-
1
-
-
0032799485
-
Progress in neuropathology of the neuronal ceroid lipofuscinoses
-
Goebel, H. H., Schochet, S. S., Jaynes, M., Bruck, W., Kohlschutter, A. and Hentati, F. (1999) Progress in neuropathology of the neuronal ceroid lipofuscinoses. Mol. Genet. Metab. 66, 367-372
-
(1999)
Mol. Genet. Metab.
, vol.66
, pp. 367-372
-
-
Goebel, H.H.1
Schochet, S.S.2
Jaynes, M.3
Bruck, W.4
Kohlschutter, A.5
Hentati, F.6
-
2
-
-
0029153109
-
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis
-
Vesa, J., Hellsten, E., Verkruyse, L. A., Camp, L. A., Rapola, J., Santavuori, P., Hofmann, S. L. and Peltonen, L. (1995) Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis. Nature (London) 376, 584-587
-
(1995)
Nature (London)
, vol.376
, pp. 584-587
-
-
Vesa, J.1
Hellsten, E.2
Verkruyse, L.A.3
Camp, L.A.4
Rapola, J.5
Santavuori, P.6
Hofmann, S.L.7
Peltonen, L.8
-
3
-
-
0030866233
-
Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis
-
Washington, D.C.
-
Sleat, D. E., Donnelly, R. J., Lackland, H., Liu, C. G., Sohar, I., Pullarkat, R. K. and Lobel, P. (1997) Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis. Science (Washington, D.C.) 277, 1802-1805
-
(1997)
Science
, vol.277
, pp. 1802-1805
-
-
Sleat, D.E.1
Donnelly, R.J.2
Lackland, H.3
Liu, C.G.4
Sohar, I.5
Pullarkat, R.K.6
Lobel, P.7
-
4
-
-
0029147298
-
Isolation of a novel gene underlying Batten disease, CLN3
-
Cambridge, Mass.
-
The International Batten Disease Consortium (1995) Isolation of a novel gene underlying Batten disease, CLN3. Cell (Cambridge, Mass.) 82, 949-957
-
(1995)
Cell
, vol.82
, pp. 949-957
-
-
-
5
-
-
0031803649
-
CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis
-
Savukoski, M., Klockars, T., Holmberg, V., Santavuori, P., Lander, E. S. and Peltonen, L. (1998) CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis. Nat. Genet. 19, 286-288
-
(1998)
Nat. Genet.
, vol.19
, pp. 286-288
-
-
Savukoski, M.1
Klockars, T.2
Holmberg, V.3
Santavuori, P.4
Lander, E.S.5
Peltonen, L.6
-
6
-
-
0036155235
-
Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse
-
Gao, H., Boustany, R. M., Espinola, J. A., Cotman, S. L., Srinidhi, L., Antonellis, K. A., Gillis, T., Qin, X., Liu, S., Donahue, L. R. et al. (2002) Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse. Am. J. Hum. Genet. 70, 324-335
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 324-335
-
-
Gao, H.1
Boustany, R.M.2
Espinola, J.A.3
Cotman, S.L.4
Srinidhi, L.5
Antonellis, K.A.6
Gillis, T.7
Qin, X.8
Liu, S.9
Donahue, L.R.10
-
7
-
-
0036155408
-
The gene mutated in variant late-infantile neuronal ceroid lipofuscinosis (CLN6) and in nclf mutant mice encodes a novel predicted transmembrane protein
-
Wheeler, R. B., Sharp, J. D., Schultz, R. A., Joslin, J. M., Williams, R. E. and Mole, S. E. (2002) The gene mutated in variant late-infantile neuronal ceroid lipofuscinosis (CLN6) and in nclf mutant mice encodes a novel predicted transmembrane protein. Am. J. Hum. Genet. 70, 537-542
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 537-542
-
-
Wheeler, R.B.1
Sharp, J.D.2
Schultz, R.A.3
Joslin, J.M.4
Williams, R.E.5
Mole, S.E.6
-
8
-
-
0032831071
-
The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations on CLN8
-
Ranta, S., Zhang, Y., Ross, B., Lonka, L., Takkunen, E., Messer, A., Sharp, J., Wheeler, R., Kusumi, K., Mole, S. et al. (1999) The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations on CLN8. Nat. Genet. 23, 233-236
-
(1999)
Nat. Genet.
