-
1
-
-
79957583944
-
Genetic modifiers of neurological disease
-
doi:10.1016/j.gde.2010.12.007. PubMed: 21251811
-
Kearney JA (2011) Genetic modifiers of neurological disease. Curr Opin Genet Dev 21: 349-353. doi:10.1016/j.gde.2010.12.007. PubMed: 21251811.
-
(2011)
Curr Opin Genet Dev
, vol.21
, pp. 349-353
-
-
Kearney, J.A.1
-
2
-
-
84876883390
-
Mechanisms underlying synaptic vulnerability and degeneration in neurodegenerative disease
-
n/a-n/a
-
Gillingwater TH, Wishart TM (2013) Mechanisms underlying synaptic vulnerability and degeneration in neurodegenerative disease. Neuropathology and Applied Neurobiology: n/a-n/a.
-
(2013)
Neuropathology and Applied Neurobiology
-
-
Gillingwater, T.H.1
Wishart, T.M.2
-
3
-
-
78650034178
-
Ubiquitin/proteasome pathway impairment in neurodegeneration: Therapeutic implications
-
doi:10.1007/s10495-010-0466-z. PubMed: 20131003
-
Huang Q, Figueiredo-Pereira ME (2010) Ubiquitin/proteasome pathway impairment in neurodegeneration: therapeutic implications. Apoptosis 15: 1292-1311. doi:10.1007/s10495-010-0466-z. PubMed: 20131003.
-
(2010)
Apoptosis
, vol.15
, pp. 1292-1311
-
-
Huang, Q.1
Figueiredo-Pereira, M.E.2
-
4
-
-
58149159907
-
Dysfunction of the ubiquitin-proteasome system in multiple disease conditions: Therapeutic approaches
-
doi:10.1002/bies.20852. PubMed: 18937370
-
Paul S (2008) Dysfunction of the ubiquitin-proteasome system in multiple disease conditions: therapeutic approaches. Bioessays 30: 1172-1184. doi:10.1002/bies.20852. PubMed: 18937370.
-
(2008)
Bioessays
, vol.30
, pp. 1172-1184
-
-
Paul, S.1
-
5
-
-
33847069643
-
Redox proteomics identification of oxidatively modified brain proteins in inherited Alzheimer's disease: An initial assessment
-
PubMed: 17183150
-
Butterfield DA, Gnjec A, Poon HF, Castegna A, Pierce WM et al. (2006) Redox proteomics identification of oxidatively modified brain proteins in inherited Alzheimer's disease: An initial assessment. J Alzheimers Dis 10: 391-397. PubMed: 17183150.
-
(2006)
J Alzheimers Dis
, vol.10
, pp. 391-397
-
-
Butterfield, D.A.1
Gnjec, A.2
Poon, H.F.3
Castegna, A.4
Pierce, W.M.5
-
6
-
-
0036733145
-
Proteomic identification of oxidatively modified proteins in Alzheimer's disease brain. Part II: Dihydropyrimidinase-related protein 2, α-enolase and heat shock cognate 71
-
doi:10.1046/j.1471-4159.2002.01103.x. PubMed: 12354300
-
Castegna A, Aksenov M, Thongboonkerd V, Klein JB, Pierce WM et al. (2002) Proteomic identification of oxidatively modified proteins in Alzheimer's disease brain. Part II: dihydropyrimidinase-related protein 2, α-enolase and heat shock cognate 71. J Neurochem 82: 1524-1532. doi:10.1046/j.1471-4159. 2002.01103.x. PubMed: 12354300.
-
(2002)
J Neurochem
, vol.82
, pp. 1524-1532
-
-
Castegna, A.1
Aksenov, M.2
Thongboonkerd, V.3
Klein, J.B.4
Pierce, W.M.5
-
7
-
-
1842581669
-
Oxidative Modifications and Down-regulation of Ubiquitin Carboxyl-terminal Hydrolase L1 Associated with Idiopathic Parkinson's and Alzheimer's Diseases
-
PubMed: 14722078
-
Choi J, Levey AI, Weintraub ST, Rees HD, Gearing M et al. (2004) Oxidative Modifications and Down-regulation of Ubiquitin Carboxyl-terminal Hydrolase L1 Associated with Idiopathic Parkinson's and Alzheimer's Diseases. J Biol Chem 279: 13256-13264. PubMed: 14722078.
