-
2
-
-
0033365230
-
Proteolipoprotein gene analysis in 82 patients with sporadic pelizaeus- merzbacher disease: Duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not
-
DOI 10.1086/302483
-
Mimault C, Giraud G, Courtois V, et al. Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher Disease: duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not. The Clinical European Network on Brain Dysmyelinating Disease. Am J Hum Genet 1999; 65 (2): 360-9. (Pubitemid 30462994)
-
(1999)
American Journal of Human Genetics
, vol.65
, Issue.2
, pp. 360-369
-
-
Mimault, C.1
Giraud, G.2
Courtois, V.3
Cailloux, F.4
Boire, J.Y.5
Dastugue, B.6
Boespflug-Tanguy, O.7
-
3
-
-
0033678145
-
Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating Disease
-
Cailloux F, Gauthier-Barichard F, Mimault C, et al. Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating Disease. Eur J Hum Genet 2000; 8 (11): 837-45.
-
(2000)
Eur J Hum Genet
, vol.8
, Issue.11
, pp. 837-845
-
-
Cailloux, F.1
Gauthier-Barichard, F.2
Mimault, C.3
-
4
-
-
0031801082
-
Duplication of the proteolipid protein gene is the major cause of Pelizaeus-Merzbacher disease
-
Sistermans EA, de Coo RF, De Wijs IJ, Van Oost BA. Duplication of the proteolipid protein gene is the major cause of Pelizaeus-Merzbacher disease. Neurology 1998; 50 (6): 1749-54. (Pubitemid 28283246)
-
(1998)
Neurology
, vol.50
, Issue.6
, pp. 1749-1754
-
-
Sistermans, E.A.1
De Coo, R.F.M.2
De Wijs, I.J.3
Van Oost, B.A.4
-
5
-
-
0028240173
-
Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease [3]
-
DOI 10.1038/ng0494-333
-
Ellis D, Malcolm S. Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease. Nat Genet 1994; 6 (4): 333-4. (Pubitemid 24190013)
-
(1994)
Nature Genetics
, vol.6
, Issue.4
, pp. 333-334
-
-
Ellis, D.1
Malcolm, S.2
-
6
-
-
0030964590
-
Molecular genetics of krabbe disease (Globoid cell Leukodystrophy): Diagnostic and clinical implications
-
DOI 10.1002/(SICI)1098-1004(1997)10:4<268::AID-HUMU2>3.0.CO;2-D
-
Wenger DA, Rafi MA, Luzi P. Molecular genetics of Krabbe disease (globoid cell leukodystrophy): diagnostic and clinical implications. Hum Mutat 1997; 10 (4): 268-79. (Pubitemid 27430501)
-
(1997)
Human Mutation
, vol.10
, Issue.4
, pp. 268-279
-
-
Wenger, D.A.1
Rafi, M.A.2
Luzi, P.3
-
7
-
-
0025329012
-
Reversal of early neurologic and neuroradiologic manifestations of X-linked adrenoleukodystrophy by bone marrow transplantation
-
Aubourg P, Blanche S, Jambaque I, et al. Reversal of early neurologic and neuroradiologic manifestations of X-linked adrenoleukodystrophy by bone marrow transplantation. N Engl J Med 1990; 322 (26): 1860-6. (Pubitemid 20200413)
-
(1990)
New England Journal of Medicine
, vol.322
, Issue.26
, pp. 1860-1866
-
-
Aubourg, P.1
Blanche, S.2
Jambaque, I.3
Rocchiccioli, F.4
Kalifa, G.5
Naud-Saudreau, C.6
Rolland, M.-O.7
Debre, M.8
Chaussain, J.-L.9
Griscelli, C.10
Fischer, A.11
Bougneres, P.-F.12
-
8
-
-
20844453744
-
Transplantation of umbilical-cord blood in babies with infantile Krabbe's disease
-
DOI 10.1056/NEJMoa042604
-
Escolar ML, Poe MD, Provenzale JM, et al. Transplantation of umbilical-cord blood in babies with infantile Krabbes disease. N Engl J Med 2005; 352 (20): 2069-81. (Pubitemid 40664308)
-
(2005)
New England Journal of Medicine
, vol.352
, Issue.20
, pp. 2069-2081
-
-
Escolar, M.L.1
Poe, M.D.2
Provenzale, J.M.3
Richards, K.C.4
Allison, J.5
Wood, S.6
Wenger, D.A.7
Pietryga, D.8
Wall, D.9
Champagne, M.10
Morse, R.11
Krivit, W.12
Kurtzberg, J.13
-
9
-
-
0030793307
-
A mouse model for X-linked adrenoleukodystrophy
-
DOI 10.1073/pnas.94.17.9366
-
Lu JF, Lawler AM, Watkins PA, et al. A mouse model for X-linked adrenoleukodystrophy. Proc Natl Acad Sci USA 1997; 94 (17): 9366-71. (Pubitemid 27357835)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.17
, pp. 9366-9371
-
-
Lu, J.-F.1
Lawler, A.M.2
Watkins, P.A.3
Powers, J.M.4
Moser, A.B.5
Moser, H.W.6
Smith, K.D.7
-
10
-
-
0030689779
-
Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice
-
Forss-Petter S, Werner H, Berger J, et al. Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice. J Neurosci Res 1997; 50 (5): 829-43.
