-
2
-
-
0034992601
-
Axonal and neuronal degeneration in multiple sclerosis: Mechanisms and functional consequences
-
Bjartmar, C. & Trapp, B.D. Axonal and neuronal degeneration in multiple sclerosis: mechanisms and functional consequences. Curr. Opin. Neurol. 14, 271-278 (2001).
-
(2001)
Curr. Opin. Neurol
, vol.14
, pp. 271-278
-
-
Bjartmar, C.1
Trapp, B.D.2
-
3
-
-
0032576752
-
Axonal transection in the lesions of multiple sclerosis
-
Trapp, B.D. et al. Axonal transection in the lesions of multiple sclerosis. N. Engl. J. Med. 338, 278-285 (1998).
-
(1998)
N. Engl. J. Med
, vol.338
, pp. 278-285
-
-
Trapp, B.D.1
-
4
-
-
0032486428
-
Axonal swellings and degeneration in mice lacking the major proteolipid of myelin
-
Griffiths, I. et al. Axonal swellings and degeneration in mice lacking the major proteolipid of myelin. Science 280, 1610-1613 (1998).
-
(1998)
Science
, vol.280
, pp. 1610-1613
-
-
Griffiths, I.1
-
5
-
-
0037370361
-
Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination
-
Lappe-Siefke, C. et al. Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination. Nat. Genet. 33, 366-374 (2003).
-
(2003)
Nat. Genet
, vol.33
, pp. 366-374
-
-
Lappe-Siefke, C.1
-
6
-
-
0141833983
-
Disease mechanisms in inherited neuropathies
-
Suter, U. & Scherer, S.S. Disease mechanisms in inherited neuropathies. Nat. Rev. Neurosci. 4, 714-726 (2003).
-
(2003)
Nat. Rev. Neurosci
, vol.4
, pp. 714-726
-
-
Suter, U.1
Scherer, S.S.2
-
7
-
-
3142674927
-
Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia
-
Edgar, J.M. et al. Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia. J. Cell Biol. 166, 121-131 (2004).
-
(2004)
J. Cell Biol
, vol.166
, pp. 121-131
-
-
Edgar, J.M.1
-
8
-
-
1342310772
-
Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport
-
Ferreirinha, F. et al. Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport. J. Clin. Invest. 113, 231-242 (2004).
-
(2004)
J. Clin. Invest
, vol.113
, pp. 231-242
-
-
Ferreirinha, F.1
-
9
-
-
8644221211
-
Mammalian peroxisomes and reactive oxygen species
-
Schrader, M. & Fahimi, H.D. Mammalian peroxisomes and reactive oxygen species. Histochem. Cell Biol. 122, 383-393 (2004).
-
(2004)
Histochem. Cell Biol
, vol.122
, pp. 383-393
-
-
Schrader, M.1
Fahimi, H.D.2
-
10
-
-
4744371532
-
Peroxisomes, lipid metabolism, and peroxisomal disorders
-
Wanders, R.J. Peroxisomes, lipid metabolism, and peroxisomal disorders. Mol. Genet. Metab. 83, 16-27 (2004).
-
(2004)
Mol. Genet. Metab
, vol.83
, pp. 16-27
-
-
Wanders, R.J.1
-
11
-
-
16944361876
-
A mouse model for Zellweger syndrome
-
Baes, M. et al. A mouse model for Zellweger syndrome. Nat. Genet. 17, 49-57 (1997).
-
(1997)
Nat. Genet
, vol.17
, pp. 49-57
-
-
Baes, M.1
-
12
-
-
0036328365
-
Oligodendroglial cells in culture effectively dispose of exogenous hydrogen peroxide: Comparison with cultured neurones, astroglial and microglial cells
-
Hirrlinger, J., Resch, A., Gutterer, J.M. & Dringen, R. Oligodendroglial cells in culture effectively dispose of exogenous hydrogen peroxide: comparison with cultured neurones, astroglial and microglial cells. J. Neurochem. 82, 635-644 (2002).
