-
1
-
-
38349006201
-
Polyunsaturated fatty acids induce alpha-synuclein-related pathogenic changes in neuronal cells
-
Assayag, K., Yakunin, E., Loeb, V., Selkoe, D. J. and Sharon, R. (2007). Polyunsaturated fatty acids induce alpha-synuclein-related pathogenic changes in neuronal cells. Am. J. Pathol. 171, 2000-2011.
-
(2007)
Am. J. Pathol.
, vol.171
, pp. 2000-2011
-
-
Assayag, K.1
Yakunin, E.2
Loeb, V.3
Selkoe, D.J.4
Sharon, R.5
-
2
-
-
0030226044
-
Genetic analysis of the lozenge gene complex in drosophila melanogaster: Adult visual system phenotypes
-
Batterham, P., and Crew, J. R., Sokac, A. M., Andrews, J. R., Pasquini, G. M. F., Davies, A. G., Stocker, R. F. and Pollock, J. A. (1996). Genetic analysis of the lozenge gene complex in Drosophila melanogaster: adult visual system phenotypes. J. Neurogenet. 10, 193-220.
-
(1996)
J. Neurogenet.
, vol.10
, pp. 193-220
-
-
Batterham, P.1
Crew, J.R.2
Sokac, A.M.3
Andrews, J.R.4
Pasquini, G.M.F.5
Davies, A.G.6
Stocker, R.F.7
Pollock, J.A.8
-
3
-
-
20444504698
-
The genetic epidemiology of neurodegenerative disease
-
Bertram, L. and Tanzi, R. E. (2005). The genetic epidemiology of neurodegenerative disease. J. Clin. Invest. 115, 1449-1457.
-
(2005)
J. Clin. Invest.
, vol.115
, pp. 1449-1457
-
-
Bertram, L.1
Tanzi, R.E.2
-
4
-
-
45749083772
-
De novo CoA biosynthesis is required to maintain DNA integrity during development of the drosophila nervous system
-
Bosveld, F., Rana, A., van der Wouden, P. E., Lemstra, W., Ritsema, M., Kampinga, H. H. and Sibon, O. C. M. (2008). De novo CoA biosynthesis is required to maintain DNA integrity during development of the Drosophila nervous system. Hum. Mol. Genet. 17, 2058-2069.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 2058-2069
-
-
Bosveld, F.1
Rana, A.2
Van Der Wouden, P.E.3
Lemstra, W.4
Ritsema, M.5
Kampinga, H.H.6
Sibon, O.C.M.7
-
5
-
-
0024377179
-
The emergence of order in the drosophila pupal retina
-
Cagan, R. L. and Ready, D. F. (1989). The emergence of order in the Drosophila pupal retina. Dev. Biol. 136, 346-362.
-
(1989)
Dev. Biol.
, vol.136
, pp. 346-362
-
-
Cagan, R.L.1
Ready, D.F.2
-
6
-
-
0027445946
-
The strawberry notch gene functions with notch in common developmental pathways
-
Coyle-Thompson, C. A. and Banerjee, U. (1993). The strawberry notch gene functions with Notch in common developmental pathways. Development 119, 377-395.
-
(1993)
Development
, vol.119
, pp. 377-395
-
-
Coyle-Thompson, C.A.1
Banerjee, U.2
-
7
-
-
84864603834
-
Drosophila fatty acid transport protein regulates rhodopsin-1 metabolism and is required for photoreceptor neuron survival
-
Dourlen, P., Bertin, B., Chatelain, G., Robin, M., Napoletano, F., Roux, M. J. and Mollereau, B. (2012). Drosophila fatty acid transport protein regulates rhodopsin-1 metabolism and is required for photoreceptor neuron survival. PLoS Genet. 8, e1002833.
-
(2012)
PLoS Genet.
, vol.8
-
-
Dourlen, P.1
Bertin, B.2
Chatelain, G.3
Robin, M.4
Napoletano, F.5
Roux, M.J.6
Mollereau, B.7
-
8
-
-
84944755190
-
Fatty acid transport proteins in disease: New insights from invertebrate models
-
Dourlen, P., Sujkowski, A., Wessells, R. and Mollereau, B. (2015). Fatty acid transport proteins in disease: new insights from invertebrate models. Prog. Lipid Res. 60, 30-40.
-
(2015)
Prog. Lipid Res.
, vol.60
, pp. 30-40
-
-
Dourlen, P.1
Sujkowski, A.2
Wessells, R.3
Mollereau, B.4
-
9
-
-
16344362289
-
Adrenal insufficiency in asymptomatic adrenoleukodystrophy patients identified by very long-chain fatty acid screening
-
Dubey, P., and Raymond, G. V., Moser, A. B., Kharkar, S., Bezman, L. and Moser, H. W. (2005). Adrenal insufficiency in asymptomatic adrenoleukodystrophy patients identified by very long-chain fatty acid screening. J. Pediatr. 146, 528-532.
