The HSPB8‐BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases (English)
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- New search for: Seidel, K.
- New search for: Vinet, J.
- New search for: den Dunnen, W. F. A.
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- New search for: Meister, M.
- New search for: Boncoraglio, A.
- New search for: Zijlstra, M. P.
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In:
Neuropathology and Applied Neurobiology
;
38
, 1
;
39-53
;
2012
- Article (Journal) / Electronic Resource
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Title:The HSPB8‐BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases
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Contributors:Seidel, K. ( author ) / Vinet, J. ( author ) / den Dunnen, W. F. A. ( author ) / Brunt, E. R. ( author ) / Meister, M. ( author ) / Boncoraglio, A. ( author ) / Zijlstra, M. P. ( author ) / Boddeke, H. W. G. M. ( author ) / Rüb, U. ( author ) / Kampinga, H. H. ( author )
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Published in:Neuropathology and Applied Neurobiology ; 38, 1 ; 39-53
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Publisher:
- New search for: Blackwell Publishing Ltd
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Publication date:2012-02-01
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Size:15 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Keywords:
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Source:
Table of contents – Volume 38, Issue 1
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1
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In this issue| 2012
- 4
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The neuropathology, pathophysiology and genetics of multiple system atrophyAhmed, Z. / Asi, Y. T. / Sailer, A. / Lees, A. J. / Houlden, H. / Revesz, T. / Holton, J. L. et al. | 2012
- 25
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A quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP‐43 proteinopathy (FTLD‐TDP)Armstrong, R. A. / Carter, D. / Cairns, N. J. et al. | 2012
- 39
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The HSPB8‐BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseasesSeidel, K. / Vinet, J. / den Dunnen, W. F. A. / Brunt, E. R. / Meister, M. / Boncoraglio, A. / Zijlstra, M. P. / Boddeke, H. W. G. M. / Rüb, U. / Kampinga, H. H. et al. | 2012
- 54
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Co‐occurrence of argyrophilic grain disease in sporadic amyotrophic lateral sclerosisSoma, K. / Fu, Y.‐J. / Wakabayashi, K. / Onodera, O. / Kakita, A. / Takahashi, H. et al. | 2012
- 61
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Loss of neurofilaments in the neuromuscular junction in a rat model of proximal axonopathySoler‐Martín, C. / Vilardosa, Ú. / Saldaña‐Ruíz, S. / Garcia, N. / Llorens, J. et al. | 2012
- 72
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Post‐mortem findings in 10 patients with presumed normal‐pressure hydrocephalus and review of the literatureLeinonen, V. / Koivisto, A. M. / Savolainen, S. / Rummukainen, J. / Sutela, A. / Vanninen, R. / Jääskeläinen, J. E. / Soininen, H. / Alafuzoff, I. et al. | 2012
- 87
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Utility of Ki67 immunostaining in the grading of pineal parenchymal tumours: a multicentre studyFèvre‐Montange, M. / Vasiljevic, A. / Frappaz, D. / Champier, J. / Szathmari, A. / Aubriot Lorton, M.‐H. / Chapon, F. / Coulon, A. / Quintin Roué, I. / Delisle, M.‐B. et al. | 2012
- 95
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Adult onset leucodystrophy with neuroaxonal spheroids and pigmented glia (ALSP): report of a new kindredTan, K. / Brewer, J. / Rowe, D. B. / Jenkins, B. / Powers, J. M. / Buckland, M. E. et al. | 2012
- 101
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Frontotemporal lobar degeneration in a very young patient is associated with fused in sarcoma (FUS) pathological changesBaborie, A. / Jaros, E. / Griffiths, T. D. / Momeni, P. / Perry, R. / Mann, D. M. A. et al. | 2012
- 105
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Recurrent anaplastic meningioma treated by sunitinib based on results from quantitative proteomicsYoshikawa, A. / Nakada, M. / Ohtsuki, S. / Hayashi, Y. / Obuchi, W. / Sato, Y. / Ikeda, C. / Watanabe, T. / Kawahara, Y. / Hasegawa, T. et al. | 2012
- 111
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Primary meningeal histiocytic sarcoma: a report of two unusual casesBell, S. L. / Hanzely, Z. / Alakandy, L. M. / Jackson, R. / Stewart, W. et al. | 2012