-
1
-
-
67650138617
-
Sporadic inclusion body myositis: An unsolved mystery
-
Machado P, Miller A, Holton J, Hanna M. Sporadic inclusion body myositis: an unsolved mystery. Acta Reumatol Port 2009; 34 (2A):161-182.
-
(2009)
Acta Reumatol Port
, vol.34
, Issue.2
, pp. 161-182
-
-
MacHado, P.1
Miller, A.2
Holton, J.3
Hanna, M.4
-
2
-
-
0028961960
-
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): Immunocytochemical and genetic analyses
-
Arahata K, Ishihara T, Fukunaga H, et al. Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses. Muscle Nerve 1995; 2:S56-S66.
-
(1995)
Muscle Nerve
, vol.2
-
-
Arahata, K.1
Ishihara, T.2
Fukunaga, H.3
-
4
-
-
33646483653
-
Brachio-cervical inflammatory myopathies: Clinical, immune, and myopathologic features
-
Pestronk A, Kos K, Lopate G, Al-Lozi MT. Brachio-cervical inflammatory myopathies: clinical, immune, and myopathologic features. Arthritis Rheum 2006; 54:1687-1696.
-
(2006)
Arthritis Rheum
, vol.54
, pp. 1687-1696
-
-
Pestronk, A.1
Kos, K.2
Lopate, G.3
Al-Lozi, M.T.4
-
5
-
-
0024604938
-
Major histocompatibility complex class i antigen expression, immunolocalization of interferon subtypes, and T cell-mediated cytotoxicity in myopathies
-
Emslie-Smith AM, Arahata K, Engel AG. Major histocompatibility complex class I antigen expression, immunolocalization of interferon subtypes, and T cell-mediated cytotoxicity in myopathies. Hum Pathol 1989; 20:224-231.
-
(1989)
Hum Pathol
, vol.20
, pp. 224-231
-
-
Emslie-Smith, A.M.1
Arahata, K.2
Engel, A.G.3
-
6
-
-
0017861736
-
Inclusion body myositis: A distinct variety of idiopathic inflammatory myopathy
-
Carpenter S, Karpati G, Heller I, Eisen A. Inclusion body myositis: a distinct variety of idiopathic inflammatory myopathy. Neurology 1978; 28:8-17.
-
(1978)
Neurology
, vol.28
, pp. 8-17
-
-
Carpenter, S.1
Karpati, G.2
Heller, I.3
Eisen, A.4
-
7
-
-
0024340503
-
Inclusion body myositis. Observations in 40 patients
-
Lotz BP, Engel AG, Nishino H, et al. Inclusion body myositis. Observations in 40 patients. Brain 1989; 112 (Pt 3):727-747.
-
(1989)
Brain
, vol.112
, Issue.PART 3
, pp. 727-747
-
-
Lotz, B.P.1
Engel, A.G.2
Nishino, H.3
-
8
-
-
0026327717
-
Amyloid filaments in inclusion body myositis. Novel findings provide insight into nature of filaments
-
Mendell JR, Sahenk Z, Gales T, Paul L. Amyloid filaments in inclusion body myositis. Novel findings provide insight into nature of filaments. Arch Neurol 1991; 48:1229-1234.
-
(1991)
Arch Neurol
, vol.48
, pp. 1229-1234
-
-
Mendell, J.R.1
Sahenk, Z.2
Gales, T.3
Paul, L.4
-
9
-
-
0027240930
-
Enhanced detection of congo-red-positive amyloid deposits in muscle fibers of inclusion body myositis and brain of Alzheimer;s disease using fluorescence technique
-
Askanas V, Engel WK, Alvarez RB. Enhanced detection of congo-red-positive amyloid deposits in muscle fibers of inclusion body myositis and brain of Alzheimer;s disease using fluorescence technique. Neurology 1993; 43:1265-1267.
-
(1993)
Neurology
, vol.43
, pp. 1265-1267
-
-
Askanas, V.1
Engel, W.K.2
Alvarez, R.B.3
-
10
-
-
0026695045
-
Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis
-
Askanas V, Engel WK, Alvarez RB. Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis. Am J Pathol 1992; 141:31-36.
-
(1992)
Am J Pathol
, vol.141
, pp. 31-36
-
-
Askanas, V.1
Engel, W.K.2
Alvarez, R.B.3
-
11
-
-
59149088668
-
Inclusion body myositis: Review of recent literature
-
Greenberg SA. Inclusion body myositis: review of recent literature. Curr Neurol Neurosci Rep 2009; 9:83-89.
