-
1
-
-
39049085666
-
Delayed functional expression of neuronal chemokine receptors following focal nerve demyelination in the rat: A mechanism for the development of chronic sensitization of peripheral nociceptors
-
Bhangoo S., Ren D., Miller R. J., et al,. (2007a) Delayed functional expression of neuronal chemokine receptors following focal nerve demyelination in the rat: a mechanism for the development of chronic sensitization of peripheral nociceptors. Mol. Pain 3, 38.
-
(2007)
Mol. Pain
, vol.3
, pp. 38
-
-
Bhangoo, S.1
Ren, D.2
Miller, R.J.3
-
2
-
-
34249737450
-
CXCR4 chemokine receptor signaling mediates pain hypersensitivity in association with antiretroviral toxic neuropathy
-
Bhangoo S. K., Ren D., Miller R. J., Chan D. M., Ripsch M. S., Weiss C., McGinnis C., and, White F. A., (2007b) CXCR4 chemokine receptor signaling mediates pain hypersensitivity in association with antiretroviral toxic neuropathy. Brain Behav. Immun. 21, 581-591.
-
(2007)
Brain Behav. Immun.
, vol.21
, pp. 581-591
-
-
Bhangoo, S.K.1
Ren, D.2
Miller, R.J.3
Chan, D.M.4
Ripsch, M.S.5
Weiss, C.6
McGinnis, C.7
White, F.A.8
-
3
-
-
70349446343
-
Targeting neuroprotection as an alternative approach to preventing and treating neuropathic pain
-
Bordet T., and, Pruss R. M., (2009) Targeting neuroprotection as an alternative approach to preventing and treating neuropathic pain. Neurotherapeutics 6, 648-662.
-
(2009)
Neurotherapeutics
, vol.6
, pp. 648-662
-
-
Bordet, T.1
Pruss, R.M.2
-
4
-
-
0026693754
-
Cardiovascular effects of omega-conopeptides in conscious rats: Mechanisms of action
-
Bowersox S. S., Singh T., Nadasdi L., Zukowska-Grojec Z., Valentino K., and, Hoffman B. B., (1992) Cardiovascular effects of omega-conopeptides in conscious rats: mechanisms of action. J. Cardiovasc. Pharmacol. 20, 756-764.
-
(1992)
J. Cardiovasc. Pharmacol.
, vol.20
, pp. 756-764
-
-
Bowersox, S.S.1
Singh, T.2
Nadasdi, L.3
Zukowska-Grojec, Z.4
Valentino, K.5
Hoffman, B.B.6
-
5
-
-
80054817553
-
Neuroprotection against traumatic brain injury by a peptide derived from the collapsin response mediator protein 2 (CRMP2)
-
Brittain J. M., Chen L., Wilson S. M., et al,. (2011a) Neuroprotection against traumatic brain injury by a peptide derived from the collapsin response mediator protein 2 (CRMP2). J. Biol. Chem. 286, 37778-37792.
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 37778-37792
-
-
Brittain, J.M.1
Chen, L.2
Wilson, S.M.3
-
6
-
-
79960115452
-
Suppression of inflammatory and neuropathic pain by uncoupling CRMP-2 from the presynaptic Ca(2)(+) channel complex
-
Brittain J. M., Duarte D. B., Wilson S. M., et al,. (2011b) Suppression of inflammatory and neuropathic pain by uncoupling CRMP-2 from the presynaptic Ca(2)(+) channel complex. Nat. Med. 17, 822-829.
-
(2011)
Nat. Med.
, vol.17
, pp. 822-829
-
-
Brittain, J.M.1
Duarte, D.B.2
Wilson, S.M.3
-
7
-
-
84860334997
-
Disruption of NMDAR-CRMP-2 signaling protects against focal cerebral ischemic damage in the rat middle cerebral artery occlusion model
-
Brittain J. M., Pan R., You H., Brustovetsky T., Brustovetsky N., Zamponi G. W., Lee W. H., and, Khanna R., (2012) Disruption of NMDAR-CRMP-2 signaling protects against focal cerebral ischemic damage in the rat middle cerebral artery occlusion model. Channels (Austin) 6, 52-59.
-
(2012)
Channels (Austin)
, vol.6
, pp. 52-59
-
-
Brittain, J.M.1
Pan, R.2
You, H.3
Brustovetsky, T.4
Brustovetsky, N.5
Zamponi, G.W.6
Lee, W.H.7
Khanna, R.8
-
8
-
-
0034926291
-
The vanilloid receptor: A molecular gateway to the pain pathway
-
Caterina M. J., and, Julius D., (2001) The vanilloid receptor: a molecular gateway to the pain pathway. Annu. Rev. Neurosci. 24, 487-517.