-
(2005)
J. Pediatr.
, vol.146
, pp. 528-532
-
-
Dubey, P.1
Raymond, G.V.2
Moser, A.B.3
Kharkar, S.4
Bezman, L.5
Moser, H.W.6
-
10
-
-
84961761070
-
Glial expression of swiss cheese (SWS), the drosophila orthologue of neuropathy target esterase (NTE), is required for neuronal ensheathment and function
-
Dutta, S., Rieche, F., Eckl, N., Duch, C. and Kretzschmar, D. (2016). Glial expression of Swiss cheese (SWS), the Drosophila orthologue of neuropathy target esterase (NTE), is required for neuronal ensheathment and function. Dis. Model. Mech. 9, 283-294.
-
(2016)
Dis. Model. Mech.
, vol.9
, pp. 283-294
-
-
Dutta, S.1
Rieche, F.2
Eckl, N.3
Duch, C.4
Kretzschmar, D.5
-
11
-
-
0034704752
-
A drosophila model of Parkinson's disease
-
Feany, M. B. and Bender, W. W. (2000). A Drosophila model of Parkinson's disease. Nature 404, 394-398.
-
(2000)
Nature
, vol.404
, pp. 394-398
-
-
Feany, M.B.1
Bender, W.W.2
-
12
-
-
0034523144
-
Apoptosis in the central nervous system of cerebral adrenoleukodystrophy patients
-
Feigenbaum, V., Gelot, A., Casanova, P., Daumas-Duport, C., Aubourg, P. and Dubois-Dalcq, M. (2000). Apoptosis in the central nervous system of cerebral adrenoleukodystrophy patients. Neurobiol. Dis. 7, 600-612.
-
(2000)
Neurobiol. Dis.
, vol.7
, pp. 600-612
-
-
Feigenbaum, V.1
Gelot, A.2
Casanova, P.3
Daumas-Duport, C.4
Aubourg, P.5
Dubois-Dalcq, M.6
-
13
-
-
33947200308
-
Phosphatidylcholine synthesis and its catabolism by yeast neuropathy target esterase 1
-
Fernandez-Murray, J. P. and McMaster, C. R. (2007). Phosphatidylcholine synthesis and its catabolism by yeast neuropathy target esterase 1. Biochim. Biophys. Acta 1771, 331-336.
-
(2007)
Biochim. Biophys. Acta
, vol.1771
, pp. 331-336
-
-
Fernandez-Murray, J.P.1
McMaster, C.R.2
-
14
-
-
0030689779
-
Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice
-
Forss-Petter, S., Werner, H., Berger, J., Lassmann, H., Molzer, B., and Schwab, M. H., Bernheimer, H., Zimmermann, F. and Nave, K.-A. (1997). Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice. J. Neurosci. Res. 50, 829-843.
-
(1997)
J. Neurosci. Res.
, vol.50
, pp. 829-843
-
-
Forss-Petter, S.1
Werner, H.2
Berger, J.3
Lassmann, H.4
Molzer, B.5
Schwab, M.H.6
Bernheimer, H.7
Zimmermann, F.8
Nave, K.-A.9
-
15
-
-
24344508083
-
Neuropathy target esterase and phospholipid deacylation
-
Glynn, P. (2005). Neuropathy target esterase and phospholipid deacylation. Biochim. Biophys. Acta 1736, 87-93.
-
(2005)
Biochim. Biophys. Acta
, vol.1736
, pp. 87-93
-
-
Glynn, P.1
-
16
-
-
0037418177
-
Ends-out, or replacement, gene targeting in drosophila
-
Gong, W. J. and Golic, K. G. (2003). Ends-out, or replacement, gene targeting in Drosophila. Proc. Natl. Acad. Sci. USA 100, 2556-2561.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 2556-2561
-
-
Gong, W.J.1
Golic, K.G.2
-
17
-
-
84928534730
-
The leukodystrophies
-
Gordon, H. B., Letsou, A. and Bonkowsky, J. L. (2014). The leukodystrophies. Semin. Neurol. 34, 312-320.
-
(2014)
Semin. Neurol.
, vol.34
, pp. 312-320
-
-
Gordon, H.B.1
Letsou, A.2
Bonkowsky, J.L.3
-
18
-
-
5444246172
-
Am not I afly like thee? From genes in fruit flies to behavior in humans
-
Greenspan, R. J. and Dierick, H. A. (2004). 'Am not I afly like thee?' From genes in fruit flies to behavior in humans. Hum. Mol. Genet. 13 Suppl. 2, R267-R273.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. R267-R273
-
-
Greenspan, R.J.1
Dierick, H.A.2
-
19
-
-
0022551325
-
Lignoceroyl-coash ligase: Enzyme defect in fatty acid beta-oxidation system in X-linked childhood adrenoleukodystrophy
-
Hashmi, M., Stanley, W. and Singh, I. (1986). Lignoceroyl-CoASH ligase: enzyme defect in fatty acid beta-oxidation system in X-linked childhood adrenoleukodystrophy. FEBS Lett. 196, 247-250.
-
(1986)
FEBS Lett.
