Publications:

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Sirtuins at the Crossroads between Mitochondrial Quality Control and Neurodegenerative Diseases: Structure, Regulation, Modifications, and Modulators.

Aging And Disease

Xu, Hui H; Liu, Yi-Yang YY; Li, Lin-Seng LS; Liu, You-Shuo YS

Publication Date: 2023-06-01

Variant appearance in text: rs2970848

PubMed Link: 37191431

Variant Present in the following documents:

• Main text
• ad-14-3-794.pdf

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Mitochondrial protein dysfunction in pathogenesis of neurological diseases.

Frontiers In Molecular Neuroscience

Wang, Liang L; Yang, Ziyun Z; He, Xiumei X; Pu, Shiming S; Yang, Cheng C; Wu, Qiong Q; Zhou, Zuping Z; Cen, Xiaobo X; Zhao, Hongxia H

Publication Date: 2022

Variant appearance in text: rs2970848

PubMed Link: 36157077

Variant Present in the following documents:

• Main text
• fnmol-15-974480.pdf

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Emerging Therapeutic Strategies for Parkinson's Disease and Future Prospects: A 2021 Update.

Biomedicines

Gouda, Noha A NA; Elkamhawy, Ahmed A; Cho, Jungsook J

Publication Date: 2022-02-03

Variant appearance in text: rs2970848

PubMed Link: 35203580

Variant Present in the following documents:

• Main text
• biomedicines-10-00371.pdf

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PGC-1s in the Spotlight with Parkinson's Disease.

International Journal Of Molecular Sciences

Piccinin, Elena E; Sardanelli, Anna Maria AM; Seibel, Peter P; Moschetta, Antonio A; Cocco, Tiziana T; Villani, Gaetano G

Publication Date: 2021-03-28

Variant appearance in text: rs2970848

PubMed Link: 33800548

Variant Present in the following documents:

• Main text
• ijms-22-03487.pdf

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Hypermethylation of the Gene Coding for PGC-1α in Peripheral Blood Leukocytes of Patients With Parkinson's Disease.

Frontiers In Neuroscience

Yang, Xiaodong X; Xu, Shaoqing S; Qian, Yiwei Y; He, Xiaoqin X; Chen, Shengdi S; Xiao, Qin Q

Publication Date: 2020

Variant appearance in text: rs2970848

PubMed Link: 32174806

Variant Present in the following documents:

• Main text
• fnins-14-00097.pdf

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Analysis of Single Nucleotide Polymorphisms of STK32B, PPARGC1A and CTNNA3 Gene With Sporadic Parkinson's Disease Susceptibility in Chinese Han Population.

Frontiers In Neurology

Shi, Chang-He CH; Cheng, Yuan Y; Tang, Mi-Bo MB; Liu, Yu-Tao YT; Yang, Zhi-Hua ZH; Li, Fang F; Fan, Yu Y; Yang, Jing J; Xu, Yu-Ming YM

Publication Date: 2018

Variant appearance in text: rs2970848

PubMed Link: 29899728

Variant Present in the following documents:

• Main text
• fneur-09-00387.pdf

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NFE2L2, PPARGC1α, and pesticides and Parkinson's disease risk and progression.

Mechanisms Of Ageing And Development

Paul, Kimberly C KC; Sinsheimer, Janet S JS; Cockburn, Myles M; Bronstein, Jeff M JM; Bordelon, Yvette Y; Ritz, Beate B

Publication Date: 2018-07

Variant appearance in text: rs2970848

PubMed Link: 29630901

Variant Present in the following documents:

• Main text

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The impact of mitochondrial DNA and nuclear genes related to mitochondrial functioning on the risk of Parkinson's disease.

Current Genomics

Gaweda-Walerych, Katarzyna K; Zekanowski, Cezary C

Publication Date: 2013-12

Variant appearance in text: rs2970848

PubMed Link: 24532986

Variant Present in the following documents:

• Main text

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A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort.

Bmc Neurology

Weydt, Patrick P; Soyal, Selma M SM; Landwehrmeyer, G Bernhard GB; Patsch, Wolfgang W; ,

Publication Date: 2014-01-02

Variant appearance in text: rs2970848

PubMed Link: 24383721

Variant Present in the following documents:

• Main text
• 1471-2377-14-1.pdf

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DNA sequence variants in PPARGC1A, a gene encoding a coactivator of the ω-3 LCPUFA sensing PPAR-RXR transcription complex, are associated with NV AMD and AMD-associated loci in genes of complement and VEGF signaling pathways.

Plos One

SanGiovanni, John Paul JP; Chen, Jing J; Sapieha, Przemyslaw P; Aderman, Christopher M CM; Stahl, Andreas A; Clemons, Traci E TE; Chew, Emily Y EY; Smith, Lois E H LE

Publication Date: 2013

Variant appearance in text: rs2970848

PubMed Link: 23335958

Variant Present in the following documents:

• Main text
• pone.0053155.pdf

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Association of PGC-1alpha polymorphisms with age of onset and risk of Parkinson's disease.

Bmc Medical Genetics

Clark, Joanne J; Reddy, Sonika S; Zheng, Kangni K; Betensky, Rebecca A RA; Simon, David K DK

Publication Date: 2011-05-19

Variant appearance in text: rs2970848

PubMed Link: 21595954

Variant Present in the following documents:

• Main text
• 1471-2350-12-69.pdf

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Localization of sequence variations in PGC-1α influence their modifying effect in Huntington disease.

Molecular Neurodegeneration

Che, Hong Van B HV; Metzger, Silke S; Portal, Esteban E; Deyle, Carolin C; Riess, Olaf O; Nguyen, Huu Phuc HP

Publication Date: 2011-01-06

Variant appearance in text: rs2970848

PubMed Link: 21211002

Variant Present in the following documents:

• Main text
• 1750-1326-6-1.pdf

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PGC-1alpha as modifier of onset age in Huntington disease.

Molecular Neurodegeneration

Taherzadeh-Fard, Elahe E; Saft, Carsten C; Andrich, Jürgen J; Wieczorek, Stefan S; Arning, Larissa L

Publication Date: 2009-02-06

Variant appearance in text: rs2970848

PubMed Link: 19200361

Variant Present in the following documents:

• Main text
• 1750-1326-4-10.pdf

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