-
(2002)
J. Neurochem
, vol.82
, pp. 635-644
-
-
Hirrlinger, J.1
Resch, A.2
Gutterer, J.M.3
Dringen, R.4
-
13
-
-
0036273592
-
Opinion: Peroxisomal-protein import: is it really that complex?
-
Gould, S.J. & Collins, C.S. Opinion: peroxisomal-protein import: is it really that complex? Nat. Rev. Mol. Cell Biol. 3, 382-389 (2002).
-
(2002)
Nat. Rev. Mol. Cell Biol
, vol.3
, pp. 382-389
-
-
Gould, S.J.1
Collins, C.S.2
-
14
-
-
0028817372
-
Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
-
Dodt, G. et al. Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders. Nat. Genet. 9, 115-125 (1995).
-
(1995)
Nat. Genet
, vol.9
, pp. 115-125
-
-
Dodt, G.1
-
15
-
-
0036198394
-
Generation of Pex5-loxP mice allowing the conditional elimination of peroxisomes
-
Baes, M., Dewerchin, M., Janssen, A., Collen, D. & Carmeliet, P. Generation of Pex5-loxP mice allowing the conditional elimination of peroxisomes. Genesis 32, 177-178 (2002).
-
(2002)
Genesis
, vol.32
, pp. 177-178
-
-
Baes, M.1
Dewerchin, M.2
Janssen, A.3
Collen, D.4
Carmeliet, P.5
-
16
-
-
0033047785
-
Metabolic control of peroxisome abundance
-
Chang, C.C. et al. Metabolic control of peroxisome abundance. J. Cell Sci. 112, 1579-1590 (1999).
-
(1999)
J. Cell Sci
, vol.112
, pp. 1579-1590
-
-
Chang, C.C.1
-
17
-
-
20044370505
-
High cholesterol level is essential for myelin membrane growth
-
Saher, G. et al. High cholesterol level is essential for myelin membrane growth. Nat. Neurosci. 8, 468-475 (2005).
-
(2005)
Nat. Neurosci
, vol.8
, pp. 468-475
-
-
Saher, G.1
-
18
-
-
0022537701
-
Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly
-
Zoeller, R.A. & Raetz, C.R. Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly. Proc. Natl. Acad. Sci. USA 83, 5170-5174 (1986).
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 5170-5174
-
-
Zoeller, R.A.1
Raetz, C.R.2
-
19
-
-
0042131525
-
Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in mice
-
Rodemer, C. et al. Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in mice. Hum. Mol. Genet. 12, 1881-1895 (2003).
-
(2003)
Hum. Mol. Genet
, vol.12
, pp. 1881-1895
-
-
Rodemer, C.1
-
20
-
-
0026183566
-
Peroxisomal disorders
-
Moser, H.W., Bergin, A. & Cornblath, D. Peroxisomal disorders. Biochem. Cell Biol. 69, 463-474 (1991).
-
(1991)
Biochem. Cell Biol
, vol.69
, pp. 463-474
-
-
Moser, H.W.1
Bergin, A.2
Cornblath, D.3
-
21
-
-
14244267510
-
Peroxisomal disorders I: Biochemistry and genetics of peroxisome biogenesis disorders
-
Wanders, R.J. & Waterham, H.R. Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders. Clin. Genet. 67, 107-133 (2005).
-
(2005)
Clin. Genet
, vol.67
, pp. 107-133
-
-
Wanders, R.J.1
Waterham, H.R.2
-
22
-
-
0030689779
-
Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice
-
Forss-Petter, S. et al. Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice. J. Neurosci. Res. 50, 829-843 (1997).
-
(1997)
J. Neurosci. Res
, vol.50
, pp. 829-843
-
-
Forss-Petter, S.1
-
23
-
-
0030793307
-
A mouse model for X-linked adrenoleukodystrophy
-
Lu, J.F. et al. A mouse model for X-linked adrenoleukodystrophy. Proc. Natl. Acad. Sci. USA 94, 9366-9371 (1997).