-
(2001)
Annu. Rev. Neurosci.
, vol.24
, pp. 487-517
-
-
Caterina, M.J.1
Julius, D.2
-
9
-
-
3543122391
-
Intrathecal ziconotide for refractory pain
-
Doggrell S. A., (2004) Intrathecal ziconotide for refractory pain. Expert Opin. Investig. Drugs 13, 875-877.
-
(2004)
Expert Opin. Investig. Drugs
, vol.13
, pp. 875-877
-
-
Doggrell, S.A.1
-
10
-
-
34250835903
-
A comprehensive model for the cellular uptake of cationic cell-penetrating peptides
-
Duchardt F., Fotin-Mleczek M., Schwarz H., Fischer R., and, Brock R., (2007) A comprehensive model for the cellular uptake of cationic cell-penetrating peptides. Traffic 8, 848-866.
-
(2007)
Traffic
, vol.8
, pp. 848-866
-
-
Duchardt, F.1
Fotin-Mleczek, M.2
Schwarz, H.3
Fischer, R.4
Brock, R.5
-
11
-
-
70350368006
-
Gabapentin receptor alpha2delta-1 is a neuronal thrombospondin receptor responsible for excitatory CNS synaptogenesis
-
Eroglu C., Allen N. J., Susman M. W., et al,. (2009) Gabapentin receptor alpha2delta-1 is a neuronal thrombospondin receptor responsible for excitatory CNS synaptogenesis. Cell 139, 380-392.
-
(2009)
Cell
, vol.139
, pp. 380-392
-
-
Eroglu, C.1
Allen, N.J.2
Susman, M.W.3
-
12
-
-
1542327642
-
Pathway for polyarginine entry into mammalian cells
-
Fuchs S. M., and, Raines R. T., (2004) Pathway for polyarginine entry into mammalian cells. Biochemistry 43, 2438-2444.
-
(2004)
Biochemistry
, vol.43
, pp. 2438-2444
-
-
Fuchs, S.M.1
Raines, R.T.2
-
13
-
-
0036048640
-
CRMP-2 binds to tubulin heterodimers to promote microtubule assembly
-
Fukata Y., Itoh T. J., Kimura T., et al,. (2002) CRMP-2 binds to tubulin heterodimers to promote microtubule assembly. Nat. Cell Biol. 4, 583-591.
-
(2002)
Nat. Cell Biol.
, vol.4
, pp. 583-591
-
-
Fukata, Y.1
Itoh, T.J.2
Kimura, T.3
-
14
-
-
0029975930
-
The novel anticonvulsant drug, gabapentin (Neurontin), binds to the alpha2delta subunit of a calcium channel
-
Gee N. S., Brown J. P., Dissanayake V. U., Offord J., Thurlow R., and, Woodruff G. N., (1996) The novel anticonvulsant drug, gabapentin (Neurontin), binds to the alpha2delta subunit of a calcium channel. J. Biol. Chem. 271, 5768-5776.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 5768-5776
-
-
Gee, N.S.1
Brown, J.P.2
Dissanayake, V.U.3
Offord, J.4
Thurlow, R.5
Woodruff, G.N.6
-
15
-
-
80053510653
-
Pain as a global public health priority
-
Goldberg D. S., and, McGee S. J., (2011) Pain as a global public health priority. BMC Public Health 11, 770.
-
(2011)
BMC Public Health
, vol.11
, pp. 770
-
-
Goldberg, D.S.1
McGee, S.J.2
-
16
-
-
0035837299
-
Changes in cytosolic calcium in response to noxious heat and their relationship to vanilloid receptors in rat dorsal root ganglion neurons
-
Greffrath W., Kirschstein T., Nawrath H., and, Treede R., (2001) Changes in cytosolic calcium in response to noxious heat and their relationship to vanilloid receptors in rat dorsal root ganglion neurons. Neuroscience 104, 539-550.
-
(2001)
Neuroscience
, vol.104
, pp. 539-550
-
-
Greffrath, W.1
Kirschstein, T.2
Nawrath, H.3
Treede, R.4
-
17
-
-
0345459935
-
How prevalent is chronic pain?
-
Harstall C., (2003) How prevalent is chronic pain? Pain Clin. Updates vol XI, 1-4.