, vol.23
, pp. 233-236
-
-
Ranta, S.1
Zhang, Y.2
Ross, B.3
Lonka, L.4
Takkunen, E.5
Messer, A.6
Sharp, J.7
Wheeler, R.8
Kusumi, K.9
Mole, S.10
-
9
-
-
0026539541
-
Mitochondrial ATP synthase subunit c storage in the ceroid- lipofuscinoses (Batten disease)
-
Palmer, D. N., Fearnley, I. M., Walker, J. E., Hall, N. A., Lake, B. D., Wolfe, L. S., Haltia, M., Martinus, R. D. and Jolly, R. D. (1992) Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease). Am. J. Med. Genet. 42, 561-567
-
(1992)
Am. J. Med. Genet.
, vol.42
, pp. 561-567
-
-
Palmer, D.N.1
Fearnley, I.M.2
Walker, J.E.3
Hall, N.A.4
Lake, B.D.5
Wolfe, L.S.6
Haltia, M.7
Martinus, R.D.8
Jolly, R.D.9
-
10
-
-
0030845481
-
Different patterns of hydrophobic protein storage in different forms of neuronal ceroid lipofuscinosis (NCL, Batten disease)
-
Palmer, D. N., Jolly, R. D., van Mil, H. C., Tyynelä, J. and Westlake, V. J. (1997) Different patterns of hydrophobic protein storage in different forms of neuronal ceroid lipofuscinosis (NCL, Batten disease). Neuropediatrics 28, 45-48
-
(1997)
Neuropediatrics
, vol.28
, pp. 45-48
-
-
Palmer, D.N.1
Jolly, R.D.2
Van Mil, H.C.3
Tyynelä, J.4
Westlake, V.J.5
-
11
-
-
0030722899
-
Variant late infantile neuronal ceroid-lipofuscinosis: Pathomorphology and biochemistry
-
Tyynelä, J., Suopanki, J., Santavuori, P., Baumann, M. and Haltia, M. (1997) Variant late infantile neuronal ceroid-lipofuscinosis: Pathomorphology and biochemistry. J. Neuropatho. Exp. Neurol. 56, 369-375
-
(1997)
J. Neuropatho. Exp. Neurol.
, vol.56
, pp. 369-375
-
-
Tyynelä, J.1
Suopanki, J.2
Santavuori, P.3
Baumann, M.4
Haltia, M.5
-
12
-
-
0034112242
-
Northern epilepsy: A novel form of neuronal ceroid-lipofuscinosis
-
Herva, R., Tyynela, J., Hirvasniemi, A., Syrjakallio-Ylitalo, M. and Haltia, M. (2000) Northern epilepsy: a novel form of neuronal ceroid-lipofuscinosis. Brain Pathol. 10, 215-222
-
(2000)
Brain Pathol.
, vol.10
, pp. 215-222
-
-
Herva, R.1
Tyynela, J.2
Hirvasniemi, A.3
Syrjakallio-Ylitalo, M.4
Haltia, M.5
-
13
-
-
0034659833
-
A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration
-
Tyynela, J., Sonar, I., Sleat, D. E., Gin, R. M., Donnelly, R. J., Baumann, M., Haltia, M. and Lobel, P. (2000) A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration. EMBO J. 19, 2786-2792
-
(2000)
EMBO J.
, vol.19
, pp. 2786-2792
-
-
Tyynela, J.1
Sonar, I.2
Sleat, D.E.3
Gin, R.M.4
Donnelly, R.J.5
Baumann, M.6
Haltia, M.7
Lobel, P.8
-
14
-
-
0034666116
-
Cathepsin D deficiency induces lysosomal storage with ceroid lipofuscin in mouse CNS neurons
-
Koike, M., Nakanishi, H., Saftig, P., Ezaki, J., Isahara, K., Ohsawa, Y., Schulz-Schaeffer, W., Watanabe, T., Waguri, S., Kametaka, S. et al. (2000) Cathepsin D deficiency induces lysosomal storage with ceroid lipofuscin in mouse CNS neurons. J. Neurosci. 20, 6898-6906
-
(2000)