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 9366-9371
-
-
Lu, J.F.1
-
24
-
-
0031587790
-
Adrenoleukodystrophy protein-deficient mice represent abnormality of very long chain fatty acid metabolism
-
Kobayashi, T., Shinnoh, N., Kondo, A. & Yamada, T. Adrenoleukodystrophy protein-deficient mice represent abnormality of very long chain fatty acid metabolism. Biochem. Biophys. Res. Commun. 232, 631-636 (1997).
-
(1997)
Biochem. Biophys. Res. Commun
, vol.232
, pp. 631-636
-
-
Kobayashi, T.1
Shinnoh, N.2
Kondo, A.3
Yamada, T.4
-
25
-
-
0032522207
-
Expression of monocyte chemoattractant protein-1 and other beta-chemokines by resident glia and inflammatory cells in multiple sclerosis lesions
-
Simpson, J.E., Newcombe, J., Cuzner, M.L. & Woodroofe, M.N. Expression of monocyte chemoattractant protein-1 and other beta-chemokines by resident glia and inflammatory cells in multiple sclerosis lesions. J. Neuroimmunol. 84, 238-249 (1998).
-
(1998)
J. Neuroimmunol
, vol.84
, pp. 238-249
-
-
Simpson, J.E.1
Newcombe, J.2
Cuzner, M.L.3
Woodroofe, M.N.4
-
26
-
-
0032100683
-
MCP-1, MCP-2 and MCP-3 expression in multiple sclerosis lesions: An immunohistochemical and in situ hybridization study
-
McManus, C. et al. MCP-1, MCP-2 and MCP-3 expression in multiple sclerosis lesions: an immunohistochemical and in situ hybridization study. J. Neuroimmunol. 86, 20-29 (1998).
-
(1998)
J. Neuroimmunol
, vol.86
, pp. 20-29
-
-
McManus, C.1
-
27
-
-
5644259586
-
Comparison of myelin, axon, lipid, and immunopathology in the central nervous system of differentially myelin-compromised mutant mice: A morphological and biochemical study
-
Loers, G., Aboul-Enein, F., Bartsch, U., Lassmann, H. & Schachner, M. Comparison of myelin, axon, lipid, and immunopathology in the central nervous system of differentially myelin-compromised mutant mice: a morphological and biochemical study. Mol. Cell. Neurosci. 27, 175-189 (2004).
-
(2004)
Mol. Cell. Neurosci
, vol.27
, pp. 175-189
-
-
Loers, G.1
Aboul-Enein, F.2
Bartsch, U.3
Lassmann, H.4
Schachner, M.5
-
28
-
-
0037135989
-
Notch1 control of oligodendrocyte differentiation in the spinal cord
-
Genoud, S. et al. Notch1 control of oligodendrocyte differentiation in the spinal cord. J. Cell Biol. 158, 709-718 (2002).
-
(2002)
J. Cell Biol
, vol.158
, pp. 709-718
-
-
Genoud, S.1
-
30
-
-
0041624042
-
Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy
-
Loes, D.J. et al. Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy. Neurology 61, 369-374 (2003).
-
(2003)
Neurology
, vol.61
, pp. 369-374
-
-
Loes, D.J.1
-
31
-
-
10744220226
-
Quantitative proton magnetic resonance spectroscopy of children with adrenoleukodystrophy before and after hematopoietic stem cell transplantation
-
Wilken, B. et al. Quantitative proton magnetic resonance spectroscopy of children with adrenoleukodystrophy before and after hematopoietic stem cell transplantation. Neuropediatrics 34, 237-246 (2003).
-
(2003)
Neuropediatrics
, vol.34
, pp. 237-246
-
-
Wilken, B.1
-
32
-
-
0032995794
-
The neurobiology of X-linked adrenoleukodystrophy, a demyelinating peroxisomal disorder
-
Dubois-Dalcq, M., Feigenbaum, V. & Aubourg, P. The neurobiology of X-linked adrenoleukodystrophy, a demyelinating peroxisomal disorder. Trends Neurosci. 22, 4-12 (1999).
