Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: Disease and ND5[original query] |
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The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations. Journal of cardiac failure 2001 1 6 (4): 321-9. Marin-Garcia J, Goldenthal M J, Ananthakrishnan R, Pierpont M |
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 polymorphisms and risk of Parkinson's disease in Spanish population. Journal of the neurological sciences 2005 Sep 236 (1-2): 49-54. Huerta Cecilia, Castro Mónica G, Coto Eliecer, Blázquez Marta, Ribacoba René, Guisasola Luis M, Salvador Carlos, Martínez Carmen, Lahoz Carlos H, Alvarez Victor |
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease. Journal of medical genetics 2007 Apr 44 (4): e74. Blok M J, Spruijt L, de Coo I F M, Schoonderwoerd K, Hendrickx A, Smeets H |
Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation. American journal of human genetics 2008 Dec 83 (6): 760-8. Ji Yanli, Zhang A-Mei, Jia Xiaoyun, Zhang Ya-Ping, Xiao Xueshan, Li Shiqiang, Guo Xiangming, Bandelt Hans-Jürgen, Zhang Qingjiong, Yao Yong-Ga |
Evaluating mitochondrial DNA in patients with breast cancer and benign breast disease. Journal of cancer research and clinical oncology 2011 Apr 137 (4): 669-75. Shen Lijun, Wei Jia, Chen Tao, He Jing, Qu Jianchun, He Xiumei, Jiang Luxi, Qu Yemin, Fang Hezhi, Chen Guorong, Lu Jianxin, Bai Yido |
Mitochondrial genome variations in advanced stage endometriosis: a study in South Indian population. PloS one 2012 7 (7): e40668. Govatati Suresh, Tipirisetti Nageswara Rao, Perugu Shyam, Kodati Vijaya Lakshmi, Deenadayal Mamata, Satti Vishnupriya, Bhanoori Manjula, Shivaji |
Mitochondrial DNA variation analysis in cervical cancer. Mitochondrion 2014 May 16 73-82. Kabekkodu Shama Prasada, Bhat Samatha, Mascarenhas Roshan, Mallya Sandeep, Bhat Manoj, Pandey Deeksha, Kushtagi Pralhad, Thangaraj Kumarasamy, Gopinath P M, Satyamoorthy Kapaet |
Mitochondrial DNA variations in myelodysplastic syndrome. Annals of hematology 2013 Jul 92 (7): 871-6. Gupta Maya, Madkaikar Manisha, Rao Vundinti Babu, Mishra Anju, Govindaraj Periyasamy, Thangaraj Kumarasamy, Ghosh Kanjaks |
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 |
Analyses of the mitochondrial mutations in the Chinese patients with sporadic Creutzfeldt-Jakob disease. European journal of human genetics : EJHG 2015 Jan 23 (1): 86-91. Zhang Jin, Zhang Zhi-Xia, Du Peng-Chen, Zhou Wei, Wu Su-Dong, Wang Qi-Ling, Chen Cao, Shi Qi, Chen Chen, Gao Chen, Tian Chan, Dong Xiao-Pi |
Analysis of mitochondrial DNA heteroplasmic mutations A1555G, C3256T, T3336C, ?5178?, G12315A, G13513A, G14459A, G14846? and G15059A in CHD patients with the history of myocardial infarction. Experimental and molecular pathology 2015 Dec . Mitrofanov Konstantin Y, Zhelankin Andrey V, Shiganova G M, Sazonova Margarita A, Bobryshev Yuri V, Postnov Anton Y, Sobenin I ? Igor A, Orekhov Alexander |
Correlational study on mitochondrial DNA mutations as potential risk factors in breast cancer. Oncotarget 2016 Apr . Li Linhai, Chen Lidan, Li Jun, Zhang Weiyun, Liao Yang, Chen Jianyun, Sun Zhaoh |
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 |
A novel mutation in the mitochondrial MT-ND5 gene in a family with MELAS. The relevance of genetic analysis on targeted tissues. Mitochondrion 2019 10 50 14-18. Panadés-de Oliveira Luísa, Montoya Julio, Emperador Sonia, Ruiz-Pesini Eduardo, Jericó Ivonne, Arenas Joaquín, Hernández-Lain Aurelio, Blázquez Alberto, Martín Miguel Á, Domínguez-González Cristi |
Cardiomyopathy in children with mitochondrial disease: Prognosis and genetic background. International journal of cardiology 2019 1 279 115-121. Imai-Okazaki Atsuko, Kishita Yoshihito, Kohda Masakazu, Mizuno Yosuke, Fushimi Takuya, Matsunaga Ayako, Yatsuka Yukiko, Hirata Tomoko, Harashima Hiroko, Takeda Atsuhito, Nakaya Akihiro, Sakata Yasushi, Kogaki Shigetoyo, Ohtake Akira, Murayama Kei, Okazaki Yasus |
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 |
MELAS/LS Overlap Syndrome Associated With Mitochondrial DNA Mutations: Clinical, Genetic, and Radiological Studies. Frontiers in neurology 2021 5 12 648740. Wei Yanping, Huang Yan, Yang Yingmai, Qian M |
Examining the Association between Mitochondrial Genome Variation and Coronary Artery Disease. Genes 2022 3 13 (3): . Vilne Baiba, Sawant Aniket, Rudaka Iri |
Mitochondrial DNA haplogroup analysis in Saudi Arab patients with multiple sclerosis. PloS one 2022 12 17 (12): e0279237. Al-Kafaji Ghada, Alwehaidah Materah Salem, Alsabbagh Manahel Mahmood, Alharbi Maram A, Bakhiet Mo |
[Leber's hereditary optic neuropathy clinical features in patients with mitochondrial DNA m.13513G>A candidate mutation]. Vestnik oftalmologii 2022 10 138 (5. Vyp. 2): 208-214. Andreeva N A, Murakhovskaya Yu K, Tsygankova P G, Krilova T D, Sheremet N |
Use of dual genomic sequencing to screen mitochondrial diseases in pediatrics: a retrospective analysis. Scientific reports 2023 3 13 (1): 4193. Wu Teng-Hui, Peng Jing, Yang Li, Chen Yan-Hui, Lu Xiu-Lan, Huang Jiao-Tian, You Jie-Yu, Ou-Yang Wen-Xian, Sun Yue-Yu, Xue Yi-Nan, Mao Xiao, Yan Hui-Ming, Ren Rong-Na, Xie Jing, Chen Zhi-Heng, Zhang Victor-Wei, Lyu Gui-Zhen, He Fa |
"Mitochondrial pathogenic mutations and metabolic alterations associated with COVID-19 disease severity". Journal of medical virology 2023 2 95 (2): e28553. Kumari Diksha, Singh Yamini, Singh Sayar, Dogra Vikas, Srivastava Ashish Kumar, Srivastava Swati, Garg Iti, Bargotya Mona, Hussain Javid, Ganju Lilly, Varshney Raje |
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia. International journal of molecular sciences 2023 1 24 (2): . Kistol Denis, Tsygankova Polina, Krylova Tatiana, Bychkov Igor, Itkis Yulia, Nikolaeva Ekaterina, Mikhailova Svetlana, Sumina Maria, Pechatnikova Natalia, Kurbatov Sergey, Bostanova Fatima, Migiaev Ochir, Zakharova Ekateri |
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