-
1
-
-
84893649256
-
State of play in amyotrophic lateral sclerosis genetics
-
Renton AE, Chiò A, Traynor BJ (2014) State of play in amyotrophic lateral sclerosis genetics. Nat Neurosci 17(1):17-23.
-
(2014)
Nat Neurosci
, vol.17
, Issue.1
, pp. 17-23
-
-
Renton, A.E.1
Chiò, A.2
Traynor, B.J.3
-
2
-
-
2142655789
-
Regulation of ganglioside biosynthesis in the nervous system
-
Yu RK, Bieberich E, Xia T, Zeng G (2004) Regulation of ganglioside biosynthesis in the nervous system. J Lipid Res 45(5):783-793.
-
(2004)
J Lipid Res
, vol.45
, Issue.5
, pp. 783-793
-
-
Yu, R.K.1
Bieberich, E.2
Xia, T.3
Zeng, G.4
-
3
-
-
84875418118
-
Neuronal expression of glucosylceramide synthase in central nervous system regulates body weight and energy homeostasis
-
Nordström V, et al. (2013) Neuronal expression of glucosylceramide synthase in central nervous system regulates body weight and energy homeostasis. PLoS Biol 11(3):e1001506.
-
(2013)
PLoS Biol
, vol.11
, Issue.3
-
-
Nordström, V.1
-
4
-
-
34248228704
-
Inhibiting glycosphingolipid synthesis improves glycemic control and insulin sensitivity in animal models of type 2 diabetes
-
Zhao H, et al. (2007) Inhibiting glycosphingolipid synthesis improves glycemic control and insulin sensitivity in animal models of type 2 diabetes. Diabetes 56(5):1210-1218.
-
(2007)
Diabetes
, vol.56
, Issue.5
, pp. 1210-1218
-
-
Zhao, H.1
-
5
-
-
67650088127
-
Neurotrophic and neuroprotective actions of an enhancer of ganglioside biosynthesis
-
Inokuchi J (2009) Neurotrophic and neuroprotective actions of an enhancer of ganglioside biosynthesis. Int Rev Neurobiol 85:319-336.
-
(2009)
Int Rev Neurobiol
, vol.85
, pp. 319-336
-
-
Inokuchi, J.1
-
6
-
-
0028322086
-
Differentiation of oligodendrocytes cultured from developing rat brain is enhanced by exogenous GM3 ganglioside
-
Yim SH, Farrer RG, Hammer JA, Yavin E, Quarles RH (1994) Differentiation of oligodendrocytes cultured from developing rat brain is enhanced by exogenous GM3 ganglioside. J Neurosci Res 38(3):268-281.
-
(1994)
J Neurosci Res
, vol.38
, Issue.3
, pp. 268-281
-
-
Yim, S.H.1
Farrer, R.G.2
Hammer, J.A.3
Yavin, E.4
Quarles, R.H.5
-
7
-
-
65549146461
-
Ganglioside GM3 and its biological functions
-
Prokazova NV, Samovilova NN, Gracheva EV, Golovanova NK (2009) Ganglioside GM3 and its biological functions. Biochem Biokhim 74(3):235-249.
-
(2009)
Biochem Biokhim
, vol.74
, Issue.3
, pp. 235-249
-
-
Prokazova, N.V.1
Samovilova, N.N.2
Gracheva, E.V.3
Golovanova, N.K.4
-
8
-
-
40849120250
-
The Yin and Yang of lactosylceramide metabolism: Implications in cell function
-
Chatterjee S, Pandey A (2008) The Yin and Yang of lactosylceramide metabolism: Implications in cell function. Biochim Biophys Acta 1780(3):370-382.
-
(2008)
Biochim Biophys Acta
, vol.1780
, Issue.3
, pp. 370-382
-
-
Chatterjee, S.1
Pandey, A.2
-
10
-
-
0021203563
-
Gangliosides of human spinal cord: Aberrant composition of cords from patients with amyotrophic lateral sclerosis
-
Dawson G, Stefansson K (1984) Gangliosides of human spinal cord: Aberrant composition of cords from patients with amyotrophic lateral sclerosis. J Neurosci Res 12(2-3):213-220.
-
(1984)
J Neurosci Res
, vol.12
, Issue.2-3
, pp. 213-220
-
-
Dawson, G.1
Stefansson, K.2
-
11
-
-
0025272484
-
Polyclonal IgM anti-GM1 ganglioside antibody in patients with motor neuron disease and variants
-
Salazar-Grueso EF, Routbort MJ, Martin J, Dawson G, Roos RP (1990) Polyclonal IgM anti-GM1 ganglioside antibody in patients with motor neuron disease and variants. Ann Neurol 27(5):558-563.
