A citation-based method for searching scientific literature

Libin Cui, Hyunkyung Jeong, Fran Borovecki, Christopher N Parkhurst, Naoko Tanese, Dimitri Krainc. Cell 2006
Times Cited: 757







List of co-cited articles
1713 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mutant huntingtin binds the mitochondrial fission GTPase dynamin-related protein-1 and increases its enzymatic activity.
Wenjun Song, Jin Chen, Alejandra Petrilli, Geraldine Liot, Eva Klinglmayr, Yue Zhou, Patrick Poquiz, Jonathan Tjong, Mahmoud A Pouladi, Michael R Hayden,[...]. Nat Med 2011
369
24

Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1alpha in Huntington's disease neurodegeneration.
Patrick Weydt, Victor V Pineda, Anne E Torrence, Randell T Libby, Terrence F Satterfield, Eduardo R Lazarowski, Merle L Gilbert, Gregory J Morton, Theodor K Bammler, Andrew D Strand,[...]. Cell Metab 2006
443
22

Suppression of reactive oxygen species and neurodegeneration by the PGC-1 transcriptional coactivators.
Julie St-Pierre, Stavit Drori, Marc Uldry, Jessica M Silvaggi, James Rhee, Sibylle Jäger, Christoph Handschin, Kangni Zheng, Jiandie Lin, Wenli Yang,[...]. Cell 2006
21

PGC-1alpha expression decreases in the Alzheimer disease brain as a function of dementia.
Weiping Qin, Vahram Haroutunian, Pavel Katsel, Christopher P Cardozo, Lap Ho, Joseph D Buxbaum, Giulio M Pasinetti. Arch Neurol 2009
253
19

PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease.
Bin Zheng, Zhixiang Liao, Joseph J Locascio, Kristen A Lesniak, Sarah S Roderick, Marla L Watt, Aron C Eklund, Yanli Zhang-James, Peter D Kim, Michael A Hauser,[...]. Sci Transl Med 2010
526
18


Mitochondrial loss, dysfunction and altered dynamics in Huntington's disease.
Jinho Kim, Jennifer P Moody, Christina K Edgerly, Olivia L Bordiuk, Kerry Cormier, Karen Smith, M Flint Beal, Robert J Ferrante. Hum Mol Genet 2010
214
16

Defects in adaptive energy metabolism with CNS-linked hyperactivity in PGC-1alpha null mice.
Jiandie Lin, Pei-Hsuan Wu, Paul T Tarr, Katrin S Lindenberg, Julie St-Pierre, Chen-Yu Zhang, Vamsi K Mootha, Sibylle Jäger, Claudia R Vianna, Richard M Reznick,[...]. Cell 2004
911
16

Mutant huntingtin directly increases susceptibility of mitochondria to the calcium-induced permeability transition and cytochrome c release.
Yeun Su Choo, Gail V W Johnson, Marcy MacDonald, Peter J Detloff, Mathieu Lesort. Hum Mol Genet 2004
351
15

PARIS (ZNF746) repression of PGC-1α contributes to neurodegeneration in Parkinson's disease.
Joo-Ho Shin, Han Seok Ko, Hochul Kang, Yunjong Lee, Yun-Il Lee, Olga Pletinkova, Juan C Troconso, Valina L Dawson, Ted M Dawson. Cell 2011
634
15

Mutant huntingtin's interaction with mitochondrial protein Drp1 impairs mitochondrial biogenesis and causes defective axonal transport and synaptic degeneration in Huntington's disease.
Ulziibat P Shirendeb, Marcus J Calkins, Maria Manczak, Vishwanath Anekonda, Brett Dufour, Jodi L McBride, Peizhong Mao, P Hemachandra Reddy. Hum Mol Genet 2012
230
15

Metabolic control through the PGC-1 family of transcription coactivators.
Jiandie Lin, Christoph Handschin, Bruce M Spiegelman. Cell Metab 2005
14

VCP recruitment to mitochondria causes mitophagy impairment and neurodegeneration in models of Huntington's disease.
Xing Guo, XiaoYan Sun, Di Hu, Ya-Juan Wang, Hisashi Fujioka, Rajan Vyas, Sudha Chakrapani, Amit Umesh Joshi, Yu Luo, Daria Mochly-Rosen,[...]. Nat Commun 2016
93
15

Mitochondrial defect in Huntington's disease caudate nucleus.
M Gu, M T Gash, V M Mann, F Javoy-Agid, J M Cooper, A H Schapira. Ann Neurol 1996
543
13

