A citation-based method for searching scientific literature

Leen Vendredy, Elias Adriaenssens, Vincent Timmerman. Cell Stress Chaperones 2020
Times Cited: 20







List of co-cited articles
124 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Small Heat Shock Proteins, Big Impact on Protein Aggregation in Neurodegenerative Disease.
Jack M Webster, April L Darling, Vladimir N Uversky, Laura J Blair. Front Pharmacol 2019
56
35

Mutations in HspB1 and hereditary neuropathies.
Lydia K Muranova, Maria V Sudnitsyna, Sergei V Strelkov, Nikolai B Gusev. Cell Stress Chaperones 2020
12
50

Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.
Oleg V Evgrafov, Irena Mersiyanova, Joy Irobi, Ludo Van Den Bosch, Ines Dierick, Conrad L Leung, Olga Schagina, Nathalie Verpoorten, Katrien Van Impe, Valeriy Fedotov,[...]. Nat Genet 2004
437
25

Hsp27 chaperones FUS phase separation under the modulation of stress-induced phosphorylation.
Zhenying Liu, Shengnan Zhang, Jinge Gu, Yilun Tong, Yichen Li, Xinrui Gui, Houfang Long, Chuchu Wang, Chunyu Zhao, Jinxia Lu,[...]. Nat Struct Mol Biol 2020
44
20

ATPase-Modulated Stress Granules Contain a Diverse Proteome and Substructure.
Saumya Jain, Joshua R Wheeler, Robert W Walters, Anurag Agrawal, Anthony Barsic, Roy Parker. Cell 2016
689
20

Characterization of human small heat shock protein HSPB1 α-crystallin domain localized mutants associated with hereditary motor neuron diseases.
Stephen D Weeks, Lydia K Muranova, Michelle Heirbaut, Steven Beelen, Sergei V Strelkov, Nikolai B Gusev. Sci Rep 2018
24
20

A Surveillance Function of the HSPB8-BAG3-HSP70 Chaperone Complex Ensures Stress Granule Integrity and Dynamism.
Massimo Ganassi, Daniel Mateju, Ilaria Bigi, Laura Mediani, Ina Poser, Hyun O Lee, Samuel J Seguin, Federica F Morelli, Jonathan Vinet, Giuseppina Leo,[...]. Mol Cell 2016
164
20

HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1-induced Charcot-Marie-Tooth disease.
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
301
20

A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8.
Delphine Bouhy, Manisha Juneja, Istvan Katona, Anne Holmgren, Bob Asselbergh, Vicky De Winter, Tino Hochepied, Steven Goossens, Jody J Haigh, Claude Libert,[...]. Acta Neuropathol 2018
37
20


Small Heat Shock Proteins and Human Neurodegenerative Diseases.
L K Muranova, A S Ryzhavskaya, M V Sudnitsyna, V M Shatov, N B Gusev. Biochemistry (Mosc) 2019
13
23


Cellular Functions and Mechanisms of Action of Small Heat Shock Proteins.
Axel Mogk, Carmen Ruger-Herreros, Bernd Bukau. Annu Rev Microbiol 2019
59
15

N- and C-terminal regions of αB-crystallin and Hsp27 mediate inhibition of amyloid nucleation, fibril binding, and fibril disaggregation.
Emily E Selig, Courtney O Zlatic, Dezerae Cox, Yee-Foong Mok, Paul R Gooley, Heath Ecroyd, Michael D W Griffin. J Biol Chem 2020
13
23

Charcot-Marie-Tooth 2F (Hsp27 mutations): A review.
Nicholas U Schwartz. Neurobiol Dis 2019
7
42

Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies.
Mansour Haidar, Bob Asselbergh, Elias Adriaenssens, Vicky De Winter, Jean-Pierre Timmermans, Michaela Auer-Grumbach, Manisha Juneja, Vincent Timmerman. Autophagy 2019
27
15



Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interaction.
Margit Fuchs, Dominic J Poirier, Samuel J Seguin, Herman Lambert, Serena Carra, Steve J Charette, Jacques Landry. Biochem J 2009
120
15

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
33
15

Competing protein-protein interactions regulate binding of Hsp27 to its client protein tau.
Rebecca Freilich, Miguel Betegon, Eric Tse, Sue-Ann Mok, Olivier Julien, David A Agard, Daniel R Southworth, Koh Takeuchi, Jason E Gestwicki. Nat Commun 2018
47
15

Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy.
Leonardo Almeida-Souza, Sofie Goethals, Vicky de Winter, Ines Dierick, Rodrigo Gallardo, Joost Van Durme, Joy Irobi, Jan Gettemans, Frederic Rousseau, Joost Schymkowitz,[...]. J Biol Chem 2010
75
15


Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease.
Thomas Geuens, Vicky De Winter, Nicholas Rajan, Tilmann Achsel, Ligia Mateiu, Leonardo Almeida-Souza, Bob Asselbergh, Delphine Bouhy, Michaela Auer-Grumbach, Claudia Bagni,[...]. Acta Neuropathol Commun 2017
16
18

Mutations in BAG3 cause adult-onset Charcot-Marie-Tooth disease.
Michael Shy, Adriana P Rebelo, Shawna Me Feely, Lisa A Abreu, Feifei Tao, Andrea Swenson, Chelsea Bacon, Stephan Zuchner. J Neurol Neurosurg Psychiatry 2018
21
15


Interplay of disordered and ordered regions of a human small heat shock protein yields an ensemble of 'quasi-ordered' states.
Amanda F Clouser, Hannah Er Baughman, Benjamin Basanta, Miklos Guttman, Abhinav Nath, Rachel E Klevit. Elife 2019
24
15

Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases.
Serena Carra, Alessandra Boncoraglio, Bart Kanon, Jeanette F Brunsting, Melania Minoia, Anil Rana, Michel J Vos, Kay Seidel, Ody C M Sibon, Harm H Kampinga. J Biol Chem 2010
65
15

Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in Japan.
Hajime Tanabe, Yujiro Higuchi, Jun-Hui Yuan, Akihiro Hashiguchi, Akiko Yoshimura, Satoshi Ishihara, Satoshi Nozuma, Yuji Okamoto, Eiji Matsuura, Hiroyuki Ishiura,[...]. J Peripher Nerv Syst 2018
9
33

HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients.
Simona Capponi, Alessandro Geroldi, Paola Fossa, Marina Grandis, Paola Ciotti, Rossella Gulli, Angelo Schenone, Paola Mandich, Emilia Bellone. J Peripher Nerv Syst 2011
46
15

An aberrant phase transition of stress granules triggered by misfolded protein and prevented by chaperone function.
Daniel Mateju, Titus M Franzmann, Avinash Patel, Andrii Kopach, Edgar E Boczek, Shovamayee Maharana, Hyun O Lee, Serena Carra, Anthony A Hyman, Simon Alberti. EMBO J 2017
226
15

Increased expression and retention of the secretory chaperone proSAAS following cell stress.
Manita Shakya, Taha Yildirim, Iris Lindberg. Cell Stress Chaperones 2020
4
50

Molecular chaperone functions in protein folding and proteostasis.
Yujin E Kim, Mark S Hipp, Andreas Bracher, Manajit Hayer-Hartl, F Ulrich Hartl. Annu Rev Biochem 2013
856
10

ProSAAS-derived peptides are colocalized with neuropeptide Y and function as neuropeptides in the regulation of food intake.
Jonathan H Wardman, Iryna Berezniuk, Shi Di, Jeffrey G Tasker, Lloyd D Fricker. PLoS One 2011
37
10

