-
1
-
-
2342544939
-
Monitoring the 3-year efficacy of enzyme replacement therapy in Fabry disease by repeated skin biopsies
-
Thurberg BL, Byers HR, Granter SR, et al: Monitoring the 3-year efficacy of enzyme replacement therapy in Fabry disease by repeated skin biopsies. J Invest Dermatol 2004;122:900-908.
-
(2004)
J. Invest. Dermatol.
, vol.122
, pp. 900-908
-
-
Thurberg, B.L.1
Byers, H.R.2
Granter, S.R.3
-
2
-
-
0037452544
-
Fabry disease, an under-recognized multisystemic disorder: Expert recommendations for diagnosis, management, and enzyme replacement therapy
-
Desnick RJ, Brady R, Barranger J, et al: Fabry disease, an under-recognized multisystemic disorder: Expert recommendations for diagnosis, management, and enzyme replacement therapy. Ann Intern Med 2003;138:338-346.
-
(2003)
Ann. Intern. Med.
, vol.138
, pp. 338-346
-
-
Desnick, R.J.1
Brady, R.2
Barranger, J.3
-
3
-
-
12144287518
-
Fabry disease defined: Baseline clinical manifestations of 366 patients in the Fabry Outcome Survey
-
Mehta A, Ricci R, Widmer U, et al: Fabry disease defined: Baseline clinical manifestations of 366 patients in the Fabry Outcome Survey. Eur J Clin Invest 2004;34:236-244.
-
(2004)
Eur. J. Clin. Invest.
, vol.34
, pp. 236-244
-
-
Mehta, A.1
Ricci, R.2
Widmer, U.3
-
4
-
-
4644316602
-
Enzyme therapy for Fabry disease: Neutralizing antibodies toward agalsidase alpha and beta
-
Linthorst GE, Hollak CE, Donker-Koopman WE, et al: Enzyme therapy for Fabry disease: Neutralizing antibodies toward agalsidase alpha and beta. Kidney Int 2004;66:1589-1595.
-
(2004)
Kidney Int.
, vol.66
, pp. 1589-1595
-
-
Linthorst, G.E.1
Hollak, C.E.2
Donker-Koopman, W.E.3
-
5
-
-
0037453003
-
Long-term correction of globotriaosylceramide storage in Fabry mice by recombinant adeno-associated virus-mediated gene transfer
-
Park J, Murray GJ, Limaye A, et al: Long-term correction of globotriaosylceramide storage in Fabry mice by recombinant adeno-associated virus-mediated gene transfer. Proc Natl Acad Sci USA 2003;100:3450-3454.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 3450-3454
-
-
Park, J.1
Murray, G.J.2
Limaye, A.3
-
6
-
-
10744219813
-
AAV2 vector harboring a liver-restricted promoter facilitates sustained expression of therapeutic levels of α-galactosidase A and the induction of immune tolerance in Fabry mice
-
Ziegler RJ, Lonning SM, Armentano D, et al: AAV2 vector harboring a liver-restricted promoter facilitates sustained expression of therapeutic levels of α-galactosidase A and the induction of immune tolerance in Fabry mice. Mol Ther 2003;9:231-240.
-
(2003)
Mol. Ther.
, vol.9
, pp. 231-240
-
-
Ziegler, R.J.1
Lonning, S.M.2
Armentano, D.3
-
7
-
-
0035811674
-
Improvement in cardiac function in the cardiac variant of Fabry's disease with galactose-infusion therapy
-
Frustaci A, Chimenti C, Ricci R, et al: Improvement in cardiac function in the cardiac variant of Fabry's disease with galactose-infusion therapy. N Engl J Med 2001;345:25-32.
-
(2001)
N. Engl. J. Med.
, vol.345
, pp. 25-32
-
-
Frustaci, A.1
Chimenti, C.2
Ricci, R.3
-
8
-
-
0033018496
-
Accelerated transport and maturation of lysosomal alpha-galactosidase A in Fabry lymphoblasts by an enzyme inhibitor
-
Fan JQ, Ishii S, Asano N, Suzuki Y: Accelerated transport and maturation of lysosomal alpha-galactosidase A in Fabry lymphoblasts by an enzyme inhibitor. Nat Med 1999;5:112-115.