J. Neurosci.
, vol.20
, pp. 6898-6906
-
-
Koike, M.1
Nakanishi, H.2
Saftig, P.3
Ezaki, J.4
Isahara, K.5
Ohsawa, Y.6
Schulz-Schaeffer, W.7
Watanabe, T.8
Waguri, S.9
Kametaka, S.10
-
15
-
-
0031846129
-
The locus for ovine ceroid lipofuscinosis is syntenic to the human Batten disease variant CLN6
-
Broom, M. F., Zhou, C., Broom, J. E., Barwell, K. J., Jolly, R. D. and Hill, D. F. (1998) The locus for ovine ceroid lipofuscinosis is syntenic to the human Batten disease variant CLN6. J. Med. Genet. 35, 717-721
-
(1998)
J. Med. Genet.
, vol.35
, pp. 717-721
-
-
Broom, M.F.1
Zhou, C.2
Broom, J.E.3
Barwell, K.J.4
Jolly, R.D.5
Hill, D.F.6
-
16
-
-
0036560569
-
Neuronal ceroid lipofuscinosis in Merino sheep
-
Cook, R. W., Jolly, R. D., Palmer, D. N., Tammen, I., Broom, M. F. and McKinnon, R. (2002) Neuronal ceroid lipofuscinosis in Merino sheep. Aust. Vet. J. 80, 292-297
-
(2002)
Aust. Vet. J.
, vol.80
, pp. 292-297
-
-
Cook, R.W.1
Jolly, R.D.2
Palmer, D.N.3
Tammen, I.4
Broom, M.F.5
McKinnon, R.6
-
17
-
-
0024336199
-
Ceroid-lipofuscinosis (Batten's disease): Pathogenesis and sequential neuropathological changes in the ovine model
-
Jolly, R. D., Shimada, A., Dopfmer, I., Slack, P. M., Birtles, M. J. and Palmer, D. N. (1989) Ceroid-lipofuscinosis (Batten's disease): pathogenesis and sequential neuropathological changes in the ovine model. Neuropathol. Appl. Neurobiol. 15, 371-383
-
(1989)
Neuropathol. Appl. Neurobiol.
, vol.15
, pp. 371-383
-
-
Jolly, R.D.1
Shimada, A.2
Dopfmer, I.3
Slack, P.M.4
Birtles, M.J.5
Palmer, D.N.6
-
18
-
-
0022367967
-
Ceroid-lipofuscinosis (Batten's disease): Pathogenesis of blindness in the ovine model
-
Mayhew, I. G., Jolly, R. D., Pickett, B. T. and Slack, P. M. (1985) Ceroid-lipofuscinosis (Batten's disease): pathogenesis of blindness in the ovine model. Neuropathol. Appl. Neurobiol. 11, 273-290
-
(1985)
Neuropathol. Appl. Neurobiol.
, vol.11
, pp. 273-290
-
-
Mayhew, I.G.1
Jolly, R.D.2
Pickett, B.T.3
Slack, P.M.4
-
20
-
-
0025290956
-
The sequence of the major protein stored in ovine ceroid-lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase
-
Fearnley, I. M., Walker, J. E., Martinus, R. D., Jolly, R. D., Kirkland, K. B., Shaw, G. J. and Palmer, D. N. (1990) The sequence of the major protein stored in ovine ceroid-lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase. Biochem. J. 268, 751-758
-
(1990)
Biochem. J.
, vol.268
, pp. 751-758
-
-
Fearnley, I.M.1
Walker, J.E.2
Martinus, R.D.3
Jolly, R.D.4
Kirkland, K.B.5
Shaw, G.J.6
Palmer, D.N.7
-
22
-
-
0028108204
-
Oxidants induce transcriptional activation of manganese superoxide dismutase in glomerular cells
-
Yoshioka, T., Homma, T., Meyrick, B., Takeda, M., Moore-Jarrett, T., Kon, V. and Ichikawa, I. (1994) Oxidants induce transcriptional activation of manganese superoxide dismutase in glomerular cells. Kidney Int. 46, 405-413
-
(1994)
Kidney Int.