-
(2009)
Curr Neurol Neurosci Rep
, vol.9
, pp. 83-89
-
-
Greenberg, S.A.1
-
12
-
-
68149144251
-
How citation distortions create unfounded authority: Analysis of a citation network
-
Greenberg SA. How citation distortions create unfounded authority: analysis of a citation network. BMJ 2009; 339:b2680.
-
(2009)
BMJ
, vol.339
-
-
Greenberg, S.A.1
-
13
-
-
70349322489
-
Nature of ;Tau; immunoreactivity in normal myonuclei and inclusion body myositis
-
Salajegheh M, Pinkus JL, Nazareno R, et al. Nature of ;Tau; immunoreactivity in normal myonuclei and inclusion body myositis. Muscle Nerve 2009; 40:520-528.
-
(2009)
Muscle Nerve
, vol.40
, pp. 520-528
-
-
Salajegheh, M.1
Pinkus, J.L.2
Nazareno, R.3
-
14
-
-
67650264666
-
Sarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositis
-
Salajegheh M, Pinkus JL, Taylor JP, et al. Sarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositis. Muscle Nerve 2009; 40: 19-31.
-
(2009)
Muscle Nerve
, vol.40
, pp. 19-31
-
-
Salajegheh, M.1
Pinkus, J.L.2
Taylor, J.P.3
-
15
-
-
58749094423
-
Inflammatory myopathies with mitochondrial pathology and protein aggregates
-
Temiz P, Weihl CC, Pestronk A. Inflammatory myopathies with mitochondrial pathology and protein aggregates. J Neurol Sci 2009; 278:25-29.
-
(2009)
J Neurol Sci
, vol.278
, pp. 25-29
-
-
Temiz, P.1
Weihl, C.C.2
Pestronk, A.3
-
16
-
-
0029019593
-
Mitochondrial DNA deletions in muscle fibers in inclusion body myositis
-
Oldfors A, Moslemi AR, Fyhr IM, et al. Mitochondrial DNA deletions in muscle fibers in inclusion body myositis. J Neuropathol Exp Neurol 1995; 54:581-587.
-
(1995)
J Neuropathol Exp Neurol
, vol.54
, pp. 581-587
-
-
Oldfors, A.1
Moslemi, A.R.2
Fyhr, I.M.3
-
17
-
-
8944243541
-
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients
-
Santorelli FM, Sciacco M, Tanji K, et al. Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients. Ann Neurol 1996; 39:789-795.
-
(1996)
Ann Neurol
, vol.39
, pp. 789-795
-
-
Santorelli, F.M.1
Sciacco, M.2
Tanji, K.3
-
18
-
-
0031044461
-
Polymyositis with cytochrome oxidase negative muscle fibres. Early quadriceps weakness and poor response to immunosuppressive therapy
-
Blume G, Pestronk A, Frank B, Johns DR. Polymyositis with cytochrome oxidase negative muscle fibres. Early quadriceps weakness and poor response to immunosuppressive therapy. Brain 1997; 120 (Pt 1):39-45.
-
(1997)
Brain
, vol.120
, Issue.PART 1
, pp. 39-45
-
-
Blume, G.1
Pestronk, A.2
Frank, B.3
Johns, D.R.4
-
19
-
-
0037135111
-
The amyloid hypothesis of Alzheimer;s disease: Progress and problems on the road to therapeutics
-
Hardy J, Selkoe DJ. The amyloid hypothesis of Alzheimer;s disease: progress and problems on the road to therapeutics. Science 2002; 297:353-356.
-
(2002)
Science
, vol.297
, pp. 353-356
-
-
Hardy, J.1
Selkoe, D.J.2
-
20
-
-
76449085569
-
Gamma-secretases: From cell biology to therapeutic strategies
-
Bergmans BA, De Strooper B. gamma-secretases: from cell biology to therapeutic strategies. Lancet Neurol 2010; 9:215-226.
-
(2010)
Lancet Neurol
, vol.9
, pp. 215-226
-
-
Bergmans, B.A.1
De Strooper, B.2
-
21
-
-
0021256895
-
Alzheimer;s disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid protein
-
Glenner GG, Wong CW. Alzheimer;s disease: initial report of the purification and characterization of a novel cerebrovascular amyloid protein. Biochem Biophys Res Commun 1984; 120:885-890.
