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



Maria Patron, Hans-Georg Sprenger, Thomas Langer. Cell Res 2018
Times Cited: 45




List of shared articles



Times cited

Mitochondrial proteases in human diseases.
Maria Gomez-Fabra Gala, Friederike-Nora Vögtle. FEBS Lett 2021
5

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

ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy.
Leonardo Caporali, Stefania Magri, Andrea Legati, Valentina Del Dotto, Francesca Tagliavini, Francesca Balistreri, Alessia Nasca, Chiara La Morgia, Michele Carbonelli, Maria L Valentino,[...]. Ann Neurol 2020
9

Expanding the clinical and genetic heterogeneity of SPAX5.
Claudia Dosi, Daniele Galatolo, Anna Rubegni, Stefano Doccini, Rosa Pasquariello, Claudia Nesti, Federico Sicca, Melissa Barghigiani, Roberta Battini, Alessandra Tessa,[...]. Ann Clin Transl Neurol 2020
4

A novel AFG3L2 mutation close to AAA domain leads to aberrant OMA1 and OPA1 processing in a family with optic atrophy.
Valentina Baderna, Joshua Schultz, Lisa S Kearns, Michael Fahey, Bryony A Thompson, Jonathan B Ruddle, Aamira Huq, Francesca Maltecca. Acta Neuropathol Commun 2020
2


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

Mitochondrial Proteolysis and Metabolic Control.
Sofia Ahola, Thomas Langer, Thomas MacVicar. Cold Spring Harb Perspect Biol 2019
9

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

Spinocerebellar Ataxia Type 28-Phenotypic and Molecular Characterization of a Family with Heterozygous and Compound-Heterozygous Mutations in AFG3L2.
Sinem Tunc, Marija Dulovic-Mahlow, Hauke Baumann, Magdalena Khira Baaske, Magdalena Jahn, Johanna Junker, Alexander Münchau, Norbert Brüggemann, Katja Lohmann. Cerebellum 2019
6

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

The machineries, regulation and cellular functions of mitochondrial calcium.
Carlotta Giorgi, Saverio Marchi, Paolo Pinton. Nat Rev Mol Cell Biol 2018
218

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

Mitochondrial calcium signalling and neurodegenerative diseases.
Elena Britti, Fabien Delaspre, Jordi Tamarit, Joaquim Ros. Neuronal Signal 2018
15