-
1
-
-
0014207442
-
Myxovirus-like structures in a case of human chronic polymyositis
-
Chou S. Myxovirus-like structures in a case of human chronic polymyositis. Science 1967; 158: 1453-5
-
(1967)
Science
, vol.158
, pp. 1453-1455
-
-
Chou, S.1
-
2
-
-
0015129206
-
Inclusion body myositis
-
Yunis E, Samaha F. Inclusion body myositis. Lab Invest 1971; 25: 240-8
-
(1971)
Lab Invest
, vol.25
, pp. 240-248
-
-
Yunis, E.1
Samaha, F.2
-
3
-
-
0034649445
-
Epidemiology of inclusion body myositis in the Netherlands: A nationwide study
-
Badrising U, Maat-Schieman M, van Duinen S, Breedveld F, van Doorn P, van Engelen B, van den Hoogen F, Hoogendijk J, Höweler C, de Jager A, Jennekens F, Koehler P, van der Leeuw H, de Visser M, Verschuuren J, Wintzen A. Epidemiology of inclusion body myositis in the Netherlands: a nationwide study. Neurology 2000; 55: 1385-7
-
(2000)
Neurology
, vol.55
, pp. 1385-1387
-
-
Badrising, U.1
Maat-Schieman, M.2
Van Duinen, S.3
Breedveld, F.4
Van Doorn, P.5
Van Engelen, B.6
Van Den Hoogen, F.7
Hoogendijk, J.8
Höweler, C.9
De Jager, A.10
Jennekens, F.11
Koehler, P.12
Van Der Leeuw, H.13
De Visser, M.14
Verschuuren, J.15
Wintzen, A.16
-
4
-
-
0028787389
-
Inclusion body myositis and myopathies
-
Griggs R, Askanas V, DiMauro S, Engel A, Karpati G, Mendell J, Rowland L. Inclusion body myositis and myopathies. Neurol Prog 1995; 38: 705-13
-
(1995)
Neurol Prog
, vol.38
, pp. 705-713
-
-
Griggs, R.1
Askanas, V.2
DiMauro, S.3
Engel, A.4
Karpati, G.5
Mendell, J.6
Rowland, L.7
-
5
-
-
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
-
6
-
-
0000788880
-
Inclusion-body myositis: Pathologic changes
-
Eds V Askanas, G Serratrice, W Engel. Cambridge: Cambridge University Press
-
Figarella-Branger D, Baeta-Machado A, Putzu G, Pellissier JF. Inclusion-body myositis: pathologic changes. In Inclusion-Body Myositis and Myopathies. Eds V Askanas, G Serratrice, W Engel. Cambridge: Cambridge University Press, 1998; 137-55
-
(1998)
Inclusion-Body Myositis and Myopathies
, pp. 137-155
-
-
Figarella-Branger, D.1
Baeta-Machado, A.2
Putzu, G.3
Pellissier, J.F.4
-
7
-
-
0030933296
-
Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9
-
Ikeuchi T, Asaka T, Saito M, Tanaka H, Higuchi S, Tanaka K, Saida K, Uyama E, Mizusawa H, Fukuhara N, Nonaka I, Takamori M, Tsuji S. Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9. Ann Neurol 1997; 41: 432-7
-
(1997)
Ann Neurol
, vol.41
, pp. 432-437
-
-
Ikeuchi, T.1
Asaka, T.2
Saito, M.3
Tanaka, H.4
Higuchi, S.5
Tanaka, K.6
Saida, K.7
Uyama, E.8
Mizusawa, H.9
Fukuhara, N.10
Nonaka, I.11
Takamori, M.12
Tsuji, S.13
-
8
-
-
18244381306
-
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: Hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia
-
Kovach MJ, Waggoner B, Leal SM, Gelber D, Khardori R, Levenstien MA, Shanks CA, Gregg G, Al-Lozi MT, Miller T, Rakowicz W, Lopate G, Florence J, Glosser G, Simmons Z, Morris JC, Whyte MP, Pestronk A, Kimonis VE. Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia. Mol Genet Metab 2001; 74: 458-75
-
(2001)
Mol Genet Metab
, vol.74
, pp. 458-475
-
-
Kovach, M.J.1