, vol.46
, pp. 405-413
-
-
Yoshioka, T.1
Homma, T.2
Meyrick, B.3
Takeda, M.4
Moore-Jarrett, T.5
Kon, V.6
Ichikawa, I.7
-
23
-
-
0025337812
-
Regulation of manganese superoxide dismutase by lipopolysaccharide, interleukin-1, and tumor necrosis factor. Role in the acute inflammatory response
-
Visner, G. A., Dougall, W. C., Wilson, J. M., Burr, I. A. and Nick, H. S. (1990) Regulation of manganese superoxide dismutase by lipopolysaccharide, interleukin-1, and tumor necrosis factor. Role in the acute inflammatory response. J. Biol. Chem. 265, 2856-2864
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 2856-2864
-
-
Visner, G.A.1
Dougall, W.C.2
Wilson, J.M.3
Burr, I.A.4
Nick, H.S.5
-
24
-
-
0024202127
-
Induction of manganous superoxide dismutase by tumor necrosis factor: Possible protective mechanism
-
Washington, D.C.
-
Wong, G. H. and Goeddel, D. V. (1988) Induction of manganous superoxide dismutase by tumor necrosis factor: possible protective mechanism. Science (Washington, D.C.) 242, 941-944
-
(1988)
Science
, vol.242
, pp. 941-944
-
-
Wong, G.H.1
Goeddel, D.V.2
-
25
-
-
0030951610
-
Follow-up study of subunit c of mitochondrial ATP synthase (SCMAS) in Batten disease and in unrelated lysosomal disorders
-
Elleder, M., Sokolova, J. and Hrebicek, M. (1997) Follow-up study of subunit c of mitochondrial ATP synthase (SCMAS) in Batten disease and in unrelated lysosomal disorders. Acta Neuropathol. 93, 379-390
-
(1997)
Acta Neuropathol.
, vol.93
, pp. 379-390
-
-
Elleder, M.1
Sokolova, J.2
Hrebicek, M.3
-
26
-
-
0032973867
-
A lysosomal proteinase, the late infantile neuronal ceroid lipofuscinosis gene (CLN2) product, is essential for degradation of a hydrophobic protein, the subunit c of ATP synthase
-
Ezaki, J., Tanida, I., Kanehagi, N. and Kominami, E. (1999) A lysosomal proteinase, the late infantile neuronal ceroid lipofuscinosis gene (CLN2) product, is essential for degradation of a hydrophobic protein, the subunit c of ATP synthase, J. Neurochem. 72, 2573-2582
-
(1999)
J. Neurochem.
, vol.72
, pp. 2573-2582
-
-
Ezaki, J.1
Tanida, I.2
Kanehagi, N.3
Kominami, E.4
-
27
-
-
0346490223
-
2-D Electrophoresis using immobilized pH gradients
-
Edition AB 80-6429-60, Amersham Pharmacia Biotech Inc.
-
Berkelman, T. and Stenstedt, T. (1998) 2-D Electrophoresis using immobilized pH gradients. In Principles and Methods, Edition AB 80-6429-60, Amersham Pharmacia Biotech Inc.
-
(1998)
Principles and Methods
-
-
Berkelman, T.1
Stenstedt, T.2
-
28
-
-
0023190840
-
Increase in manganese superoxide dismutase activity in the mouse heart after X-irradiation
-
Oberley, L. W., St Clair, D. K., Autor, A. P. and Oberley, T. D. (1987) Increase in manganese superoxide dismutase activity in the mouse heart after X-irradiation. Arch. Biochem. Biophys. 254, 69-80
-
(1987)
Arch. Biochem. Biophys.
, vol.254
, pp. 69-80
-
-
Oberley, L.W.1
St Clair, D.K.2
Autor, A.P.3
Oberley, T.D.4
-
29
-
-
0015153416
-
Superoxide dismutase: Improved assays and an assay applicable to acrylamide gels
-
Beauchamp, C. and Fridovich, I. (1971) Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal. Biochem. 44, 276-287
-
(1971)
Anal. Biochem.
, vol.44
, pp. 276-287
-
-
Beauchamp, C.1
Fridovich, I.2
-
30
-
-
0029053451
-
Superoxide radical and superoxide dismutases
-
Fridovich, I. (1995) Superoxide radical and superoxide dismutases. Annu. Rev. Biochem. 64, 97-112
-
(1995)
Annu. Rev. Biochem.
