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Mitochondrial DNA
The Journal of DNA Mapping, Sequencing, and Analysis
Volume 26, 2015 - Issue 4
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Research Article

Usage of mitochondrial D-loop variation to predict risk for Huntington disease

Kazem MousavizadehDepartment of Molecular Medicine, Iran University of Medical Sciences, Tehran, Iran,
,
Peyman RajabiDepartment of Molecular Medicine, Iran University of Medical Sciences, Tehran, Iran, ;Department of Medical Biotechnology, Tehran University of Medical Sciences, Tehran, Iran,
,
Mahsa AlaeeDepartment of Molecular Medicine, Iran University of Medical Sciences, Tehran, Iran, ;Department of Medical Biotechnology, Tehran University of Medical Sciences, Tehran, Iran,
,
Sepideh DadgarDepartment of Genetics, Special Medical Center, Tehran, Iran, and
&
Massoud HoushmandDepartment of Genetics, Special Medical Center, Tehran, Iran, and ;Department of Medical Genetics, National Institute for Genetic Engineering and Biotechnology, Tehran, IranCorrespondence[email protected]
Pages 579-582 | Received 16 Oct 2013, Accepted 22 Dec 2013, Published online: 29 Jan 2014

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Read on this site (2)

S. Rodrigues-Antunes & B. N. Borges. (2019) Alterations in mtDNA, gastric carcinogenesis and early diagnosis. Mitochondrial DNA Part A 30:2, pages 226-233.
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Masoumeh Falah, Mohammad Farhadi, Seyed Kamran Kamrava, Saeid Mahmoudian, Ahmad Daneshi, Maryam Balali, Alimohamad Asghari & Massoud Houshmand. (2017) Association of genetic variations in the mitochondrial DNA control region with presbycusis. Clinical Interventions in Aging 12, pages 459-465.
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Articles from other publishers (8)

Heriberto Santander-Lucio, Armando Totomoch-Serra, María de Lourdes Muñoz, Normand García-Hernández, Gerardo Pérez-Ramírez, Adán Valladares-Salgado & Ashael Alfredo Pérez-Muñoz. (2023) Variants in the Control Region of Mitochondrial Genome Associated with type 2 Diabetes in a Cohort of Mexican Mestizos. Archives of Medical Research 54:2, pages 113-123.
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Ghada Al-Kafaji, Halla F. Bakheit, Faisal AlAli, Mina Fattah, Saad Alhajeri, Maram A. Alharbi, Abdulqader Daif, Manahel Mahmood Alsabbagh, Materah Salem Alwehaidah & Moiz Bakhiet. (2022) Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis. PLOS ONE 17:2, pages e0263606.
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Vellingiri Balachandar, Kamarajan Rajagopalan, Kaavya Jayaramayya, Madesh Jeevanandam & Mahalaxmi Iyer. (2021) Mitochondrial dysfunction: A hidden trigger of autism?. Genes & Diseases 8:5, pages 629-639.
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Yoon-ha Jang, Sae Ryun Ahn, Ji-yeon Shim & Kwang-il Lim. (2021) Engineering Genetic Systems for Treating Mitochondrial Diseases. Pharmaceutics 13:6, pages 810.
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Ana Victoria Lechuga‐Vieco, Raquel Justo‐Méndez & José Antonio Enríquez. (2020) Not all mitochondrial DNAs are made equal and the nucleus knows it . IUBMB Life 73:3, pages 511-529.
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Tobore Onojighofia Tobore. (2019) Towards a comprehensive understanding of the contributions of mitochondrial dysfunction and oxidative stress in the pathogenesis and pathophysiology of Huntington's disease. Journal of Neuroscience Research 97:11, pages 1455-1468.
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Huanzheng Li, Jesse Slone, Lin Fei & Taosheng Huang. (2019) Mitochondrial DNA Variants and Common Diseases: A Mathematical Model for the Diversity of Age-Related mtDNA Mutations. Cells 8:6, pages 608.
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Sharareh Kamfar, Seyed Moayed Alavian, Kambiz Hasrak, Massoud Houshmand, Bahram Seifi Zarei, Alireza Khalaj, Forough Homaunpur & Massoud Saidijam. (2019) Analysis of Mitochondrial 4977-bp Deletion and D-Loop Variation in Iranian Non-Alcoholic Fatty Liver Disease Patients. Hepatitis Monthly In Press:In Press.
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