-
(1990)
Ann Neurol
, vol.27
, Issue.5
, pp. 558-563
-
-
Salazar-Grueso, E.F.1
Routbort, M.J.2
Martin, J.3
Dawson, G.4
Roos, R.P.5
-
12
-
-
0027467549
-
A characteristic ganglioside antibody pattern in the CSF of patients with amyotrophic lateral sclerosis
-
Stevens A, Weller M, Wiethölter H (1993) A characteristic ganglioside antibody pattern in the CSF of patients with amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry 56(4):361-364.
-
(1993)
J Neurol Neurosurg Psychiatry
, vol.56
, Issue.4
, pp. 361-364
-
-
Stevens, A.1
Weller, M.2
Wiethölter, H.3
-
13
-
-
0021886401
-
Ganglioside patterns in amyotrophic lateral sclerosis brain regions
-
Rapport MM, Donnenfeld H, Brunner W, Hungund B, Bartfeld H (1985) Ganglioside patterns in amyotrophic lateral sclerosis brain regions. Ann Neurol 18(1):60-67.
-
(1985)
Ann Neurol
, vol.18
, Issue.1
, pp. 60-67
-
-
Rapport, M.M.1
Donnenfeld, H.2
Brunner, W.3
Hungund, B.4
Bartfeld, H.5
-
14
-
-
0035093829
-
Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I
-
Dawkins JL, Hulme DJ, Brahmbhatt SB, Auer-Grumbach M, Nicholson GA (2001) Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I. Nat Genet 27(3):309-312.
-
(2001)
Nat Genet
, vol.27
, Issue.3
, pp. 309-312
-
-
Dawkins, J.L.1
Hulme, D.J.2
Brahmbhatt, S.B.3
Auer-Grumbach, M.4
Nicholson, G.A.5
-
15
-
-
84863980515
-
Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASAH1
-
Zhou J, et al. (2012) Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASAH1. Am J Hum Genet 91(1):5-14.
-
(2012)
Am J Hum Genet
, vol.91
, Issue.1
, pp. 5-14
-
-
Zhou, J.1
-
16
-
-
84880305974
-
Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia
-
Boukhris A, et al. (2013) Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia. Am J Hum Genet 93(1):118-123.
-
(2013)
Am J Hum Genet
, vol.93
, Issue.1
, pp. 118-123
-
-
Boukhris, A.1
-
17
-
-
84873707921
-
Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia
-
Martin E, et al. (2013) Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia. Am J Hum Genet 92(2):238-244.
-
(2013)
Am J Hum Genet
, vol.92
, Issue.2
, pp. 238-244
-
-
Martin, E.1
-
18
-
-
0021835619
-
Motor neuron disease and adult hexosaminidase A deficiency in two families: Evidence for multisystem degeneration
-
Mitsumoto H, et al. (1985) Motor neuron disease and adult hexosaminidase A deficiency in two families: Evidence for multisystem degeneration. Ann Neurol 17(4):378-385.
-
(1985)
Ann Neurol
, vol.17
, Issue.4
, pp. 378-385
-
-
Mitsumoto, H.1
-
19
-
-
0020331661
-
Adult GM2 gangliosidosis masquerading as slowly progressive muscular atrophy: Motor neuron disease phenotype
-
Jellinger K, Anzil AP, Seemann D, Bernheimer H (1982) Adult GM2 gangliosidosis masquerading as slowly progressive muscular atrophy: Motor neuron disease phenotype. Clin Neuropathol 1(1):31-44.
-
(1982)
Clin Neuropathol
, vol.1
, Issue.1
, pp. 31-44
-
-
Jellinger, K.1
Anzil, A.P.2
Seemann, D.3
Bernheimer, H.4
-
20
-
-
0021270792
-
Clinical and genetic variations in the syndrome of adult GM2 gangliosidosis resulting from hexosaminidase A deficiency
-
Argov Z, Navon R (1984) Clinical and genetic variations in the syndrome of adult GM2 gangliosidosis resulting from hexosaminidase A deficiency. Ann Neurol 16(1):14-20.
-
(1984)
Ann Neurol
, vol.16
, Issue.1
, pp. 14-20
-
-
Argov, Z.1
Navon, R.2
-
21
-
-
0035194691
-
Disease mechanisms revealed by transcription profiling in SOD1-G93A transgenic mouse spinal cord
-
Olsen MK, et al. (2001) Disease mechanisms revealed by transcription profiling in SOD1-G93A transgenic mouse spinal cord. Ann Neurol 50(6):730-740.