, vol.196
, pp. 247-250
-
-
Hashmi, M.1
Stanley, W.2
Singh, I.3
-
20
-
-
44849118490
-
Toxic effects of X-linked adrenoleukodystrophy-associated, very long chain fatty acids on glial cells and neurons from rat hippocampus in culture
-
Hein, S., Schonfeld, P., Kahlert, S. and Reiser, G. (2008). Toxic effects of X-linked adrenoleukodystrophy-associated, very long chain fatty acids on glial cells and neurons from rat hippocampus in culture. Hum. Mol. Genet. 17, 1750-1761.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 1750-1761
-
-
Hein, S.1
Schonfeld, P.2
Kahlert, S.3
Reiser, G.4
-
21
-
-
0038778368
-
A very long-chain acyl-coa synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy
-
Heinzer, A. K., and Watkins, P. A., Lu, J.-F., Kemp, S., and Moser, A. B., Li, Y. Y., Mihalik, S., Powers, J. M. and Smith, K. D. (2003). A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy. Hum. Mol. Genet. 12, 1145-1154.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 1145-1154
-
-
Heinzer, A.K.1
Watkins, P.A.2
Lu, J.-F.3
Kemp, S.4
Moser, A.B.5
Li, Y.Y.6
Mihalik, S.7
Powers, J.M.8
Smith, K.D.9
-
22
-
-
36148978574
-
Drosophila niemann-pick type C-2 genes control sterol homeostasis and steroid biosynthesis: A model of human neurodegenerative disease
-
Huang, X., and Warren, J. T., Buchanan, J., Gilbert, L. I. and Scott, M. P. (2007). Drosophila Niemann-Pick type C-2 genes control sterol homeostasis and steroid biosynthesis: a model of human neurodegenerative disease. Development 134, 3733-3742.
-
(2007)
Development
, vol.134
, pp. 3733-3742
-
-
Huang, X.1
Warren, J.T.2
Buchanan, J.3
Gilbert, L.I.4
Scott, M.P.5
-
23
-
-
0017265264
-
Fatty acid abnormality in adrenoleukodystrophy
-
Igarashi, M., and Schaumburg, H. H., Powers, J., Kishimoto, Y., Koilodny, E. and Suzuki, K. (1976). Fatty acid abnormality in adrenoleukodystrophy. J. Neurochem. 26, 851-860.
-
(1976)
J. Neurochem.
, vol.26
, pp. 851-860
-
-
Igarashi, M.1
Schaumburg, H.H.2
Powers, J.3
Kishimoto, Y.4
Koilodny, E.5
Suzuki, K.6
-
24
-
-
0034810289
-
Potential environmental and host participants in the early white matter lesion of adreno-leukodystrophy: Morphologic evidence for CD8 cytotoxic T cells, cytolysis of oligodendrocytes, and CD1-mediated lipid antigen presentation
-
Ito, M., and Blumberg, B. M., Mock, D. J., Goodman, A. D., and Moser, A. B., Moser, H. W., Smith, K. D. and Powers, J. M. (2001). Potential environmental and host participants in the early white matter lesion of adreno-leukodystrophy: morphologic evidence for CD8 cytotoxic T cells, cytolysis of oligodendrocytes, and CD1-mediated lipid antigen presentation. J. Neuropathol. Exp. Neurol. 60 1004-1019.
-
(2001)
J. Neuropathol. Exp. Neurol.
, vol.60
, pp. 1004-1019
-
-
Ito, M.1
Blumberg, B.M.2
Mock, D.J.3
Goodman, A.D.4
Moser, A.B.5
Moser, H.W.6
Smith, K.D.7
Powers, J.M.8
-
25
-
-
12844267552
-
Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophy
-
Kemp, S., Valianpour, F., Denis, S., Ofman, R., Sanders, R.-J., Mooyer, P., Barth, P. G. and Wanders, R. J. A. (2005). Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophy. Mol. Genet. Metab. 84 144-151.
-
(2005)
Mol. Genet. Metab.
, vol.84
, pp. 144-151
-
-
Kemp, S.1
Valianpour, F.2
Denis, S.3
Ofman, R.4
Sanders, R.-J.5
Mooyer, P.6
Barth, P.G.7
Wanders, R.J.A.8
-
26
-
-
84870592909
-
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences
-
Labate, A., Tarantino, P., Viri, M., Mumoli, L., Gagliardi, M., Romeo, A., Zara, F., Annesi, G. and Gambardella, A. (2012). Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences. Epilepsia 53, e196-e199.
-
(2012)
Epilepsia
, vol.53
, pp. e196-e199
-
-
Labate, A.1
Tarantino, P.2
Viri, M.3
Mumoli, L.4
Gagliardi, M.5
Romeo, A.6
Zara, F.7
Annesi, G.8
Gambardella, A.9
-
27
-
-
0001112876
-
Peroxisomal lignoceroyl-coa ligase deficiency in childhood adrenoleukodystrophy and adrenomyeloneuropathy
-
Lazo, O., Contreras, M., Hashmi, M., Stanley, W., Irazu, C. and Singh, I. (1988). Peroxisomal lignoceroyl-CoA ligase deficiency in childhood adrenoleukodystrophy and adrenomyeloneuropathy. Proc. Natl. Acad. Sci. USA 85, 7647-7651.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 7647-7651
-
-
Lazo, O.1
Contreras, M.2
Hashmi, M.3
Stanley, W.4
Irazu, C.5
Singh, I.6
-
28
-
-
84920995154
-
Glial lipid droplets and ROS induced by mitochondrial defects promote neurodegeneration
-
Liu, L., Zhang, K., Sandoval, H., Yamamoto, S., Jaiswal, M., Sanz, E., Li, Z., Hui, J., Graham, B. H., Quintana, A. et al. (2015). Glial lipid droplets and ROS induced by mitochondrial defects promote neurodegeneration. Cell 160, 177-190.