-
(2004)
J Biol Chem
, vol.279
, pp. 13256-13264
-
-
Choi, J.1
Levey, A.I.2
Weintraub, S.T.3
Rees, H.D.4
Gearing, M.5
-
8
-
-
0032190090
-
The ubiquitin pathway in Parkinson's disease
-
doi:10.1038/26652. PubMed: 9774100
-
Leroy E, Boyer R, Auburger G, Leube B, Ulm G et al. (1998) The ubiquitin pathway in Parkinson's disease. Nature 395: 451-452. doi:10.1038/26652. PubMed: 9774100.
-
(1998)
Nature
, vol.395
, pp. 451-452
-
-
Leroy, E.1
Boyer, R.2
Auburger, G.3
Leube, B.4
Ulm, G.5
-
9
-
-
34547535639
-
The functions of UCH-L1 and its relation to neurodegenerative diseases
-
doi:10.1016/j.neuint.2007.05.007. PubMed: 17586089
-
Setsuie R, Wada K (2007) The functions of UCH-L1 and its relation to neurodegenerative diseases. Neurochem Int 51: 105-111. doi:10.1016/j.neuint. 2007.05.007. PubMed: 17586089.
-
(2007)
Neurochem Int
, vol.51
, pp. 105-111
-
-
Setsuie, R.1
Wada, K.2
-
10
-
-
80052580969
-
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
-
doi:10.1038/nature10353. PubMed: 21857683
-
Deng H-X, Chen W, Hong S-T, Boycott KM, Gorrie GH et al. (2011) Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature 477: 211-215. doi:10.1038/nature10353. PubMed: 21857683.
-
(2011)
Nature
, vol.477
, pp. 211-215
-
-
Deng, H.-X.1
Chen, W.2
Hong, S.-T.3
Boycott, K.M.4
Gorrie, G.H.5
-
11
-
-
38749120297
-
Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy
-
doi:10.1016/j.ajhg.2007.09.009. PubMed: 18179898
-
Ramser J, Ahearn ME, Lenski C, Yariz KO, Hellebrand H et al. (2008) Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy. Am J Hum Genet 82: 188-193. doi:10.1016/j.ajhg.2007.09. 009. PubMed: 18179898.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 188-193
-
-
Ramser, J.1
Ahearn, M.E.2
Lenski, C.3
Yariz, K.O.4
Hellebrand, H.5
-
12
-
-
33847410541
-
Emerging roles for ubiquitin and protein degradation in neuronal function
-
doi:10.1124/pr.59.1.4. PubMed: 17329546
-
Yi JJ, Ehlers MD (2007) Emerging roles for ubiquitin and protein degradation in neuronal function. Pharmacol Rev 59: 14-39. doi:10.1124/pr.59.1. 4. PubMed: 17329546.
-
(2007)
Pharmacol Rev
, vol.59
, pp. 14-39
-
-
Yi, J.J.1
Ehlers, M.D.2
-
13
-
-
67650620318
-
Regulation and cellular roles of ubiquitin-specific deubiquitinating enzymes
-
doi:10.1146/annurev.biochem.78.082307.091526. PubMed: 19489724
-
Reyes-Turcu FE, Ventii KH, Wilkinson KD (2009) Regulation and cellular roles of ubiquitin-specific deubiquitinating enzymes. Annu Rev Biochem 78: 363-397. doi:10.1146/annurev.biochem.78.082307.091526. PubMed: 19489724.
-
(2009)
Annu Rev Biochem
, vol.78
, pp. 363-397
-
-
Reyes-Turcu, F.E.1
Ventii, K.H.2
Wilkinson, K.D.3
-
14
-
-
0036842130
-
Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease
-
doi:10.1038/ng1006. PubMed: 12368914
-
Wilson SM, Bhattacharyya B, Rachel RA, Coppola V, Tessarollo L et al. (2002) Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease. Nat Genet 32: 420-425. doi:10.1038/ng1006. PubMed: 12368914.
-
(2002)
Nat Genet
, vol.32
, pp. 420-425
-
-
Wilson, S.M.1
Bhattacharyya, B.2
Rachel, R.A.3
Coppola, V.4
Tessarollo, L.5
-
15
-
-
84863082577
-
Altered neurotransmitter release machinery in mice deficient for the deubiquitinating enzyme Usp14
-
PubMed: 22075695
-
Bhattacharyya BJ, Wilson SM, Jung H, Miller RJ (2012) Altered neurotransmitter release machinery in mice deficient for the deubiquitinating enzyme Usp14. Am J Physiol Cell Physiol 302: C698-C708. PubMed: 22075695.
