A citation-based method for searching scientific literature

Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, Massimo Plumari, Giorgio Battaglia, Annalisa Pastore, Adele Finardi, Claudia Cagnoli, Filippo Tempia, Marina Frontali, Liana Veneziano, Tiziana Sacco, Enrica Boda, Alessandro Brussino, Florian Bonn, Barbara Castellotti, Silvia Baratta, Caterina Mariotti, Cinzia Gellera, Valentina Fracasso, Stefania Magri, Thomas Langer, Paolo Plevani, Stefano Di Donato, Marco Muzi-Falconi, Franco Taroni. Nat Genet 2010
Times Cited: 208



Mirko Koppen, Metodi D Metodiev, Giorgio Casari, Elena I Rugarli, Thomas Langer. Mol Cell Biol 2007
Times Cited: 133




List of shared articles



Times cited

The Power of Yeast in Modelling Human Nuclear Mutations Associated with Mitochondrial Diseases.
Camilla Ceccatelli Berti, Giulia di Punzio, Cristina Dallabona, Enrico Baruffini, Paola Goffrini, Tiziana Lodi, Claudia Donnini. Genes (Basel) 2021
3

Mitochondrial ATP-Dependent Proteases-Biological Function and Potential Anti-Cancer Targets.
Yue Feng, Kazem Nouri, Aaron D Schimmer. Cancers (Basel) 2021
0

Mitochondrial Proteases: Multifaceted Regulators of Mitochondrial Plasticity.
Soni Deshwal, Kai Uwe Fiedler, Thomas Langer. Annu Rev Biochem 2020
26

Impaired flickering of the permeability transition pore causes SPG7 spastic paraplegia.
Irene Sambri, Filomena Massa, Francesca Gullo, Simone Meneghini, Laura Cassina, Michela Carraro, Giorgia Dina, Angelo Quattrini, Lorenzo Patanella, Annamaria Carissimo,[...]. EBioMedicine 2020
3


Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity.
Cecilia Mancini, Eriola Hoxha, Luisa Iommarini, Alessandro Brussino, Uwe Richter, Francesca Montarolo, Claudia Cagnoli, Roberta Parolisi, Diana Iulia Gondor Morosini, Valentina Nicolò,[...]. Neurobiol Dis 2019
12

Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment.
Alessia Catania, Andrea Legati, Lorenzo Peverelli, Lorenzo Nanetti, Silvia Marchet, Nadia Zanetti, Costanza Lamperti, Daniele Ghezzi. Am J Med Genet A 2019
2

Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation.
Susanna Tulli, Andrea Del Bondio, Valentina Baderna, Davide Mazza, Franca Codazzi, Tyler Mark Pierson, Alessandro Ambrosi, Dagmar Nolte, Cyril Goizet, Camilo Toro,[...]. J Med Genet 2019
10

Astrocyte-specific deletion of the mitochondrial m-AAA protease reveals glial contribution to neurodegeneration.
Sara Murru, Simon Hess, Esther Barth, Eva R Almajan, Désirée Schatton, Steffen Hermans, Susanne Brodesser, Thomas Langer, Peter Kloppenburg, Elena I Rugarli. Glia 2019
15

Unique Structural Features of the Mitochondrial AAA+ Protease AFG3L2 Reveal the Molecular Basis for Activity in Health and Disease.
Cristina Puchades, Bojian Ding, Albert Song, R Luke Wiseman, Gabriel C Lander, Steven E Glynn. Mol Cell 2019
27


Mitochondrial Nascent Chain Quality Control Determines Organelle Form and Function.
Brendan J Battersby, Uwe Richter, Omid Safronov. ACS Chem Biol 2019
3

m-AAA proteases, mitochondrial calcium homeostasis and neurodegeneration.
Maria Patron, Hans-Georg Sprenger, Thomas Langer. Cell Res 2018
45


Dissecting Substrate Specificities of the Mitochondrial AFG3L2 Protease.
Bojian Ding, Dwight W Martin, Anthony J Rampello, Steven E Glynn. Biochemistry 2018
7

Coordinating Mitochondrial Biology Through the Stress-Responsive Regulation of Mitochondrial Proteases.
Justine Lebeau, T Kelly Rainbolt, R Luke Wiseman. Int Rev Cell Mol Biol 2018
11

AAA Proteases: Guardians of Mitochondrial Function and Homeostasis.
Magdalena Opalińska, Hanna Jańska. Cells 2018
14

SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy.
Kirsten Svenstrup, Troels Tolstrup Nielsen, Frederik Aidt, Nina Rostgaard, Morten Duno, Flemming Wibrand, Tua Vinther-Jensen, Ian Law, John Vissing, Peter Roos,[...]. Cerebellum 2017
11

Multifunctional Mitochondrial AAA Proteases.
Steven E Glynn. Front Mol Biosci 2017
30

Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies.
Eleni Bagli, Anastasia K Zikou, Niki Agnantis, Georgios Kitsos. In Vivo 2017
12

Mitochondrial Quality Control Proteases in Neuronal Welfare.
Roman M Levytskyy, Edward M Germany, Oleh Khalimonchuk. J Neuroimmune Pharmacol 2016
20

Movement disorders in mitochondrial diseases.
C Tranchant, M Anheim. Rev Neurol (Paris) 2016
29

The m-AAA Protease Associated with Neurodegeneration Limits MCU Activity in Mitochondria.
Tim König, Simon E Tröder, Kavya Bakka, Anne Korwitz, Ricarda Richter-Dennerlein, Philipp A Lampe, Maria Patron, Mareike Mühlmeister, Sergio Guerrero-Castillo, Ulrich Brandt,[...]. Mol Cell 2016
91

Caveolin-1 controls mitochondrial function through regulation of m-AAA mitochondrial protease.
Daniela Volonte, Zhongmin Liu, Sruti Shiva, Ferruccio Galbiati. Aging (Albany NY) 2016
16

The Mitochondrial m-AAA Protease Prevents Demyelination and Hair Greying.
Shuaiyu Wang, Julie Jacquemyn, Sara Murru, Paola Martinelli, Esther Barth, Thomas Langer, Carien M Niessen, Elena I Rugarli. PLoS Genet 2016
14