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Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients

Joy Irobi, Anne Holmgren, Vicky De Winter, Bob Asselbergh, Jan Gettemans UGent, Dirk Adriaensen, Chantal Ceuterick-de Groote, Rudy Van Coster UGent, Peter De Jonghe and Vincent Timmerman (2012) NEUROMUSCULAR DISORDERS. 22(8). p.699-711
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
HSP27, GENE, HMN-II, CELL-DEATH, MISSENSE MUTATION, ALZHEIMERS-DISEASE, DYSFUNCTION, MISFOLDED PROTEINS, MARIE-TOOTH-DISEASE, HEAT-SHOCK-PROTEIN, Protein aggregation and mitochondrial depolarization, Small heat shock protein HSPB8, Dermal biopsy, Hereditary motor neuropathy
journal title
NEUROMUSCULAR DISORDERS
Neuromusc. Disord.
volume
22
issue
8
pages
699 - 711
Web of Science type
Article
Web of Science id
000307619900004
JCR category
CLINICAL NEUROLOGY
JCR impact factor
3.464 (2012)
JCR rank
42/190 (2012)
JCR quartile
1 (2012)
ISSN
0960-8966
DOI
10.1016/j.nmd.2012.04.005
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
2999720
handle
http://hdl.handle.net/1854/LU-2999720
date created
2012-09-26 15:16:24
date last changed
2012-09-27 10:55:58
@article{2999720,
  author       = {Irobi, Joy and Holmgren, Anne and De Winter, Vicky and Asselbergh, Bob and Gettemans, Jan and Adriaensen, Dirk and Ceuterick-de Groote, Chantal and Van Coster, Rudy and De Jonghe, Peter and Timmerman, Vincent},
  issn         = {0960-8966},
  journal      = {NEUROMUSCULAR DISORDERS},
  keyword      = {HSP27,GENE,HMN-II,CELL-DEATH,MISSENSE MUTATION,ALZHEIMERS-DISEASE,DYSFUNCTION,MISFOLDED PROTEINS,MARIE-TOOTH-DISEASE,HEAT-SHOCK-PROTEIN,Protein aggregation and mitochondrial depolarization,Small heat shock protein HSPB8,Dermal biopsy,Hereditary motor neuropathy},
  language     = {eng},
  number       = {8},
  pages        = {699--711},
  title        = {Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients},
  url          = {http://dx.doi.org/10.1016/j.nmd.2012.04.005},
  volume       = {22},
  year         = {2012},
}

Chicago
Irobi, Joy, Anne Holmgren, Vicky De Winter, Bob Asselbergh, Jan Gettemans, Dirk Adriaensen, Chantal Ceuterick-de Groote, Rudy Van Coster, Peter De Jonghe, and Vincent Timmerman. 2012. “Mutant HSPB8 Causes Protein Aggregates and a Reduced Mitochondrial Membrane Potential in Dermal Fibroblasts from Distal Hereditary Motor Neuropathy Patients.” Neuromuscular Disorders 22 (8): 699–711.
APA
Irobi, J., Holmgren, A., De Winter, V., Asselbergh, B., Gettemans, J., Adriaensen, D., Ceuterick-de Groote, C., et al. (2012). Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients. NEUROMUSCULAR DISORDERS, 22(8), 699–711.
Vancouver
1.
Irobi J, Holmgren A, De Winter V, Asselbergh B, Gettemans J, Adriaensen D, et al. Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients. NEUROMUSCULAR DISORDERS. 2012;22(8):699–711.
MLA
Irobi, Joy, Anne Holmgren, Vicky De Winter, et al. “Mutant HSPB8 Causes Protein Aggregates and a Reduced Mitochondrial Membrane Potential in Dermal Fibroblasts from Distal Hereditary Motor Neuropathy Patients.” NEUROMUSCULAR DISORDERS 22.8 (2012): 699–711. Print.