-
1
-
-
0344442325
-
Pharmacological manipulation of glutamate transport
-
Beretta S, Begni B, Ferrarese C. Pharmacological manipulation of glutamate transport. Drug News Perspect 2003; 16: 435-45.
-
(2003)
Drug News Perspect
, vol.16
, pp. 435-445
-
-
Beretta, S.1
Begni, B.2
Ferrarese, C.3
-
2
-
-
0033522924
-
Titrating the effects of mitochondrial complex I impairment in the cell physiology
-
Barrientos A, Moraes CT. Titrating the effects of mitochondrial complex I impairment in the cell physiology. J Biol Chem 1999; 274: 16188-97.
-
(1999)
J Biol Chem
, vol.274
, pp. 16188-16197
-
-
Barrientos, A.1
Moraes, C.T.2
-
3
-
-
0032937403
-
A pharmacological review of competitive inhibitors and substrates of high-affinity, sodium-dependent glutamate transport in the central nervous system
-
Bridges RJ, Kavanaugh MP, Chamberlin AR. A pharmacological review of competitive inhibitors and substrates of high-affinity, sodium-dependent glutamate transport in the central nervous system. Curr Pharm Des 1999; 5: 363-79.
-
(1999)
Curr Pharm des
, vol.5
, pp. 363-379
-
-
Bridges, R.J.1
Kavanaugh, M.P.2
Chamberlin, A.R.3
-
4
-
-
0033137153
-
The enigmatic relationship between mitochondrial dysfunction and Leber's hereditary optic neruopathy
-
Brown MD. The enigmatic relationship between mitochondrial dysfunction and Leber's hereditary optic neruopathy. J Neurol Sci 1999; 165: 1-5.
-
(1999)
J Neurol Sci
, vol.165
, pp. 1-5
-
-
Brown, M.D.1
-
5
-
-
0034704125
-
Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation
-
Brown MD, Trounce IA, Jun AS, Allen JC, Wallace DC. Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation. J Biol Chem 2000; 275: 39831-36.
-
(2000)
J Biol Chem
, vol.275
, pp. 39831-39836
-
-
Brown, M.D.1
Trounce, I.A.2
Jun, A.S.3
Allen, J.C.4
Wallace, D.C.5
-
6
-
-
77957170634
-
Leber's hereditary optic neuropathy
-
Schapira AHV, DiMauro S, editors. Boston: Butterworth-Heinemann
-
Carelli V. Leber's hereditary optic neuropathy. In: Schapira AHV, DiMauro S, editors. Mitochondrial disorders in neurology. 2nd ed. Boston: Butterworth-Heinemann; 2002. p. 115-42.
-
(2002)
Mitochondrial Disorders in Neurology. 2nd Ed.
, pp. 115-142
-
-
Carelli, V.1
-
7
-
-
18744426519
-
Leber's hereditary optic neuropathy: Biochemical effect of the 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype
-
Carelli V, Ghelli A, Ratta M, Bacchilega E, Sangiorgi S, Mancini R, et al. Leber's hereditary optic neuropathy: biochemical effect of the 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype. Neurology 1997; 48: 1623-32.
-
(1997)
Neurology
, vol.48
, pp. 1623-1632
-
-
Carelli, V.1
Ghelli, A.2
Ratta, M.3
Bacchilega, E.4
Sangiorgi, S.5
Mancini, R.6
-
8
-
-
0033028388
-
Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy
-
Carelli V, Ghelli A, Bucchi L, Montagna P, De Negri A, Leuzzi V, et al. Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy. Ann Neurol 1999; 45: 320-8.
-
(1999)
Ann Neurol
, vol.45
, pp. 320-328
-
-
Carelli, V.1
Ghelli, A.2
Bucchi, L.3
Montagna, P.4
De Negri, A.5
Leuzzi, V.6
-
9
-
-
0842300125
-
Reactive oxygen species in the pathogenesis of Leber's hereditary optic neuropathy
-
Arvo Abstract #1650
-
Carelli V, Sadun AA, Ross-Cisneros FN, Rao N, Qi X, Guy J. Reactive oxygen species in the pathogenesis of Leber's hereditary optic neuropathy [Arvo Abstract #1650]. Invest Ophthalmol Vis Sci 2000; 41: S312.