-
(2015)
Cell
, vol.160
, pp. 177-190
-
-
Liu, L.1
Zhang, K.2
Sandoval, H.3
Yamamoto, S.4
Jaiswal, M.5
Sanz, E.6
Li, Z.7
Hui, J.8
Graham, B.H.9
Quintana, A.10
-
29
-
-
0030793307
-
A mouse model for X-linked adrenoleukodystrophy
-
Lu, J.-F., Lawler, A. M., and Watkins, P. A., Powers, J. M., Moser, A. B., Moser, H. W. and Smith, K. D. (1997). A mouse model for X-linked adrenoleukodystrophy. Proc. Natl. Acad. Sci. USA 94, 9366-9371.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, 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
-
30
-
-
68849116829
-
Arabidopsis CER8 encodes LONG-CHAIN ACYL-COA SYNTHETASE 1 (LACS1) that has overlapping functions with LACS2 in plant wax and cutin synthesis
-
Lu, S., Song, T., Kosma, D. K., and Parsons, E. P., Rowland, O. and Jenks, M. A. (2009). Arabidopsis CER8 encodes LONG-CHAIN ACYL-COA SYNTHETASE 1 (LACS1) that has overlapping functions with LACS2 in plant wax and cutin synthesis. Plant J. 59, 553-564.
-
(2009)
Plant J.
, vol.59
, pp. 553-564
-
-
Lu, S.1
Song, T.2
Kosma, D.K.3
Parsons, E.P.4
Rowland, O.5
Jenks, M.A.6
-
31
-
-
80052301114
-
A drosophila model for the zellweger spectrum of peroxisome biogenesis disorders
-
Mast, F. D., Li, J., Virk, M. K., Hughes, S. C, Simmonds, A. J. and Rachubinski, R. A. (2011). A Drosophila model for the Zellweger spectrum of peroxisome biogenesis disorders. Dis. Model. Mech. 4, 659-672.
-
(2011)
Dis. Model. Mech.
, vol.4
, pp. 659-672
-
-
Mast, F.D.1
Li, J.2
Virk, M.K.3
Hughes, S.C.4
Simmonds, A.J.5
Rachubinski, R.A.6
-
32
-
-
0033581027
-
Preventing neurodegeneration in the drosophila mutant bubblegum [see comments]
-
Min, K.-T. and Benzer, S. (1999). Preventing neurodegeneration in the Drosophila mutant bubblegum [see comments]. Science 284, 1985-1988.
-
(1999)
Science
, vol.284
, pp. 1985-1988
-
-
Min, K.-T.1
Benzer, S.2
-
33
-
-
0030860131
-
Adrenoleukodystrophy: Phenotype, genetics, pathogenesis and therapy
-
Moser, H. W. (1997). Adrenoleukodystrophy: phenotype, genetics, pathogenesis and therapy. Brain 120, 1485-1508.
-
(1997)
Brain
, vol.120
, pp. 1485-1508
-
-
Moser, H.W.1
-
34
-
-
0018973786
-
Adrenoleukodystrophy: Elevated C26 fatty acid in cultured skin fibroblasts
-
Moser, H. W., and Moser, A. B., Kawamura, N., Murphy, J., Suzuki, K., Schaumburg, H. and Kishimoto, Y. (1980). Adrenoleukodystrophy: elevated C26 fatty acid in cultured skin fibroblasts. Ann. Neurol. 7, 542-549.
-
(1980)
Ann. Neurol.
, vol.7
, pp. 542-549
-
-
Moser, H.W.1
Moser, A.B.2
Kawamura, N.3
Murphy, J.4
Suzuki, K.5
Schaumburg, H.6
Kishimoto, Y.7
-
35
-
-
0032932397
-
Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls
-
Moser, A. B., Kreiter, N., Bezman, L., Lu, S.-E., and Raymond, G. V., Naidu, S. and Moser, H. W. (1999). Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls. Ann. Neurol. 45, 100-110.
-
(1999)
Ann. Neurol.
, vol.45
, pp. 100-110
-
-
Moser, A.B.1
Kreiter, N.2
Bezman, L.3
Lu, S.-E.4
Raymond, G.V.5
Naidu, S.6
Moser, H.W.7
-
36
-
-
29544446329
-
Adrenoleukodystrophy: New approaches to a neurodegenerative disease
-
Moser, H. W., Raymond, G. V. and Dubey, P. (2005). Adrenoleukodystrophy: new approaches to a neurodegenerative disease. JAMA 294, 3131-3134.
-
(2005)
JAMA
, vol.294
, pp. 3131-3134
-
-
Moser, H.W.1
Raymond, G.V.2
Dubey, P.3
-
37
-
-
35348876033
-
Lorenzo's oil therapy for X-linked adrenoleukodystrophy: Rationale and current assessment of efficacy
-
Moser, H. W., and Moser, A. B., Hollandsworth, K., Brereton, N. H. and Raymond, G. V. (2007). "Lorenzo's oil" therapy for X-linked adrenoleukodystrophy: rationale and current assessment of efficacy. J. Mol. Neurosci. 33, 105-113.