-
(1997)
J Neurosci Res
, vol.50
, Issue.5
, pp. 829-843
-
-
Forss-Petter, S.1
Werner, H.2
Berger, J.3
-
11
-
-
0036501313
-
Late onset neurological phenotype of the X-ALD gene inactivation in mice: A mouse model for adrenomyeloneuropathy
-
Pujol A, Hindelang C, Callizot N, Bartsch U, Schachner M, Mandel JL. Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathy. Hum Mol Genet 2002; 11 (5): 499-505. (Pubitemid 34257486)
-
(2002)
Human Molecular Genetics
, vol.11
, Issue.5
, pp. 499-505
-
-
Pujol, A.1
Hindelang, C.2
Callizot, N.3
Bartsch, U.4
Schachner, M.5
Mandel, J.L.6
-
12
-
-
10544235699
-
Phenotype of arylsulfatase A-deficient mice: Relationship to human metachromatic leukodystrophy
-
DOI 10.1073/pnas.93.25.14821
-
Hess B, Saftig P, Hartmann D, et al. Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy. Proc Natl Acad Sci USA 1996; 93 (25): 14821-6. (Pubitemid 26419053)
-
(1996)
Proceedings of the National Academy of Sciences of the United States of America
, vol.93
, Issue.25
, pp. 14821-14826
-
-
Hess, B.1
Saftig, P.2
Hartmann, D.3
Coenen, R.4
Lullmann-Rauch, R.5
Goebel, H.H.6
Evers, M.7
Von Figura, K.8
D'Hooge, R.9
Nagels, G.10
De Deyn, P.11
Peters, C.12
Gieselmann, V.13
-
13
-
-
33750597616
-
Gene therapy of metachromatic leukodystrophy reverses neurological damage and deficits in mice
-
DOI 10.1172/JCI28873
-
Biffi A, Capotondo A, Fasano S, et al. Gene therapy of metachromatic leukodystrophy reverses neurological damage and deficits in mice. J Clin Invest 2006; 116 (11): 3070-82. (Pubitemid 44684492)
-
(2006)
Journal of Clinical Investigation
, vol.116
, Issue.11
, pp. 3070-3082
-
-
Biffi, A.1
Capotondo, A.2
Fasano, S.3
Del Carro, U.4
Marchesini, S.5
Azuma, H.6
Malaguti, M.C.7
Amadio, S.8
Brambilla, R.9
Grompe, M.10
Bordignon, C.11
Quattrini, A.12
Naldini, L.13
-
14
-
-
0023778163
-
Transplantation of oligodendrocytes and Schwann cells into the spinal cord of the myelin-deficient rat
-
Duncan ID, Hammang JP, Jackson KF, Wood PM, Bunge RP, Langford L. Transplantation of oligodendrocytes and Schwann cells into the spinal cord of the myelin-deficient rat. J Neurocytol 1988; 17 (3): 351-60.
-
(1988)
J Neurocytol
, vol.17
, Issue.3
, pp. 351-360
-
-
Duncan, I.D.1
Hammang, J.P.2
Jackson, K.F.3
Wood, P.M.4
Bunge, R.P.5
Langford, L.6
-
15
-
-
0028134894
-
Transplantation of an oligodendrocyte cell line leading to extensive myelination
-
DOI 10.1073/pnas.91.24.11616
-
Tontsch U, Archer DR, Dubois-Dalcq M, Duncan ID. Transplantation of an oligodendrocyte cell line leading to extensive myelination. Proc Natl Acad Sci USA 1994; 91 (24): 11616-20. (Pubitemid 24356395)
-
(1994)
Proceedings of the National Academy of Sciences of the United States of America
, vol.91
, Issue.24
, pp. 11616-11620
-
-
Tontsch, U.1
Archer, D.R.2
Dubois-Dalcq, M.3
Duncan, I.D.4
-
16
-
-
0033618593
-
Embryonic stem cell-derived glial precursors: A source of myelinating transplants
-
Brustle O, Jones KN, Learish RD, et al. Embryonic stem cell-derived glial precursors: a source of myelinating transplants. Science 1999; 285 (5428): 754-6.