-
(2000)
Invest Ophthalmol Vis Sci
, vol.41
-
-
Carelli, V.1
Sadun, A.A.2
Ross-Cisneros, F.N.3
Rao, N.4
Qi, X.5
Guy, J.6
-
11
-
-
0032993159
-
Clinical, biochemical and molecular genetic features of Leber's hereditary optic neuropathy
-
Chalmers RM, Schapira AH. Clinical, biochemical and molecular genetic features of Leber's hereditary optic neuropathy. Biochim Biophys Acta 1999; 1410: 147-58.
-
(1999)
Biochim Biophys Acta
, vol.1410
, pp. 147-158
-
-
Chalmers, R.M.1
Schapira, A.H.2
-
12
-
-
0033137096
-
Functional consequences of the 3460-bp mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
Cock HR, Cooper JM, Schapira AHV. Functional consequences of the 3460-bp mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. J Neurol Sci 1999; 165: 10-7.
-
(1999)
J Neurol Sci
, vol.165
, pp. 10-17
-
-
Cock, H.R.1
Cooper, J.M.2
Schapira, A.H.V.3
-
13
-
-
0037155221
-
Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-induced apoptosis
-
Danielson SR, Wong A, Carelli V, Martinuzzi A, Schapira AHV, Cortopassi AG. Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-induced apoptosis. J Biol Chem 2002; 277: 5810-5.
-
(2002)
J Biol Chem
, vol.277
, pp. 5810-5815
-
-
Danielson, S.R.1
Wong, A.2
Carelli, V.3
Martinuzzi, A.4
Schapira, A.H.V.5
Cortopassi, A.G.6
-
14
-
-
0027964504
-
Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy
-
Degli Esposti M, Carelli V, Ghelli A, Ratta M, Crimi M, Sangiorgi S, et al. Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy. FEBS Lett 1994; 352: 375-9.
-
(1994)
FEBS Lett
, vol.352
, pp. 375-379
-
-
Degli Esposti, M.1
Carelli, V.2
Ghelli, A.3
Ratta, M.4
Crimi, M.5
Sangiorgi, S.6
-
15
-
-
0141521643
-
New insights into the bioenergetics of mitochondrial disorders using intracellular ATP reporters
-
Gajewski CD, Yang L, Schon EA, Manfredi G. New insights into the bioenergetics of mitochondrial disorders using intracellular ATP reporters. Mol Biol Cell 2003; 14: 3628-35.
-
(2003)
Mol Biol Cell
, vol.14
, pp. 3628-3635
-
-
Gajewski, C.D.1
Yang, L.2
Schon, E.A.3
Manfredi, G.4
-
16
-
-
0141792570
-
Mitochondrial production of oxygen radical species and the role of Coenzyme Q as an antioxidant
-
Maywood
-
Genova ML, Pich MM, Biondi A, Bernacchia A, Falasca A, Bovina C, et al. Mitochondrial production of oxygen radical species and the role of Coenzyme Q as an antioxidant. Exp Biol Med (Maywood) 2003; 228: 506-13.
-
(2003)
Exp Biol Med
, vol.228
, pp. 506-513
-
-
Genova, M.L.1
Pich, M.M.2
Biondi, A.3
Bernacchia, A.4
Falasca, A.5
Bovina, C.6
-
17
-
-
0037423202
-
Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium
-
Ghelli A, Zanna C, Porcelli AM, Schapira AH, Martinuzzi A, Carelli V, et al. Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium. J Biol Chem 2003; 278: 4145-50.
-
(2003)
J Biol Chem
, vol.278
, pp. 4145-4150
-
-
Ghelli, A.1
Zanna, C.2
Porcelli, A.M.3
Schapira, A.H.4
Martinuzzi, A.5
Carelli, V.6
-
18
-
-
0345535774
-
Sodium-dependent glutamate transport in Muller glial cells: Regulation by phorbol esters
-
Gonzalez MI, Lopez-Colom AM, Ortega A. Sodium-dependent glutamate transport in Muller glial cells: regulation by phorbol esters. Brain Res 1999; 831: 140-5.