-
(2001)
Ann Neurol
, vol.50
, Issue.6
, pp. 730-740
-
-
Olsen, M.K.1
-
22
-
-
34250656185
-
Toxicity from different SOD1 mutants dysregulates the complement system and the neuronal regenerative response in ALS motor neurons
-
Lobsiger CS, Boillée S, Cleveland DW (2007) Toxicity from different SOD1 mutants dysregulates the complement system and the neuronal regenerative response in ALS motor neurons. Proc Natl Acad Sci USA 104(18):7319-7326.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, Issue.18
, pp. 7319-7326
-
-
Lobsiger, C.S.1
Boillée, S.2
Cleveland, D.W.3
-
23
-
-
82655173728
-
Disease progression in a mouse model of amyotrophic lateral sclerosis: The influence of chronic stress and corticosterone
-
Fidler JA, et al. (2011) Disease progression in a mouse model of amyotrophic lateral sclerosis: The influence of chronic stress and corticosterone. FASEB J 25(12):4369-4377.
-
(2011)
FASEB J
, vol.25
, Issue.12
, pp. 4369-4377
-
-
Fidler, J.A.1
-
24
-
-
0035206768
-
Ganglioside patterns in human spinal cord
-
Vorwerk CK (2001) Ganglioside patterns in human spinal cord. Spinal Cord 39(12):628-632.
-
(2001)
Spinal Cord
, vol.39
, Issue.12
, pp. 628-632
-
-
Vorwerk, C.K.1
-
25
-
-
80051514415
-
Many ceramides
-
Hannun YA, Obeid LM (2011) Many ceramides. J Biol Chem 286(32):27855-27862.
-
(2011)
J Biol Chem
, vol.286
, Issue.32
, pp. 27855-27862
-
-
Hannun, Y.A.1
Obeid, L.M.2
-
26
-
-
84865084107
-
Systemic delivery of a glucosylceramide synthase inhibitor reduces CNS substrates and increases lifespan in a mouse model of type 2 Gaucher disease
-
Cabrera-Salazar MA, et al. (2012) Systemic delivery of a glucosylceramide synthase inhibitor reduces CNS substrates and increases lifespan in a mouse model of type 2 Gaucher disease. PLoS ONE 7(8):e43310.
-
(2012)
PLoS ONE
, vol.7
, Issue.8
-
-
Cabrera-Salazar, M.A.1
-
27
-
-
34249306894
-
A specific and potent inhibitor of glucosylceramide synthase for substrate inhibition therapy of Gaucher disease
-
McEachern KA, et al. (2007) A specific and potent inhibitor of glucosylceramide synthase for substrate inhibition therapy of Gaucher disease. Mol Genet Metab 91(3):259-267.
-
(2007)
Mol Genet Metab
, vol.91
, Issue.3
, pp. 259-267
-
-
McEachern, K.A.1
-
28
-
-
34249861059
-
A missense mutation in the 3-ketodihydrosphingosine reductase FVT1 as candidate causal mutation for bovine spinal muscular atrophy
-
Krebs S, Medugorac I, Röther S, Strässer K, Förster M (2007) A missense mutation in the 3-ketodihydrosphingosine reductase FVT1 as candidate causal mutation for bovine spinal muscular atrophy. Proc Natl Acad Sci USA 104(16):6746-6751.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, Issue.16
, pp. 6746-6751
-
-
Krebs, S.1
Medugorac, I.2
Röther, S.3
Strässer, K.4
Förster, M.5
-
29
-
-
0036789845
-
Evidence that accumulation of ceramides and cholesterol esters mediates oxidative stress-induced death of motor neurons in amyotrophic lateral sclerosis
-
Cutler RG, Pedersen WA, Camandola S, Rothstein JD, Mattson MP (2002) Evidence that accumulation of ceramides and cholesterol esters mediates oxidative stress-induced death of motor neurons in amyotrophic lateral sclerosis. Ann Neurol 52(4):448-457.
-
(2002)
Ann Neurol
, vol.52
, Issue.4
, pp. 448-457
-
-
Cutler, R.G.1
Pedersen, W.A.2
Camandola, S.3
Rothstein, J.D.4
Mattson, M.P.5
-
30
-
-
0031661695
-
Variations among cell lines in the synthesis of sphingolipids in de novo and recycling pathways
-
Gillard BK, Clement RG, Marcus DM (1998) Variations among cell lines in the synthesis of sphingolipids in de novo and recycling pathways. Glycobiology 8(9):885-890.