-
(2007)
J. Mol. Neurosci.
, vol.33
, pp. 105-113
-
-
Moser, H.W.1
Moser, A.B.2
Hollandsworth, K.3
Brereton, N.H.4
Raymond, G.V.5
-
38
-
-
0027532282
-
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
-
Mosser, J., Douar, A.-M., Sarde, C.-O., Kioschis, P., Feil, R., Moser, H., Poustka, A.-M., Mandel, J.-L. and Aubourg, P. (1993). Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters. Nature 361, 726-730.
-
(1993)
Nature
, vol.361
, pp. 726-730
-
-
Mosser, J.1
Douar, A.-M.2
Sarde, C.-O.3
Kioschis, P.4
Feil, R.5
Moser, H.6
Poustka, A.-M.7
Mandel, J.-L.8
Aubourg, P.9
-
39
-
-
15244351250
-
Loss of swiss cheese/neuropathy target esterase activity causes disruption of phosphatidylcholine homeostasis and neuronal and glial death in adult drosophila
-
Muhlig-Versen, M., da Cruz, A. B., Tschape, J.-A., Moser, M., Buttner, R., Athenstaedt, K., Glynn, P. and Kretzschmar, D. (2005). Loss of Swiss cheese/neuropathy target esterase activity causes disruption of phosphatidylcholine homeostasis and neuronal and glial death in adult Drosophila. J. Neurosci. 25, 2865-2873.
-
(2005)
J. Neurosci.
, vol.25
, pp. 2865-2873
-
-
Muhlig-Versen, M.1
Da Cruz, A.B.2
Tschape, J.-A.3
Moser, M.4
Buttner, R.5
Athenstaedt, K.6
Glynn, P.7
Kretzschmar, D.8
-
40
-
-
79961096053
-
Drosophila carrying pex3 or pex16 mutations are models of zellweger syndrome that reflect its symptoms associated with the absence of peroxisomes
-
Nakayama, M., Sato, H., Okuda, T., Fujisawa, N., Kono, N., Arai, H., Suzuki, E., Umeda, M., Ishikawa, H. O. and Matsuno, K. (2011). Drosophila carrying pex3 or pex16 mutations are models of Zellweger syndrome that reflect its symptoms associated with the absence of peroxisomes. PLoS ONE 6, e22984.
-
(2011)
PLoS ONE
, vol.6
-
-
Nakayama, M.1
Sato, H.2
Okuda, T.3
Fujisawa, N.4
Kono, N.5
Arai, H.6
Suzuki, E.7
Umeda, M.8
Ishikawa, H.O.9
Matsuno, K.10
-
41
-
-
78149433845
-
Myelination and support of axonal integrity by glia
-
Nave, K.-A. (2010). Myelination and support of axonal integrity by glia. Nature 468, 244-252.
-
(2010)
Nature
, vol.468
, pp. 244-252
-
-
Nave, K.-A.1
-
42
-
-
0036021395
-
Temperature-sensitive paralytic mutants are enriched for those causing neurodegeneration in drosophila
-
Palladino, M. J., Hadley, T. J. and Ganetzky, B. (2002). Temperature-sensitive paralytic mutants are enriched for those causing neurodegeneration in Drosophila. Genetics 161, 1197-1208.
-
(2002)
Genetics
, vol.161
, pp. 1197-1208
-
-
Palladino, M.J.1
Hadley, T.J.2
Ganetzky, B.3
-
43
-
-
0037075580
-
Crumbs, the drosophila homologue of human CRB1/RP12, is essential for photoreceptor morphogenesis
-
Pellikka, M., Tanentzapf, G., Pinto, M., Smith, C, and McGlade, C. J., Ready, D. F. and Tepass, U. (2002). Crumbs, the Drosophila homologue of human CRB1/RP12, is essential for photoreceptor morphogenesis. Nature 416, 143-149.
-
(2002)
Nature
, vol.416
, pp. 143-149
-
-
Pellikka, M.1
Tanentzapf, G.2
Pinto, M.3
Smith, C.4
McGlade, C.J.5
Ready, D.F.6
Tepass, U.7
-
44
-
-
48549102737
-
Neuronal loss of drosophila NPC1a causes cholesterol aggregation and age-progressive neurodegeneration
-
Phillips, S. E., and Woodruff, E. A., III, Liang, P., Patten, M. and Broadie, K. (2008). Neuronal loss of Drosophila NPC1a causes cholesterol aggregation and age-progressive neurodegeneration. J. Neurosci. 28, 6569-6582.
-
(2008)
J. Neurosci.
, vol.28
, pp. 6569-6582
-
-
Phillips, S.E.1
Woodruff, E.A.2
Liang, P.3
Patten, M.4
Broadie, K.5
-
45
-
-
0019431106
-
The testis in adreno-leukodystrophy
-
Powers, J. M. and Schaumburg, H. H. (1981). The testis in adreno-leukodystrophy. Am. J. Pathol. 102, 90-98.
-
(1981)
Am. J. Pathol.