-
(2012)
Am J Physiol Cell Physiol
, vol.302
-
-
Bhattacharyya, B.J.1
Wilson, S.M.2
Jung, H.3
Miller, R.J.4
-
16
-
-
82555200901
-
Ubiquitin homeostasis is critical for synaptic development and function
-
doi:10.1523/JNEUROSCI.2922-11.2011. PubMed: 22131412
-
Chen PC, Bhattacharyya BJ, Hanna J, Minkel H, Wilson JA et al. (2011) Ubiquitin homeostasis is critical for synaptic development and function. J Neurosci 31: 17505-17513. doi:10.1523/JNEUROSCI.2922-11.2011. PubMed: 22131412.
-
(2011)
J Neurosci
, vol.31
, pp. 17505-17513
-
-
Chen, P.C.1
Bhattacharyya, B.J.2
Hanna, J.3
Minkel, H.4
Wilson, J.A.5
-
17
-
-
69749110327
-
The proteasome-associated deubiquitinating enzyme Usp14 is essential for the maintenance of synaptic ubiquitin levels and the development of neuromuscular junctions
-
doi:10.1523/JNEUROSCI.2635-09.2009. PubMed: 19726649
-
Chen PC, Qin LN, Li XM, Walters BJ, Wilson JA et al. (2009) The proteasome-associated deubiquitinating enzyme Usp14 is essential for the maintenance of synaptic ubiquitin levels and the development of neuromuscular junctions. J Neurosci 29: 10909-10919. doi:10.1523/JNEUROSCI.2635-09.2009. PubMed: 19726649.
-
(2009)
J Neurosci
, vol.29
, pp. 10909-10919
-
-
Chen, P.C.1
Qin, L.N.2
Li, X.M.3
Walters, B.J.4
Wilson, J.A.5
-
18
-
-
27644477433
-
Loss of Usp14 results in reduced levels of ubiquitin in ataxia mice
-
doi:10.1111/j.1471-4159.2005.03409.x. PubMed: 16190881
-
Anderson C, Crimmins S, Wilson JA, Korbel GA, Ploegh HL et al. (2005) Loss of Usp14 results in reduced levels of ubiquitin in ataxia mice. J Neurochem 95: 724-731. doi:10.1111/j.1471-4159.2005.03409.x. PubMed: 16190881.
-
(2005)
J Neurochem
, vol.95
, pp. 724-731
-
-
Anderson, C.1
Crimmins, S.2
Wilson, J.A.3
Korbel, G.A.4
Ploegh, H.L.5
-
19
-
-
33750935146
-
Transgenic rescue of ataxia mice with neuronal-specific expression of ubiquitin-specific protease 14
-
doi:10.1523/JNEUROSCI.3600-06.2006. PubMed: 17079671
-
Crimmins S, Jin Y, Wheeler C, Huffman AK, Chapman C et al. (2006) Transgenic rescue of ataxia mice with neuronal-specific expression of ubiquitin-specific protease 14. J Neurosci 26: 11423-11431. doi:10.1523/ JNEUROSCI.3600-06.2006. PubMed: 17079671.
-
(2006)
J Neurosci
, vol.26
, pp. 11423-11431
-
-
Crimmins, S.1
Jin, Y.2
Wheeler, C.3
Huffman, A.K.4
Chapman, C.5
-
20
-
-
84865097380
-
Pla2g12b and Hpn Are Genes Identified by Mouse ENU Mutagenesis That Affect HDL Cholesterol
-
doi:10.1371/journal.pone.0043139. PubMed: 22912808
-
Aljakna A, Choi S, Savage H, Hageman Blair R, Gu T et al. (2012) Pla2g12b and Hpn Are Genes Identified by Mouse ENU Mutagenesis That Affect HDL Cholesterol. PLOS ONE 7: e43139. doi:10.1371/journal.pone.0043139. PubMed: 22912808.
