Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Disease and ND3[original query] |
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Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. American journal of human genetics 2003 Apr 72 (4): 804-11. van der Walt Joelle M, Nicodemus Kristin K, Martin Eden R, Scott William K, Nance Martha A, Watts Ray L, Hubble Jean P, Haines Jonathan L, Koller William C, Lyons Kelly, Pahwa Rajesh, Stern Matthew B, Colcher Amy, Hiner Bradley C, Jankovic Joseph, Ondo William G, Allen Fred H, Goetz Christopher G, Small Gary W, Mastaglia Frank, Stajich Jeffrey M, McLaurin Adam C, Middleton Lefkos T, Scott Burton L, Schmechel Donald E, Pericak-Vance Margaret A, Vance Jeffery |
De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency. Annals of neurology 2004 1 55 (1): 58-64. McFarland Robert, Kirby Denise M, Fowler Kerry J, Ohtake Akira, Ryan Michael T, Amor David J, Fletcher Janice M, Dixon Joanne W, Collins Felicity A, Turnbull Douglass M, Taylor Robert W, Thorburn David |
Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians. European journal of human genetics : EJHG 2005 Jun 13 (6): 748-52. Ghezzi Daniele, Marelli Cecilia, Achilli Alessandro, Goldwurm Stefano, Pezzoli Gianni, Barone Paolo, Pellecchia Maria Teresa, Stanzione Paolo, Brusa Livia, Bentivoglio Anna Rita, Bonuccelli Ubaldo, Petrozzi Lucia, Abbruzzese Giovanni, Marchese Roberta, Cortelli Pietro, Grimaldi Daniela, Martinelli Paolo, Ferrarese Carlo, Garavaglia Barbara, Sangiorgi Simonetta, Carelli Valerio, Torroni Antonio, Albanese Alberto, Zeviani Massi |
The interactive effect of SIRT1 promoter region polymorphism on type 2 diabetes susceptibility in the North Indian population. PloS one 2012 7 (11): e48621. Rai Ekta, Sharma Swarkar, Kaul Surabhi, Jain Kamal, Matharoo Kawaljit, Bhanwer Amarjit S, Bamezai Rameshwar N |
Mitochondrial complex I gene variations; as a potential genetic risk factor in pathogenesis of multiple sclerosis. Journal of the neurological sciences 2014 Oct 345 (1-2): 220-3. Poursadegh Zonouzi Ahmad, Ghorbian Saeid, Abkar Morteza, Poursadegh Zonouzi Ali Akbar, Azadi A |
Mitochondrial NADH Dehydrogenase Subunit 3 Polymorphism Associated with an Earlier Age at Onset in Male Machado-Joseph disease Patients. CNS neuroscience & therapeutics 2015 Sep . Chen Sheng, Gan Shi-Rui, Cai Ping-Ping, Ni Wang, Zhou Qi, Dong Yi, Wang Ning, Wu Zhi-Yi |
Mitochondrial genome mutations in 13 subunits of respiratory chain complexes in Chinese Han and Mongolian hypertensive individuals. Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2017 11 29 (7): 1090-1099. Zhao Ying, Chen Xi, Li Haide, Zhu Chao, Li Yang, Liu Yu |
Four novel mutations in the mitochondrial ND4 gene of complex I in patients with multiple sclerosis. Biomedical reports 2019 12 11 (6): 257-268. Alharbi Maram Atallah, Al-Kafaji Ghada, Khalaf Noureddine Ben, Messaoudi Safia Abdulsalam, Taha Safa, Daif Abdulqader, Bakhiet Mo |
Genomic profiling of mitochondrial DNA reveals novel complex gene mutations in familial type 2 diabetes mellitus individuals from Mizo ethnic population, Northeast India. Mitochondrion 2019 Dec 51 7-14. Lalrohlui Freda, Zohmingthanga John, Hruaii Vanlal, Kumar Nachimuthu Senth |
