1 - 25 of 38 results for author:"Whitby F.G." in Literature citations
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| UNC119 is required for G protein trafficking in sensory neurons. Zhang H., Constantine R., Vorobiev S., Chen Y., Seetharaman J., Huang Y.J., Xiao R., Montelione G.T., Gerstner C.D., Davis M.W. et al. Nat. Neurosci. 14:874-880(2011) · UniProtKB (4) · Mapped (10) |
| Crystal structures of a halophilic archaeal malate synthase from Haloferax volcanii and comparisons with isoforms A and G. Bracken C.D., Neighbor A.M., Lamlenn K.K., Thomas G.C., Schubert H.L., Whitby F.G., Howard B.R. BMC Struct. Biol. 11:23-23(2011) · UniProtKB (1) |
| Structure of a Blm10 complex reveals common mechanisms for proteasome binding and gate opening. Sadre-Bazzaz K., Whitby F.G., Robinson H., Formosa T., Hill C.P. Mol. Cell 37:728-735(2010) · Mapped (15) |
| Structural models for interactions between the 20S proteasome and its PAN/19S activators. Stadtmueller B.M., Ferrell K., Whitby F.G., Heroux A., Robinson H., Myszka D.G., Hill C.P. J. Biol. Chem. 285:13-17(2010) · UniProtKB (3) · Mapped (13) |
| X-ray structures of the hexameric building block of the HIV capsid. Pornillos O., Ganser-Pornillos B.K., Kelly B.N., Hua Y., Whitby F.G., Stout C.D., Sundquist W.I., Hill C.P., Yeager M. Cell 137:1282-1292(2009) · Mapped (1) |
| Substrate shuttling between active sites of uroporphyrinogen decarboxylase is not required to generate coproporphyrinogen. Phillips J.D., Warby C.A., Whitby F.G., Kushner J.P., Hill C.P. J. Mol. Biol. 389:306-314(2009) · Mapped (1) |
| A general mechanism for transcription regulation by Oct1 and Oct4 in response to genotoxic and oxidative stress. Kang J., Gemberling M., Nakamura M., Whitby F.G., Handa H., Fairbrother W.G., Tantin D. Genes Dev. 23:208-222(2009) · Mapped (64) |
| Biochemical and structural studies of yeast Vps4 oligomerization. Gonciarz M.D., Whitby F.G., Eckert D.M., Kieffer C., Heroux A., Sundquist W.I., Hill C.P. J. Mol. Biol. 384:878-895(2008) · Mapped (1) |
| ALIX-CHMP4 interactions in the human ESCRT pathway. McCullough J., Fisher R.D., Whitby F.G., Sundquist W.I., Hill C.P. Proc. Natl. Acad. Sci. U.S.A. 105:7687-7691(2008) · UniProtKB (4) · Mapped (1) |
| Structures of prostacyclin synthase and its complexes with substrate analog and inhibitor reveal a ligand-specific heme conformation change. Li Y.C., Chiang C.W., Yeh H.C., Hsu P.Y., Whitby F.G., Wang L.H., Chan N.L. J. Biol. Chem. 283:2917-2926(2008) · UniProtKB (1) · Mapped (1) |
| Two novel uroporphyrinogen decarboxylase (URO-D) mutations causing hepatoerythropoietic porphyria (HEP). Phillips J.D., Whitby F.G., Stadtmueller B.M., Edwards C.Q., Hill C.P., Kushner J.P. Transl. Res. 149:85-91(2007) · UniProtKB (1) |
| Structural basis for ubiquitin recognition by the human ESCRT-II EAP45 GLUE domain. Alam S.L., Langelier C., Whitby F.G., Koirala S., Robinson H., Hill C.P., Sundquist W.I. Nat. Struct. Mol. Biol. 13:1029-1030(2006) · UniProtKB (1) · Mapped (2) |
| A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome. Toydemir R.M., Brassington A.E., Bayrak-Toydemir P., Krakowiak P.A., Jorde L.B., Whitby F.G., Longo N., Viskochil D.H., Carey J.C., Bamshad M.J. Am. J. Hum. Genet. 79:935-941(2006) · UniProtKB (1) · Mapped (9) |
| Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome. Toydemir R.M., Rutherford A., Whitby F.G., Jorde L.B., Carey J.C., Bamshad M.J. |
| Investigation of treatment failure in neonatal echovirus 7 infection. Rentz A.C., Libbey J.E., Fujinami R.S., Whitby F.G., Byington C.L. Pediatr. Infect. Dis. J. 25:259-262(2006) · UniProtKB (1) |
| Structural and mechanistic studies of VPS4 proteins. Scott A., Chung H.Y., Gonciarz-Swiatek M., Hill G.C., Whitby F.G., Gaspar J., Holton J.M., Viswanathan R., Ghaffarian S., Hill C.P. et al. |
| The 1.9 A structure of a proteasome-11S activator complex and implications for proteasome-PAN/PA700 interactions. Forster A., Masters E.I., Whitby F.G., Robinson H., Hill C.P. |
| Crystal structure of the oxygen-dependant coproporphyrinogen oxidase (Hem13p) of Saccharomyces cerevisiae. Phillips J.D., Whitby F.G., Warby C.A., Labbe P., Yang C., Pflugrath J.W., Ferrara J.D., Robinson H., Kushner J.P., Hill C.P. J. Biol. Chem. 279:38960-38968(2004) · UniProtKB (1) |
| Structural basis for tetrapyrrole coordination by uroporphyrinogen decarboxylase. Phillips J.D., Whitby F.G., Kushner J.P., Hill C.P. EMBO J. 22:6225-6233(2003) · UniProtKB (1) |
| The pore of activated 20S proteasomes has an ordered 7-fold symmetric conformation. Forster A., Whitby F.G., Hill C.P. EMBO J. 22:4356-4364(2003) · Mapped (14) |
| Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes. Sung S.S., Brassington A.-M.E., Grannatt K., Rutherford A., Whitby F.G., Krakowiak P.A., Jorde L.B., Carey J.C., Bamshad M. Am. J. Hum. Genet. 72:681-690(2003) · UniProtKB (2) · Mapped (3) |
| Crystal structure of a biliverdin IXalpha reductase enzyme-cofactor complex. Whitby F.G., Phillips J.D., Hill C.P., McCoubrey W.K. Jr., Maines M.D. J. Mol. Biol. 319:1199-1210(2002) · UniProtKB (1) · Mapped (6) |
| Myosin light chain mutation causes autosomal recessive cardiomyopathy with mid-cavitary hypertrophy and restrictive physiology. Olson T.M., Karst M.L., Whitby F.G., Driscoll D.J. Circulation 105:2337-2340(2002) · UniProtKB (1) |
| Functional consequences of naturally occurring mutations in human uroporphyrinogen decarboxylase. Phillips J.D., Parker T.L., Schubert H.L., Whitby F.G., Hill C.P., Kushner J.P. Blood 98:3179-3185(2001) · UniProtKB (1) |
| Crystal structure of human uroporphyrinogen III synthase. Mathews M.A., Schubert H.L., Whitby F.G., Alexander K.J., Schadick K., Bergonia H.A., Phillips J.D., Hill C.P. EMBO J. 20:5832-5839(2001) · UniProtKB (1) |