Waggoner, B.2
Leal, S.M.3
Gelber, D.4
Khardori, R.5
Levenstien, M.A.6
Shanks, C.A.7
Gregg, G.8
Al-Lozi, M.T.9
Miller, T.10
Rakowicz, W.11
Lopate, G.12
Florence, J.13
Glosser, G.14
Simmons, Z.15
Morris, J.C.16
Whyte, M.P.17
Pestronk, A.18
Kimonis, V.E.19
-
9
-
-
17944366749
-
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
-
Eisenberg I, Avidan N, Potikha T, Hochner H, Chen M, Olender T, Barash M, Shemesh M, Sadeh M, Grabov-Nardini G, Shmilevich I, Friedmann A, Karpati G, Bradley WG, Baumbach L, Lancet D, Asher EB, Beckmann JS, Argov Z, Mitrani-Rosenbaum S. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy. Nat Genet 2001; 29: 83-7
-
(2001)
Nat Genet
, vol.29
, pp. 83-87
-
-
Eisenberg, I.1
Avidan, N.2
Potikha, T.3
Hochner, H.4
Chen, M.5
Olender, T.6
Barash, M.7
Shemesh, M.8
Sadeh, M.9
Grabov-Nardini, G.10
Shmilevich, I.11
Friedmann, A.12
Karpati, G.13
Bradley, W.G.14
Baumbach, L.15
Lancet, D.16
Asher, E.B.17
Beckmann, J.S.18
Argov, Z.19
Mitrani-Rosenbaum, S.20
more..
-
10
-
-
0034687697
-
Autosomal dominant myopathy: Missense mutation (Glu706→Lys) in the myosin heavy chain IIa gene
-
Martinsson A, Oldfors A, Darin N, Berg K, Tajsharghi H, Kyllerman M, Wahlstrom J. Autosomal dominant myopathy: missense mutation (Glu706→Lys) in the myosin heavy chain IIa gene. Proc Natl Acad Sci USA 2000; 97: 14614-9
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 14614-14619
-
-
Martinsson, A.1
Oldfors, A.2
Darin, N.3
Berg, K.4
Tajsharghi, H.5
Kyllerman, M.6
Wahlstrom, J.7
-
11
-
-
0037066098
-
Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age
-
Tajsharghi H, Thornell LE, Darin N, Martinsson T, Kyllerman M, Wahlstrom J, Oldfors A. Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age. Neurology 2002; 58: 780-6
-
(2002)
Neurology
, vol.58
, pp. 780-786
-
-
Tajsharghi, H.1
Thornell, L.E.2
Darin, N.3
Martinsson, T.4
Kyllerman, M.5
Wahlstrom, J.6
Oldfors, A.7
-
12
-
-
0035144844
-
Autosomal dominant distal myopathy: Further evidence of a chromosome 14 locus
-
Voit T, Kutz P, Leube B, Neuen-Jacob B, Schroder J, Cavalotti D, Vaccario M, Schaper J, Broich P, Cohn R, Baethmann M, Gohlich-Ratmann G, Scoppetta C, Herrmann R. Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus. Neuromuscul Disord 2001; 11: 11-9
-
(2001)
Neuromuscul Disord
, vol.11
, pp. 11-19
-
-
Voit, T.1
Kutz, P.2
Leube, B.3
Neuen-Jacob, B.4
Schroder, J.5
Cavalotti, D.6
Vaccario, M.7
Schaper, J.8
Broich, P.9
Cohn, R.10
Baethmann, M.11
Gohlich-Ratmann, G.12
Scoppetta, C.13
Herrmann, R.14
-
13
-
-
0020045356
-
Inclusion-body myositis: Clinicopathological studies and isolation of an adenovirus type 2 from muscle biopsy specimen
-
Mikol J, Felten-Papaiconomou A, Ferchal F, Perol Y, Gautier B, Haguenau M, Pepin B. Inclusion-body myositis: clinicopathological studies and isolation of an adenovirus type 2 from muscle biopsy specimen. Ann Neurol 1982;11:576-81
-
(1982)
Ann Neurol
, vol.11
, pp. 576-581
-
-
Mikol, J.1
Felten-Papaiconomou, A.2
Ferchal, F.3
Perol, Y.4
Gautier, B.5
Haguenau, M.6
Pepin, B.7
-
14
-
-
0022538255
-
Inclusion body myositis: A chronic persistent mumps myositis?
