Human Genome Epidemiology Literature Finder
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Records 1 - 28 (of 28 Records) |
| Query Trace: Disease and ND1[original query] |
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| 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 |
| Mitochondrial polymorphisms as risk factors for endometrial cancer in southwest China. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 0 16 (4): 1661-7. Xu L, Hu Y, Chen B, Tang W, Han X, Yu H, Xiao |
| Complex I polymorphisms, bigenomic heterogeneity, and family history in Virginians with Parkinson's disease. Journal of the neurological sciences 2006 Sep 247 (2): 224-30. Swerdlow Russell H, Weaver Bradley, Grawey Amy, Wenger Connie, Freed Eric, Worrall Bradford |
| Complex insertion/deletion polymorphism in NOD1 (CARD4) is not associated with inflammatory bowel disease susceptibility in East Anglia panel. Inflammatory bowel diseases 2006 Oct 12 (10): 967-71. Tremelling Mark, Hancock Laura, Bredin Francesca, Sharpstone Daniel, Bingham Shiela A, Parkes Mil |
| Variation of mitochondrial gene and the association with type 2 diabetes mellitus in a Chinese population. Diabetes research and clinical practice 2006 Jul 73 (1): 77-82. Tang Dong-Ling, Zhou Xin, Li Xia, Zhao Lei, Liu Fa |
| Leukocyte mitochondrial DNA alteration in systemic lupus erythematosus and its relevance to the susceptibility to lupus nephritis. International journal of molecular sciences 2012 13 (7): 7. Lee HT, Lin CS, Chen WS, Liao HT, Tsai CY, Wei YH |
| Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans. Proceedings of the National Academy of Sciences of the United States of America 2012 May 109 (19): 7391-6. Ji Fuyun, Sharpley Mark S, Derbeneva Olga, Alves Leonardo Scherer, Qian Pin, Wang Yaoli, Chalkia Dimitra, Lvova Maria, Xu Jiancheng, Yao Wei, Simon Mariella, Platt Julia, Xu Shiqin, Angelin Alessia, Davila Antonio, Huang Taosheng, Wang Ping H, Chuang Lee-Ming, Moore Lorna G, Qian Guisheng, Wallace Douglas |
| [Study on three common mitochondrial DNA mutations in Leber's hereditary optic neuropathy]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2012 Oct 29 (5): 519-23. Ma Yun-xia, Zhou Yon-gan, Zhang Jing-ping, Zhang Quan-bin, Liu Wei-la, Ren Cai-fen, Li Xiao- |
| 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 |
| Mitochondrial DNA T4216C and A4917G variations in multiple sclerosis. Journal of the neurological sciences 2015 Sep 356 (1-2): 55-60. Andalib Sasan, Talebi Mahnaz, Sakhinia Ebrahim, Farhoudi Mehdi, Sadeghi-Bazargani Homayoun, Gjedde Albe |
| Genetic aetiology of ophthalmological manifestations in children - a focus on mitochondrial disease-related symptoms. Acta ophthalmologica 2015 Oct . Widgren Paula, Hurme Anri, Falck Aura, Keski-Filppula Riikka, Remes Anne M, Moilanen Jukka, Majamaa Kari, Kervinen Marko, Uusimaa Johan |
| Mitochondrial complex I and V gene polymorphisms in type II diabetes mellitus among high risk Mizo-Mongoloid population, Northeast India. Genes and environment : the official journal of the Japanese Environmental Mutagen Society 2016 38 5. Lalrohlui Freda, Thapa Sunaina, Ghatak Souvik, Zohmingthanga John, Senthil Kumar Nachimut |
| Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India. Investigative ophthalmology & visual science 2017 8 58 (10): 3923-3930. Khan Nahid Akhtar, Govindaraj Periyasamy, Soumittra Nagasamy, Sharma Sonika, Srilekha Sundaramoorthy, Ambika Selvakumar, Vanniarajan Ayyasamy, Meena Angamuthu Kanikannan, Uppin Megha S, Sundaram Challa, Bindu Parayil Sankaran, Gayathri Narayanappa, Taly Arun B, Thangaraj Kumarasa |
| 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 |
| Long-term screening for primary mitochondrial DNA variants associated with Leber hereditary optic neuropathy: incidence, penetrance and clinical features. Mitochondrion 2020 8 54 128-132. Marotta Rosetta, Chin Judy, Chiotis Maria, Shuey Neil, Collins Steven |
| Frequency and spectrum of MT-TT variants associated with Leber's hereditary optic neuropathy in a Chinese cohort of subjects. Mitochondrial DNA. Part B, Resources 2020 12 4 (2): 2266-2280. Lyu Yuanyuan, Xu Man, Chen Jie, Ji YanChun, Guan Min-Xin, Zhang Juanju |
| Differential mitochondrial genome in patients with Rheumatoid Arthritis. Autoimmunity 2020 11 54 (1): 1-12. Jaiswal Kumar Sagar, Khanna Shweta, Ghosh Arup, Padhan Prasanta, Raghav Sunil Kumar, Gupta Bhaw |
| 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 |
| The association between multiple risk factors, clinical correlations and molecular insights in Parkinson's disease patients from Tamil Nadu population, India. Neuroscience letters 2021 4 755 135903. Venkatesan Dhivya, Iyer Mahalaxmi, S Robert Wilson, G Lakshmipathy, Vellingiri Balachand |
| Mild Leber hereditary optic neuropathy (LHON) in a Western European family due to the rare Asian m.14502T>C variant in the MT-ND6 gene. Ophthalmic genetics 2021 4 42 (4): 440-445. Vandeputte Justine, Van Heetvelde Mattias, Van Cauwenbergh Caroline, Seneca Sara, De Baere Elfride, Leroy Bart P, De Zaeytijd Jul |
| [Risk of Multiple Sclerosis: Analysis of Interactions Between Variants of Nuclear and Mitochondrial Genomes]. Molekuliarnaia biologiia 0 55 (6): 956-964. Kozin M S, Kiselev I S, Baulina N M, Pavlova G V, Boyko A N, Kulakova O G, Favorova O |
| First mitochondrial genome-wide association study with metabolomics. Human molecular genetics 2021 10 31 (19): 3367-3376. Aboulmaouahib Brahim, Kastenmüller Gabi, Suhre Karsten, Zöllner Sebastian, Weissensteiner Hansi, Prehn Cornelia, Adamski Jerzy, Gieger Christian, Wang-Sattler Rui, Lichtner Peter, Strauch Konstantin, Flaquer Antòn |
| Mitochondrial DNA variants in a cohort from Argentina with suspected Leber's hereditary optic neuropathy (LHON). PloS one 2023 2 18 (2): e0275703. Buonfiglio Paula I, Menazzi Sebastián, Francipane Liliana, Lotersztein Vanesa, Ferreiro Verónica, Elgoyhen Ana Belén, Dalamón Vivia |
| Mitochondrial Pathogenic Mutations and Expression Pattern of Oxidative Phosphorylation Genes in COVID-19 Patients. Iranian journal of allergy, asthma, and immunology 2024 11 23 (4): 374-392. Milad Shokuhi Nia, Dormohammad Kordi Tamandani, Mohammad Kazem Momeni, Zakaria Bame |
| Screening for mitochondrial tRNA variants in 200 patients with systemic lupus erythematosus. Human heredity 2024 11 1-19. Dan Xuan, Fuyong Qiang, Hui Xu, Li Wang, Yonghui X |
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