, vol.64
, pp. 97-112
-
-
Fridovich, I.1
-
31
-
-
0026484388
-
The oxidant stress hypothesis in Parkinson's disease: Evidence supporting it
-
Fahn, S, and Cohen, G. (1992) The oxidant stress hypothesis in Parkinson's disease: evidence supporting it. Ann. Neurol. 32, 804-812
-
(1992)
Ann. Neurol.
, vol.32
, pp. 804-812
-
-
Fahn, S.1
Cohen, G.2
-
32
-
-
0030813067
-
Evidence of increased oxidative damage in both sporadic and familial amyotrophic lateral sclerosis
-
Ferrante, R. J., Browne, S. E., Shinobu, L. A., Bowling, A. C., Baik, M. J., MacGarvey, U., Kowall, N. W., Brown, Jr, R. H. and Beal, M. F. (1997) Evidence of increased oxidative damage in both sporadic and familial amyotrophic lateral sclerosis. J. Neurochem. 69, 2064-2074
-
(1997)
J. Neurochem.
, vol.69
, pp. 2064-2074
-
-
Ferrante, R.J.1
Browne, S.E.2
Shinobu, L.A.3
Bowling, A.C.4
Baik, M.J.5
MacGarvey, U.6
Kowall, N.W.7
Brown Jr., R.H.8
Beal, M.F.9
-
33
-
-
0023811053
-
Normal oxidative damage to mitochondrial and nuclear DNA is extensive
-
Richter, C., Park, J. W. and Ames, B. N. (1988) Normal oxidative damage to mitochondrial and nuclear DNA is extensive. Proc. Natl. Acad. Sci. U.S.A. 85, 6465-6467
-
(1988)
Proc. Natl. Acad. Sci. U.S.A.
, vol.85
, pp. 6465-6467
-
-
Richter, C.1
Park, J.W.2
Ames, B.N.3
-
34
-
-
0028239794
-
The voltage sensor of the mitochondrial permeability transition pore is tuned by the oxidation-reduction state of vicinal thiols. Increase of the gating potential by oxidants and its reversal by reducing agents
-
Petronilli, V., Costantini, P., Scorrano, L., Colonna, R., Passamonti, S. and Bernardi, P. (1994) The voltage sensor of the mitochondrial permeability transition pore is tuned by the oxidation-reduction state of vicinal thiols. Increase of the gating potential by oxidants and its reversal by reducing agents. J. Biol. Chem. 269, 16638-16642
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 16638-16642
-
-
Petronilli, V.1
Costantini, P.2
Scorrano, L.3
Colonna, R.4
Passamonti, S.5
Bernardi, P.6
-
35
-
-
0030581151
-
Induction of apoptotic program in cell-free extracts: Requirement for dATP and cytochrome c
-
Cambridge, Mass.
-
Liu, X., Kim, C. N., Yang, J., Jemmerson, R. and Wang, X. (1996) Induction of apoptotic program in cell-free extracts: Requirement for dATP and cytochrome c. Cell (Cambridge, Mass.) 86, 147-157
-
(1996)
Cell
, vol.86
, pp. 147-157
-
-
Liu, X.1
Kim, C.N.2
Yang, J.3
Jemmerson, R.4
Wang, X.5
-
36
-
-
0024308039
-
Superoxide dismutases. An adaptation to a paramagnetic gas
-
Fridovich, I. (1989) Superoxide dismutases. An adaptation to a paramagnetic gas. J. Biol. Chem. 264, 7761-7764
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 7761-7764
-
-
Fridovich, I.1
-
37
-
-
0345654322
-
Neuronal apoptosis in Creutzfeldt-Jakob disease
-
Gray, F., Chretien, F., Adle-Biassette, H., Dorandeu, A., Ereau, T., Delisle, M. B., Kopp, N., Ironside, J. W. and Vital, C. (1999) Neuronal apoptosis in Creutzfeldt-Jakob disease. J. Neuropathol. Exp. Neurol. 58, 321-328
-
(1999)
J. Neuropathol. Exp. Neurol.
, vol.58
, pp. 321-328
-
-
Gray, F.1
Chretien, F.2
Adle-Biassette, H.3
Dorandeu, A.4
Ereau, T.5
Delisle, M.B.6
Kopp, N.7
Ironside, J.W.8
Vital, C.9
-
38
-
-
0028833215
-
Cell death in Alzheimer's disease evaluated by DNA fragmentation in situ
-
Berl.
