Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 85 Records) |
Query Trace: ND1[original query] |
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Mitochondrial DNA associations with East Asian metabolic syndrome. Biochimica et biophysica acta. Bioenergetics 2018 7 1859 (9): 878-892. Chalkia Dimitra, Chang Yi-Cheng, Derbeneva Olga, Lvova Maria, Wang Ping, Mishmar Dan, Liu Xiaogang, Singh Larry N, Chuang Lee-Ming, Wallace Douglas |
D-loop Mutations in Renal Cell Carcinoma Improve Predictive Accuracy for Cancer-Related Death by Integrating with Mutations in the NADH Dehydrogenase Subunit 1 Gene. Genes 2019 12 10 (12): . Kim Hakushi, Komiyama Tomoyoshi, Nitta Masahiro, Kawamura Yoshiaki, Hasegawa Masanori, Shoji Sunao, Orihashi Yasushi, Inomoto Chie, Kajiwara Hiroshi, Nakamura Naoya, Kobayashi Hiroyuki, Miyajima Aki |
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 |
IgA nephropathy is associated with elevated urinary mitochondrial DNA copy numbers. Scientific reports 2019 11 9 (1): 16068. Yu Byung Chul, Cho Nam-Jun, Park Samel, Kim Hyoungnae, Choi Soo Jeong, Kim Jin Kuk, Hwang Seung Duk, Gil Hyo-Wook, Lee Eun Young, Jeon Jin Seok, Noh Hyunjin, Han Dong Cheol, Kim Yon Hee, Jin So-Young, Park Moo Yong, Kwon Soon H |
Digital PCR-based plasma cell-free DNA mutation analysis for early-stage pancreatic tumor diagnosis and surveillance. Journal of gastroenterology 2020 9 55 (12): 1183-1193. Okada Tetsuhiro, Mizukami Yusuke, Ono Yusuke, Sato Hiroki, Hayashi Akihiro, Kawabata Hidemasa, Koizumi Kazuya, Masuda Sakue, Teshima Shinichi, Takahashi Kuniyuki, Katanuma Akio, Omori Yuko, Iwano Hirotoshi, Yamada Masataka, Yokochi Tomoki, Asahara Shingo, Kawakubo Kazumichi, Kuwatani Masaki, Sakamoto Naoya, Enomoto Katsuro, Goto Takuma, Sasajima Junpei, Fujiya Mikihiro, Ueda Jun, Matsumoto Seiji, Taniue Kenzui, Sugitani Ayumu, Karasaki Hidenori, Okumura Toshikat |
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 |
A novel m.11406 T > A mutation in mitochondrial ND4 gene causes MELAS syndrome. Mitochondrion 2020 7 54 57-64. Lin Yan, Xu Xuebi, Zhao Dandan, Liu Fuchen, Luo Yuebei, Du Jixiang, Wang Dongdong, Ji Kunqian, Zhao Yuying, Yan Chuanz |
Associations of mitochondrial DNA 3777-4679 region mutations with maternally inherited essential hypertensive subjects in China. BMC medical genetics 2020 May 21 (1): 105. Zhu Ye, You Jia, Xu Chao, Gu Xia |
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 |
The relationship between mitochondrial ND5 gene polymorphisms and in vitro embryo production in Sanjabi sheep. Zygote (Cambridge, England) 2021 Sep 1-3. Teymouri Fereshteh, Foroutanifar Saheb, Abdolmohammadi Alireza, Hajarian Ha |
Dysfunction in Mitochondrial Electron Transport Chain Complex I, Pyruvate Dehydrogenase Activity, and Mutations in ND1 and ND4 Gene in Autism Spectrum Disorder Subjects from Tamil Nadu Population, India. Molecular neurobiology 2021 Jul . Mahalaxmi Iyer, Subramaniam Mohana Devi, Gopalakrishnan Abilash Valsala, Vellingiri Balachand |
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 |
Quantitative detection of circulating MT-ND1 as a potential biomarker for colorectal cancer. Bosnian journal of basic medical sciences 2021 4 21 (5): 577-586. Xu Yichun, Zhou Jiajing, Yuan Qing, Su Jun, Li Qian, Lu Xiaoliang, Zhang Liwen, Cai Zhai, Han Junso |
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 |
The ND1 and CYTB genes polymorphisms associated with in vitro early embryo development of Sanjabi sheep. Animal biotechnology 2021 12 1-5. Mardani Pejman, Foroutanifar Saheb, Abdolmohammadi Alireza, Hajarian Ha |
[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 |
A Pilot Mitochondrial Genome-Wide Association on Migraine Among Saudi Arabians. International journal of general medicine 2022 7 15 6249-6258. Al Asoom Lubna, Khan Johra, Al Sunni Ahmad, Rafique Nazish, Latif Rabia, Alabdali Majed, AbdulAzeez Sayed, Borgio J Franc |
RNA-seq and Mitochondrial DNA Analysis of Adrenal Gland Metastatic Tissue in a Patient with Renal Cell Carcinoma. Biology 2022 4 11 (4): . Komiyama Tomoyoshi, Kim Hakushi, Tanaka Masayuki, Isaki Sanae, Yokoyama Keiko, Miyajima Akira, Kobayashi Hiroyu |
Mutation profile of neurodegenerative mitochondriopathy - LHON in Southern India. Gene 2022 Apr 819 146202. Gowri Poigaialwar, Sathish Ponraj, Mahesh Kumar Shanmugam, Sundaresan Periasa |
The serotonin reuptake transporter modulates mitochondrial copy number and mitochondrial respiratory complex gene expression in the frontal cortex and cerebellum in a sexually dimorphic manner. Journal of neuroscience research 2022 1 100 (3): 869-879. Thorne Bryony N, Ellenbroek Bart A, Day Darren |
Prevalence of primary mutations in Leber hereditary optic neuropathy: A five-year report from a tertiary eye care center in India. Molecular vision 2022 1 27 718-724. Sundaramurthy Srilekha, Selvakumar Ambika, Dharani Vidhya, Soumittra Nagasamy, Mani Jayaprakash, Thirumalai Karthiyayini, Periyasamy Porkodi, Mathavan Sinnakaruppan, Sripriya Sarangapa |
Evaluating the role of selection in the evolution of mitochondrial genomes of aboriginal peoples of Siberia. Vavilovskii zhurnal genetiki i selektsii 2023 6 27 (3): 218-223. B A Malyarchuk, M V Deren |
Mitochondria-wide association study observed significant interactions of mitochondrial respiratory and the inflammatory in the development of anxiety and depression. Translational psychiatry 2023 6 13 (1): 216. Li Liu, Shiqiang Cheng, Xin Qi, Peilin Meng, Xuena Yang, Chuyu Pan, Yujing Chen, Huijie Zhang, Zhen Zhang, Jingxi Zhang, Chune Li, Yan Wen, Yumeng Jia, Bolun Cheng, Feng Zha |
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 Genome Alterations, Cytochrome C Oxidase Activity, and Oxidative Stress: Implications in Primary Open-angle Glaucoma. Journal of current glaucoma practice 2023 2 16 (3): 158-165. Mohanty Kuldeep, Mishra Swetasmita, Dada Rima, Dada Tan |
Association of Mitochondrial Variants with the Joint Occurrence of Polycystic Ovary Syndrome and Hashimoto's Thyroiditis. Antioxidants (Basel, Switzerland) 2023 11 12 (11): . Natalia Zeber-Lubecka, Maria Kulecka, Katarzyna Suchta, Michalina D?browska, Micha? Ciebiera, Ewa E Henn |
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- Page last updated:Apr 29, 2024
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