-
(2003)
Pain Clin. Updates
, vol.11
, pp. 1-4
-
-
Harstall, C.1
-
18
-
-
0036260775
-
The arginine-rich hexapeptide R4W2 is a stereoselective antagonist at the vanilloid receptor 1: A Ca2+ imaging study in adult rat dorsal root ganglion neurons
-
Himmel H. M., Kiss T., Borvendeg S. J., Gillen C., and, Illes P., (2002) The arginine-rich hexapeptide R4W2 is a stereoselective antagonist at the vanilloid receptor 1: a Ca2+ imaging study in adult rat dorsal root ganglion neurons. J. Pharmacol. Exp. Ther. 301, 981-986.
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.301
, pp. 981-986
-
-
Himmel, H.M.1
Kiss, T.2
Borvendeg, S.J.3
Gillen, C.4
Illes, P.5
-
19
-
-
0346724920
-
Novel mechanism of enhanced nociception in a model of AIDS therapy-induced painful peripheral neuropathy in the rat
-
Joseph E. K., Chen X., Khasar S. G., and, Levine J. D., (2004) Novel mechanism of enhanced nociception in a model of AIDS therapy-induced painful peripheral neuropathy in the rat. Pain 107, 147-158.
-
(2004)
Pain
, vol.107
, pp. 147-158
-
-
Joseph, E.K.1
Chen, X.2
Khasar, S.G.3
Levine, J.D.4
-
20
-
-
0027941058
-
Voltage-sensitive calcium channels in spinal nociceptive processing: Blockade of N- and P-type channels inhibits formalin-induced nociception
-
Malmberg A. B., and, Yaksh T. L., (1994) Voltage-sensitive calcium channels in spinal nociceptive processing: blockade of N- and P-type channels inhibits formalin-induced nociception. J. Neurosci. 14, 4882-4890.
-
(1994)
J. Neurosci.
, vol.14
, pp. 4882-4890
-
-
Malmberg, A.B.1
Yaksh, T.L.2
-
21
-
-
33846238159
-
Alpha2delta and the mechanism of action of gabapentin in the treatment of pain
-
Maneuf Y. P., Luo Z. D., and, Lee K., (2006) alpha2delta and the mechanism of action of gabapentin in the treatment of pain. Semin. Cell Dev. Biol. 17, 565-570.
-
(2006)
Semin. Cell Dev. Biol.
, vol.17
, pp. 565-570
-
-
Maneuf, Y.P.1
Luo, Z.D.2
Lee, K.3
-
22
-
-
0033794501
-
Polyarginine enters cells more efficiently than other polycationic homopolymers
-
Mitchell D. J., Kim D. T., Steinman L., Fathman C. G., and, Rothbard J. B., (2000) Polyarginine enters cells more efficiently than other polycationic homopolymers. J. Pept. Res. 56, 318-325.
-
(2000)
J. Pept. Res.
, vol.56
, pp. 318-325
-
-
Mitchell, D.J.1
Kim, D.T.2
Steinman, L.3
Fathman, C.G.4
Rothbard, J.B.5
-
23
-
-
84867432306
-
CRMP-2 peptide mediated decrease of high and low voltage-activated calcium channels, attenuation of nociceptor excitability, and anti-nociception in a model of AIDS therapy-induced painful peripheral neuropathy
-
Piekarz A. D., Due M. R., Khanna M., et al,. (2012) CRMP-2 peptide mediated decrease of high and low voltage-activated calcium channels, attenuation of nociceptor excitability, and anti-nociception in a model of AIDS therapy-induced painful peripheral neuropathy. Mol. Pain 8, 54.
-
(2012)
Mol. Pain
, vol.8
, pp. 54
-
-
Piekarz, A.D.1
Due, M.R.2
Khanna, M.3
-
24
-
-
0034666364
-
Arginine-rich peptides are blockers of VR-1 channels with analgesic activity
-
Planells-Cases R., Aracil A., Merino J. M., Gallar J., Perez-Paya E., Belmonte C., Gonzalez-Ros J. M., and, Ferrer-Montiel A. V., (2000) Arginine-rich peptides are blockers of VR-1 channels with analgesic activity. FEBS Lett. 481, 131-136.
-
(2000)
FEBS Lett.
, vol.481
, pp. 131-136
-
-
Planells-Cases, R.1
Aracil, A.2
Merino, J.M.3
Gallar, J.4
Perez-Paya, E.5
Belmonte, C.6
Gonzalez-Ros, J.M.7
Ferrer-Montiel, A.V.8
-
25
-
-
84858405523
-
A peptide uncoupling CRMP-2 from the presynaptic Ca2 + channel complex demonstrate efficacy in animal models of migraine and AIDS therapy-induced neuropathy
-
Ripsch M. S., Ballard C. J., Khanna M., Hurley J. H., White F. A., and, Khanna R., (2012) A peptide uncoupling CRMP-2 from the presynaptic Ca2 + channel complex demonstrate efficacy in animal models of migraine and AIDS therapy-induced neuropathy. Transl. Neurosci. 3, 1-8.