-
(2012)
PLOS ONE
, vol.7
-
-
Aljakna, A.1
Choi, S.2
Savage, H.3
Hageman Blair, R.4
Gu, T.5
-
21
-
-
80052898518
-
An ENU-Induced Mutation of Nrg1 Causes Dilated Pupils and a Reduction in Muscarinic Receptors in the Sphincter Pupillae
-
doi:10.1371/journal.pone.0025176. PubMed: 21949880
-
Chen B, Li K, Zhang F, Zhai G, Gong W et al. (2011) An ENU-Induced Mutation of Nrg1 Causes Dilated Pupils and a Reduction in Muscarinic Receptors in the Sphincter Pupillae. PLOS ONE 6: e25176. doi:10.1371/journal.pone.0025176. PubMed: 21949880.
-
(2011)
PLOS ONE
, vol.6
-
-
Chen, B.1
Li, K.2
Zhang, F.3
Zhai, G.4
Gong, W.5
-
22
-
-
84865424405
-
A Splice Site Mutation in Laminin Results in a Severe Muscular Dystrophy and Growth Abnormalities in Zebrafish
-
doi:10.1371/journal.pone.0043794. PubMed: 22952766
-
Gupta VA, Kawahara G, Myers JA, Chen AT, Hall TE et al. (2012) A Splice Site Mutation in Laminin Results in a Severe Muscular Dystrophy and Growth Abnormalities in Zebrafish. PLOS ONE 7: e43794. doi:10.1371/journal.pone. 0043794. PubMed: 22952766.
-
(2012)
PLOS ONE
, vol.7
-
-
Gupta, V.A.1
Kawahara, G.2
Myers, J.A.3
Chen, A.T.4
Hall, T.E.5
-
23
-
-
85047690932
-
ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease
-
doi:10.1172/JCI200419574. PubMed: 14755340
-
Wu J-Y, Kao H-J, Li S-C, Stevens R, Hillman S et al. (2004) ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease. J Clin Invest 113: 434-440. doi:10.1172/JCI200419574. PubMed: 14755340.
-
(2004)
J Clin Invest
, vol.113
, pp. 434-440
-
-
Wu, J.-Y.1
Kao, H.-J.2
Li, S.-C.3
Stevens, R.4
Hillman, S.5
-
24
-
-
0036753063
-
Multiple Associated Proteins Regulate Proteasome Structure and Function
-
doi:10.1016/S1097-2765(02)00638-X. PubMed: 12408819
-
Leggett DS, Hanna J, Borodovsky A, Crosas B, Schmidt M et al. (2002) Multiple Associated Proteins Regulate Proteasome Structure and Function. Mol Cell 10: 495-507. doi:10.1016/S1097-2765(02)00638-X. PubMed: 12408819.
-
(2002)
Mol Cell
, vol.10
, pp. 495-507
-
-
Leggett, D.S.1
Hanna, J.2
Borodovsky, A.3
Crosas, B.4
Schmidt, M.5
-
25
-
-
34250007128
-
The mouse polyubiquitin gene UbC is essential for fetal liver development, cell-cycle progression and stress tolerance
-
doi:10.1038/sj.emboj.7601722. PubMed: 17491588
-
Ryu K-Y, Maehr R, Gilchrist CA, Long MA, Bouley DM et al. (2007) The mouse polyubiquitin gene UbC is essential for fetal liver development, cell-cycle progression and stress tolerance. EMBO J 26: 2693-2706. doi:10.1038/sj.emboj.7601722. PubMed: 17491588.
-
(2007)
EMBO J
, vol.26
, pp. 2693-2706
-
-
Ryu, K.-Y.1
Maehr, R.2
Gilchrist, C.A.3
Long, M.A.4
Bouley, D.M.5
-
26
-
-
0028935061
-
Acetylcholine receptor gene expression at the developing neuromuscular junction
-
PubMed: 7724666
-
Duclert A, Changeux JP (1995) Acetylcholine receptor gene expression at the developing neuromuscular junction. Physiol Rev 75: 339-368. PubMed: 7724666.
-
(1995)
Physiol Rev
, vol.75
, pp. 339-368
-
-
Duclert, A.1
Changeux, J.P.2
-
27
-
-
0029937936
-
Involvement of protein kinases in the upregulation of acetylcholine release at endplates of alpha-bungarotoxin-treated rats
-
PubMed: 8735703
-
Plomp JJ, Molenaar PC (1996) Involvement of protein kinases in the upregulation of acetylcholine release at endplates of alpha-bungarotoxin-treated rats. J Physiol 493: 175-186. PubMed: 8735703.