-
(1999)
Trends Neurosci
, vol.22
, pp. 4-12
-
-
Dubois-Dalcq, M.1
Feigenbaum, V.2
Aubourg, P.3
-
33
-
-
0027532282
-
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
-
Mosser, J. et al. Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters. Nature 361, 726-730 (1993).
-
(1993)
Nature
, vol.361
, pp. 726-730
-
-
Mosser, J.1
-
34
-
-
33846942956
-
X-linked adrenoleukodystrophy: Very long-chain fatty acid metabolism, ABC half-transporters and the complicated route to treatment
-
Kemp, S. & Wanders, R.J. X-linked adrenoleukodystrophy: Very long-chain fatty acid metabolism, ABC half-transporters and the complicated route to treatment. Mol. Genet. Metab. 90, 268-276 (2007).
-
(2007)
Mol. Genet. Metab
, vol.90
, pp. 268-276
-
-
Kemp, S.1
Wanders, R.J.2
-
35
-
-
0036501313
-
Late onset neurological phenotype of the X-ALD gene inactivation in mice: A mouse model for adrenomyeloneuropathy
-
Pujol, A. et al. Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathy. Hum. Mol. Genet. 11, 499-505 (2002).
-
(2002)
Hum. Mol. Genet
, vol.11
, pp. 499-505
-
-
Pujol, A.1
-
36
-
-
33845955516
-
Immunopathogenesis of adrenoleukodystrophy: Current understanding
-
Hudspeth, M.P. & Raymond, G.V. Immunopathogenesis of adrenoleukodystrophy: current understanding. J. Neuroimmunol. 182, 5-12 (2006).
-
(2006)
J. Neuroimmunol
, vol.182
, pp. 5-12
-
-
Hudspeth, M.P.1
Raymond, G.V.2
-
37
-
-
0035846634
-
Late onset white matter disease in peroxisome biogenesis disorder
-
Barth, P.G. et al. Late onset white matter disease in peroxisome biogenesis disorder. Neurology 57, 1949-1955 (2001).
-
(2001)
Neurology
, vol.57
, pp. 1949-1955
-
-
Barth, P.G.1
-
38
-
-
0031737638
-
Clinical approach to inherited peroxisomal disorders: A series of 27 patients
-
Baumgartner, M.R. et al. Clinical approach to inherited peroxisomal disorders: a series of 27 patients. Ann. Neurol. 44, 720-730 (1998).
-
(1998)
Ann. Neurol
, vol.44
, pp. 720-730
-
-
Baumgartner, M.R.1
-
39
-
-
21044452485
-
+ T cells in multiple sclerosis and its animal models
-
+ T cells in multiple sclerosis and its animal models. Curr. Drug Targets Inflamm. Allergy 4, 239-245 (2005).
-
(2005)
Curr. Drug Targets Inflamm. Allergy
, vol.4
, pp. 239-245
-
-
Goverman, J.1
-
40
-
-
1642281535
-
Relapsing and remitting multiple sclerosis: Pathology of the newly forming lesion
-
Barnett, M.H. & Prineas, J.W. Relapsing and remitting multiple sclerosis: pathology of the newly forming lesion. Ann. Neurol. 55, 458-468 (2004).
-
(2004)
Ann. Neurol
, vol.55
, pp. 458-468
-
-
Barnett, M.H.1
Prineas, J.W.2
-
41
-
-
0032146068
-
Immune surveillance in the injured nervous system: T-lymphocytes invade the axotomized mouse facial motor nucleus and aggregate around sites of neuronal degeneration
-
Raivich, G. et al. Immune surveillance in the injured nervous system: T-lymphocytes invade the axotomized mouse facial motor nucleus and aggregate around sites of neuronal degeneration. J. Neurosci. 18, 5804-5816 (1998).
-
(1998)
J. Neurosci
, vol.18
, pp. 5804-5816
-
-
Raivich, G.1
-
42
-
-
33748138567
-
Immune cells contribute to myelin degeneration and axonopathic changes in mice overexpressing proteolipid protein in oligodendrocytes
-
Ip, C.W. et al. Immune cells contribute to myelin degeneration and axonopathic changes in mice overexpressing proteolipid protein in oligodendrocytes. J. Neurosci. 26, 8206-8216 (2006).