-
(1999)
Nat. Med.
, vol.5
, pp. 112-115
-
-
Fan, J.Q.1
Ishii, S.2
Asano, N.3
Suzuki, Y.4
-
9
-
-
0037419009
-
Chemical chaperones - A new concept in drug research
-
Kolter T, Wendeler M: Chemical chaperones - A new concept in drug research. Chembiochemistry 2003;4:260-264.
-
(2003)
Chembiochemistry
, vol.4
, pp. 260-264
-
-
Kolter, T.1
Wendeler, M.2
-
10
-
-
7044284796
-
Transgenic mouse expressing human mutant alpha-galactosidase A in an endogenous enzyme deficient background: A biochemical animal model for studying active-site specific chaperone therapy for Fabry disease
-
Ishii S, Yoshioka H, Mannen K, et al: Transgenic mouse expressing human mutant alpha-galactosidase A in an endogenous enzyme deficient background: A biochemical animal model for studying active-site specific chaperone therapy for Fabry disease. Biochim Biophys Acta 2004;1690:250-257.
-
(2004)
Biochim. Biophys. Acta
, vol.1690
, pp. 250-257
-
-
Ishii, S.1
Yoshioka, H.2
Mannen, K.3
-
11
-
-
0036941003
-
Motoneuron death in normal and spinal muscular atrophy-affected human fetuses
-
Fidzianska A, Rafalowska J: Motoneuron death in normal and spinal muscular atrophy-affected human fetuses. Acta Neuropathol (Berl) 2002;104:363-368.
-
(2002)
Acta Neuropathol. (Berl.)
, vol.104
, pp. 363-368
-
-
Fidzianska, A.1
Rafalowska, J.2
-
12
-
-
16644394038
-
Spinal muscular atrophy: Survival pattern and functional status
-
Chung BH, Wong VC, Ip P: Spinal muscular atrophy: Survival pattern and functional status. Pediatrics 2004;114:e548-e553.
-
(2004)
Pediatrics
, vol.114
-
-
Chung, B.H.1
Wong, V.C.2
Ip, P.3
-
13
-
-
0032471510
-
Intragenic telSMN mutations: Frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number
-
Parsons DW, McAndrew PE, Iannaccone ST, et al: Intragenic telSMN mutations: Frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number. Am J Hum Genet 1998;63:1712-1723.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1712-1723
-
-
Parsons, D.W.1
McAndrew, P.E.2
Iannaccone, S.T.3
-
14
-
-
0032567036
-
A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing
-
Pellizzoni L, Kataoka N, Charroux B, Dreyfuss G: A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing. Cell 1998;95:615-624.
-
(1998)
Cell
, vol.95
, pp. 615-624
-
-
Pellizzoni, L.1
Kataoka, N.2
Charroux, B.3
Dreyfuss, G.4
-
15
-
-
0035971112
-
A cell system with targeted disruption of the SMN gene
-
Wang J, Dreyfuss G: A cell system with targeted disruption of the SMN gene. J Biol Chem 2001;276:9599-9605.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 9599-9605
-
-
Wang, J.1
Dreyfuss, G.2
-
16
-
-
0030818315
-
Genomic variation and gene conversion in spinal muscular atrophy: Implications for disease process and clinical phenotype
-
Campbell L, Potter A, Ignatius J, et al: Genomic variation and gene conversion in spinal muscular atrophy: Implications for disease process and clinical phenotype. Am J Hum Genet 1997;61:40-50.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 40-50
-
-
Campbell, L.1
Potter, A.2
Ignatius, J.3
-
18
-
-
4744368810
-
Homozygous SMN1 deletions in unaffected family members and modification of the phenotype by SMN2
-
Prior TW, Swoboda KJ, Scott HD, Hejmanowski AQ: Homozygous SMN1 deletions in unaffected family members and modification of the phenotype by SMN2. Am J Med Genet 2004;130A:307-310.
-
(2004)
Am. J. Med. Genet.
