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Times Cited: 48
Times Cited: 48
Constantin d'Ydewalle, Jyothsna Krishnan, Driss M Chiheb, Philip Van Damme, Joy Irobi, Alan P Kozikowski, Pieter Vanden Berghe, Vincent Timmerman, Wim Robberecht, Ludo Van Den Bosch. Nat Med 2011
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Times Cited: 311
List of shared articles
Times cited
Chaperonopathies: Spotlight on Hereditary Motor Neuropathies.
Vincenzo Lupo, Carmen Aguado, Erwin Knecht, Carmen Espinós. Front Mol Biosci 2016
Vincenzo Lupo, Carmen Aguado, Erwin Knecht, Carmen Espinós. Front Mol Biosci 2016
Human HspB1, HspB3, HspB5 and HspB8: Shaping these disease factors during vertebrate evolution.
Rainer Benndorf, Ryan Velazquez, Jordan D Zehr, Sergei L Kosakovsky Pond, Jody L Martin, Alexander G Lucaci. Cell Stress Chaperones 2022
Rainer Benndorf, Ryan Velazquez, Jordan D Zehr, Sergei L Kosakovsky Pond, Jody L Martin, Alexander G Lucaci. Cell Stress Chaperones 2022
Mutations in HspB1 and hereditary neuropathies.
Lydia K Muranova, Maria V Sudnitsyna, Sergei V Strelkov, Nikolai B Gusev. Cell Stress Chaperones 2020
Lydia K Muranova, Maria V Sudnitsyna, Sergei V Strelkov, Nikolai B Gusev. Cell Stress Chaperones 2020
Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New Results.
Jaakko Sarparanta, Per Harald Jonson, Sabita Kawan, Bjarne Udd. Int J Mol Sci 2020
Jaakko Sarparanta, Per Harald Jonson, Sabita Kawan, Bjarne Udd. Int J Mol Sci 2020
Proline isomerization in the C-terminal region of HSP27.
T Reid Alderson, Justin L P Benesch, Andrew J Baldwin. Cell Stress Chaperones 2017
T Reid Alderson, Justin L P Benesch, Andrew J Baldwin. Cell Stress Chaperones 2017
A novel p.T139M mutation in HSPB1 highlighting the phenotypic spectrum in a family.
Jakkrit Amornvit, Mehmet E Yalvac, Lei Chen, Zarife Sahenk. Brain Behav 2017
Jakkrit Amornvit, Mehmet E Yalvac, Lei Chen, Zarife Sahenk. Brain Behav 2017
Mutations of small heat shock proteins and human congenital diseases.
P N Datskevich, V V Nefedova, M V Sudnitsyna, N B Gusev. Biochemistry (Mosc) 2012
P N Datskevich, V V Nefedova, M V Sudnitsyna, N B Gusev. Biochemistry (Mosc) 2012
Neuropathy- and myopathy-associated mutations in human small heat shock proteins: Characteristics and evolutionary history of the mutation sites.
Rainer Benndorf, Jody L Martin, Sergei L Kosakovsky Pond, Joel O Wertheim. Mutat Res Rev Mutat Res 2014
Rainer Benndorf, Jody L Martin, Sergei L Kosakovsky Pond, Joel O Wertheim. Mutat Res Rev Mutat Res 2014
Mitochondrial deficits and abnormal mitochondrial retrograde axonal transport play a role in the pathogenesis of mutant Hsp27-induced Charcot Marie Tooth Disease.
Bernadett Kalmar, Amy Innes, Klaus Wanisch, Alicia Koyen Kolaszynska, Amelie Pandraud, Gavin Kelly, Andrey Y Abramov, Mary M Reilly, Giampietro Schiavo, Linda Greensmith. Hum Mol Genet 2017
Bernadett Kalmar, Amy Innes, Klaus Wanisch, Alicia Koyen Kolaszynska, Amelie Pandraud, Gavin Kelly, Andrey Y Abramov, Mary M Reilly, Giampietro Schiavo, Linda Greensmith. Hum Mol Genet 2017
Small Heat Shock Proteins and Distal Hereditary Neuropathies.