, vol.102
, pp. 90-98
-
-
Powers, J.M.1
Schaumburg, H.H.2
-
46
-
-
0026469051
-
The inflammatory myelinopathy of adreno-leukodystrophy: Cells, effector molecules, and pathogenetic implications
-
Powers, J. M., Liu, Y., Moser, A. B. and Moser, H. W. (1992). The inflammatory myelinopathy of adreno-leukodystrophy: cells, effector molecules, and pathogenetic implications. J. Neuropathol. Exp. Neurol. 51, 630-643.
-
(1992)
J. Neuropathol. Exp. Neurol.
, vol.51
, pp. 630-643
-
-
Powers, J.M.1
Liu, Y.2
Moser, A.B.3
Moser, H.W.4
-
47
-
-
33644793371
-
Adreno-leukodystrophy: Oxidative stress of mice and men
-
Powers, J. M., Pei, Z., Heinzer, A. K., Deering, R., and Moser, A. B., Moser, H. W., Watkins, P. A. and Smith, K. D. (2005). Adreno-leukodystrophy: oxidative stress of mice and men. J. Neuropathol. Exp. Neurol. 64, 1067-1079.
-
(2005)
J. Neuropathol. Exp. Neurol.
, vol.64
, pp. 1067-1079
-
-
Powers, J.M.1
Pei, Z.2
Heinzer, A.K.3
Deering, R.4
Moser, A.B.5
Moser, H.W.6
Watkins, P.A.7
Smith, K.D.8
-
48
-
-
41149133870
-
Neuropathy target esterase gene mutations cause motor neuron disease
-
Rainier, S., Bui, M., Mark, E., Thomas, D., Tokarz, D., Ming, L., Delaney, C., and Richardson, R. J., Albers, J. W., Matsunami, N. et al. (2008). Neuropathy target esterase gene mutations cause motor neuron disease. Am. J. Hum. Genet. 82, 780-785.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 780-785
-
-
Rainier, S.1
Bui, M.2
Mark, E.3
Thomas, D.4
Tokarz, D.5
Ming, L.6
Delaney, C.7
Richardson, R.J.8
Albers, J.W.9
Matsunami, N.10
-
49
-
-
74849096077
-
Head trauma can initiate the onset of adreno-leukodystrophy
-
Raymond, G. V., Seidman, R., Monteith, T. S., Kolodny, E., Sathe, S., Mahmood, A. and Powers, J. M. (2010). Head trauma can initiate the onset of adreno-leukodystrophy. J. Neurol. Sci. 290, 70-74.
-
(2010)
J. Neurol. Sci.
, vol.290
, pp. 70-74
-
-
Raymond, G.V.1
Seidman, R.2
Monteith, T.S.3
Kolodny, E.4
Sathe, S.5
Mahmood, A.6
Powers, J.M.7
-
50
-
-
70349113908
-
Neuropathy target esterase is required for adult vertebrate axon maintenance
-
Read, D. J., Li, Y., Chao, M. V., Cavanagh, J. B. and Glynn, P. (2009). Neuropathy target esterase is required for adult vertebrate axon maintenance. J. Neurosci. 29, 11594-11600.
-
(2009)
J. Neurosci.
, vol.29
, pp. 11594-11600
-
-
Read, D.J.1
Li, Y.2
Chao, M.V.3
Cavanagh, J.B.4
Glynn, P.5
-
51
-
-
33644508363
-
Mechanism of toxicity of the branched-chain fatty acid phytanic acid, amarker of refsum disease, in astrocytes involves mitochondrial impairment
-
Reiser, G., Schonfeld, P. and Kahlert, S. (2006). Mechanism of toxicity of the branched-chain fatty acid phytanic acid, amarker of Refsum disease, in astrocytes involves mitochondrial impairment. Int. J. Dev. Neurosci. 24, 113-122.
-
(2006)
Int. J. Dev. Neurosci.
, vol.24
, pp. 113-122
-
-
Reiser, G.1
Schonfeld, P.2
Kahlert, S.3
-
52
-
-
0031723632
-
Localization of nervonic acid beta-oxidation in human and rodent peroxisomes: Impaired oxidation in zellweger syndrome and X-linked adrenoleukodystrophy
-
Sandhir, R., Khan, M., Chahal, A. and Singh, I. (1998). Localization of nervonic acid beta-oxidation in human and rodent peroxisomes: impaired oxidation in Zellweger syndrome and X-linked adrenoleukodystrophy. J. Lipid Res. 39, 2161-2171.
-
(1998)
J. Lipid Res.
, vol.39
, pp. 2161-2171
-
-
Sandhir, R.1
Khan, M.2
Chahal, A.3
Singh, I.4
-
53
-
-
0035989399
-
Rugose (rg), aDrosophila A kinase anchor protein, is required for retinal pattern formation and interacts genetically with multiple signaling pathways
-
Shamloula, H. K., and Mbogho, M. P., Pimentel, A. C., Chrzanowska-Lightowlers, Z. M., Hyatt, V., Okano, H. and Venkatesh, T. R. (2002). rugose (rg), aDrosophila A kinase anchor protein, is required for retinal pattern formation and interacts genetically with multiple signaling pathways. Genetics 161, 693-710.