, vol.130 A
, pp. 307-310
-
-
Prior, T.W.1
Swoboda, K.J.2
Scott, H.D.3
Hejmanowski, A.Q.4
-
19
-
-
10744229981
-
Phenylbutyrate increases SMN expression in vitro: Relevance for treatment of spinal muscular atrophy
-
Andreassi C, Angelozzi C, Tiziano FD, et al: Phenylbutyrate increases SMN expression in vitro: Relevance for treatment of spinal muscular atrophy. Eur J Hum Genet 2004;12:59-65.
-
(2004)
Eur. J. Hum. Genet.
, vol.12
, pp. 59-65
-
-
Andreassi, C.1
Angelozzi, C.2
Tiziano, F.D.3
-
20
-
-
9144269242
-
Pilot trial of phenylbutyrate in spinal muscular atrophy
-
Mercuri E, Bertini E, Messina S, et al: Pilot trial of phenylbutyrate in spinal muscular atrophy. Neuromuscul Disord 2004; 14:130-135.
-
(2004)
Neuromuscul. Disord.
, vol.14
, pp. 130-135
-
-
Mercuri, E.1
Bertini, E.2
Messina, S.3
-
21
-
-
0242290062
-
Valproic acid increases SMN levels in spinal muscular atorphy patient cells
-
Sumner CJ, Huynh TN, Markowitz JA, et al: Valproic acid increases SMN levels in spinal muscular atorphy patient cells. Ann Neurol 2003;54:647-654.
-
(2003)
Ann. Neurol.
, vol.54
, pp. 647-654
-
-
Sumner, C.J.1
Huynh, T.N.2
Markowitz, J.A.3
-
22
-
-
0027366552
-
Inherited primary peripheral neuropathies. Molecular genetics and clinical implications
-
Lupski JR, Chance PF, Garcia CA: Inherited primary peripheral neuropathies. Molecular genetics and clinical implications. JAMA 1993;270:2326-2330.
-
(1993)
JAMA
, vol.270
, pp. 2326-2330
-
-
Lupski, J.R.1
Chance, P.F.2
Garcia, C.A.3
-
23
-
-
0028810444
-
Analysis of the CMT1A-REP repeat: Mapping crossover breakpoints in CMT1A and HNPP
-
Kiyosawa H, Lensch MW, Chance PF: Analysis of the CMT1A-REP repeat: Mapping crossover breakpoints in CMT1A and HNPP. Hum Mol Genet 1995;4:2327-2334.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2327-2334
-
-
Kiyosawa, H.1
Lensch, M.W.2
Chance, P.F.3
-
24
-
-
0028950408
-
Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: Modulation of cell growth
-
Zoidl G, Blass-Kampmann S, D'Urso D, et al: Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: Modulation of cell growth. EMBO J 1995;14:1122-1128.
-
(1995)
EMBO J.
, vol.14
, pp. 1122-1128
-
-
Zoidl, G.1
Blass-Kampmann, S.2
D'Urso, D.3
-
25
-
-
0036788455
-
PMP22 overexpression causes dysmyelination in mice
-
Robaglia-Schlupp A, Pizant J, Norreel JC, et al: PMP22 overexpression causes dysmyelination in mice. Brain 2002;125:2213-2221.
-
(2002)
Brain
, vol.125
, pp. 2213-2221
-
-
Robaglia-Schlupp, A.1
Pizant, J.2
Norreel, J.C.3
-
26
-
-
0021254127
-
Schwann cell galactocerebroside induced by derivatives of adenosine-3′,5′-monophosphate
-
Sobue G, Pleasure D: Schwann cell galactocerebroside induced by derivatives of adenosine-3′,5′-monophosphate. Science 1984;224:72-74.
-
(1984)
Science
, vol.224
, pp. 72-74
-
-
Sobue, G.1
Pleasure, D.2
-
27
-
-
0023864835
-
Axons regulate Schwann cell expression of the major myelin and NGF receptor genes
-
Lemke G, Chao M: Axons regulate Schwann cell expression of the major myelin and NGF receptor genes. Development 1988; 102:499-504.
-
(1988)
Development
, vol.102
, pp. 499-504
-
-
Lemke, G.1
Chao, M.2
-
28
-
-
0342803695
-
Molecular dissection of the Schwann cell specific promoter of the PMP22 gene
-
Saberan-Djoneidi D, Sanguedolce V, Assouline Z, et al: Molecular dissection of the Schwann cell specific promoter of the PMP22 gene. Gene 2000;248:223-231.