PGC-1α rescues Huntington's disease proteotoxicity by preventing oxidative stress and promoting TFEB function.
Taiji Tsunemi, Travis D Ashe, Bradley E Morrison, Kathryn R Soriano, Jonathan Au, Ruben A Vázquez Roque, Eduardo R Lazarowski, Vincent A Damian, Eliezer Masliah, Albert R La Spada. Sci Transl Med 2012
302
13

Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines.
Alexander V Panov, Claire-Anne Gutekunst, Blair R Leavitt, Michael R Hayden, James R Burke, Warren J Strittmatter, J Timothy Greenamyre. Nat Neurosci 2002
751
13

Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia.
S E Browne, A C Bowling, U MacGarvey, M J Baik, S C Berger, M M Muqit, E D Bird, M F Beal. Ann Neurol 1997
645
13

Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage.
Ulziibat Shirendeb, Arubala P Reddy, Maria Manczak, Marcus J Calkins, Peizhong Mao, Danilo A Tagle, P Hemachandra Reddy. Hum Mol Genet 2011
254
13

N-terminal mutant huntingtin associates with mitochondria and impairs mitochondrial trafficking.
Adam L Orr, Shihua Li, Chuan-En Wang, He Li, Jianjun Wang, Juan Rong, Xingshun Xu, Pier Giorgio Mastroberardino, J Timothy Greenamyre, Xiao-Jiang Li. J Neurosci 2008
286
12

PGC-1α, mitochondrial dysfunction, and Huntington's disease.
Ashu Johri, Abhishek Chandra, M Flint Beal. Free Radic Biol Med 2013
120
12

Huntington disease.
Gillian P Bates, Ray Dorsey, James F Gusella, Michael R Hayden, Chris Kay, Blair R Leavitt, Martha Nance, Christopher A Ross, Rachael I Scahill, Ronald Wetzel,[...]. Nat Rev Dis Primers 2015
615
12

The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription.
J S Steffan, A Kazantsev, O Spasic-Boskovic, M Greenwald, Y Z Zhu, H Gohler, E E Wanker, G P Bates, D E Housman, L M Thompson. Proc Natl Acad Sci U S A 2000
789
11


Inhibition of mitochondrial protein import by mutant huntingtin.
Hiroko Yano, Sergei V Baranov, Oxana V Baranova, Jinho Kim, Yanchun Pan, Svitlana Yablonska, Diane L Carlisle, Robert J Ferrante, Albert H Kim, Robert M Friedlander. Nat Neurosci 2014
128
11

PINK1-induced mitophagy promotes neuroprotection in Huntington's disease.
B Khalil, N El Fissi, A Aouane, M-J Cabirol-Pol, T Rival, J-C Liévens. Cell Death Dis 2015
127
11

Mutant huntingtin disrupts mitochondrial proteostasis by interacting with TIM23.
Svitlana Yablonska, Vinitha Ganesan, Lisa M Ferrando, JinHo Kim, Anna Pyzel, Oxana V Baranova, Nicolas K Khattar, Timothy M Larkin, Sergei V Baranov, Ning Chen,[...]. Proc Natl Acad Sci U S A 2019
30
36



Cargo recognition failure is responsible for inefficient autophagy in Huntington's disease.
Marta Martinez-Vicente, Zsolt Talloczy, Esther Wong, Guomei Tang, Hiroshi Koga, Susmita Kaushik, Rosa de Vries, Esperanza Arias, Spike Harris, David Sulzer,[...]. Nat Neurosci 2010
554
10

Mutant HTT (huntingtin) impairs mitophagy in a cellular model of Huntington disease.
Sandra Franco-Iborra, Ainhoa Plaza-Zabala, Marta Montpeyo, David Sebastian, Miquel Vila, Marta Martinez-Vicente. Autophagy 2021
47
21

Mitochondrial dysfunction in neurodegenerative diseases.
Ashu Johri, M Flint Beal. J Pharmacol Exp Ther 2012
379
10

Inhibition of mitochondrial fragmentation diminishes Huntington's disease-associated neurodegeneration.
Xing Guo, Marie-Helene Disatnik, Marie Monbureau, Mehrdad Shamloo, Daria Mochly-Rosen, Xin Qi. J Clin Invest 2013
228
10

Huntington's disease: from molecular pathogenesis to clinical treatment.
Christopher A Ross, Sarah J Tabrizi. Lancet Neurol 2011
933
9

Huntington's disease: a clinical review.
P McColgan, S J Tabrizi. Eur J Neurol 2018
310
9

Mitophagy inhibits amyloid-β and tau pathology and reverses cognitive deficits in models of Alzheimer's disease.
Evandro F Fang, Yujun Hou, Konstantinos Palikaras, Bryan A Adriaanse, Jesse S Kerr, Beimeng Yang, Sofie Lautrup, Md Mahdi Hasan-Olive, Domenica Caponio, Xiuli Dan,[...]. Nat Neurosci 2019
513
9