-
(2012)
Transl. Neurosci.
, vol.3
, pp. 1-8
-
-
Ripsch, M.S.1
Ballard, C.J.2
Khanna, M.3
Hurley, J.H.4
White, F.A.5
Khanna, R.6
-
26
-
-
0035872936
-
Suppression of inflammatory and neuropathic pain symptoms in mice lacking the N-type Ca2 + channel
-
Saegusa H., Kurihara T., Zong S., Kazuno A., Matsuda Y., Nonaka T., Han W., Toriyama H., and, Tanabe T., (2001) Suppression of inflammatory and neuropathic pain symptoms in mice lacking the N-type Ca2 + channel. EMBO J. 20, 2349-2356.
-
(2001)
EMBO J.
, vol.20
, pp. 2349-2356
-
-
Saegusa, H.1
Kurihara, T.2
Zong, S.3
Kazuno, A.4
Matsuda, Y.5
Nonaka, T.6
Han, W.7
Toriyama, H.8
Tanabe, T.9
-
27
-
-
78649974515
-
The pharmacokinetics of cell-penetrating peptides
-
Sarko D., Beijer B., Garcia B. R., Nothelfer E. M., Leotta K., Eisenhut M., Altmann A., Haberkorn U., and, Mier W., (2010) The pharmacokinetics of cell-penetrating peptides. Mol. Pharm. 7, 2224-2231.
-
(2010)
Mol. Pharm.
, vol.7
, pp. 2224-2231
-
-
Sarko, D.1
Beijer, B.2
Garcia, B.R.3
Nothelfer, E.M.4
Leotta, K.5
Eisenhut, M.6
Altmann, A.7
Haberkorn, U.8
Mier, W.9
-
28
-
-
77951652246
-
Ziconotide for treatment of severe chronic pain
-
Schmidtko A., Lotsch J., Freynhagen R., and, Geisslinger G., (2010) Ziconotide for treatment of severe chronic pain. Lancet 375, 1569-1577.
-
(2010)
Lancet
, vol.375
, pp. 1569-1577
-
-
Schmidtko, A.1
Lotsch, J.2
Freynhagen, R.3
Geisslinger, G.4
-
29
-
-
75349110400
-
Large A-fiber activity is required for microglial proliferation and p38 MAPK activation in the spinal cord: Different effects of resiniferatoxin and bupivacaine on spinal microglial changes after spared nerve injury
-
Suter M. R., Berta T., Gao Y. J., Decosterd I., and, Ji R. R., (2009) Large A-fiber activity is required for microglial proliferation and p38 MAPK activation in the spinal cord: different effects of resiniferatoxin and bupivacaine on spinal microglial changes after spared nerve injury. Mol. Pain 5 (53), 53.
-
(2009)
Mol. Pain
, vol.5
, Issue.53
, pp. 53
-
-
Suter, M.R.1
Berta, T.2
Gao, Y.J.3
Decosterd, I.4
Ji, R.R.5
-
30
-
-
42149127014
-
Live-cell analysis of cell penetration ability and toxicity of oligo-arginines
-
Tunnemann G., Ter-Avetisyan G., Martin R. M., Stockl M., Herrmann A., and, Cardoso M. C., (2008) Live-cell analysis of cell penetration ability and toxicity of oligo-arginines. J. Pept. Sci. 14, 469-476.
-
(2008)
J. Pept. Sci.
, vol.14
, pp. 469-476
-
-
Tunnemann, G.1
Ter-Avetisyan, G.2
Martin, R.M.3
Stockl, M.4
Herrmann, A.5
Cardoso, M.C.6
-
31
-
-
79959205997
-
Merging structural motifs of functionalized amino acids and alpha-aminoamides results in novel anticonvulsant compounds with significant effects on slow and fast inactivation of voltage-gated sodium channels and in the treatment of neuropathic pain
-
Wang Y., Wilson S. M., Brittain J. M., Ripsch M. S., Salome C., Park K. D., White F. A., Khanna R., and, Kohn H., (2011) Merging structural motifs of functionalized amino acids and alpha-aminoamides results in novel anticonvulsant compounds with significant effects on slow and fast inactivation of voltage-gated sodium channels and in the treatment of neuropathic pain. ACS Chem. Neurosci. 2, 317-322.
-
(2011)
ACS Chem. Neurosci.