-
(2000)
Gene
, vol.248
, pp. 223-231
-
-
Saberan-Djoneidi, D.1
Sanguedolce, V.2
Assouline, Z.3
-
29
-
-
0028073907
-
Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters
-
Suter U, Snipes GJ, Schoener-Scott R, et al: Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters. J Biol Chem 1994;269:25795-25808.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 25795-25808
-
-
Suter, U.1
Snipes, G.J.2
Schoener-Scott, R.3
-
30
-
-
1942422646
-
Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease
-
Passage E, Norreel JC, Noack-Fraissignes P, et al: Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease. Nat Med 2004;10:396-401.
-
(2004)
Nat. Med.
, vol.10
, pp. 396-401
-
-
Passage, E.1
Norreel, J.C.2
Noack-Fraissignes, P.3
-
31
-
-
0034043493
-
Triplet repeat expansion in neuromuscular disease
-
Lieberman AP, Fischbeck KH: Triplet repeat expansion in neuromuscular disease. Muscle Nerve 2000;23:843-850.
-
(2000)
Muscle Nerve
, vol.23
, pp. 843-850
-
-
Lieberman, A.P.1
Fischbeck, K.H.2
-
32
-
-
0034255678
-
Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: A clinical and molecular study of 30 families
-
Mariotti C, Castellotti B, Pareyson D, et al: Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: A clinical and molecular study of 30 families. Neuromuscul Disord 2000; 10:391-397.
-
(2000)
Neuromuscul. Disord.
, vol.10
, pp. 391-397
-
-
Mariotti, C.1
Castellotti, B.2
Pareyson, D.3
-
33
-
-
0037444446
-
Heat shock protein 70 chaperone overexpression ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model by reducing nuclear-localized mutant androgen receptor protein
-
Adachi H, Katsuno M, Minamiyama M, et al: Heat shock protein 70 chaperone overexpression ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model by reducing nuclear-localized mutant androgen receptor protein. J Neurosci 2003;23:2203-2211.
-
(2003)
J. Neurosci.
, vol.23
, pp. 2203-2211
-
-
Adachi, H.1
Katsuno, M.2
Minamiyama, M.3
-
34
-
-
2942733520
-
Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy
-
Minamiyama M, Katsuno M, Adachi H et al: Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy. Hum Mol Genet 2004;13:1183-1192.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 1183-1192
-
-
Minamiyama, M.1
Katsuno, M.2
Adachi, H.3
-
35
-
-
3042717240
-
Cellular toxicity of polyglutamine expansion proteins: Mechanism of transcription factor deactivation
-
Schaffer G, Breuer P, Boteva R, et al: Cellular toxicity of polyglutamine expansion proteins: Mechanism of transcription factor deactivation. Mol Cell 2004;15:95-105.
-
(2004)
Mol. Cell
, vol.15
, pp. 95-105
-
-
Schaffer, G.1
Breuer, P.2
Boteva, R.3
-
36
-
-
12144286872
-
Androgen receptor YAC transgenic mice recapitulate SBMA motor neuronopathy and implicate VEGF164 in the motor neuron degeneration
-
Sopher BL, Thomas PS Jr, LaFebre-Bernt MA, et al: Androgen receptor YAC transgenic mice recapitulate SBMA motor neuronopathy and implicate VEGF164 in the motor neuron degeneration. Neuron 2004;41:687-699.
-
(2004)
Neuron
, vol.41
, pp. 687-699
-
-
Sopher, B.L.1
Thomas Jr., P.S.2
LaFebre-Bernt, M.A.3
-
37
-
-
1542298945
-
Polyglutamine diminishes VEGF; passage to motor neuron death?
-
Katsuno M, Sobue G: Polyglutamine diminishes VEGF; passage to motor neuron death? Neuron 2004;41:677-679.
-
(2004)
Neuron
, vol.41
, pp. 677-679
-
-
Katsuno, M.1
Sobue, G.2
-
38
-
-
4444377607
-
Effects of vascular endothelial growth factor (VEGF) on motor neuron degeneration
-
van Den Bosch L, Storkebaum E, Vleminckx V, et al: Effects of vascular endothelial growth factor (VEGF) on motor neuron degeneration. Neurobiol Dis 2004;17:21-28.