-
(1996)
J Physiol
, vol.493
, pp. 175-186
-
-
Plomp, J.J.1
Molenaar, P.C.2
-
29
-
-
0013832488
-
Neuropathologic alterations in the ataxia (paralytic) mouse
-
PubMed: 5855800
-
D'Amato CJ, Hicks SP (1965) Neuropathologic alterations in the ataxia (paralytic) mouse. Arch Pathol 80: 604-612. PubMed: 5855800.
-
(1965)
Arch Pathol
, vol.80
, pp. 604-612
-
-
D'Amato, C.J.1
Hicks, S.P.2
-
30
-
-
0032769571
-
Genetics of familial ALS and consequences for diagnosis
-
French ALS Research Group. doi:10.1016/S0022-510X(99)00022-2. PubMed: 10448977
-
Camu W, Khoris J, Moulard B, Salachas F, Briolotti V et al. (1999) Genetics of familial ALS and consequences for diagnosis. French ALS Research Group. J Neurol Sci 165: S21-S26. doi:10.1016/S0022-510X(99)00022-2. PubMed: 10448977.
-
(1999)
J Neurol Sci
, vol.165
-
-
Camu, W.1
Khoris, J.2
Moulard, B.3
Salachas, F.4
Briolotti, V.5
-
31
-
-
24044471670
-
Background and gender effects on survival in the TgN(SOD1-G93A)1Gur mouse model of ALS
-
doi:10.1016/j.jns.2005.02.006. PubMed: 16024047
-
Heiman-Patterson TD, Deitch JS, Blankenhorn EP, Erwin KL, Perreault MJ et al. (2005) Background and gender effects on survival in the TgN(SOD1-G93A)1Gur mouse model of ALS. J Neurol Sci 236: 1-7. doi:10.1016/j.jns.2005.02.006. PubMed: 16024047.
-
(2005)
J Neurol Sci
, vol.236
, pp. 1-7
-
-
Heiman-Patterson, T.D.1
Deitch, J.S.2
Blankenhorn, E.P.3
Erwin, K.L.4
Perreault, M.J.5
-
32
-
-
0141834020
-
Evidence for a modifying pathway in SMA discordant families: Reduced SMN level decreases the amount of its interacting partners and Htra2-beta1
-
doi:10.1007/s00439-003-1025-2. PubMed: 14520560
-
Helmken C, Hofmann Y, Schoenen F, Oprea G, Raschke H et al. (2003) Evidence for a modifying pathway in SMA discordant families: reduced SMN level decreases the amount of its interacting partners and Htra2-beta1. Hum Genet 114: 11-21. doi:10.1007/s00439-003-1025-2. PubMed: 14520560.
-
(2003)
Hum Genet
, vol.114
, pp. 11-21
-
-
Helmken, C.1
Hofmann, Y.2
Schoenen, F.3
Oprea, G.4
Raschke, H.5
-
33
-
-
33749049581
-
Deubiquitinating enzyme Ubp6 functions noncatalytically to delay proteasomal degradation
-
doi:10.1016/j.cell.2006.07.038. PubMed: 17018280
-
Hanna J, Hathaway NA, Tone Y, Crosas B, Elsasser S et al. (2006) Deubiquitinating enzyme Ubp6 functions noncatalytically to delay proteasomal degradation. Cell 127: 99-111. doi:10.1016/j.cell.2006.07.038. PubMed: 17018280.
-
(2006)
Cell
, vol.127
, pp. 99-111
-
-
Hanna, J.1
Hathaway, N.A.2
Tone, Y.3
Crosas, B.4
Elsasser, S.5
-
34
-
-
77956527159
-
Enhancement of proteasome activity by a small-molecule inhibitor of USP14
-
doi:10.1038/nature09299. PubMed: 20829789
-
Lee BH, Lee MJ, Park S, Oh DC, Elsasser S et al. (2010) Enhancement of proteasome activity by a small-molecule inhibitor of USP14. Nature 467: 179-184. doi:10.1038/nature09299. PubMed: 20829789.
-
(2010)
Nature
, vol.467
, pp. 179-184
-
-
Lee, B.H.1
Lee, M.J.2
Park, S.3
Oh, D.C.4
Elsasser, S.5
-
35
-
-
84868121623
-
Usp14 deficiency increases tau phosphorylation without altering tau degradation or causing tau-dependent deficits
-
PubMed: 23144711
-
Jin YN, Chen PC, Watson JA, Walters BJ, Phillips SE et al. (2012) Usp14 deficiency increases tau phosphorylation without altering tau degradation or causing tau-dependent deficits. PLOS ONE 7: 29. PubMed: 23144711.