-
(1999)
Brain Res
, vol.831
, pp. 140-145
-
-
Gonzalez, M.I.1
Lopez-Colom, A.M.2
Ortega, A.3
-
19
-
-
13144267708
-
Functions of the two glutamate transporters GLAST and GLT-1 in the retina
-
Harada T, Harada C, Watanabe M, Inoue Y, Sakagawa T, Nakayama N, et al. Functions of the two glutamate transporters GLAST and GLT-1 in the retina. Proc Natl Acad Sci USA 1998; 95: 4663-6.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 4663-4666
-
-
Harada, T.1
Harada, C.2
Watanabe, M.3
Inoue, Y.4
Sakagawa, T.5
Nakayama, N.6
-
20
-
-
15844414869
-
Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy
-
Hofhaus G, Johns DR, Hurko O, Attardi G, Chomyn A. Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy. J Biol Chem 1996; 271: 13155-61.
-
(1996)
J Biol Chem
, vol.271
, pp. 13155-13161
-
-
Hofhaus, G.1
Johns, D.R.2
Hurko, O.3
Attardi, G.4
Chomyn, A.5
-
21
-
-
0003272485
-
Leber hereditary optic neuropathy: A model system for mitochondrial dysfunction and neurodegeneration
-
Beal MF, Howell N, Bodis-Wollner I, editors. New York: Wiley-Liss
-
Howell N. Leber hereditary optic neuropathy: a model system for mitochondrial dysfunction and neurodegeneration. In: Beal MF, Howell N, Bodis-Wollner I, editors. Mitochondria and free radicals in neurodegen-erative diseases. New York: Wiley-Liss; 1997. p. 247-69.
-
(1997)
Mitochondria and Free Radicals in Neurodegen-erative Diseases
, pp. 247-269
-
-
Howell, N.1
-
22
-
-
0032078333
-
Leber hereditary optic neuropathy: Respiratory chain dysfunction and degeneration of the optic nerve
-
Howell N. Leber hereditary optic neuropathy: respiratory chain dysfunction and degeneration of the optic nerve. Vision Res 1998; 38: 1495-504.
-
(1998)
Vision Res
, vol.38
, pp. 1495-1504
-
-
Howell, N.1
-
23
-
-
0041784445
-
LHON and other optic nerve atrophies: The mitochondrial connection
-
Howell N. LHON and other optic nerve atrophies: the mitochondrial connection. Dev Ophthalmol 2003; 37: 94-108.
-
(2003)
Dev Ophthalmol
, vol.37
, pp. 94-108
-
-
Howell, N.1
-
24
-
-
0034607082
-
Specific antagonists of NMDA receptors prevent osteoclast sealing zone formation required for bone resorption
-
Itzstein C, Espinosa L, Delmas PD, Chenu C. Specific antagonists of NMDA receptors prevent osteoclast sealing zone formation required for bone resorption. Biochem Biophys Res Commun 2003; 268: 201-9.
-
(2003)
Biochem Biophys Res Commun
, vol.268
, pp. 201-209
-
-
Itzstein, C.1
Espinosa, L.2
Delmas, P.D.3
Chenu, C.4
-
25
-
-
0024448458
-
Human cells lacking mtDNA: Repopulation with exogenous mitochondria by complementation
-
King MP, Attardi G. Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation. Science 1989; 246: 500-3.
-
(1989)
Science
, vol.246
, pp. 500-503
-
-
King, M.P.1
Attardi, G.2
-
26
-
-
1042301416
-
Characterization of superoxide-producing sites in isolated brain mitochondria
-
Kudin AP, Bimpong-Buta NY, Vielhaber S, Elger CE, Kunz WS. Characterization of superoxide-producing sites in isolated brain mitochondria. J Biol Chem 2004; 279: 4127-35.
-
(2004)
J Biol Chem
, vol.279
, pp. 4127-4135
-
-
Kudin, A.P.1
Bimpong-Buta, N.Y.2
Vielhaber, S.3
Elger, C.E.4
Kunz, W.S.5
-
27
-
-
0025936841
-
Lebers hereditary optic neuropathy and complex I deficiency in muscle
-
Larsson N-G, Andersen O, Holme E, Oldfors A, Wahlstrom J. Lebers hereditary optic neuropathy and complex I deficiency in muscle. Ann Neurol 1991; 30: 701-8.