-
Chou S. Inclusion body myositis: a chronic persistent mumps myositis? Hum Pathol 1986; 17: 765-77
-
(1986)
Hum Pathol
, vol.17
, pp. 765-777
-
-
Chou, S.1
-
15
-
-
0029908563
-
The immunopathologic and inflammatory differences between dermatomyositis, polymyositis and sporadic inclusion body myositis
-
Dalakas M, Sivakumar K. The immunopathologic and inflammatory differences between dermatomyositis, polymyositis and sporadic inclusion body myositis. Curr Opin Neurol 1996; 9: 235-9
-
(1996)
Curr Opin Neurol
, vol.9
, pp. 235-239
-
-
Dalakas, M.1
Sivakumar, K.2
-
16
-
-
0036158812
-
Clinical and serological characteristics of 125 Dutch myositis patients
-
Hengstman G, Brouwer R, Vree Egberts W, Seelig H, Jongen P, van Venrooij B, van Engelen B. Clinical and serological characteristics of 125 Dutch myositis patients. J Neurol 2002; 249: 69-75
-
(2002)
J Neurol
, vol.249
, pp. 69-75
-
-
Hengstman, G.1
Brouwer, R.2
Vree Egberts, W.3
Seelig, H.4
Jongen, P.5
Van Venrooij, B.6
Van Engelen, B.7
-
17
-
-
0029938020
-
Cytochrome C oxydase deficiencies in the muscle of patients with inflammatory myopathies
-
Chariot P, Ruet E, Authier J, Labes D, Poron F, Gherardi R. Cytochrome C oxydase deficiencies in the muscle of patients with inflammatory myopathies. Acta Neuropathol 1996; 91: 530-6
-
(1996)
Acta Neuropathol
, vol.91
, pp. 530-536
-
-
Chariot, P.1
Ruet, E.2
Authier, J.3
Labes, D.4
Poron, F.5
Gherardi, R.6
-
18
-
-
0030836286
-
Analysis of multiple mitochondrial DNA deletions in inclusion body myositis
-
Moslemi A, Lindberg C, Oldfors A. Analysis of multiple mitochondrial DNA deletions in inclusion body myositis. Hum Mutat 1997; 10: 381-6
-
(1997)
Hum Mutat
, vol.10
, pp. 381-386
-
-
Moslemi, A.1
Lindberg, C.2
Oldfors, A.3
-
19
-
-
0031808684
-
Characterization of the mitochondrial DNA abnormalities in the skeletal muscle of patients with inclusion body myositis
-
Horvath R, Fu K, Johns T, Genge A, Karpati G, Shoubridge E. Characterization of the mitochondrial DNA abnormalities in the skeletal muscle of patients with inclusion body myositis. J Neuropathol Exp Neurol 1998; 57: 396-403
-
(1998)
J Neuropathol Exp Neurol
, vol.57
, pp. 396-403
-
-
Horvath, R.1
Fu, K.2
Johns, T.3
Genge, A.4
Karpati, G.5
Shoubridge, E.6
-
20
-
-
0028230941
-
Conspicuous accumulation of a single-stranded DNA binding protein in skeletal muscle fibers in inclusion body myositis
-
Nalbantoglu J, Karpati G, Carpenter S. Conspicuous accumulation of a single-stranded DNA binding protein in skeletal muscle fibers in inclusion body myositis. Am J Pathol 1994; 144: 874-82
-
(1994)
Am J Pathol
, vol.144
, pp. 874-882
-
-
Nalbantoglu, J.1
Karpati, G.2
Carpenter, S.3
-
22
-
-
9444226061
-
Myosite à inclusions et maladies neuromusculaires à vacuoles bordées
-
Eds G Serratrice, J Pellissier, J Pouget, O Blin, D Figarella-Branger, F Billé-Turc, J Azulay. Paris: Expansion Scientifique Francaise
-
Pellissier JF, Figarella-Branger D, Pouget J, Serratrice G. Myosite à inclusions et maladies neuromusculaires à vacuoles bordées. In Nervous System, Muscles and Systemic Diseases. Eds G Serratrice, J Pellissier, J Pouget, O Blin, D Figarella-Branger, F Billé-Turc, J Azulay. Paris: Expansion Scientifique Francaise, 1993; 99-108