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits. American journal of human genetics 2019 Jan 104 (1): 112-138. Kraja Aldi T, Liu Chunyu, Fetterman Jessica L, Graff Mariaelisa, Have Christian Theil, Gu Charles, Yanek Lisa R, Feitosa Mary F, Arking Dan E, Chasman Daniel I, Young Kristin, Ligthart Symen, Hill W David, Weiss Stefan, Luan Jian'an, Giulianini Franco, Li-Gao Ruifang, Hartwig Fernando P, Lin Shiow J, Wang Lihua, Richardson Tom G, Yao Jie, Fernandez Eliana P, Ghanbari Mohsen, Wojczynski Mary K, Lee Wen-Jane, Argos Maria, Armasu Sebastian M, Barve Ruteja A, Ryan Kathleen A, An Ping, Baranski Thomas J, Bielinski Suzette J, Bowden Donald W, Broeckel Ulrich, Christensen Kaare, Chu Audrey Y, Corley Janie, Cox Simon R, Uitterlinden Andre G, Rivadeneira Fernando, Cropp Cheryl D, Daw E Warwick, van Heemst Diana, de Las Fuentes Lisa, Gao He, Tzoulaki Ioanna, Ahluwalia Tarunveer S, de Mutsert Renée, Emery Leslie S, Erzurumluoglu A Mesut, Perry James A, Fu Mao, Forouhi Nita G, Gu Zhenglong, Hai Yang, Harris Sarah E, Hemani Gibran, Hunt Steven C, Irvin Marguerite R, Jonsson Anna E, Justice Anne E, Kerrison Nicola D, Larson Nicholas B, Lin Keng-Hung, Love-Gregory Latisha D, Mathias Rasika A, Lee Joseph H, Nauck Matthias, Noordam Raymond, Ong Ken K, Pankow James, Patki Amit, Pattie Alison, Petersmann Astrid, Qi Qibin, Ribel-Madsen Rasmus, Rohde Rebecca, Sandow Kevin, Schnurr Theresia M, Sofer Tamar, Starr John M, Taylor Adele M, Teumer Alexander, Timpson Nicholas J, de Haan Hugoline G, Wang Yujie, Weeke Peter E, Williams Christine, Wu Hongsheng, Yang Wei, Zeng Donglin, Witte Daniel R, Weir Bruce S, Wareham Nicholas J, Vestergaard Henrik, Turner Stephen T, Torp-Pedersen Christian, Stergiakouli Evie, Sheu Wayne Huey-Herng, Rosendaal Frits R, Ikram M Arfan, Franco Oscar H, Ridker Paul M, Perls Thomas T, Pedersen Oluf, Nohr Ellen A, Newman Anne B, Linneberg Allan, Langenberg Claudia, Kilpeläinen Tuomas O, Kardia Sharon L R, Jørgensen Marit E, Jørgensen Torben, Sørensen Thorkild I A, Homuth Georg, Hansen Torben, Goodarzi Mark O, Deary Ian J, Christensen Cramer, Chen Yii-Der Ida, Chakravarti Aravinda, Brandslund Ivan, Bonnelykke Klaus, Taylor Kent D, Wilson James G, Rodriguez Santiago, Davies Gail, Horta Bernardo L, Thyagarajan Bharat, Rao D C, Grarup Niels, Davila-Roman Victor G, Hudson Gavin, Guo Xiuqing, Arnett Donna K, Hayward Caroline, Vaidya Dhananjay, Mook-Kanamori Dennis O, Tiwari Hemant K, Levy Daniel, Loos Ruth J F, Dehghan Abbas, Elliott Paul, Malik Afshan N, Scott Robert A, Becker Diane M, de Andrade Mariza, Province Michael A, Meigs James B, Rotter Jerome I, North Kari |
Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I. BMC pediatrics 2020 1 20 (1): 41. Danhelovska Tereza, Kolarova Hana, Zeman Jiri, Hansikova Hana, Vaneckova Manuela, Lambert Lukas, Kucerova-Vidrova Vendula, Berankova Kamila, Honzik Tomas, Tesarova Marke |
NGS-based mtDNA Profiling Could Reveal Genetic Alterations in Schizophrenia. Current topics in medicinal chemistry 2021 6 21 (11): 938-948. Ivanova Elena Mihailova, Kandilarova Snezhina Mihailova, Lukanov Tzvetelin Ivanov, Naumova Elissaveta Jordanova, Akabalieva Katerina Valentinova, Milanova Vihra Krumo |
Examining the Association between Mitochondrial Genome Variation and Coronary Artery Disease. Genes 2022 3 13 (3): . Vilne Baiba, Sawant Aniket, Rudaka Iri |
Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis. PloS one 2022 17 (2): e0263606. Al-Kafaji Ghada, Bakheit Halla F, AlAli Faisal, Fattah Mina, Alhajeri Saad, Alharbi Maram A, Daif Abdulqader, Alsabbagh Manahel Mahmood, Alwehaidah Materah Salem, Bakhiet Mo |
Modeling of mitochondrial genetic polymorphisms reveals induction of heteroplasmy by pleiotropic disease locus 10398A>G. Scientific reports 2023 6 13 (1): 10405. Molly Smullen, Meagan N Olson, Liam F Murray, Madhusoodhanan Suresh, Guang Yan, Pepper Dawes, Nathaniel J Barton, Jivanna N Mason, Yucheng Zhang, Aria A Fernandez-Fontaine, George M Church, Diego Mastroeni, Qi Wang, Elaine T Lim, Yingleong Chan, Benjamin Readhe |
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