Sushi repeat-containing protein 1: a novel disease-associated molecule in cerebral amyloid angiopathy.
Yasuteru Inoue, Mitsuharu Ueda, Masayoshi Tasaki, Akari Takeshima, Akihito Nagatoshi, Teruaki Masuda, Yohei Misumi, Takayuki Kosaka, Toshiya Nomura, Mayumi Mizukami,[...]. Acta Neuropathol 2017
19
10

Embryonic gene expression and pro-protein processing of proSAAS during rodent development.
Daniel J Morgan, Nino Mzhavia, Bonnie Peng, Hui Pan, Lakshmi A Devi, John E Pintar. J Neurochem 2005
18
11

Sequestration of toxic oligomers by HspB1 as a cytoprotective mechanism.
Juhi Ojha, Gunasingh Masilamoni, David Dunlap, Ross A Udoff, Anil G Cashikar. Mol Cell Biol 2011
71
10

Cerebrospinal fluid proteomics implicates the granin family in Parkinson's disease.
Melissa S Rotunno, Monica Lane, Wenfei Zhang, Pavlina Wolf, Petra Oliva, Catherine Viel, Anne-Marie Wills, Roy N Alcalay, Clemens R Scherzer, Lamya S Shihabuddin,[...]. Sci Rep 2020
26
10

Small heat-shock proteins: paramedics of the cell.
Gillian R Hilton, Hadi Lioe, Florian Stengel, Andrew J Baldwin, Justin L P Benesch. Top Curr Chem 2013
82
10


In vivo aspects of protein folding and quality control.
David Balchin, Manajit Hayer-Hartl, F Ulrich Hartl. Science 2016
668
10

Identification of novel cerebrospinal fluid biomarker candidates for dementia with Lewy bodies: a proteomic approach.
Inger van Steenoven, Marleen J A Koel-Simmelink, Leonie J M Vergouw, Betty M Tijms, Sander R Piersma, Thang V Pham, Claire Bridel, Gian-Luca Ferri, Cristina Cocco, Barbara Noli,[...]. Mol Neurodegener 2020
20
10

Protein transmission in neurodegenerative disease.
Chao Peng, John Q Trojanowski, Virginia M-Y Lee. Nat Rev Neurol 2020
143
10

MALDI imaging mass spectrometry to investigate endogenous peptides in an animal model of Usher's disease.
Bijon Chatterji, Clarissa Dickhut, Svenja Mielke, Jonas Krüger, Ingo Just, Silke Glage, Martin Meier, Dirk Wedekind, Andreas Pich. Proteomics 2014
13
15

Molecular chaperones in protein folding and proteostasis.
F Ulrich Hartl, Andreas Bracher, Manajit Hayer-Hartl. Nature 2011
10

Conditional Disorder in Small Heat-shock Proteins.
T Reid Alderson, Jinfa Ying, Ad Bax, Justin L P Benesch, Andrew J Baldwin. J Mol Biol 2020
12
16

Clusterin as a therapeutic target.
Mark R Wilson, Amina Zoubeidi. Expert Opin Ther Targets 2017
70
10

A comprehensive systematic review of CSF proteins and peptides that define Alzheimer's disease.
Cristina M Pedrero-Prieto, Sonia García-Carpintero, Javier Frontiñán-Rubio, Emilio Llanos-González, Cristina Aguilera García, Francisco J Alcaín, Iris Lindberg, Mario Durán-Prado, Juan R Peinado, Yoana Rabanal-Ruiz. Clin Proteomics 2020
19
10

Pathways of cellular proteostasis in aging and disease.
Courtney L Klaips, Gopal Gunanathan Jayaraj, F Ulrich Hartl. J Cell Biol 2018
318
10

A novel function for proSAAS as an amyloid anti-aggregant in Alzheimer's disease.
Akina Hoshino, Michael Helwig, Sina Rezaei, Casey Berridge, Jason L Eriksen, Iris Lindberg. J Neurochem 2014
27
10


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.