-
(2004)
Neurobiol. Dis.
, vol.17
, pp. 21-28
-
-
van Den Bosch, L.1
Storkebaum, E.2
Vleminckx, V.3
-
39
-
-
0034526311
-
VEGF enhances intraneural angiogenesis and improves nerve regeneration after axotomy
-
Hobson MI, Green CJ, Terenghi G: VEGF enhances intraneural angiogenesis and improves nerve regeneration after axotomy. J Anat 2000;197:591-605.
-
(2000)
J. Anat.
, vol.197
, pp. 591-605
-
-
Hobson, M.I.1
Green, C.J.2
Terenghi, G.3
-
40
-
-
0035023584
-
Reversal of experimental diabetic neuropathy by VEGF gene transfer
-
Schratzberger P, Walter DH, Rittig K, et al: Reversal of experimental diabetic neuropathy by VEGF gene transfer. J Clin Invest 2001;107:1083-1092.
-
(2001)
J. Clin. Invest.
, vol.107
, pp. 1083-1092
-
-
Schratzberger, P.1
Walter, D.H.2
Rittig, K.3
-
41
-
-
2342667384
-
New roles for VEGF in nervous tissue - Beyond blood vessels
-
Rosenstein JM, Krum JM: New roles for VEGF in nervous tissue - Beyond blood vessels. Exp Neurol 2004;187:246-253.
-
(2004)
Exp. Neurol.
, vol.187
, pp. 246-253
-
-
Rosenstein, J.M.1
Krum, J.M.2
-
42
-
-
0034978562
-
Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration
-
Oosthuyse B, Moons L, Storkebaum E, et al: Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration. Nat Genet 2001;128:131-138.
-
(2001)
Nat. Genet.
, vol.128
, pp. 131-138
-
-
Oosthuyse, B.1
Moons, L.2
Storkebaum, E.3
-
43
-
-
3242701496
-
Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondria
-
5-17
-
Liu J, Lillo C, Jonsson PA, et al: Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondria Neuron 2004;43:5-17.
-
(2004)
Neuron
, vol.43
-
-
Liu, J.1
Lillo, C.2
Jonsson, P.A.3
-
44
-
-
0141861939
-
Hypoxic induction of vascular endothelial growth factor is selectively impaired in mice carrying the mutant SOD1 gene
-
Murakami T, Ilieva H, Shiote M, et al: Hypoxic induction of vascular endothelial growth factor is selectively impaired in mice carrying the mutant SOD1 gene. Brain Res 2003;989:231-237.
-
(2003)
Brain Res.
, vol.989
, pp. 231-237
-
-
Murakami, T.1
Ilieva, H.2
Shiote, M.3
-
45
-
-
2642526164
-
VEGF delivery with retrogradely transported lentivector prolongs survival in a mouse ALS model
-
Azzouz M, Ralph GS, Storkebaum E, et al: VEGF delivery with retrogradely transported lentivector prolongs survival in a mouse ALS model. Nature 2004;429:413-417.
-
(2004)
Nature
, vol.429
, pp. 413-417
-
-
Azzouz, M.1
Ralph, G.S.2
Storkebaum, E.3
-
46
-
-
4844227301
-
Vascular endothelial growth factor prolongs survival in a transgenic mouse model of ALS
-
Zheng C, Nennesmo I, Fadeel B, Henter JI: Vascular endothelial growth factor prolongs survival in a transgenic mouse model of ALS. Ann Neurol 2004;56:564-567.
-
(2004)
Ann. Neurol.
, vol.56
, pp. 564-567
-
-
Zheng, C.1
Nennesmo, I.2
Fadeel, B.3
Henter, J.I.4
-
47
-
-
16644382257
-
Treatment of motoneuron degeneration by intracerebroventricular delivery of VEGF in a rat model of ALS
-
Storkebaum E, Lambrechts D, Dewerchin M, et al: Treatment of motoneuron degeneration by intracerebroventricular delivery of VEGF in a rat model of ALS. Nat Neurosci 2005;8:85-92.
-
(2005)
Nat. Neurosci.