-
(1991)
Ann Neurol
, vol.30
, pp. 701-708
-
-
Larsson, N.-G.1
Andersen, O.2
Holme, E.3
Oldfors, A.4
Wahlstrom, J.5
-
28
-
-
0035958729
-
Intracellular generation of free radicals and modifications of detoxifying enzymes in cultured neurons from the developing rat forebrain in response to transient hypoxia
-
Lievre V, Becuwe P, Bianchi A, Bossenmeyer-Pourie C, Koziel V, Franck P, et al. Intracellular generation of free radicals and modifications of detoxifying enzymes in cultured neurons from the developing rat forebrain in response to transient hypoxia. Neuroscience 2001; 105: 287-97.
-
(2001)
Neuroscience
, vol.105
, pp. 287-297
-
-
Lievre, V.1
Becuwe, P.2
Bianchi, A.3
Bossenmeyer-Pourie, C.4
Koziel, V.5
Franck, P.6
-
29
-
-
0034667741
-
Acrolein, a product of lipid peroxidation, inhibits glucose and glutamate uptake in primary neuronal cultures
-
Lovell MA, Xie C, Markesbery WR. Acrolein, a product of lipid peroxidation, inhibits glucose and glutamate uptake in primary neuronal cultures. Free Radic Biol Med 2000; 29: 714-20.
-
(2000)
Free Radic Biol Med
, vol.29
, pp. 714-720
-
-
Lovell, M.A.1
Xie, C.2
Markesbery, W.R.3
-
30
-
-
84948011844
-
The toxic effect of sodium L-glutamate on the inner layers of the retina
-
Lucas DR, Newhouse JP. The toxic effect of sodium L-glutamate on the inner layers of the retina. Arch Ophthalmol 1957; 58: 193-201.
-
(1957)
Arch Ophthalmol
, vol.58
, pp. 193-201
-
-
Lucas, D.R.1
Newhouse, J.P.2
-
31
-
-
0035073291
-
Selective excitotoxic degeneration of adult pig retinal ganglion cells in vitro
-
Luo X, Heidinger V, Picaud S, Lambrou G, Dreyfus H, Sahel J, et al. Selective excitotoxic degeneration of adult pig retinal ganglion cells in vitro. Invest Ophthalmol Vis Sci 2001; 42: 1096-06.
-
(2001)
Invest Ophthalmol Vis Sci
, vol.42
, pp. 1096-1106
-
-
Luo, X.1
Heidinger, V.2
Picaud, S.3
Lambrou, G.4
Dreyfus, H.5
Sahel, J.6
-
32
-
-
0025995774
-
Electron transfer properties of NADH: Ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)
-
Majander A, Huoponen K, Savontaus ML, Nikoskelainen E, Wikstrom M. Electron transfer properties of NADH: ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON). FEBS Lett 1991; 292: 289-92.
-
(1991)
FEBS Lett
, vol.292
, pp. 289-292
-
-
Majander, A.1
Huoponen, K.2
Savontaus, M.L.3
Nikoskelainen, E.4
Wikstrom, M.5
-
33
-
-
0037322524
-
The epidemiology of Leber hereditary optic neuropathy in the North East of England
-
Man PY, Griffiths PG, Brown DT, Howell N, Turnbull DM, Chinnery PF. The epidemiology of Leber hereditary optic neuropathy in the North East of England. Am J Hum Genet 2003; 72: 333-9.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 333-339
-
-
Man, P.Y.1
Griffiths, P.G.2
Brown, D.T.3
Howell, N.4
Turnbull, D.M.5
Chinnery, P.F.6
-
34
-
-
0027944004
-
Overexpression of BCL-2 in transgenic mice protects neurons from naturally occurring cell death and experimental ischemia
-
Martinou JC, Dubois-Dauphin M, Staple JK, Rodriguez I, Frankowski H, Missotten M, et al. Overexpression of BCL-2 in transgenic mice protects neurons from naturally occurring cell death and experimental ischemia. Neuron 1994; 13: 1017-30.