-
(1999)
Science
, vol.285
, Issue.5428
, pp. 754-756
-
-
Brustle, O.1
Jones, K.N.2
Learish, R.D.3
-
17
-
-
0024570219
-
Myelin formation in myelin-deficient rat spinal cord following transplantation of normal fetal spinal cord
-
DOI 10.1016/0304-3940(89)90135-3
-
Rosenbluth J, Hasegawa M, Schiff R. Myelin formation in myelin-deficient rat spinal cord following transplantation of normal fetal spinal cord. Neurosci Lett 1989; 97 (1-2): 35-40. (Pubitemid 19048907)
-
(1989)
Neuroscience Letters
, vol.97
, Issue.1-2
, pp. 35-40
-
-
Rosenbluth, J.1
Hasegawa, M.2
Schiff, R.3
-
18
-
-
0031015174
-
Myelination of the canine central nervous system by glial cell transplantation: A model for repair of human myelin disease
-
DOI 10.1038/nm0197-54
-
Archer DR, Cuddon PA, Lipsitz D, Duncan ID. Myelination of the canine central nervous system by glial cell transplantation: a model for repair of human myelin disease. Nat Med 1997; 3 (1): 54-9. (Pubitemid 27019141)
-
(1997)
Nature Medicine
, vol.3
, Issue.1
, pp. 54-59
-
-
Archer, D.R.1
Cuddon, P.A.2
Lipsitz, D.3
Duncan, I.D.4
-
19
-
-
0019790884
-
Shaking pups: A disorder of central myelination in the spaniel dog. II. Ultrastructural observations on the white matter of the cervical spinal cord
-
Griffiths IR, Duncan ID, McCulloch M. Shaking pups: a disorder of central myelination in the spaniel dog. II. Ultrastructural observations on the white matter of the cervical spinal cord. J Neurocytol 1981; 10 (5): 847-58. (Pubitemid 12233858)
-
(1981)
Journal of Neurocytology
, vol.10
, Issue.5
, pp. 847-858
-
-
Griffiths, I.R.1
Duncan, I.D.2
McCulloch, M.3
-
20
-
-
0020595713
-
Survival and differentiation of oligodendrocytes from neural tissue transplanted into new-born mouse brain
-
DOI 10.1016/0304-3940(83)90449-4
-
Gumpel M, Baumann N, Raoul M, Jacque C. Survival and differentiation of oligodendrocytes from neural tissue transplanted into new-born mouse brain. Neurosci Lett 1983; 37 (3): 307-11. (Pubitemid 13062411)
-
(1983)
Neuroscience Letters
, vol.37
, Issue.3
, pp. 307-311
-
-
Gumpel, M.1
Baumann, N.2
Raoul, M.3
Jacque, C.4
-
21
-
-
0030087510
-
Cell-cell interactions during the migration of myelin-forming cells transplanted in the demyelinated spinal cord
-
DOI 10.1002/(SICI)1098-1136(199602)16:2<147::AID-GLIA7>3.0.CO;2-0
-
Baron-Van Evercooren A, Avellana-Adalid V, Ben Younes-Chennoufi A, Gansmuller A, Nait-Oumesmar B, Vignais L. Cell-cell interactions during the migration of myelin-forming cells transplanted in the demyelinated spinal cord. Glia 1996; 16 (2): 147-64. (Pubitemid 26309477)
-
(1996)
GLIA
, vol.16
, Issue.2
, pp. 147-164
-
-
Baron-Van Evercooren, A.1
Avellana-Adalid, V.2
Younes-Chennoufi, A.B.3
Gansmuller, A.4
Nait-Oumesmar, B.5
Vignais, L.6
-
22
-
-
1542336187
-
Fetal and adult human oligodendrocyte progenitor cell isolates myelinate the congenitally dysmyelinated brain
-
DOI 10.1038/nm974
-
Windrem MS, Nunes MC, Rashbaum WK, et al. Fetal and adult human oligodendrocyte progenitor cell isolates myelinate the congenitally dysmyelinated brain. Nat Med 2004; 10 (1): 93-7. (Pubitemid 38524704)
-
(2004)
Nature Medicine
, vol.10
, Issue.1
, pp. 93-97
-
-
Windrem, M.S.1
Nunes, M.C.2
Rashbaum, W.K.3
Schwartz, T.H.4
Goodman, R.A.5
McKhann II, G.6
Roy, N.S.7