, vol.8
, pp. 85-92
-
-
Storkebaum, E.1
Lambrechts, D.2
Dewerchin, M.3
-
48
-
-
2942627907
-
Low levels of the vascular endothelial growth factor in CSF from early ALS patients
-
Devos D, Moreau C, Lassalle P, et al: Low levels of the vascular endothelial growth factor in CSF from early ALS patients. Neurology 2004;62:2127-2129.
-
(2004)
Neurology
, vol.62
, pp. 2127-2129
-
-
Devos, D.1
Moreau, C.2
Lassalle, P.3
-
49
-
-
0041903805
-
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death
-
Lambrechts D, Storkebaum E, Morimoto M, et al: VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death. Nat Genet 2003;34:383-394.
-
(2003)
Nat. Genet.
, vol.34
, pp. 383-394
-
-
Lambrechts, D.1
Storkebaum, E.2
Morimoto, M.3
-
50
-
-
0042166179
-
A new piece of the ALS puzzle
-
Cleveland JL: A new piece of the ALS puzzle. Nat Genet 2003;34:357-358.
-
(2003)
Nat. Genet.
, vol.34
, pp. 357-358
-
-
Cleveland, J.L.1
-
52
-
-
0036842205
-
Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy
-
Plante-Bordeneuve V, Said G: Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy. Muscle Nerve 2002;26:608-621.
-
(2002)
Muscle Nerve
, vol.26
, pp. 608-621
-
-
Plante-Bordeneuve, V.1
Said, G.2
-
54
-
-
2942558484
-
The phosphodiesterase inhibitor rolipram delivered after a spinal cord lesion promotes axonal regeneration and functional recovery
-
Nikulina E, Tidwell JL, Dai HN, et al: The phosphodiesterase inhibitor rolipram delivered after a spinal cord lesion promotes axonal regeneration and functional recovery. Proc Natl Acad Sci U S A 2004;101:8786-8790.
-
(2004)
Proc. Natl. Acad. Sci. U. S. A.
, vol.101
, pp. 8786-8790
-
-
Nikulina, E.1
Tidwell, J.L.2
Dai, H.N.3
-
55
-
-
2342472526
-
Axonal growth of embryonic stem cell-derived motoneurons in vitro and in motoneuron-injured adult rats
-
Harper JM, Krishnan C, Darman JS, et al: Axonal growth of embryonic stem cell-derived motoneurons in vitro and in motoneuron-injured adult rats. Proc Natl Acad Sci U S A 2004;101:7123-7128.
-
(2004)
Proc. Natl. Acad. Sci. U. S. A.
, vol.101
, pp. 7123-7128
-
-
Harper, J.M.1
Krishnan, C.2
Darman, J.S.3
-
56
-
-
0025168927
-
Delayed wallerian degeneration in sciatic nerves of C57BL/Ola mice is associated with impaired regeneration of sensory axons
-
Bisby MA, Chen S: Delayed wallerian degeneration in sciatic nerves of C57BL/Ola mice is associated with impaired regeneration of sensory axons. Brain Res 1990;530:117-120.
-
(1990)
Brain Res.
, vol.530
, pp. 117-120
-
-
Bisby, M.A.1
Chen, S.2
-
57
-
-
0025764472
-
Delayed response to denervation in muscles of C57BL/Ola mice
-
Brown MC, Booth CM, Lunn ER, Perry VH: Delayed response to denervation in muscles of C57BL/Ola mice. Neuroscience 1991;43:279-283.
-
(1991)
Neuroscience
, vol.43
, pp. 279-283
-
-
Brown, M.C.1
Booth, C.M.2
Lunn, E.R.3
Perry, V.H.4
-
59
-
-
0344950387
-
Inhibiting axon degeneration and synapse loss attenuates apoptosis and disease progression in a mouse model of motoneuron disease
-
Ferri A, Sanes JR, Coleman MP, et al: Inhibiting axon degeneration and synapse loss attenuates apoptosis and disease progression in a mouse model of motoneuron disease. Curr Biol 2003;13:669-673.
-
(2003)
Curr. Biol.