-
(1984)
Biochem Biophys Res Commun
, vol.120
, pp. 885-890
-
-
Glenner, G.G.1
Wong, C.W.2
-
22
-
-
64449088789
-
Amyloid-beta42 is preferentially accumulated in muscle fibers of patients with sporadic inclusion-body myositis
-
Vattemi G, Nogalska A, King Engel W, et al. Amyloid-beta42 is preferentially accumulated in muscle fibers of patients with sporadic inclusion-body myositis. Acta Neuropathol 2009; 117:569-574.
-
(2009)
Acta Neuropathol
, vol.117
, pp. 569-574
-
-
Vattemi, G.1
Nogalska, A.2
King Engel, W.3
-
23
-
-
0028169901
-
Expression of beta-amyloid precursor protein gene is developmentally regulated in human muscle fibers in vivo and in vitro
-
Sarkozi E, Askanas V, Johnson SA, et al. Expression of beta-amyloid precursor protein gene is developmentally regulated in human muscle fibers in vivo and in vitro. Exp Neurol 1994; 128:27-33.
-
(1994)
Exp Neurol
, vol.128
, pp. 27-33
-
-
Sarkozi, E.1
Askanas, V.2
Johnson, S.A.3
-
24
-
-
0029971055
-
Difference in expression of phosphorylated tau epitopes between sporadic inclusion-body myositis and hereditary inclusion-body myopathies
-
Mirabella M, Alvarez RB, Bilak M, et al. Difference in expression of phosphorylated tau epitopes between sporadic inclusion-body myositis and hereditary inclusion-body myopathies. J Neuropathol Exp Neurol 1996; 55:774-786.
-
(1996)
J Neuropathol Exp Neurol
, vol.55
, pp. 774-786
-
-
Mirabella, M.1
Alvarez, R.B.2
Bilak, M.3
-
25
-
-
41949119043
-
TDP-43 A315T mutation in familial motor neuron disease
-
Gitcho MA, Baloh RH, Chakraverty S, et al. TDP-43 A315T mutation in familial motor neuron disease. Ann Neurol 2008; 63:535-538.
-
(2008)
Ann Neurol
, vol.63
, pp. 535-538
-
-
Gitcho, M.A.1
Baloh, R.H.2
Chakraverty, S.3
-
26
-
-
42649120983
-
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
-
Kabashi E, Valdmanis PN, Dion P, et al. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. NatGenet 2008; 40:572-574.
-
(2008)
NatGenet
, vol.40
, pp. 572-574
-
-
Kabashi, E.1
Valdmanis, P.N.2
Dion, P.3
-
27
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
Sreedharan J, Blair IP, Tripathi VB, et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 2008; 319:1668-1672.
-
(2008)
Science
, vol.319
, pp. 1668-1672
-
-
Sreedharan, J.1
Blair, I.P.2
Tripathi, V.B.3
-
28
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann M, Sampathu DM, Kwong LK, et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 2006; 314:130-133.
-
(2006)
Science
, vol.314
, pp. 130-133
-
-
Neumann, M.1
Sampathu, D.M.2
Kwong, L.K.3
-
29
-
-
59249094498
-
TDP-43 accumulation is common in myopathies with rimmed vacuoles
-
Kusters B, van Hoeve BJ, Schelhaas HJ, et al. TDP-43 accumulation is common in myopathies with rimmed vacuoles. Acta Neuropathol 2009; 117:209-211.
-
(2009)
Acta Neuropathol
, vol.117
, pp. 209-211
-
-
Kusters, B.1
Van Hoeve, B.J.2
Schelhaas, H.J.3
-
30
-
-
65349175153
-
TAR DNA-binding protein 43 accumulation in protein aggregate myopathies
-
Olive M, Janue A, Moreno D, et al. TAR DNA-binding protein 43 accumulation in protein aggregate myopathies. J Neuropathol Exp Neurol 2009; 68:262-273.
-
(2009)
J Neuropathol Exp Neurol
, vol.68
, pp. 262-273
-
-
Olive, M.1
Janue, A.2
Moreno, D.3
-
31
-
-
53149138951
-
TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia
-
Weihl CC, Temiz P, Miller SE, et al. TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia. J Neurol Neurosurg Psychiatry 2008; 79:1186-1189.