-
(2002)
Genetics
, vol.161
, pp. 693-710
-
-
Shamloula, H.K.1
Mbogho, M.P.2
Pimentel, A.C.3
Chrzanowska-Lightowlers, Z.M.4
Hyatt, V.5
Okano, H.6
Venkatesh, T.R.7
-
54
-
-
82955214822
-
Impaired coenzyme ametabolism affects histone and tubulin acetylation in drosophila and human cell models of pantothenate kinase associated neurodegeneration
-
Siudeja, K., Srinivasan, B., Xu, L., Rana, A., de Jong, J., Nollen, E. A. A., Jackowski, S., Sanford, L., Hayflick, S. and Sibon, O. C. M. (2011). Impaired Coenzyme Ametabolism affects histone and tubulin acetylation in Drosophila and human cell models of pantothenate kinase associated neurodegeneration. EMBO Mol. Med. 3, 755-766.
-
(2011)
EMBO Mol. Med.
, vol.3
, pp. 755-766
-
-
Siudeja, K.1
Srinivasan, B.2
Xu, L.3
Rana, A.4
De Jong, J.5
Nollen, E.A.A.6
Jackowski, S.7
Sanford, L.8
Hayflick, S.9
Sibon, O.C.M.10
-
55
-
-
80052458730
-
X-linked adrenoleukodystrophy
-
(ed. R. A. Pagon, M. P. Adam, H. H. Ardinger, S. E. Wallace, A. Amemiya, L. J. H. Bean, T. D. Bird, C. R. Dolan, C. T. Fong, R. J. H. Smith et al.)
-
Steinberg, S. J., Moser, A. B. and Raymond, G. V. (2015). X-Linked Adrenoleukodystrophy. In GeneReviews [Internet] (ed. R. A. Pagon, M. P. Adam, H. H. Ardinger, S. E. Wallace, A. Amemiya, L. J. H. Bean, T. D. Bird, C. R. Dolan, C. T. Fong, R. J. H. Smith et al.).
-
(2015)
GeneReviews [Internet]
-
-
Steinberg, S.J.1
Moser, A.B.2
Raymond, G.V.3
-
56
-
-
0033551122
-
Human very-long-chain acyl-coa synthetase: Cloning, topography, and relevance to branched-chain fatty acid metabolism
-
Seattle, WA. Steinberg, S. J., Wang, S. J., Kim, D. G., Mihalik, S.J. and Watkins, P.A. (1999a). Human very-long-chain acyl-CoA synthetase: cloning, topography, and relevance to branched-chain fatty acid metabolism. Biochem. Biophys. Res. Commun. 257, 615-621.
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.257
, pp. 615-621
-
-
Seattle, W.A.1
Steinberg, S.J.2
Wang, S.J.3
Kim, D.G.4
Mihalik, S.J.5
Watkins, P.A.6
-
57
-
-
0032887065
-
Human liver-specific very-long-chain acyl-coenzyme A synthetase: Cdna cloning and characterization of a second enzymatically active protein
-
Steinberg, S. J., and Wang, S. J., McGuinness, M. C. and Watkins, P. A. (1999b). Human liver-specific very-long-chain acyl-coenzyme A synthetase: cDNA cloning and characterization of a second enzymatically active protein. Mol. Genet. Metab. 68, 323-328.
-
(1999)
Mol. Genet. Metab.
, vol.68
, pp. 323-328
-
-
Steinberg, S.J.1
Wang, S.J.2
McGuinness, M.C.3
Watkins, P.A.4
-
58
-
-
0034717047
-
The human liver-specific homolog of very long-chain acyl-coa synthetase is cholate: CoA ligase
-
Steinberg, S. J., and Mihalik, S. J., Kim, D. G., Cuebas, D. A. and Watkins, P. A. (2000). The human liver-specific homolog of very long-chain acyl-CoA synthetase is cholate: CoA ligase. A. J. Biol. Chem. 275, 15605-15608.
-
(2000)
A. J. Biol. Chem.
, vol.275
, pp. 15605-15608
-
-
Steinberg, S.J.1
Mihalik, S.J.2
Kim, D.G.3
Cuebas, D.A.4
Watkins, P.A.5
-
59
-
-
84866422755
-
The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions
-
Steinlein, O. K., Villain, M. and Korenke, C. (2012). The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions. Seizure 21, 740-742.
-
(2012)
Seizure
, vol.21
, pp. 740-742
-
-
Steinlein, O.K.1
Villain, M.2
Korenke, C.3
-
60
-
-
0037249406
-
The flybase database of the drosophila genome projects and community literature
-
The FlyBase Consortium (2003). The Flybase database of the Drosophila genome projects and community literature. Nucleic Acids Res. 31, 172-175.
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 172-175
-
-
-
61
-
-
36048969072
-
No influence of indy on lifespan in drosophila after correction for genetic and cytoplasmic background effects
-
Toivonen, J. M., and Walker, G. A., Martinez-Diaz, P., Bjedov, I., Driege, Y., Jacobs, H. T., Gems, D. and Partridge, L. (2007). No influence of Indy on lifespan in Drosophila after correction for genetic and cytoplasmic background effects. PLoS Genet. 3, e95.
-
(2007)
PLoS Genet.
