Literature DB >> 22398449

Neurodegeneration: Trouble in the cell's powerhouse.

Derek P Narendra, Richard J Youle.   

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Year:  2012        PMID: 22398449      PMCID: PMC4746717          DOI: 10.1038/nature10952

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


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  13 in total

1.  ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF.

Authors:  J C Engert; P Bérubé; J Mercier; C Doré; P Lepage; B Ge; J P Bouchard; J Mathieu; S B Melançon; M Schalling; E S Lander; K Morgan; T J Hudson; A Richter
Journal:  Nat Genet       Date:  2000-02       Impact factor: 38.330

2.  Mitochondrial dysfunction and Purkinje cell loss in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS).

Authors:  Martine Girard; Roxanne Larivière; David A Parfitt; Emily C Deane; Rebecca Gaudet; Nadya Nossova; Francois Blondeau; George Prenosil; Esmeralda G M Vermeulen; Michael R Duchen; Andrea Richter; Eric A Shoubridge; Kalle Gehring; R Anne McKinney; Bernard Brais; J Paul Chapple; Peter S McPherson
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-17       Impact factor: 11.205

3.  Fission and selective fusion govern mitochondrial segregation and elimination by autophagy.

Authors:  Gilad Twig; Alvaro Elorza; Anthony J A Molina; Hibo Mohamed; Jakob D Wikstrom; Gil Walzer; Linsey Stiles; Sarah E Haigh; Steve Katz; Guy Las; Joseph Alroy; Min Wu; Bénédicte F Py; Junying Yuan; Jude T Deeney; Barbara E Corkey; Orian S Shirihai
Journal:  EMBO J       Date:  2008-01-17       Impact factor: 11.598

4.  Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin.

Authors:  M Babcock; D de Silva; R Oaks; S Davis-Kaplan; S Jiralerspong; L Montermini; M Pandolfo; J Kaplan
Journal:  Science       Date:  1997-06-13       Impact factor: 47.728

5.  OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.

Authors:  C Alexander; M Votruba; U E Pesch; D L Thiselton; S Mayer; A Moore; M Rodriguez; U Kellner; B Leo-Kottler; G Auburger; S S Bhattacharya; B Wissinger
Journal:  Nat Genet       Date:  2000-10       Impact factor: 38.330

6.  Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants.

Authors:  Jessica C Greene; Alexander J Whitworth; Isabella Kuo; Laurie A Andrews; Mel B Feany; Leo J Pallanck
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-17       Impact factor: 11.205

7.  Autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Authors:  J P Bouchard; A Barbeau; R Bouchard; R W Bouchard
Journal:  Can J Neurol Sci       Date:  1978-02       Impact factor: 2.104

8.  Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice.

Authors:  Naotada Ishihara; Masatoshi Nomura; Akihiro Jofuku; Hiroki Kato; Satoshi O Suzuki; Keiji Masuda; Hidenori Otera; Yae Nakanishi; Ikuya Nonaka; Yu-Ichi Goto; Naoko Taguchi; Hidetaka Morinaga; Maki Maeda; Ryoichi Takayanagi; Sadaki Yokota; Katsuyoshi Mihara
Journal:  Nat Cell Biol       Date:  2009-07-05       Impact factor: 28.824

9.  POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement.

Authors:  G Van Goethem; P Luoma; M Rantamäki; A Al Memar; S Kaakkola; P Hackman; R Krahe; A Löfgren; J J Martin; P De Jonghe; A Suomalainen; B Udd; C Van Broeckhoven
Journal:  Neurology       Date:  2004-10-12       Impact factor: 9.910

10.  Dnm1 forms spirals that are structurally tailored to fit mitochondria.

Authors:  Elena Ingerman; Edward M Perkins; Michael Marino; Jason A Mears; J Michael McCaffery; Jenny E Hinshaw; Jodi Nunnari
Journal:  J Cell Biol       Date:  2005-09-26       Impact factor: 10.539

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  12 in total

Review 1.  Redox biology and the interface between bioenergetics, autophagy and circadian control of metabolism.