-
(1998)
Glycobiology
, vol.8
, Issue.9
, pp. 885-890
-
-
Gillard, B.K.1
Clement, R.G.2
Marcus, D.M.3
-
31
-
-
79551690481
-
Phosphatase and tensin homologue/protein kinase B pathway linked to motor neuron survival in human superoxide dismutase 1-related amyotrophic lateral sclerosis
-
Kirby J, et al. (2011) Phosphatase and tensin homologue/protein kinase B pathway linked to motor neuron survival in human superoxide dismutase 1-related amyotrophic lateral sclerosis. Brain 134(Pt 2):506-517.
-
(2011)
Brain
, vol.134
, Issue.2
, pp. 506-517
-
-
Kirby, J.1
-
32
-
-
38449102577
-
Lactosylceramide: A lipid second messenger in neuroinflammatory disease
-
Won JS, Singh AK, Singh I (2007) Lactosylceramide: A lipid second messenger in neuroinflammatory disease. J Neurochem 103(Suppl 1):180-191.
-
(2007)
J Neurochem
, vol.103
, pp. 180-191
-
-
Won, J.S.1
Singh, A.K.2
Singh, I.3
-
33
-
-
84895422067
-
Microglia induce motor neuron death via the classical NF-κB pathway in amyotrophic lateral sclerosis
-
Frakes AE, et al. (2014) Microglia induce motor neuron death via the classical NF-κB pathway in amyotrophic lateral sclerosis. Neuron 81(5):1009-1023.
-
(2014)
Neuron
, vol.81
, Issue.5
, pp. 1009-1023
-
-
Frakes, A.E.1
-
34
-
-
0029891216
-
Cerebrovascular complications of Fabry's disease
-
Mitsias P, Levine SR (1996) Cerebrovascular complications of Fabry's disease. Ann Neurol 40(1):8-17.
-
(1996)
Ann Neurol
, vol.40
, Issue.1
, pp. 8-17
-
-
Mitsias, P.1
Levine, S.R.2
-
35
-
-
41149097086
-
ALS-causing SOD1 mutants generate vascular changes prior to motor neuron degeneration
-
Zhong Z, et al. (2008) ALS-causing SOD1 mutants generate vascular changes prior to motor neuron degeneration. Nat Neurosci 11(4):420-422.
-
(2008)
Nat Neurosci
, vol.11
, Issue.4
, pp. 420-422
-
-
Zhong, Z.1
-
36
-
-
0141997303
-
Globoid cell leukodystrophy (Krabbe's disease): Update
-
Suzuki K (2003) Globoid cell leukodystrophy (Krabbe's disease): Update. J Child Neurol 18(9):595-603.
-
(2003)
J Child Neurol
, vol.18
, Issue.9
, pp. 595-603
-
-
Suzuki, K.1
-
37
-
-
84876900163
-
Degeneration and impaired regeneration of gray matter oligodendrocytes in amyotrophic lateral sclerosis
-
Kang SH, et al. (2013) Degeneration and impaired regeneration of gray matter oligodendrocytes in amyotrophic lateral sclerosis. Nat Neurosci 16(5):571-579.
-
(2013)
Nat Neurosci
, vol.16
, Issue.5
, pp. 571-579
-
-
Kang, S.H.1
-
38
-
-
0038491333
-
Ganglioside GM3 inhibits matrix metalloproteinase-9 activation and disrupts its association with integrin
-
Wang XQ, Sun P, Paller AS (2003) Ganglioside GM3 inhibits matrix metalloproteinase-9 activation and disrupts its association with integrin. J Biol Chem 278(28):25591-25599.
-
(2003)
J Biol Chem
, vol.278
, Issue.28
, pp. 25591-25599
-
-
Wang, X.Q.1
Sun, P.2
Paller, A.S.3
-
39
-
-
84892919280
-
Neuronal matrix metalloproteinase-9 is a determinant of selective neurodegeneration
-
Kaplan A, et al. (2014) Neuronal matrix metalloproteinase-9 is a determinant of selective neurodegeneration. Neuron 81(2):333-348.
-
(2014)
Neuron
, vol.81
, Issue.2
, pp. 333-348
-
-
Kaplan, A.1
-
40
-
-
80052783545
-
Astrocytes from familial and sporadic ALS patients are toxic to motor neurons
-
Haidet-Phillips AM, et al. (2011) Astrocytes from familial and sporadic ALS patients are toxic to motor neurons. Nat Biotechnol 29(9):824-828.
-
(2011)
Nat Biotechnol
, vol.29
, Issue.9
, pp. 824-828
-
-
Haidet-Phillips, A.M.1
-
41
-
-
84895508213
-
Necroptosis drives motor neuron death in models of both sporadic and familial ALS
-
Re DB, et al. (2014) Necroptosis drives motor neuron death in models of both sporadic and familial ALS. Neuron 81(5):1001-1008.