-
(1993)
Nervous System, Muscles and Systemic Diseases
, pp. 99-108
-
-
Pellissier, J.F.1
Figarella-Branger, D.2
Pouget, J.3
Serratrice, G.4
-
23
-
-
0028246491
-
Twisted tubulofilaments of inclusion-body myositis resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau
-
Askanas V, Engel W, Bilak M, Alvarez R, Selkoe D. Twisted tubulofilaments of inclusion-body myositis resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau. Am J Pathol 1994; 144: 177-87
-
(1994)
Am J Pathol
, vol.144
, pp. 177-187
-
-
Askanas, V.1
Engel, W.2
Bilak, M.3
Alvarez, R.4
Selkoe, D.5
-
25
-
-
0022827447
-
Identification of cDNA clones for the human microtubule associated protein tau and chromosomal location of genes for tau and microtubule-associated protein 2
-
Neve R, Harris P, Kosik K, Kurnit D, Donlon A. Identification of cDNA clones for the human microtubule associated protein tau and chromosomal location of genes for tau and microtubule-associated protein 2. Mol Brain Res 1986;1:271-80
-
(1986)
Mol Brain Res
, vol.1
, pp. 271-280
-
-
Neve, R.1
Harris, P.2
Kosik, K.3
Kurnit, D.4
Donlon, A.5
-
26
-
-
0026488111
-
Structure and novel exons of the human tau gene
-
Andreadis A, Brown W, Kosik K. Structure and novel exons of the human tau gene. Biochemistry 1992; 31: 10626-33
-
(1992)
Biochemistry
, vol.31
, pp. 10626-10633
-
-
Andreadis, A.1
Brown, W.2
Kosik, K.3
-
27
-
-
0026595846
-
Tau proteins of Alzheimer paired helical filaments: Abnormal phosphorylation of all six brain isoforms
-
Goedert M, Spillantini M, Crowther R. Tau proteins of Alzheimer paired helical filaments: abnormal phosphorylation of all six brain isoforms. Neuron 1992; 8: 159-68
-
(1992)
Neuron
, vol.8
, pp. 159-168
-
-
Goedert, M.1
Spillantini, M.2
Crowther, R.3
-
28
-
-
0033850407
-
Tau protein isoforms, phosphorylation and role in neurodegenerative disorders
-
Buée L, Bussière T, Buée-Scherrer V, Delacourte A, Hof P. Tau protein isoforms, phosphorylation and role in neurodegenerative disorders. Brain Res Rev 2000; 33: 95-130
-
(2000)
Brain Res Rev
, vol.33
, pp. 95-130
-
-
Buée, L.1
Bussière, T.2
Buée-Scherrer, V.3
Delacourte, A.4
Hof, P.5
-
29
-
-
0029971055
-
Difference in expression of phosphorylated tau epitopes between sporadic inclusion-body myosiotis and hereditary inclusion-body myopathies
-
Mirabella M, Alvarez R, Bilak M, Engel W, Askanas V. Difference in expression of phosphorylated tau epitopes between sporadic inclusion-body myosiotis and hereditary inclusion-body myopathies. J Neuropathol Exp Neurol 1996; 55: 774-86
-
(1996)
J Neuropathol Exp Neurol
, vol.55
, pp. 774-786
-
-
Mirabella, M.1
Alvarez, R.2
Bilak, M.3
Engel, W.4
Askanas, V.5
-
30
-
-
0028304713
-
Microtubule-associated protein Tau epitopes are present in fiber lesions in diverse muscle disorders
-
Lübke U, Six J, Villanova M, Boons J, Vandermeeren M, Ceuterick C, Cras P, Martin J. Microtubule-associated protein Tau epitopes are present in fiber lesions in diverse muscle disorders. Am J Pathol 1994; 145: 175-88
-
(1994)
Am J Pathol
, vol.145
, pp. 175-188
-
-
Lübke, U.1
Six, J.2
Villanova, M.3
Boons, J.4
Vandermeeren, M.5
Ceuterick, C.6
Cras, P.7