Authors:  Adam R Wende; Martin E Young; John Chatham; Jianhua Zhang; Namakkal S Rajasekaran; Victor M Darley-Usmar
Journal:  Free Radic Biol Med       Date:  2016-05-27       Impact factor: 7.376

Review 2.  Mitochondrial biogenesis: a therapeutic target for neurodevelopmental disorders and neurodegenerative diseases.

Authors:  Martine Uittenbogaard; Anne Chiaramello
Journal:  Curr Pharm Des       Date:  2014       Impact factor: 3.116

3.  The brain and eye: Treating cerebral and retinal ischemia through mitochondrial transfer.

Authors:  Matt Heyck; Brooke Bonsack; Henry Zhang; Nadia Sadanandan; Blaise Cozene; Chase Kingsbury; Jea-Young Lee; Cesar V Borlongan
Journal:  Exp Biol Med (Maywood)       Date:  2019-10-11

4.  Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder.

Authors:  Alexander J Abrams; Robert B Hufnagel; Adriana Rebelo; Claudia Zanna; Neville Patel; Michael A Gonzalez; Ion J Campeanu; Laurie B Griffin; Saskia Groenewald; Alleene V Strickland; Feifei Tao; Fiorella Speziani; Lisa Abreu; Rebecca Schüle; Leonardo Caporali; Chiara La Morgia; Alessandra Maresca; Rocco Liguori; Raffaele Lodi; Zubair M Ahmed; Kristen L Sund; Xinjian Wang; Laura A Krueger; Yanyan Peng; Carlos E Prada; Cynthia A Prows; Elizabeth K Schorry; Anthony Antonellis; Holly H Zimmerman; Omar A Abdul-Rahman; Yaping Yang; Susan M Downes; Jeffery Prince; Flavia Fontanesi; Antonio Barrientos; Andrea H Németh; Valerio Carelli; Taosheng Huang; Stephan Zuchner; Julia E Dallman
Journal:  Nat Genet       Date:  2015-07-13       Impact factor: 38.330

5.  Long non-coding RNA and alternative splicing modulations in Parkinson's leukocytes identified by RNA sequencing.

Authors:  Lilach Soreq; Alessandro Guffanti; Nathan Salomonis; Alon Simchovitz; Zvi Israel; Hagai Bergman; Hermona Soreq
Journal:  PLoS Comput Biol       Date:  2014-03-20       Impact factor: 4.475

6.  Distinct Mechanisms of Pathogenic DJ-1 Mutations in Mitochondrial Quality Control.

Authors:  Daniela Strobbe; Alexis A Robinson; Kirsten Harvey; Lara Rossi; Caterina Ferraina; Valerio de Biase; Carlo Rodolfo; Robert J Harvey; Michelangelo Campanella
Journal:  Front Mol Neurosci       Date:  2018-03-15       Impact factor: 5.639

7.  Metabolic and Organelle Morphology Defects in Mice and Human Patients Define Spinocerebellar Ataxia Type 7 as a Mitochondrial Disease.

Authors:  Jacqueline M Ward; Colleen A Stoyas; Pawel M Switonski; Farid Ichou; Weiwei Fan; Brett Collins; Christopher E Wall; Isaac Adanyeguh; Chenchen Niu; Bryce L Sopher; Chizuru Kinoshita; Richard S Morrison; Alexandra Durr; Alysson R Muotri; Ronald M Evans; Fanny Mochel; Albert R La Spada
Journal:  Cell Rep       Date:  2019-01-29       Impact factor: 9.423

8.  Analysis of mitochondrial function and localisation during human embryonic stem cell differentiation in vitro.

Authors:  Andrew B J Prowse; Fenny Chong; David A Elliott; Andrew G Elefanty; Edouard G Stanley; Peter P Gray; Trent P Munro; Geoffrey W Osborne
Journal:  PLoS One       Date:  2012-12-19       Impact factor: 3.240

Review 9.  ALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the disease.

Authors:  Elizabeth B Moloney; Fred de Winter; Joost Verhaagen
Journal:  Front Neurosci       Date:  2014-08-14       Impact factor: 4.677

10.  A method for assessing tissue respiration in anatomically defined brain regions.

Authors:  Erica Underwood; John B Redell; Jing Zhao; Anthony N Moore; Pramod K Dash
Journal:  Sci Rep       Date:  2020-08-06       Impact factor: 4.379

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