-
(2008)
J Neurol Neurosurg Psychiatry
, vol.79
, pp. 1186-1189
-
-
Weihl, C.C.1
Temiz, P.2
Miller, S.E.3
-
32
-
-
77950479450
-
Autophagy in skeletal muscle
-
Sandri M. Autophagy in skeletal muscle. FEBS Lett 2010; 584:1411-1416.
-
(2010)
FEBS Lett
, vol.584
, pp. 1411-1416
-
-
Sandri, M.1
-
33
-
-
35448981935
-
Autophagy: From phenomenology to molecular understanding in less than a decade
-
Klionsky DJ. Autophagy: from phenomenology to molecular understanding in less than a decade. Nat Rev Mol Cell Biol 2007; 8:931-937.
-
(2007)
Nat Rev Mol Cell Biol
, vol.8
, pp. 931-937
-
-
Klionsky, D.J.1
-
34
-
-
70449927247
-
Autophagy is required to maintain muscle mass
-
Masiero E, Agatea L, Mammucari C, et al. Autophagy is required to maintain muscle mass. Cell Metab 2009; 10:507-515.
-
(2009)
Cell Metab
, vol.10
, pp. 507-515
-
-
Masiero, E.1
Agatea, L.2
Mammucari, C.3
-
35
-
-
57049094929
-
Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease
-
Raben N, Hill V, Shea L, et al. Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease. Hum Mol Genet 2008; 17:3897-3908.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3897-3908
-
-
Raben, N.1
Hill, V.2
Shea, L.3
-
36
-
-
34250864795
-
Protein turnover via autophagy: Implications for metabolism
-
Mizushima N, Klionsky DJ. Protein turnover via autophagy: implications for metabolism. Annu Rev Nutr 2007; 27:19-40.
-
(2007)
Annu Rev Nutr
, vol.27
, pp. 19-40
-
-
Mizushima, N.1
Klionsky, D.J.2
-
37
-
-
34848886914
-
Autophagosome formation: Core machinery and adaptations
-
Xie Z, Klionsky DJ. Autophagosome formation: core machinery and adaptations. Nat Cell Biol 2007; 9:1102-1109.
-
(2007)
Nat Cell Biol
, vol.9
, pp. 1102-1109
-
-
Xie, Z.1
Klionsky, D.J.2
-
38
-
-
0034329418
-
LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing
-
Kabeya Y, Mizushima N, Ueno T, et al. LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing. Embo J 2000; 19:5720-5728.
-
(2000)
Embo J
, vol.19
, pp. 5720-5728
-
-
Kabeya, Y.1
Mizushima, N.2
Ueno, T.3
-
39
-
-
36849089101
-
Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice
-
Komatsu M, Waguri S, Koike M, et al. Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice. Cell 2007; 131:1149-1163.
-
(2007)
Cell
, vol.131
, pp. 1149-1163
-
-
Komatsu, M.1
Waguri, S.2
Koike, M.3
-
40
-
-
53049103308
-
Structural basis for sorting mechanism of p62 in selective autophagy
-
Ichimura Y, Kumanomidou T, Sou YS, et al. Structural basis for sorting mechanism of p62 in selective autophagy. J Biol Chem 2008; 283:22847-22857.
-
(2008)
J Biol Chem
, vol.283
, pp. 22847-22857
-
-
Ichimura, Y.1
Kumanomidou, T.2
Sou, Y.S.3
-
41
-
-
34548259958
-
P62/SQSTM1 binds directly to Atg8/ LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy
-
Pankiv S, Clausen TH, Lamark T, et al. p62/SQSTM1 binds directly to Atg8/ LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy. J Biol Chem 2007; 282:24131-24145.
-
(2007)
J Biol Chem
, vol.282
, pp. 24131-24145
-
-
Pankiv, S.1
Clausen, T.H.2
Lamark, T.3
-
42
-
-
36448940798
-
FoxO3 controls autophagy in skeletal muscle in vivo
-
Mammucari C, Milan G, Romanello V, et al. FoxO3 controls autophagy in skeletal muscle in vivo. Cell Metab 2007; 6:458-471.
-
(2007)
Cell Metab
, vol.6
, pp. 458-471
-
-
Mammucari, C.1
Milan, G.2
Romanello, V.3
-
43
-
-
38949108670
-
Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes
-
Klionsky DJ, Abeliovich H, Agostinis P, et al. Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes. Autophagy 2008; 4:151-175.