-
(2006)
J. Neurosci
, vol.26
, pp. 8206-8216
-
-
Ip, C.W.1
-
43
-
-
0037201962
-
High-resolution 3D MRI of mouse brain reveals small cerebral structures in vivo
-
Natt, O. et al. High-resolution 3D MRI of mouse brain reveals small cerebral structures in vivo. J. Neurosci. Methods 120, 203-209 (2002).
-
(2002)
J. Neurosci. Methods
, vol.120
, pp. 203-209
-
-
Natt, O.1
-
44
-
-
0018634293
-
Silver staining of myelin by means of physical development
-
Gallyas, F. Silver staining of myelin by means of physical development. Neurol. Res. 1, 203-209 (1979).
-
(1979)
Neurol. Res
, vol.1
, pp. 203-209
-
-
Gallyas, F.1
-
45
-
-
0010983211
-
Die Silberimprägnation der Neurofibrillen
-
Bielschowsky, M. Die Silberimprägnation der Neurofibrillen. J. Psychol. Neurol. 3, 169-183 (1904).
-
(1904)
J. Psychol. Neurol
, vol.3
, pp. 169-183
-
-
Bielschowsky, M.1
-
46
-
-
0029845073
-
Monoclonal antibody O10 defines a conformationally sensitive cell-surface epitope of proteolipid protein (PLP): Evidence that PLP misfolding underlies dysmyelination in mutant mice
-
Jung, M., Sommer, I., Schachner, M. & Nave, K.A. Monoclonal antibody O10 defines a conformationally sensitive cell-surface epitope of proteolipid protein (PLP): evidence that PLP misfolding underlies dysmyelination in mutant mice. J. Neurosci. 16, 7920-7929 (1996).
-
(1996)
J. Neurosci
, vol.16
, pp. 7920-7929
-
-
Jung, M.1
Sommer, I.2
Schachner, M.3
Nave, K.A.4
-
47
-
-
0015857284
-
Myelination in rat brain: Method of myelin isolation
-
Norton, W.T. & Poduslo, S.E. Myelination in rat brain: method of myelin isolation. J. Neurochem. 21, 749-757 (1973).
-
(1973)
J. Neurochem
, vol.21
, pp. 749-757
-
-
Norton, W.T.1
Poduslo, S.E.2
-
48
-
-
33845261493
-
A rapid method of total lipid extraction and purification
-
Bligh, E.G. & Dyer, W.J. A rapid method of total lipid extraction and purification. Can. J. Biochem. Physiol. 37, 911-917 (1959).
-
(1959)
Can. J. Biochem. Physiol
, vol.37
, pp. 911-917
-
-
Bligh, E.G.1
Dyer, W.J.2
-
49
-
-
0035063286
-
Quantitative determination of phospholipid compositions by ESI-MS: Effects of acyl chain length, unsaturation, and lipid concentration on instrument response
-
Koivusalo, M., Haimi, P., Heikinheimo, L., Kostiainen, R. & Somerharju, P. Quantitative determination of phospholipid compositions by ESI-MS: effects of acyl chain length, unsaturation, and lipid concentration on instrument response. J. Lipid Res. 42, 663-672 (2001).
-
(2001)
J. Lipid Res
, vol.42
, pp. 663-672
-
-
Koivusalo, M.1
Haimi, P.2
Heikinheimo, L.3
Kostiainen, R.4
Somerharju, P.5
-
50
-
-
33747623280
-
Interleukin 18-independent engagement of interleukin 18 receptor is required for autoimmune inflammation
-
Gutcher, I., Urich, E., Wolter, K., Prinz, M. & Becher, B. Interleukin 18-independent engagement of interleukin 18 receptor is required for autoimmune inflammation. Nat. Immunol. 7, 946-953 (2006).
-
(2006)
Nat. Immunol
, vol.7
, pp. 946-953
-
-
Gutcher, I.1
Urich, E.2
Wolter, K.3
Prinz, M.4
Becher, B.5
|