Martin, J.8
-
31
-
-
0025822933
-
Immunolocalization of ubiquitin in muscle biopsies of patients with inclusion body myositis and oculopharyngeal muscular dystrophy
-
Askanas V, Serdaroglu P, Engel W, Alvarez R. Immunolocalization of ubiquitin in muscle biopsies of patients with inclusion body myositis and oculopharyngeal muscular dystrophy. Neurosci Lett 1991; 130: 73-6
-
(1991)
Neurosci Lett
, vol.130
, pp. 73-76
-
-
Askanas, V.1
Serdaroglu, P.2
Engel, W.3
Alvarez, R.4
-
32
-
-
0026695045
-
Light and electron microscopic localization of β-amyloid protein in muscle biopsies of patients with inclusion-body myositis
-
Askanas V, Engel W, Alvarez R. Light and electron microscopic localization of β-amyloid protein in muscle biopsies of patients with inclusion-body myositis. Am J Pathol 1992;141:31-6
-
(1992)
Am J Pathol
, vol.141
, pp. 31-36
-
-
Askanas, V.1
Engel, W.2
Alvarez, R.3
-
33
-
-
0027444952
-
β-amyloid precursor epitopes in muscle fibers of inclusion body myositis
-
Askanas V, Alvarez R, Engel W. β-Amyloid precursor epitopes in muscle fibers of inclusion body myositis. Ann Neurol 1993; 34: 551-60
-
(1993)
Ann Neurol
, vol.34
, pp. 551-560
-
-
Askanas, V.1
Alvarez, R.2
Engel, W.3
-
34
-
-
0028123613
-
Apolipoprotein E immunoreactive deposits in inclusion-body muscle disease
-
Askanas V, Mirabella M, Engel W, Alvarez R, Weisgraber K. Apolipoprotein E immunoreactive deposits in inclusion-body muscle disease. Lancet 1994; 343; 364-5
-
(1994)
Lancet
, vol.343
, pp. 364-365
-
-
Askanas, V.1
Mirabella, M.2
Engel, W.3
Alvarez, R.4
Weisgraber, K.5
-
35
-
-
0031897126
-
Light and electron microcopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathy
-
Askanas V, Engel W, Yang C, Alvarez R, Lee V, Wisniewski T. Light and electron microcopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathy. Am J Pathol 1998; 152: 889-95
-
(1998)
Am J Pathol
, vol.152
, pp. 889-895
-
-
Askanas, V.1
Engel, W.2
Yang, C.3
Alvarez, R.4
Lee, V.5
Wisniewski, T.6
-
36
-
-
0033934231
-
Novel immunolocalization of alpha-synuclein in human muscle of inclusion-body myositis, regenerating and necrotic fibers, and at neuromuscular junctions
-
Askanas V, Engel W, Alvarez R, McFerrin J, Broccolini A. Novel immunolocalization of alpha-synuclein in human muscle of inclusion-body myositis, regenerating and necrotic fibers, and at neuromuscular junctions. J Neuropathol Exp Neurol 2000; 59: 592-8
-
(2000)
J Neuropathol Exp Neurol
, vol.59
, pp. 592-598
-
-
Askanas, V.1
Engel, W.2
Alvarez, R.3
McFerrin, J.4
Broccolini, A.5
-
37
-
-
0035830290
-
Presence of BACE1 and BACE2 in muscle fibres of patients with sporadic inclusion-body myositis
-
Vattemi G, Engel WK, McFerrin J, Buxbaum JD, Pastorino L, Askanas V. Presence of BACE1 and BACE2 in muscle fibres of patients with sporadic inclusion-body myositis. Lancet 2001; 358: 1962-4
-
(2001)
Lancet
, vol.358
, pp. 1962-1964
-
-
Vattemi, G.1
Engel, W.K.2
McFerrin, J.3
Buxbaum, J.D.4
Pastorino, L.5
Askanas, V.6
-
38
-
-
0030857085
-
βAPP gene transfer into cultured human muscle induces inclusion-body myositis aspects
-
Askanas V, McFerrin J, Alvarez R, Baque S, Engel W. βAPP gene transfer into cultured human muscle induces inclusion-body myositis aspects. Neuroreport 1997; 8: 2155-8