Involvement of PGC-1α in the formation and maintenance of neuronal dendritic spines.
Aiwu Cheng, Ruiqian Wan, Jenq-Lin Yang, Naomi Kamimura, Tae Gen Son, Xin Ouyang, Yongquan Luo, Eitan Okun, Mark P Mattson. Nat Commun 2012
224
9

Adult Conditional Knockout of PGC-1α Leads to Loss of Dopamine Neurons.
Haisong Jiang, Sung-Ung Kang, Shuran Zhang, Senthilkumar Karuppagounder, Jinchong Xu, Yong-Kyu Lee, Bong-Gu Kang, Yunjong Lee, Jianmin Zhang, Olga Pletnikova,[...]. eNeuro 2016
60
15

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice.
L Mangiarini, K Sathasivam, M Seller, B Cozens, A Harper, C Hetherington, M Lawton, Y Trottier, H Lehrach, S W Davies,[...]. Cell 1996
9

Mitochondrial DNA damage is associated with reduced mitochondrial bioenergetics in Huntington's disease.
Almas Siddiqui, Sulay Rivera-Sánchez, María del R Castro, Karina Acevedo-Torres, Anand Rane, Carlos A Torres-Ramos, David G Nicholls, Julie K Andersen, Sylvette Ayala-Torres. Free Radic Biol Med 2012
84
10

Targeting Huntingtin Expression in Patients with Huntington's Disease.
Sarah J Tabrizi, Blair R Leavitt, G Bernhard Landwehrmeyer, Edward J Wild, Carsten Saft, Roger A Barker, Nick F Blair, David Craufurd, Josef Priller, Hugh Rickards,[...]. N Engl J Med 2019
298
9

The Biology of Huntingtin.
Frédéric Saudou, Sandrine Humbert. Neuron 2016
388
9

Impaired PGC-1alpha function in muscle in Huntington's disease.
Rajnish K Chaturvedi, Peter Adhihetty, Shubha Shukla, Thomas Hennessy, Noel Calingasan, Lichuan Yang, Anatoly Starkov, Mahmoud Kiaei, Milena Cannella, Jenny Sassone,[...]. Hum Mol Genet 2009
180
9

A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis.
P Puigserver, Z Wu, C W Park, R Graves, M Wright, B M Spiegelman. Cell 1998
9

PGC-1α activity in nigral dopamine neurons determines vulnerability to α-synuclein.
Carine Ciron, Lu Zheng, Wojciech Bobela, Graham W Knott, Teresa C Leone, Daniel P Kelly, Bernard L Schneider. Acta Neuropathol Commun 2015
53
16

A Mitochondria-Associated Oxidative Stress Perspective on Huntington's Disease.
Ju Zheng, Joris Winderickx, Vanessa Franssens, Beidong Liu. Front Mol Neurosci 2018
38
21

Regulation of mitochondrial biogenesis.
François R Jornayvaz, Gerald I Shulman. Essays Biochem 2010
500
8

Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules.
Laurent R Gauthier, Bénédicte C Charrin, Maria Borrell-Pagès, Jim P Dompierre, Hélène Rangone, Fabrice P Cordelières, Jan De Mey, Marcy E MacDonald, Volkmar Lessmann, Sandrine Humbert,[...]. Cell 2004
791
8

A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset.
Selma M Soyal, Thomas K Felder, Simon Auer, Penelope Hahne, Hannes Oberkofler, Anke Witting, Markus Paulmichl, G Bernhard Landwehrmeyer, Patrick Weydt, Wolfgang Patsch. Hum Mol Genet 2012
71
11

PPARγ-coactivator-1α gene transfer reduces neuronal loss and amyloid-β generation by reducing β-secretase in an Alzheimer's disease model.
Loukia Katsouri, Yau M Lim, Katrin Blondrath, Ioanna Eleftheriadou, Laura Lombardero, Amy M Birch, Nazanin Mirzaei, Elaine E Irvine, Nicholas D Mazarakis, Magdalena Sastre. Proc Natl Acad Sci U S A 2016
79
10

The PPARGC1A locus and CNS-specific PGC-1α isoforms are associated with Parkinson's Disease.
Selma M Soyal, Greta Zara, Boris Ferger, Thomas K Felder, Markus Kwik, Charity Nofziger, Silvia Dossena, Christine Schwienbacher, Andrew A Hicks, Peter P Pramstaller,[...]. Neurobiol Dis 2019
17
47


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.