-
(1994)
Neuron
, vol.13
, pp. 1017-1030
-
-
Martinou, J.C.1
Dubois-Dauphin, M.2
Staple, J.K.3
Rodriguez, I.4
Frankowski, H.5
Missotten, M.6
-
35
-
-
0030948207
-
Mechanically regulated expression of a neural glutamate transporter in bone: A role for excitatory amino acids as osteotropic agents?
-
Mason DJ, Suva LJ, Genever PG, Patton Aj, Steuckle S, Hillam RA, et al. Mechanically regulated expression of a neural glutamate transporter in bone: a role for excitatory amino acids as osteotropic agents? Bone 1997; 20: 199-205.
-
(1997)
Bone
, vol.20
, pp. 199-205
-
-
Mason, D.J.1
Suva, L.J.2
Genever, P.G.3
Aj, P.4
Steuckle, S.5
Hillam, R.A.6
-
36
-
-
0041454624
-
Leber's optic neuropathy
-
Miller NR, Newman NJ, editors. Baltimore: Williams & Wilkins
-
Newman NJ. Leber's optic neuropathy. In: Miller NR, Newman NJ, editors. Walsh and Hoyt's clinical neuro-ophthalmology. 5th ed. Baltimore: Williams & Wilkins; 1998. p. 742-53.
-
(1998)
Walsh and Hoyt's Clinical Neuro-ophthalmology. 5th Ed.
, pp. 742-753
-
-
Newman, N.J.1
-
37
-
-
0029166941
-
Leber's 'plus': Neurological abnormalities in patients with Leber's hereditary optic neuropathy
-
Nikoskelainen EK, Marttila RJ, Huoponen K, Juvonen V, Lamminen T, Sonninen P, et al. Leber's 'plus': neurological abnormalities in patients with Leber's hereditary optic neuropathy. J Neurol Neurosurg Psychiatry 1995; 59: 160-4.
-
(1995)
J Neurol Neurosurg Psychiatry
, vol.59
, pp. 160-164
-
-
Nikoskelainen, E.K.1
Marttila, R.J.2
Huoponen, K.3
Juvonen, V.4
Lamminen, T.5
Sonninen, P.6
-
38
-
-
0027990224
-
Effects of ischaemic conditions on uptake of glutamate, aspartate, and noradrenaline by cell lines derived from the human nervous system
-
O'Neill CM, Ball SG, Vaughan PFT. Effects of ischaemic conditions on uptake of glutamate, aspartate, and noradrenaline by cell lines derived from the human nervous system. J Neurochem 1994; 63: 603-11.
-
(1994)
J Neurochem
, vol.63
, pp. 603-611
-
-
O'Neill, C.M.1
Ball, S.G.2
Vaughan, P.F.T.3
-
39
-
-
0014544544
-
Glutamate-induced retinal degeneration in neonatal mice. Electron microscopy of the acutely evolving lesion
-
Olney JW. Glutamate-induced retinal degeneration in neonatal mice. Electron microscopy of the acutely evolving lesion. J Neuropathol Exp Neurol 1969; 28: 455-74.
-
(1969)
J Neuropathol Exp Neurol
, vol.28
, pp. 455-474
-
-
Olney, J.W.1
-
40
-
-
0028041471
-
Apoptotic cell death induced by optic nerve lesion in the neonatal rat
-
Rabacchi SA, Bonfanti L, Liu XH, Maffei L. Apoptotic cell death induced by optic nerve lesion in the neonatal rat. J Neurosi 1994; 14: 5292-301.
-
(1994)
J Neurosi
, vol.14
, pp. 5292-5301
-
-
Rabacchi, S.A.1
Bonfanti, L.2
Liu, X.H.3
Maffei, L.4
-
41
-
-
0029904836
-
Differential expression of three glutamate transporter subtypes in the rat retina
-
Rauen T, Rothstein JD, Wassle H. Differential expression of three glutamate transporter subtypes in the rat retina. Cell Tissue Res 1996; 286: 325-36.
-
(1996)
Cell Tissue Res
, vol.286
, pp. 325-336
-
-
Rauen, T.1
Rothstein, J.D.2
Wassle, H.3
-
42
-
-
0034520010
-
Leber's hereditary optic neuropathy differentially affects smaller axons in the optic nerve
-
Sadun AA, Win PH, Ross-Cisneros FN, Walker SO, Carelli V. Leber's hereditary optic neuropathy differentially affects smaller axons in the optic nerve. Trans Am Ophthalmol Soc 2000; 98: 223-32.