-
(1997)
Neuroreport
, vol.8
, pp. 2155-2158
-
-
Askanas, V.1
McFerrin, J.2
Alvarez, R.3
Baque, S.4
Engel, W.5
-
39
-
-
0027467560
-
Strong immunoreactivity of α1-antichymotrypsin co-localizes with β-amyloid protein and ubiquitin in vacuolated muscle fibers of inclusion-body myositis
-
Bilak M, Askanas V, Engel W. Strong immunoreactivity of α1-antichymotrypsin co-localizes with β-amyloid protein and ubiquitin in vacuolated muscle fibers of inclusion-body myositis. Acta Neuropathol 1993; 85: 378-2
-
(1993)
Acta Neuropathol
, vol.85
, pp. 378-372
-
-
Bilak, M.1
Askanas, V.2
Engel, W.3
-
40
-
-
0033849528
-
Paired helical filaments of inclusion-body myositis contain RNA and survival motor neuron protein
-
Broccolini A, Engel W, Alvarez R, Askanas V. Paired helical filaments of inclusion-body myositis contain RNA and survival motor neuron protein. Am J Pathol 2000; 156: 1151-5
-
(2000)
Am J Pathol
, vol.156
, pp. 1151-1155
-
-
Broccolini, A.1
Engel, W.2
Alvarez, R.3
Askanas, V.4
-
41
-
-
0035145398
-
Inclusion-body myositis. Newest concepts of pathogenesis and relation to aging and Alzheimer disease
-
Askanas V, Engel W. Inclusion-body myositis. Newest concepts of pathogenesis and relation to aging and Alzheimer disease. J Neuropathol Exp Neurol 2001; 60: 1-14
-
(2001)
J Neuropathol Exp Neurol
, vol.60
, pp. 1-14
-
-
Askanas, V.1
Engel, W.2
-
42
-
-
0034782506
-
Dysregulation of human brain microtubule-associated tau mRNA maturation in myotonic dystrophy type 1
-
Sergeant N, Sablonnière B, Schraen-Maschke S, Ghestem A, Maurage CA, Wattez A, Vermersch P, Delacourte A. Dysregulation of human brain microtubule-associated tau mRNA maturation in myotonic dystrophy type 1. Hum Mol Genet 2001; 10: 2143-55
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2143-2155
-
-
Sergeant, N.1
Sablonnière, B.2
Schraen-Maschke, S.3
Ghestem, A.4
Maurage, C.A.5
Wattez, A.6
Vermersch, P.7
Delacourte, A.8
-
43
-
-
0035253794
-
Hyperphosphorylation of tau is mediated by ERK activation during anticancer drug-induced apoptosis in neuroblastoma cells
-
Guise S, Braguer D, Carles G, Delacourte A, Brinand C. Hyperphosphorylation of tau is mediated by ERK activation during anticancer drug-induced apoptosis in neuroblastoma cells. J Neurosci Res 2001; 63: 257-67
-
(2001)
J Neurosci Res
, vol.63
, pp. 257-267
-
-
Guise, S.1
Braguer, D.2
Carles, G.3
Delacourte, A.4
Brinand, C.5
-
44
-
-
0040299037
-
AD 2, a phosphorylation-dependent monoclonal antibody directed against tau proteins found in Alzheimer's disease
-
Buée-Scherrer V, Condamines O, Mourton-Gilles C, Jakes R, Goedert M, Pau B, Delacourte A. AD 2, a phosphorylation-dependent monoclonal antibody directed against tau proteins found in Alzheimer's disease. Mol Brain Res 1996; 39: 79-88
-
(1996)
Mol Brain Res
, vol.39
, pp. 79-88
-
-
Buée-Scherrer, V.1
Condamines, O.2
Mourton-Gilles, C.3
Jakes, R.4
Goedert, M.5
Pau, B.6
Delacourte, A.7
-
45
-
-
0344859874
-
Phosphorylated serine 422 on Tau proteins is a pathologic epitope found in several diseases with neurofibrillary degeneration
-
