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1
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26944457419
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Gillies R.J., Hoffman J.M., Lam K.S., Menkens A.E., Piwnica-Worms D.R., Sullivan D.C., and Weissleder R. Mol. Imaging 4 (2005) 98
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Mol. Imaging
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Gillies, R.J.1
Hoffman, J.M.2
Lam, K.S.3
Menkens, A.E.4
Piwnica-Worms, D.R.5
Sullivan, D.C.6
Weissleder, R.7
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3
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11144317860
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Handl H.L., Vagner J., Han H., Mash E., Hruby V.J., and Gillies R.J. Expert Opin. Ther. Targets 8 (2004) 565
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(2004)
Expert Opin. Ther. Targets
, vol.8
, pp. 565
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Handl, H.L.1
Vagner, J.2
Han, H.3
Mash, E.4
Hruby, V.J.5
Gillies, R.J.6
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6
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0028535271
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Sharma S.D., Granberry M.E., Jiang J., Leong S.L.P., Hadley M.E., and Hruby V.J. Bioconjug. Chem. 5 (1994) 591
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(1994)
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Sharma, S.D.1
Granberry, M.E.2
Jiang, J.3
Leong, S.L.P.4
Hadley, M.E.5
Hruby, V.J.6
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7
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0030447479
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Sharma S.D., Jiang J., Hadley M.E., Bentley D.L., and Hruby V.J. Proc. Natl. Acad. Sci. U.S.A. 93 (1996) 13715
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(1996)
Proc. Natl. Acad. Sci. U.S.A.
, vol.93
, pp. 13715
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Sharma, S.D.1
Jiang, J.2
Hadley, M.E.3
Bentley, D.L.4
Hruby, V.J.5
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12
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34249286953
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Finch C.A. (Ed), Staples Printers Ltd., Kent, England
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Moore W.R.A.D., and O'Dowd M. In: Finch C.A. (Ed). Properties and Applications of Polyvinyl Alcohol (1968), Staples Printers Ltd., Kent, England 77
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(1968)
Properties and Applications of Polyvinyl Alcohol
, pp. 77
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Moore, W.R.A.D.1
O'Dowd, M.2
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15
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34249282653
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note
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Purchased from Aldrich Chemical Company.
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16
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34249277347
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Isacesco N., Taleb-Bendiab S.-A., Chatzopoulos M., Montheard J.P., and Vergnaud J.M. C.R. Acad. Sci. C Chim. 279 (1974) 683
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(1974)
C.R. Acad. Sci. C Chim.
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Isacesco, N.1
Taleb-Bendiab, S.-A.2
Chatzopoulos, M.3
Montheard, J.P.4
Vergnaud, J.M.5
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17
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34249322612
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note
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In some runs, hydroboration was apparently incomplete. Hydrogen peroxide converted the remaining alkene moieties into epoxides, which were ring-opened by hydroxide, resulting in contamination of the hexaol 1 by heptaol and octaol impurities (from HPLC and HRMS).
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19
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34249321194
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note
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Purchased from Senn Chemicals USA.
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21
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0000448866
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The 'high-affinity' ligand employed here was based on NDP-α-MSH (Ser-Tyr-Ser-Nle-Glu-His-DPhe-Arg-Trp-Gly-Lys-Pro-Val); see
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The 'high-affinity' ligand employed here was based on NDP-α-MSH (Ser-Tyr-Ser-Nle-Glu-His-DPhe-Arg-Trp-Gly-Lys-Pro-Val); see. Sawyer T.K., Sanfilippo P.J., Hruby V.J., Engel M.H., Heward C.B., Burnett J.B., and Hadley M.E. Proc. Natl. Acad. Sci. U.S.A. 77 (1980) 5754
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(1980)
Proc. Natl. Acad. Sci. U.S.A.