, vol.3
, pp. e95
-
-
Toivonen, J.M.1
Walker, G.A.2
Martinez-Diaz, P.3
Bjedov, I.4
Driege, Y.5
Jacobs, H.T.6
Gems, D.7
Partridge, L.8
-
62
-
-
0037011118
-
The neurodegeneration mutant lochrig interferes with cholesterol homeostasis and appl processing
-
Tschape, J.-A., Hammerschmied, C., Muhlig-Versen, M., Athenstaedt, K., Daum, G. and Kretzschmar, D. (2002). The neurodegeneration mutant lochrig interferes with cholesterol homeostasis and Appl processing. EMBO J. 21, 6367-6376.
-
(2002)
EMBO J.
, vol.21
, pp. 6367-6376
-
-
Tschape, J.-A.1
Hammerschmied, C.2
Muhlig-Versen, M.3
Athenstaedt, K.4
Daum, G.5
Kretzschmar, D.6
-
63
-
-
84920269464
-
Tissue-based map of the human proteome
-
Uhlen, M., Fagerberg, L., Hallstrom, B. M., Lindskog, C., Oksvold, P., Mardinoglu, A., Sivertsson, A., Kampf, C., Sjostedt, E., Asplund, A. et al. (2015). Tissue-based map of the human proteome. Science 347, 1260419.
-
(2015)
Science
, vol.347
-
-
Uhlen, M.1
Fagerberg, L.2
Hallstrom, B.M.3
Lindskog, C.4
Oksvold, P.5
Mardinoglu, A.6
Sivertsson, A.7
Kampf, C.8
Sjostedt, E.9
Asplund, A.10
-
64
-
-
0037312853
-
Palmitic and stearic fatty acids induce caspase-dependent and -independent cell death in nerve growth factor differentiated PC12 cells
-
Ulloth, J.E., Casiano, C.A. and DeLeon, M. (2003). Palmitic and stearic fatty acids induce caspase-dependent and -independent cell death in nerve growth factor differentiated PC12 cells. J. Neurochem. 84, 655-668.
-
(2003)
J. Neurochem.
, vol.84
, pp. 655-668
-
-
Ulloth, J.E.1
Casiano, C.A.2
DeLeon, M.3
-
65
-
-
84956517188
-
A novel catastrophic presentation of X-linked adrenoleukodystrophy
-
Vawter-Lee, M. M., Hallinan, B. E., and Burrow, T. A., Spaeth, C. G. and Arthur, T. M. (2015). A novel catastrophic presentation of X-linked adrenoleukodystrophy. JIMD Rep. 24, 97-102.
-
(2015)
JIMD Rep.
, vol.24
, pp. 97-102
-
-
Vawter-Lee, M.M.1
Hallinan, B.E.2
Burrow, T.A.3
Spaeth, C.G.4
Arthur, T.M.5
-
66
-
-
0023734959
-
X-linked adrenoleukodystrophy: Identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-coa synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts
-
Wanders, R. J. A., van Roermund, C. W. T, van Wijland, M. J. A, Schutgens, R. B. H., Schram, A. W., and Tager, J. M., van den Bosch, H. and Schalkwijk, C. (1988). X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts. J. Inherit. Metab. Dis. 11 Suppl. 2, 173-177.
-
(1988)
J. Inherit. Metab. Dis.
, vol.11
, pp. 173-177
-
-
Wanders, R.J.A.1
Van Roermund, C.W.T.2
Van Wijland, M.J.A.3
Schutgens, R.B.H.4
Schram, A.W.5
Tager, J.M.6
Van Den Bosch, H.7
Schalkwijk, C.8
-
67
-
-
38349101032
-
Very-long-chain acyl-coa synthetases
-
Watkins, P. A. (2008). Very-long-chain acyl-CoA synthetases. J. Biol. Chem. 283, 1773-1777.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 1773-1777
-
-
Watkins, P.A.1
-
68
-
-
37249092959
-
Evidence for 26 distinct acyl-coenzyme A synthetase genes in the human genome
-
Watkins, P. A., Maiguel, D., Jia, Z. and Pevsner, J. (2007). Evidence for 26 distinct acyl-coenzyme A synthetase genes in the human genome. J. Lipid Res. 48, 2736-2750.
-
(2007)
J. Lipid Res.
, vol.48
, pp. 2736-2750
-
-
Watkins, P.A.1
Maiguel, D.2
Jia, Z.3
Pevsner, J.4
-
69
-
-
0026507316
-
Very-late-onset adrenoleukodystrophy: Possible precipitation of demyelination by cerebral contusion
-
Weller, M., Liedtke, W., Petersen, D., Opitz, H. and Poremba, M. (1992). Very-late-onset adrenoleukodystrophy: possible precipitation of demyelination by cerebral contusion. Neurology 42, 367-370.
-
(1992)
Neurology
, vol.42
, pp. 367-370
-
-
Weller, M.1
Liedtke, W.2
Petersen, D.3
Opitz, H.4
Poremba, M.5
-
70
-
-
0025995598
-
Cell death in normal and rough eye mutants of drosophila
-
Wolff, T. and Ready, D. F. (1991). Cell death in normal and rough eye mutants of Drosophila. Development 113, 825-839.
-
(1991)
Development
, vol.113
, pp. 825-839
-
-
Wolff, T.1
Ready, D.F.2
|