, vol.13
, pp. 669-673
-
-
Ferri, A.1
Sanes, J.R.2
Coleman, M.P.3
-
60
-
-
0037388411
-
s mutation delays robust loss of motor and sensory axons in a genetic model for myelin-related axonopathy
-
s mutation delays robust loss of motor and sensory axons in a genetic model for myelin-related axonopathy. J Neurosci 2003;23:2833-2839.
-
(2003)
J. Neurosci.
, vol.23
, pp. 2833-2839
-
-
Samsam, M.1
Mi, W.2
Wessig, C.3
-
62
-
-
0035195636
-
Wallerian degeneration of injured axons and synapses is delayed by a Ube4b/Nmnat chimeric gene
-
Mack TGA, Reiner M, Beirowski B, et al: Wallerian degeneration of injured axons and synapses is delayed by a Ube4b/Nmnat chimeric gene. Nat Neurosci 2001;4:1199-1206.
-
(2001)
Nat. Neurosci.
, vol.4
, pp. 1199-1206
-
-
Mack, T.G.A.1
Reiner, M.2
Beirowski, B.3
-
63
-
-
0242669941
-
Stable inheritance of an 85-kb triplication in C57BL/WldS mice
-
Mi W, Glass JD, Coleman MP: Stable inheritance of an 85-kb triplication in C57BL/WldS mice. Mutat Res 2003;526:33-37.
-
(2003)
Mutat. Res.
, vol.526
, pp. 33-37
-
-
Mi, W.1
Glass, J.D.2
Coleman, M.P.3
-
64
-
-
4043165678
-
Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration
-
Araki T, Sasaki Y, Milbrandt J: Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration. Science 2004;305:1010-1013.
-
(2004)
Science
, vol.305
, pp. 1010-1013
-
-
Araki, T.1
Sasaki, Y.2
Milbrandt, J.3
-
65
-
-
4243098426
-
NAD to the rescue
-
Bedalov A, Simon JA: NAD to the rescue. Science 2004;305:954-955.
-
(2004)
Science
, vol.305
, pp. 954-955
-
-
Bedalov, A.1
Simon, J.A.2
-
66
-
-
3142740860
-
Calorie restriction promotes mammalian cell survival by inducing the SIRT1 deacetylase
-
Cohen HY, Miller C, Bitterman KJ, et al: Calorie restriction promotes mammalian cell survival by inducing the SIRT1 deacetylase. Science 2004;305:390-392.
-
(2004)
Science
, vol.305
, pp. 390-392
-
-
Cohen, H.Y.1
Miller, C.2
Bitterman, K.J.3
-
67
-
-
8644224064
-
Sir2 mediates longevity in the fly through a pathway related to calorie restriction
-
Rogina B, Helfand SL: Sir2 mediates longevity in the fly through a pathway related to calorie restriction. Proc Natl Acad Sci USA 2004;101:15998-16003.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 15998-16003
-
-
Rogina, B.1
Helfand, S.L.2
-
68
-
-
1442325591
-
Role of poly(ADP-ribose) polymerase activation in diabetic neuropathy
-
Obrosova IG, Li F, Abatan OI, et al: Role of poly(ADP-ribose) polymerase activation in diabetic neuropathy. Diabetes 2004;53:711-720.
-
(2004)
Diabetes
, vol.53
, pp. 711-720
-
-
Obrosova, I.G.1
Li, F.2
Abatan, O.I.3
-
69
-
-
2442651710
-
Evaluation of orally active poly(ADP-ribose) polymerase inhibitor in streptozotocin-diabetic rat model of early peripheral neuropathy
-
710-717
-
Li F, Szabo C, Pacher P, et al: Evaluation of orally active poly(ADP-ribose) polymerase inhibitor in streptozotocin-diabetic rat model of early peripheral neuropathy. Diabetologia 2004; 47:710-717.
-
(2004)
Diabetologia
, vol.47
-
-
Li, F.1
Szabo, C.2
Pacher, P.3
-
70
-
-
0347128279
-
Calorie restriction extends yeast life span by lowering the level of NADH
-
Lin S-J, Ford E, Haigis M, et al: Calorie restriction extends yeast life span by lowering the level of NADH. Genes Dev 2004;18:12-16.
-
(2004)
Genes Dev.
, vol.18
, pp. 12-16
-
-
Lin, S.-J.1
Ford, E.2
Haigis, M.3
|