-
(2014)
Neuron
, vol.81
, Issue.5
, pp. 1001-1008
-
-
Re, D.B.1
-
42
-
-
84902191691
-
Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1
-
Kiskinis E, et al. (2014) Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1. Cell Stem Cell 14(6):781-795.
-
(2014)
Cell Stem Cell
, vol.14
, Issue.6
, pp. 781-795
-
-
Kiskinis, E.1
-
43
-
-
0033594918
-
Mice lacking complex gangliosides develop Wallerian degeneration and myelination defects
-
Sheikh KA, et al. (1999) Mice lacking complex gangliosides develop Wallerian degeneration and myelination defects. Proc Natl Acad Sci USA 96(13):7532-7537.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, Issue.13
, pp. 7532-7537
-
-
Sheikh, K.A.1
-
44
-
-
79851474972
-
Gangliosides are essential in the protection of inflammation and neurodegeneration via maintenance of lipid rafts: Elucidation by a series of ganglioside-deficient mutant mice
-
Ohmi Y, et al. (2011) Gangliosides are essential in the protection of inflammation and neurodegeneration via maintenance of lipid rafts: Elucidation by a series of ganglioside-deficient mutant mice. J Neurochem 116(5):926-935.
-
(2011)
J Neurochem
, vol.116
, Issue.5
, pp. 926-935
-
-
Ohmi, Y.1
-
45
-
-
26844440360
-
Novel role of lactosylceramide in vascular endothelial growth factor-mediated angiogenesis in human endothelial cells
-
Rajesh M, Kolmakova A, Chatterjee S (2005) Novel role of lactosylceramide in vascular endothelial growth factor-mediated angiogenesis in human endothelial cells. Circ Res 97(8):796-804.
-
(2005)
Circ Res
, vol.97
, Issue.8
, pp. 796-804
-
-
Rajesh, M.1
Kolmakova, A.2
Chatterjee, S.3
-
46
-
-
0036839943
-
Hereditary sensory neuropathy type 1 mutations confer dominant negative effects on serine palmitoyltransferase, critical for sphingolipid synthesis
-
Bejaoui K, et al. (2002) Hereditary sensory neuropathy type 1 mutations confer dominant negative effects on serine palmitoyltransferase, critical for sphingolipid synthesis. J Clin Invest 110(9):1301-1308.
-
(2002)
J Clin Invest
, vol.110
, Issue.9
, pp. 1301-1308
-
-
Bejaoui, K.1
-
47
-
-
0015498606
-
Ceramidase deficiency in Farber's disease (lipogranulomatosis)
-
Sugita M, Dulaney JT, Moser HW (1972) Ceramidase deficiency in Farber's disease (lipogranulomatosis). Science 178(4065):1100-1102.
-
(1972)
Science
, vol.178
, Issue.4065
, pp. 1100-1102
-
-
Sugita, M.1
Dulaney, J.T.2
Moser, H.W.3
-
48
-
-
80052928827
-
Dysregulation of astrocyte-motoneuron cross-talk in mutant superoxide dismutase 1-related amyotrophic lateral sclerosis
-
Ferraiuolo L, et al. (2011) Dysregulation of astrocyte-motoneuron cross-talk in mutant superoxide dismutase 1-related amyotrophic lateral sclerosis. Brain 134(Pt 9):2627-2641.
-
(2011)
Brain
, vol.134
, Issue.9
, pp. 2627-2641
-
-
Ferraiuolo, L.1
-
49
-
-
4143153013
-
Drosophila glucosylceramide synthase: A negative regulator of cell death mediated by proapoptotic factors
-
Kohyama-Koganeya A, et al. (2004) Drosophila glucosylceramide synthase: A negative regulator of cell death mediated by proapoptotic factors. J Biol Chem 279(34):35995-36002.
-
(2004)
J Biol Chem
, vol.279
, Issue.34
, pp. 35995-36002
-
-
Kohyama-Koganeya, A.1
-
50
-
-
84879528008
-
Metabolic signatures of amyotrophic lateral sclerosis reveal insights into disease pathogenesis
-
Dodge JC, et al. (2013) Metabolic signatures of amyotrophic lateral sclerosis reveal insights into disease pathogenesis. Proc Natl Acad Sci USA 110(26):10812-10817.
-
(2013)
Proc Natl Acad Sci USA
, vol.110
, Issue.26
, pp. 10812-10817
-
-
Dodge, J.C.1
|