., Anholt R.R. PLoS ONE 4:e4216-e4216(2009) · Mapped (62) |
| Development of a Rab9 transgenic mouse and its ability to increase the lifespan of a murine model of Niemann-Pick type C disease. Kaptzan T., West S.A., Holicky E.L., Wheatley C.L., Marks D.L., Wang T., Peake K.B., Vance J., Walkley S.U., Pagano R.E. Am. J. Pathol. 174:14-20(2009) · Mapped (4) |
| Identification of Holliday junction resolvases from humans and yeast. Ip S.C., Rass U., Blanco M.G., Flynn H.R., Skehel J.M., West S.C. Nature 456:357-361(2008) · Mapped (3) |
| FANCM and FAAP24 function in ATR-mediated checkpoint signaling independently of the Fanconi anemia core complex. Collis S.J., Ciccia A., Deans A.J., Horejsi Z., Martin J.S., Maslen S.L., Skehel J.M., Elledge S.J., West S.C., Boulton S.J. Mol. Cell 32:313-324(2008) · Mapped (3) |
| RTEL1 maintains genomic stability by suppressing homologous recombination. Barber L.J., Youds J.L., Ward J.D., McIlwraith M.J., O'Neil N.J., Petalcorin M.I.R., Martin J.S., Collis S.J., Cantor S.B., Auclair M. et al. |
| Transcription factor 7-like 2 (TCF7L2) polymorphism and context-specific risk of type 2 diabetes in African American and Caucasian adults: the Atherosclerosis Risk in Communities study. Yan Y., North K.E., Ballantyne C.M., Brancati F.L., Chambless L.E., Franceschini N., Heiss G., Kottgen A., Pankow J.S., Selvin E. et al. Diabetes 58:285-289(2009) · Mapped (26) |
| The effect of exercise and estrogen on osteoprotegerin in premenopausal women. West S.L., Scheid J.L., De Souza M.J. Bone 44:137-144(2009) · Mapped (1) |
| Elevated PYY is associated with energy deficiency and indices of subclinical disordered eating in exercising women with hypothalamic amenorrhea. Scheid J.L., Williams N.I., West S.L., VanHeest J.L., De Souza M.J. Appetite 52:184-192(2009) · Mapped (1) |
| Molecular mechanism of DNA deadenylation by the neurological disease protein aprataxin. Rass U., Ahel I., West S.C. J. Biol. Chem. 283:33994-34001(2008) · Mapped (7) |
| Human leukocyte antigen (HLA)-B, DRB1, and DQB1 allotypes associated with disease and protection of trachoma endemic villagers. Abbas M., Bobo L.D., Hsieh Y.H., Berka N., Dunston G., Bonney G.E., Apprey V., Quinn T.C., West S.K. Invest. Ophthalmol. Vis. Sci. 50:1734-1738(2009) · Mapped (2,074) |
| X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment. Dibbens L.M., Tarpey P.S., Hynes K., Bayly M.A., Scheffer I.E., Smith R., Bomar J., Sutton E., Vandeleur L., Shoubridge C. et al. |
| Single-stranded DNA-binding protein hSSB1 is critical for genomic stability. Richard D.J., Bolderson E., Cubeddu L., Wadsworth R.I.M., Savage K., Sharma G.G., Nicolette M.L., Tsvetanov S., McIlwraith M.J., Pandita R.K. et al. Nature 453:677-681(2008) · UniProtKB (3) |
| Poly(ADP-ribose)-binding zinc finger motifs in DNA repair/checkpoint proteins. Ahel I., Ahel D., Matsusaka T., Clark A.J., Pines J., Boulton S.J., West S.C. |
| Human Pcf11 enhances degradation of RNA polymerase II-associated nascent RNA and transcriptional termination. West S., Proudfoot N.J. Nucleic Acids Res. 36:905-914(2008) · Mapped (3) |
| RIDDLE immunodeficiency syndrome is linked to defects in 53BP1-mediated DNA damage signaling. Stewart G.S., Stankovic T., Byrd P.J., Wechsler T., Miller E.S., Huissoon A., Drayson M.T., West S.C., Elledge S.J., Taylor A.M. Proc. Natl. Acad. Sci. U.S.A. 104:16910-16915(2007) · Mapped (4) |
| Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation. Tarpey P.S., Raymond F.L., Nguyen L.S., Rodriguez J., Hackett A., Vandeleur L., Smith R., Shoubridge C., Edkins S., Stevens C. et al. |
| Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly. Field M., Tarpey P.S., Smith R., Edkins S., O'Meara S., Stevens C., Tofts C., Teague J., Butler A., Dicks E. et al. Am. J. Hum. Genet. 81:367-374(2007) · UniProtKB (1) |
| Interactions between human BRCA2 protein and the meiosis-specific recombinase DMC1. Thorslund T., Esashi F., West S.C. EMBO J. 26:2915-2922(2007) · Mapped (15) |
| Stabilization of RAD51 nucleoprotein filaments by the C-terminal region of BRCA2. Esashi F., Galkin V.E., Yu X., Egelman E.H., West S.C. Nat. Struct. Mol. Biol. 14:468-474(2007) · Mapped (17) |
| Patterns of somatic mutation in human cancer genomes. Greenman C., Stephens P., Smith R., Dalgliesh G.L., Hunter C., Bignell G., Davies H., Teague J., Butler A., Stevens C. et al. Nature 446:153-158(2007) · UniProtKB (453) |