-
(2000)
Trans Am Ophthalmol Soc
, vol.98
, pp. 223-232
-
-
Sadun, A.A.1
Win, P.H.2
Ross-Cisneros, F.N.3
Walker, S.O.4
Carelli, V.5
-
43
-
-
0029810095
-
Mitochondrial dysfunction is a primary event in glutamate neurotoxicity
-
Schinder AF, Olson EC, Spitzer NC, Montal M. Mitochondrial dysfunction is a primary event in glutamate neurotoxicity. J Neurosci 1996; 16: 6125-33.
-
(1996)
J Neurosci
, vol.16
, pp. 6125-6133
-
-
Schinder, A.F.1
Olson, E.C.2
Spitzer, N.C.3
Montal, M.4
-
44
-
-
16944363113
-
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484
-
Torroni A, Petrozzi M, D'Urbano L, Sellitto D, Zeviani M, Carrara F, et al. Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. Am J Hum Genet 1997; 60: 1107-21.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1107-1121
-
-
Torroni, A.1
Petrozzi, M.2
D'Urbano, L.3
Sellitto, D.4
Zeviani, M.5
Carrara, F.6
-
45
-
-
0029868452
-
Peroxynitrite inhibits glutamate transporter subtypes
-
Trotti D, Rossi D, Gjesdal O, Levy LM, Racagni G, Danbolt NC, et al. Peroxynitrite inhibits glutamate transporter subtypes. J Biol Chem 1996; 271: 5976-9.
-
(1996)
J Biol Chem
, vol.271
, pp. 5976-5979
-
-
Trotti, D.1
Rossi, D.2
Gjesdal, O.3
Levy, L.M.4
Racagni, G.5
Danbolt, N.C.6
-
46
-
-
0032145886
-
Glutamate transporters are oxidant-vulnerable: A molecular link between oxidative and excitotoxic neurodegeneration?
-
Trotti D, Danbolt NC, Volterra A. Glutamate transporters are oxidant-vulnerable: a molecular link between oxidative and excitotoxic neurodegeneration? Trends Pharmacol Sci 1998; 19: 328-34.
-
(1998)
Trends Pharmacol Sci
, vol.19
, pp. 328-334
-
-
Trotti, D.1
Danbolt, N.C.2
Volterra, A.3
-
47
-
-
0029118005
-
MtDNA mutations associated with Leber's hereditary optic neuropathy: Studies on cytoplasmic hybrid (cybrid) cells
-
Vergani L, Martinuzzi A, Carelli V, Cortelli P, Montagna P, Schievano G, et al. MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells. Biochem Biophys Res Commun 1995; 210: 880-8.
-
(1995)
Biochem Biophys Res Commun
, vol.210
, pp. 880-888
-
-
Vergani, L.1
Martinuzzi, A.2
Carelli, V.3
Cortelli, P.4
Montagna, P.5
Schievano, G.6
-
48
-
-
0028208495
-
Glutamate uptake inhibition by oxygen free radicals in rat cortical astrocytes
-
Volterra A, Trotti D, Tromba C, Floridi S, Racagni G. Glutamate uptake inhibition by oxygen free radicals in rat cortical astrocytes. J Neurosci 1994; 14: 2924-32.
-
(1994)
J Neurosci
, vol.14
, pp. 2924-2932
-
-
Volterra, A.1
Trotti, D.2
Tromba, C.3
Floridi, S.4
Racagni, G.5
-
49
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, et al. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science 1988; 242: 1427-30.
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, T.G.5
Lezza, A.M.6
-
50
-
-
0037084559
-
Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells
-
Wong A, Cavelier L, Collins-Schramm HE, Seldin MF, McGrogan M, Savontaus ML, et al. Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells. Hum Mol Genet 2002; 11: 431-8.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 431-438
-
-
Wong, A.1
Cavelier, L.2
Collins-Schramm, H.E.3
Seldin, M.F.4
McGrogan, M.5
Savontaus, M.L.6
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