-
(2008)
Autophagy
, vol.4
, pp. 151-175
-
-
Klionsky, D.J.1
Abeliovich, H.2
Agostinis, P.3
-
44
-
-
68349097450
-
P62/SQSTM1 is overexpressed and prominently accumulated in inclusions of sporadic inclusion-body myositis muscle fibers, and can help differentiating it from polymyositis and dermatomyositis
-
Nogalska A, Terracciano C, D;Agostino C, et al. p62/SQSTM1 is overexpressed and prominently accumulated in inclusions of sporadic inclusion-body myositis muscle fibers, and can help differentiating it from polymyositis and dermatomyositis. Acta Neuropathol 2009; 118:407-413.
-
(2009)
Acta Neuropathol
, vol.118
, pp. 407-413
-
-
Nogalska, A.1
Terracciano, C.2
D3
agostino, C.4
-
45
-
-
0036144410
-
P62 Is a common component of cytoplasmic inclusions in protein aggregation diseases
-
Zatloukal K, Stumptner C, Fuchsbichler A, et al. p62 Is a common component of cytoplasmic inclusions in protein aggregation diseases. Am J Pathol 2002; 160:255-263.
-
(2002)
Am J Pathol
, vol.160
, pp. 255-263
-
-
Zatloukal, K.1
Stumptner, C.2
Fuchsbichler, A.3
-
46
-
-
74049124412
-
Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease
-
Ju JS, Fuentealba RA, Miller SE, et al. Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease. J Cell Biol 2009; 187:875-888.
-
(2009)
J Cell Biol
, vol.187
, pp. 875-888
-
-
Ju, J.S.1
Fuentealba, R.A.2
Miller, S.E.3
-
47
-
-
34249937267
-
Beta-amyloid is a substrate of autophagy in sporadic inclusion body myositis
-
Lunemann JD, Schmidt J, Schmid D, et al. Beta-amyloid is a substrate of autophagy in sporadic inclusion body myositis. Ann Neurol 2007; 61:476-483.
-
(2007)
Ann Neurol
, vol.61
, pp. 476-483
-
-
Lunemann, J.D.1
Schmidt, J.2
Schmid, D.3
-
48
-
-
34447623544
-
Expression of autophagy-associated genes in skeletal muscle: An experimental model of chloroquineinduced myopathy
-
Kimura N, Kumamoto T, Kawamura Y, et al. Expression of autophagy-associated genes in skeletal muscle: an experimental model of chloroquineinduced myopathy. Pathobiology 2007; 74:169-176.
-
(2007)
Pathobiology
, vol.74
, pp. 169-176
-
-
Kimura, N.1
Kumamoto, T.2
Kawamura, Y.3
-
49
-
-
33644869497
-
Inclusion-body myositis: A myodegenerative conformational disorder associated with Abeta, protein misfolding, and proteasome inhibition
-
Askanas V, Engel WK. Inclusion-body myositis: a myodegenerative conformational disorder associated with Abeta, protein misfolding, and proteasome inhibition. Neurology 2006; 66:S39-48.
-
(2006)
Neurology
, vol.66
-
-
Askanas, V.1
Engel, W.K.2
-
50
-
-
0033934231
-
Novel immunolocalization of alphasynuclein in human muscle of inclusion-body myositis, regenerating and necrotic muscle fibers, and at neuromuscular junctions
-
Askanas V, Engel WK, Alvarez RB, et al. Novel immunolocalization of alphasynuclein in human muscle of inclusion-body myositis, regenerating and necrotic muscle fibers, and at neuromuscular junctions. J Neuropathol Exp Neurol 2000; 59:592-598.
-
(2000)
J Neuropathol Exp Neurol
, vol.59
, pp. 592-598
-
-
Askanas, V.1
Engel, W.K.2
Alvarez, R.B.3
-
51
-
-
0027433773
-
Prion protein is abnormally accumulated in inclusion-body myositis
-
Askanas V, Bilak M, Engel WK, et al. Prion protein is abnormally accumulated in inclusion-body myositis. Neuroreport 1993; 5:25-28.
-
(1993)
Neuroreport
, vol.5
, pp. 25-28
-
-
Askanas, V.1
Bilak, M.2
Engel, W.K.3
-
52
-
-
48949086699
-
Inflammation induces tau pathology in inclusion body myositis model via glycogen synthase kinase-3beta
-
Kitazawa M, Trinh DN, LaFerla FM. Inflammation induces tau pathology in inclusion body myositis model via glycogen synthase kinase-3beta. Ann Neurol 2008; 64:15-24.