, vol.77
, pp. 5754
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Sawyer, T.K.1
Sanfilippo, P.J.2
Hruby, V.J.3
Engel, M.H.4
Heward, C.B.5
Burnett, J.B.6
Hadley, M.E.7
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22
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0019890250
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Hadley M.E., Anderson B., Heward C.B., Sawyer T.K., and Hruby V.J. Science 213 (1981) 1025
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(1981)
Science
, vol.213
, pp. 1025
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Hadley, M.E.1
Anderson, B.2
Heward, C.B.3
Sawyer, T.K.4
Hruby, V.J.5
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25
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0023598089
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The 'low-affinity' ligand employed was based on the minimal active sequence for full agonist activity of α-MSH (His-DPhe-Arg-Trp); see
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The 'low-affinity' ligand employed was based on the minimal active sequence for full agonist activity of α-MSH (His-DPhe-Arg-Trp); see. Hruby V.J., Wilkes B.C., Hadley M.E., Al-Obeidi F., Sawyer T.K., Staples D.J., de Vaux A.E., Dym O., de Lauro Castrucci A.M., Hintz M.F., Riehm J.P., and Rao K.R. J. Med. Chem. 30 (1987) 2126
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(1987)
J. Med. Chem.
, vol.30
, pp. 2126
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Hruby, V.J.1
Wilkes, B.C.2
Hadley, M.E.3
Al-Obeidi, F.4
Sawyer, T.K.5
Staples, D.J.6
de Vaux, A.E.7
Dym, O.8
de Lauro Castrucci, A.M.9
Hintz, M.F.10
Riehm, J.P.11
Rao, K.R.12
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26
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0024562277
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Castrucci A.M.L., Hadley M.E., Sawyer T.K., Wilkes B.C., Al-Obiedi F., Staples D.J., de Vaux A.E., Dym O., Hintz M.F., Riehm J.P., Rao K.R., and Hruby V.J. Gen. Comp. Endocrinol. 73 (1989) 157
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(1989)
Gen. Comp. Endocrinol.
, vol.73
, pp. 157
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Castrucci, A.M.L.1
Hadley, M.E.2
Sawyer, T.K.3
Wilkes, B.C.4
Al-Obiedi, F.5
Staples, D.J.6
de Vaux, A.E.7
Dym, O.8
Hintz, M.F.9
Riehm, J.P.10
Rao, K.R.11
Hruby, V.J.12
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27
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0030787858
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Haskell-Luevano C., Hendrata S., North C., Sawyer T.K., Hadley M.E., Hruby V.J., Dickinson C., and Gantz I. J. Med. Chem. 40 (1997) 2133
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(1997)
J. Med. Chem.
, vol.40
, pp. 2133
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Haskell-Luevano, C.1
Hendrata, S.2
North, C.3
Sawyer, T.K.4
Hadley, M.E.5
Hruby, V.J.6
Dickinson, C.7
Gantz, I.8
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28
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0027227288
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The hMC4R vector was originally received from Dr. Ira Gantz; see
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The hMC4R vector was originally received from Dr. Ira Gantz; see. Gantz I., Miwa H., Konda Y., Shimoto Y., Tashiro T., Watson S.J., DelValle J., and Yamada T. J. Biol. Chem. 268 (1993) 15174
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(1993)
J. Biol. Chem.
, vol.268
, pp. 15174
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Gantz, I.1
Miwa, H.2
Konda, Y.3
Shimoto, Y.4
Tashiro, T.5
Watson, S.J.6
DelValle, J.7
Yamada, T.8
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29
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2942530793
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Handl H.L., Vagner J., Yamamura H.I., Hruby V.J., and Gillies R.J. Anal. Biochem. 330 (2004) 242
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(2004)
Anal. Biochem.
, vol.330
, pp. 242
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Handl, H.L.1
Vagner, J.2
Yamamura, H.I.3
Hruby, V.J.4
Gillies, R.J.5
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30
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34249301295
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note
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3 instrument using the standard Eu TRF measurement (340 nm excitation, 400 μs delay, and emission collection for 400 μs at 615 nm). Competition curves were analyzed with GraphPad Prism Software using the sigmoidal dose-response classical equation for non-linear regression analysis. Each data point represents the average of 4 samples, with the error bars indicating standard error of the mean.
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Vagner J., Handl H.L., Monguchi Y., Jana U., Begay L.J., Mash E.A., Hruby V.J., and Gillies R.J. Bioconjug. Chem. 17 (2006) 1545
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(2006)
Bioconjug. Chem.
, vol.17
, pp. 1545
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Vagner, J.1
Handl, H.L.2
Monguchi, Y.3
Jana, U.4
Begay, L.J.5
Mash, E.A.6
Hruby, V.J.7
Gillies, R.J.8
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