Bussière T, Hof P, Mailliot C, Brown C, Caillet-Boudin M, Perl D, Buée L, Delacourte A. Phosphorylated serine 422 on Tau proteins is a pathologic epitope found in several diseases with neurofibrillary degeneration. Acta Neuropathol 1999; 97: 221-30
-
(1999)
Acta Neuropathol
, vol.97
, pp. 221-230
-
-
Bussière, T.1
Hof, P.2
Mailliot, C.3
Brown, C.4
Caillet-Boudin, M.5
Perl, D.6
Buée, L.7
Delacourte, A.8
-
46
-
-
0033369257
-
Time-dependent changes in myosin heavy chain mRNA and protein isoforms in unloaded soleus muscle of rat
-
Stevens L, Sultan K, Peuker H, Gohlsch B, Mounier Y, Pette D. Time-dependent changes in myosin heavy chain mRNA and protein isoforms in unloaded soleus muscle of rat. Am J Physiol 1999; 277: C1044-9
-
(1999)
Am J Physiol
, vol.277
-
-
Stevens, L.1
Sultan, K.2
Peuker, H.3
Gohlsch, B.4
Mounier, Y.5
Pette, D.6
-
47
-
-
0033009603
-
Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: Tau pathologies with exclusively 'exon 10' isoforms
-
Sergeant N, Wattez A, Delacourte A. Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: tau pathologies with exclusively 'exon 10' isoforms. J Neurochem 1999; 72: 1243-9
-
(1999)
J Neurochem
, vol.72
, pp. 1243-1249
-
-
Sergeant, N.1
Wattez, A.2
Delacourte, A.3
-
48
-
-
0031864997
-
Accumulation of tau in autophagic vacuoles in chloroquine myopathy
-
Murakami N, Oyama F, Gu Y, McLennan I, Nonaka I, Ihara Y. Accumulation of tau in autophagic vacuoles in chloroquine myopathy. J Neuropathol Exp Neurol 1998; 57: 664-73
-
(1998)
J Neuropathol Exp Neurol
, vol.57
, pp. 664-673
-
-
Murakami, N.1
Oyama, F.2
Gu, Y.3
McLennan, I.4
Nonaka, I.5
Ihara, Y.6
-
49
-
-
0029843684
-
Tau is widely expressed in rat tissues
-
Gu Y, Oyama F, Ihara Y. Tau is widely expressed in rat tissues. J Neurochem 1996; 67: 1235-44
-
(1996)
J Neurochem
, vol.67
, pp. 1235-1244
-
-
Gu, Y.1
Oyama, F.2
Ihara, Y.3
-
51
-
-
0033572791
-
Endocytosis in skeletal muscle fibers
-
Kaisto T, Rahkila P, Marjomaki V, Parton R, Metsikko K. Endocytosis in skeletal muscle fibers. Exp Cell Res 1999; 253: 551-60
-
(1999)
Exp Cell Res
, vol.253
, pp. 551-560
-
-
Kaisto, T.1
Rahkila, P.2
Marjomaki, V.3
Parton, R.4
Metsikko, K.5
-
52
-
-
0037459791
-
Association of ATP synthase alpha-chain with neurofibrillary degeneration in Alzheimer's disease
-
Sergeant N, Wattez A, Galvan-valencia M, Ghestem A, David J, Lemoine J, Sautiere P, Dachary J, Mazat J, Michalski J, Velours J, Mena-Lopez R, Delacourte A. Association of ATP synthase alpha-chain with neurofibrillary degeneration in Alzheimer's disease. Neuroscience 2003; 17: 293-303
-
(2003)
Neuroscience
, vol.17
, pp. 293-303
-
-
Sergeant, N.1
Wattez, A.2
Galvan-Valencia, M.3
Ghestem, A.4
David, J.5
Lemoine, J.6
Sautiere, P.7
Dachary, J.8
Mazat, J.9
Michalski, J.10
Velours, J.11
Mena-Lopez, R.12
Delacourte, A.13
-
53
-
-
0029944817
-
Use of anti-neurofilament antibody to identify paired-helical filaments in inclusion-body myositis
-
Askanas V, Alvarez R, Mirabella M, Engel W. Use of anti-neurofilament antibody to identify paired-helical filaments in inclusion-body myositis. Ann Neurol 1996; 39: 389-91
-
(1996)
Ann Neurol
, vol.39
, pp. 389-391
-
-
Askanas, V.1
Alvarez, R.2
Mirabella, M.3
Engel, W.4
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