V V Nefedova, L K Muranova, M V Sudnitsyna, A S Ryzhavskaya, N B Gusev. Biochemistry (Mosc) 2015
V V Nefedova, L K Muranova, M V Sudnitsyna, A S Ryzhavskaya, N B Gusev. Biochemistry (Mosc) 2015
Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutations.
Elena Abati, Stefania Magri, Megi Meneri, Giulia Manenti, Daniele Velardo, Francesca Balistreri, Chiara Pisciotta, Paola Saveri, Nereo Bresolin, Giacomo Pietro Comi,[...]. Ann Clin Transl Neurol 2021
Elena Abati, Stefania Magri, Megi Meneri, Giulia Manenti, Daniele Velardo, Francesca Balistreri, Chiara Pisciotta, Paola Saveri, Nereo Bresolin, Giacomo Pietro Comi,[...]. Ann Clin Transl Neurol 2021
Small heat shock proteins in neurodegenerative diseases.
Leen Vendredy, Elias Adriaenssens, Vincent Timmerman. Cell Stress Chaperones 2020
Leen Vendredy, Elias Adriaenssens, Vincent Timmerman. Cell Stress Chaperones 2020
Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.
Delphine Bouhy, Vincent Timmerman. Ann Neurol 2013
Delphine Bouhy, Vincent Timmerman. Ann Neurol 2013
A novel HSPB1 mutation associated with a late onset CMT2 phenotype: Case presentation and systematic review of the literature.
Arens Taga, David R Cornblath. J Peripher Nerv Syst 2020
Arens Taga, David R Cornblath. J Peripher Nerv Syst 2020
Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel Mutations.
Andoni Echaniz-Laguna, Thomas Geuens, Philippe Petiot, Yann Péréon, Elias Adriaenssens, Mansour Haidar, Simona Capponi, Thierry Maisonobe, Emmanuel Fournier, Odile Dubourg,[...]. Hum Mutat 2017
Andoni Echaniz-Laguna, Thomas Geuens, Philippe Petiot, Yann Péréon, Elias Adriaenssens, Mansour Haidar, Simona Capponi, Thierry Maisonobe, Emmanuel Fournier, Odile Dubourg,[...]. Hum Mutat 2017
Mutations in heat shock protein beta-1 (HSPB1) are associated with a range of clinical phenotypes related to different patterns of motor neuron dysfunction: A case series.
Matthew Katz, Mark Davis, Fleur C Garton, Robert Henderson, Vanda Bharti, Naomi Wray, Pamela McCombe. J Neurol Sci 2020
Matthew Katz, Mark Davis, Fleur C Garton, Robert Henderson, Vanda Bharti, Naomi Wray, Pamela McCombe. J Neurol Sci 2020
Truncated HSPB1 causes axonal neuropathy and impairs tolerance to unfolded protein stress.
Emil Ylikallio, Svetlana Konovalova, Yogesh Dhungana, Taru Hilander, Nella Junna, Juhani V Partanen, Jussi P Toppila, Mari Auranen, Henna Tyynismaa. BBA Clin 2015
Emil Ylikallio, Svetlana Konovalova, Yogesh Dhungana, Taru Hilander, Nella Junna, Juhani V Partanen, Jussi P Toppila, Mari Auranen, Henna Tyynismaa. BBA Clin 2015
A novel p.Gln175X [corrected] premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2.
Alexander M Rossor, Gabrielle L Davidson, Julian Blake, James M Polke, Sinéad M Murphy, Henry Houlden, Amy Innes, Bernadett Kalmar, Linda Greensmith, Mary M Reilly. J Peripher Nerv Syst 2012
Alexander M Rossor, Gabrielle L Davidson, Julian Blake, James M Polke, Sinéad M Murphy, Henry Houlden, Amy Innes, Bernadett Kalmar, Linda Greensmith, Mary M Reilly. J Peripher Nerv Syst 2012