Goldman, S.A.8
-
23
-
-
29444435085
-
Galactocerebrosidase-deficient oligodendrocytes maintain stable central myelin by exogenous replacement of the missing enzyme in mice
-
DOI 10.1073/pnas.0506473102
-
Kondo Y, Wenger DA, Gallo V, Duncan ID. Galactocerebrosidase-deficient oligodendrocytes maintain stable central myelin by exogenous replacement of the missing enzyme in mice. Proc Natl Acad Sci USA 2005; 102 (51): 18670-5. (Pubitemid 43011284)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.51
, pp. 18670-18675
-
-
Kondo, Y.1
Wenger, D.A.2
Gallo, V.3
Duncan, I.D.4
-
24
-
-
0037110703
-
Expression of the green fluorescent protein in the oligodendrocyte lineage: A transgenic mouse for developmental and physiological studies
-
DOI 10.1002/jnr.10368
-
Yuan X, Chittajallu R, Belachew S, Anderson S, McBain CJ, Gallo V. Expression of the green fluorescent protein in the oligodendrocyte lineage: a transgenic mouse for developmental and physiological studies. J Neurosci Res 2002; 70 (4): 529-45. (Pubitemid 35253523)
-
(2002)
Journal of Neuroscience Research
, vol.70
, Issue.4
, pp. 529-545
-
-
Yuan, X.1
Chittajallu, R.2
Belachew, S.3
Anderson, S.4
McBain, C.J.5
Gallo, V.6
-
25
-
-
0029812943
-
Expansion of rat oligodendrocyte progenitors into proliferative 'oligospheres' that retain differentiation potential
-
DOI 10.1002/(SICI)1097-4547(19960901)45:5<558::AID-JNR6>3.0.CO;2-B
-
Avellana-Adalid V, Nait-Oumesmar B, Lachapelle F, Baron-Van Evercooren A. Expansion of rat oligodendrocyte progenitors into proliferative "oligospheres" that retain differentiation potential. J Neurosci Res 1996; 45 (5): 558-70. (Pubitemid 26293357)
-
(1996)
Journal of Neuroscience Research
, vol.45
, Issue.5
, pp. 558-570
-
-
Avellana-Adalid, V.1
Nait-Oumesmar, B.2
Lachapelle, F.3
Evercooren, A.B.-V.4
-
26
-
-
0032429864
-
Generation of oligodendroglial progenitors from neural stem cells
-
DOI 10.1023/A:1006953023845
-
Zhang SC, Lundberg C, Lipsitz D, OConnor LT, Duncan ID. Generation of oligodendroglial progenitors from neural stem cells. J Neurocytol 1998; 27 (7): 475-89. (Pubitemid 29204652)
-
(1998)
Journal of Neurocytology
, vol.27
, Issue.7
, pp. 475-489
-
-
Zhang, S.-C.1
Lundberg, C.2
Lipsitz, D.3
O'Connor, L.T.4
Duncan, I.D.5
-
27
-
-
0032532312
-
Self-renewing canine oligodendroglial progenitor expanded as oligospheres
-
DOI 10.1002/(SICI)1097-4547(19981015)54:2<181::AID-JNR6>3.0.CO;2-A
-
Zhang SC, Lipsitz D, Duncan ID. Selfrenewing canine oligodendroglial progenitor expanded as oligospheres. J Neurosci Res 1998; 54 (2): 181-90. (Pubitemid 28469059)
-
(1998)
Journal of Neuroscience Research
, vol.54
, Issue.2
, pp. 181-190
-
-
Zhang, S.-C.1
Lipsitz, D.2
Duncan, I.D.3
-
28
-
-
0344131931
-
Intraventricular transplantation of oligodendrocyte progenitors into a fetal myelin mutant results in widespread formation of myelin
-
DOI 10.1002/1531-8249(199911)46:5<716::AID-ANA6>3.0.CO;2-M
-
Learish RD, Brustle O, Zhang SC, Duncan ID. Intraventricular transplantation of oligodendrocyte progenitors into a fetal myelin mutant results in widespread formation of myelin. Ann Neurol 1999; 46 (5): 716-22. (Pubitemid 29518132)
-
(1999)
Annals of Neurology
, vol.46
, Issue.5
, pp. 716-722
-
-
Learish, R.D.1
Brustle, O.2
Zhang, S.-C.3
Duncan, I.D.4
|