-
(2008)
Ann Neurol
, vol.64
, pp. 15-24
-
-
Kitazawa, M.1
Trinh, D.N.2
Laferla, F.M.3
-
53
-
-
0037197835
-
Inclusion body myositis-like phenotype induced by transgenic overexpression of beta APP in skeletal muscle
-
Sugarman MC, Yamasaki TR, Oddo S, et al. Inclusion body myositis-like phenotype induced by transgenic overexpression of beta APP in skeletal muscle. Proc Natl Acad Sci U S A 2002; 99:6334-6339.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 6334-6339
-
-
Sugarman, M.C.1
Yamasaki, T.R.2
Oddo, S.3
-
54
-
-
67650497775
-
Secretion of amyloidogenic gelsolin progressively compromises protein homeostasis leading to the intracellular aggregation of proteins
-
Page LJ, Suk JY, Bazhenova L, et al. Secretion of amyloidogenic gelsolin progressively compromises protein homeostasis leading to the intracellular aggregation of proteins. Proc Natl Acad Sci U S A 2009; 106:11125-11130.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 11125-11130
-
-
Page, L.J.1
Suk, J.Y.2
Bazhenova, L.3
-
55
-
-
0035033712
-
Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation
-
Chiesa R, Pestronk A, Schmidt RE, et al. Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation. Neurobiol Dis 2001; 8:279-288.
-
(2001)
Neurobiol Dis
, vol.8
, pp. 279-288
-
-
Chiesa, R.1
Pestronk, A.2
Schmidt, R.E.3
-
56
-
-
67049165108
-
Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis
-
Parker KC, Kong SW, Walsh RJ, et al. Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis. Muscle Nerve 2009; 39:739-753.
-
(2009)
Muscle Nerve
, vol.39
, pp. 739-753
-
-
Parker, K.C.1
Kong, S.W.2
Walsh, R.J.3
-
57
-
-
2442651500
-
Proteasomal expression, induction of immunoproteasome subunits, and local MHC class i presentation in myofibrillar myopathy and inclusion body myositis
-
Ferrer I, Martin B, Castano JG, et al. Proteasomal expression, induction of immunoproteasome subunits, and local MHC class I presentation in myofibrillar myopathy and inclusion body myositis. J Neuropathol Exp Neurol 2004; 63:484-498.
-
(2004)
J Neuropathol Exp Neurol
, vol.63
, pp. 484-498
-
-
Ferrer, I.1
Martin, B.2
Castano, J.G.3
-
59
-
-
50249175120
-
Chemical and biological approaches synergize to ameliorate protein-folding diseases
-
Mu TW, Ong DS, Wang YJ, et al. Chemical and biological approaches synergize to ameliorate protein-folding diseases. Cell 2008; 134:769-781.
-
(2008)
Cell
, vol.134
, pp. 769-781
-
-
Mu, T.W.1
Ong, D.S.2
Wang, Y.J.3
-
60
-
-
1842483843
-
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
-
Watts GD, Wymer J, Kovach MJ, et al. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. Nat Genet 2004; 36:377-381.
-
(2004)
Nat Genet
, vol.36
, pp. 377-381
-
-
Watts, G.D.1
Wymer, J.2
Kovach, M.J.3
-
61
-
-
18544394748
-
RNA interference of valosin-containing protein (VCP/p97) reveals multiple cellular roles linked to ubiquitin/proteasome-dependent proteolysis
-
Wojcik C, Yano M, DeMartino GN. RNA interference of valosin-containing protein (VCP/p97) reveals multiple cellular roles linked to ubiquitin/ proteasome-dependent proteolysis. J Cell Sci 2004; 117 (Pt 2):281-292.
-
(2004)
J Cell Sci
, vol.117
, Issue.PART 2
, pp. 281-292
-
-
Wojcik, C.1
Yano, M.2
Demartino, G.N.3
-
62
-
-
77952533111
-
VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD
-
Tresse E, Salomons FA, Vesa J, et al. VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD. Autophagy 2010; 6:1-11.
-
(2010)
Autophagy
, vol.6
, pp. 1-11
-
-
Tresse, E.1
Salomons, F.A.2
Vesa, J.3
-
63
-
-
34447093377
-
Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice
-
WeihlCC, Miller SE, Hanson PI, Pestronk A. Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice. Hum Mol Genet 2007; 16:919-928.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 919-928
-
-
Weihlcc Miller, S.E.1
Hanson, P.I.2
Pestronk, A.3
|