-
(2012)
PLOS ONE
, vol.7
, pp. 29
-
-
Jin, Y.N.1
Chen, P.C.2
Watson, J.A.3
Walters, B.J.4
Phillips, S.E.5
-
36
-
-
56249086797
-
Differential effects of Usp14 and Uch-L1 on the ubiquitin proteasome system and synaptic activity
-
doi:10.1016/j.mcn.2008.07.028. PubMed: 18771733
-
Walters BJ, Campbell SL, Chen PC, Taylor AP, Schroeder DG et al. (2008) Differential effects of Usp14 and Uch-L1 on the ubiquitin proteasome system and synaptic activity. Mol Cell Neurosci 39: 539-548. doi:10.1016/j.mcn.2008.07.028. PubMed: 18771733.
-
(2008)
Mol Cell Neurosci
, vol.39
, pp. 539-548
-
-
Walters, B.J.1
Campbell, S.L.2
Chen, P.C.3
Taylor, A.P.4
Schroeder, D.G.5
-
37
-
-
57849104761
-
Transgenic rescue of ataxia mice reveals a male-specific sterlity defect
-
doi:10.1016/j.ydbio.2008.09.021. PubMed: 18926813
-
Crimmins S, Sutovsky M, Chen PC, Huffman AK, Wheeler C et al. (2009) Transgenic rescue of ataxia mice reveals a male-specific sterlity defect. Dev Biol 325: 33-42. doi:10.1016/j.ydbio.2008.09.021. PubMed: 18926813.
-
(2009)
Dev Biol
, vol.325
, pp. 33-42
-
-
Crimmins, S.1
Sutovsky, M.2
Chen, P.C.3
Huffman, A.K.4
Wheeler, C.5
-
38
-
-
84892632978
-
-
The Gene Expression Nervous System Atlas (GENSAT) Project, NINDS Contracts N01NS02331 & HHSN271200723701C to The Rockefeller University (New York, NY)."
-
The Gene Expression Nervous System Atlas (GENSAT) Project, NINDS Contracts N01NS02331 & HHSN271200723701C to The Rockefeller University (New York, NY)."
-
-
-
-
39
-
-
70349653545
-
The ataxia (axJ) mutation causes abnormal GABAA receptor turnover in mice
-
Lappe-Siefke C, Loebrich S, Hevers W, Waidmann OB, Schweizer M, et et al. (2009). The ataxia (axJ) mutation causes abnormal GABAA receptor turnover in mice. PLoS Genet 5(9):e1000631
-
(2009)
PLoS Genet
, vol.5
, Issue.9
-
-
Lappe-Siefke, C.1
Loebrich, S.2
Hevers, W.3
Waidmann, O.B.4
Schweizer, M.5
Al, E.E.6
-
41
-
-
10744224825
-
Ubiquitin carboxy-terminal hydrolase L1 binds to and stabilizes monoubiquitin in neuron
-
doi:10.1093/hmg/ddg211. PubMed: 12913066
-
Osaka H, Wang YL, Takada K, Takizawa S, Setsuie R et al. (2003) Ubiquitin carboxy-terminal hydrolase L1 binds to and stabilizes monoubiquitin in neuron. Hum Mol Genet 12: 1945-1958. doi:10.1093/hmg/ddg211. PubMed: 12913066.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1945-1958
-
-
Osaka, H.1
Wang, Y.L.2
Takada, K.3
Takizawa, S.4
Setsuie, R.5
-
42
-
-
76549084350
-
Ubiquitin carboxyl-terminal hydrolase L1 is required for maintaining the structure and function of the neuromuscular junction
-
doi:10.1073/pnas.0911516107. PubMed: 20080621
-
Chen F, Sugiura Y, Myers KG, Liu Y, Lin W (2010) Ubiquitin carboxyl-terminal hydrolase L1 is required for maintaining the structure and function of the neuromuscular junction. Proc of the Natl Acad of Sciences of the USA 107: 1636-1641. doi:10.1073/pnas.0911516107. PubMed: 20080621.
-
(2010)
Proc of the Natl Acad of Sciences of the USA
, vol.107
, pp. 1636-1641
-
-
Chen, F.1
Sugiura, Y.2
Myers, K.G.3
Liu, Y.4
Lin, W.5
|