, vol.2
, pp. 317-322
-
-
Wang, Y.1
Wilson, S.M.2
Brittain, J.M.3
Ripsch, M.S.4
Salome, C.5
Park, K.D.6
White, F.A.7
Khanna, R.8
Kohn, H.9
-
32
-
-
0034700141
-
The design, synthesis, and evaluation of molecules that enable or enhance cellular uptake: Peptoid molecular transporters
-
Wender P. A., Mitchell D. J., Pattabiraman K., Pelkey E. T., Steinman L., and, Rothbard J. B., (2000) The design, synthesis, and evaluation of molecules that enable or enhance cellular uptake: peptoid molecular transporters. Proc. Natl Acad. Sci. USA 97, 13003-13008.
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 13003-13008
-
-
Wender, P.A.1
Mitchell, D.J.2
Pattabiraman, K.3
Pelkey, E.T.4
Steinman, L.5
Rothbard, J.B.6
-
33
-
-
84861558035
-
Ca(V)1 and Ca(V)2 channels engage distinct modes of Ca(2+) signaling to control CREB-dependent gene expression
-
Wheeler D. G., Groth R. D., Ma H., Barrett C. F., Owen S. F., Safa P., and, Tsien R. W., (2012) Ca(V)1 and Ca(V)2 channels engage distinct modes of Ca(2+) signaling to control CREB-dependent gene expression. Cell 149, 1112-1124.
-
(2012)
Cell
, vol.149
, pp. 1112-1124
-
-
Wheeler, D.G.1
Groth, R.D.2
Ma, H.3
Barrett, C.F.4
Owen, S.F.5
Safa, P.6
Tsien, R.W.7
-
34
-
-
80052635029
-
Further insights into the antinociceptive potential of a peptide disrupting the N-type calcium channel-CRMP-2 signaling complex
-
Wilson S. M., Brittain J. M., Piekarz A. D., et al,. (2011) Further insights into the antinociceptive potential of a peptide disrupting the N-type calcium channel-CRMP-2 signaling complex. Channels (Austin) 5, 449-456.
-
(2011)
Channels (Austin)
, vol.5
, pp. 449-456
-
-
Wilson, S.M.1
Brittain, J.M.2
Piekarz, A.D.3
-
35
-
-
84867431882
-
Inhibition of transmitter release and attenuation of AIDS therapy-induced and tibial nerve injury-related painful peripheral neuropathy by novel synthetic Ca2+ channel peptides
-
Wilson S. M., Schmutzler B. S., Brittain J. M., et al,. (2012a) Inhibition of transmitter release and attenuation of AIDS therapy-induced and tibial nerve injury-related painful peripheral neuropathy by novel synthetic Ca2+ channel peptides. J. Biol. Chem. 287, 35065-35077.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 35065-35077
-
-
Wilson, S.M.1
Schmutzler, B.S.2
Brittain, J.M.3
-
36
-
-
84861192183
-
Prevention of posttraumatic axon sprouting by blocking collapsin response mediator protein 2-mediated neurite outgrowth and tubulin polymerization
-
Wilson S. M., Xiong W., Wang Y., et al,. (2012b) Prevention of posttraumatic axon sprouting by blocking collapsin response mediator protein 2-mediated neurite outgrowth and tubulin polymerization. Neuroscience 210, 451-466.
-
(2012)
Neuroscience
, vol.210
, pp. 451-466
-
-
Wilson, S.M.1
Xiong, W.2
Wang, Y.3
-
37
-
-
0025296259
-
Cellular mechanism of action of resiniferatoxin: A potent sensory neuron excitotoxin
-
Winter J., Dray A., Wood J. N., Yeats J. C., and, Bevan S., (1990) Cellular mechanism of action of resiniferatoxin: a potent sensory neuron excitotoxin. Brain Res. 520, 131-140.
-
(1990)
Brain Res.
, vol.520
, pp. 131-140
-
-
Winter, J.1
Dray, A.2
Wood, J.N.3
Yeats, J.C.4
Bevan, S.5
-
38
-
-
48349117136
-
Proteomic analysis of differential proteins related to the neuropathic pain and neuroprotection in the dorsal root ganglion following its chronic compression in rats
-
Zhang Y., Wang Y. H., Zhang X. H., Ge H. Y., Arendt-Nielsen L., Shao J. M., and, Yue S. W., (2008) Proteomic analysis of differential proteins related to the neuropathic pain and neuroprotection in the dorsal root ganglion following its chronic compression in rats. Exp. Brain Res. 189, 199-209.
-
(2008)
Exp. Brain Res.
, vol.189
, pp. 199-209
-
-
Zhang, Y.1
Wang, Y.H.2
Zhang, X.H.3
Ge, H.Y.4
Arendt-Nielsen, L.5
Shao, J.M.6
Yue, S.W.7
|