-
Lassmann, H., Bancher, C., Breitschopf, H., Wegiel, J., Bobinski, M., Jellinger, K. and Wisniewski, H. M. (1995) Cell death in Alzheimer's disease evaluated by DNA fragmentation in situ. Acta Neuropathol. (Berl.) 89, 35-41
-
(1995)
Acta Neuropathol.
, vol.89
, pp. 35-41
-
-
Lassmann, H.1
Bancher, C.2
Breitschopf, H.3
Wegiel, J.4
Bobinski, M.5
Jellinger, K.6
Wisniewski, H.M.7
-
39
-
-
0035478732
-
Involvement of nitric oxide released from microglia-macrophages in pathological changes of cathepsin D-deficient mice
-
Nakanishi, H., Zhang, J., Koike, M., Nishioku, T., Okamoto, Y., Kominami, E., von Figura, K., Peters, C., Yamamoto, K., Saftig, P. and Uchiyama, Y. (2001) Involvement of nitric oxide released from microglia-macrophages in pathological changes of cathepsin D-deficient mice. J. Neurosci. 21, 7526-7533
-
(2001)
J. Neurosci.
, vol.21
, pp. 7526-7533
-
-
Nakanishi, H.1
Zhang, J.2
Koike, M.3
Nishioku, T.4
Okamoto, Y.5
Kominami, E.6
Von Figura, K.7
Peters, C.8
Yamamoto, K.9
Saftig, P.10
Uchiyama, Y.11
-
40
-
-
0034718598
-
Microglial activation precedes acute neurodegeneration in Sandhoff disease and is suppressed by bone marrow transplantation
-
Wada, R., Tifft, C. J. and Proia, R. L. (2000) Microglial activation precedes acute neurodegeneration in Sandhoff disease and is suppressed by bone marrow transplantation. Proc. Natl. Acad. Sci. U.S.A. 97, 10954-10959
-
(2000)
Proc. Natl. Acad. Sci. U.S.A.
, vol.97
, pp. 10954-10959
-
-
Wada, R.1
Tifft, C.J.2
Proia, R.L.3
-
41
-
-
0032789944
-
Ovine ceroid lipofuscinosis (OCL6): Postulated mechanism of neurodegeneration
-
Jolly, R. D. and Walkley, S. U. (1999) Ovine ceroid lipofuscinosis (OCL6): postulated mechanism of neurodegeneration. Mol. Genet. Metab. 66, 376-380
-
(1999)
Mol. Genet. Metab.
, vol.66
, pp. 376-380
-
-
Jolly, R.D.1
Walkley, S.U.2
-
42
-
-
0035813219
-
A coding region determinant of instability regulates levels of manganese superoxide dismutase mRNA
-
Davis, C. A., Monnier, J. M. and Nick, H. S. (2001) A coding region determinant of instability regulates levels of manganese superoxide dismutase mRNA. J. Biol. Chem. 276, 37317-37326
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 37317-37326
-
-
Davis, C.A.1
Monnier, J.M.2
Nick, H.S.3
-
43
-
-
0032501998
-
Peroxynitrite-mediated inactivation of manganese superoxide dismutase involves nitration and oxidation of critical tyrosine residues
-
MacMillan-Crow, L. A., Crow, J. P. and Thompson, J. A. (1998) Peroxynitrite-mediated inactivation of manganese superoxide dismutase involves nitration and oxidation of critical tyrosine residues. Biochemistry 37, 1613-1622
-
(1998)
Biochemistry
, vol.37
, pp. 1613-1622
-
-
MacMillan-Crow, L.A.1
Crow, J.P.2
Thompson, J.A.3
-
44
-
-
0036176571
-
Mitochondrial dysfunction in the neuronal ceroid-lipofuscinoses (Batten disease)
-
Jolly, R. D., Brown, S., Das, A. M. and Walkley S. U. (2002) Mitochondrial dysfunction in the neuronal ceroid-lipofuscinoses (Batten disease). Neurochem. Int. 40, 565-571
-
(2002)
Neurochem. Int.
, vol.40
, pp. 565-571
-
-
Jolly, R.D.1
Brown, S.2
Das, A.M.3
Walkley, S.U.4
|