Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 73 Records) |
Query Trace: Disease and TRNA[original query] |
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Haplogroup Context is Less Important in the Penetrance of Mitochondrial DNA Complex I Mutations Compared to mt-tRNA Mutations. Journal of molecular evolution 2018 Jul . O'Keefe Hannah, Queen Rachel A, Meldau Surita, Lord Phillip, Elson Joanna |
Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial Patients. Frontiers in neurology 2019 3 10 160. Musumeci Olimpia, Barca Emanuele, Lamperti Costanza, Servidei Serenella, Comi Giacomo Pietro, Moggio Maurizio, Mongini Tiziana, Siciliano Gabriele, Filosto Massimiliano, Pegoraro Elena, Primiano Guido, Ronchi Dario, Vercelli Liliana, Orsucci Daniele, Bello Luca, Zeviani Massimo, Mancuso Michelangelo, Toscano Anton |
The mitochondrial tRNA 5587T>C and tRNA 12280A>G mutations may be associated with hypertension in a Chinese family. Experimental and therapeutic medicine 2019 2 17 (3): 1855-1862. Lin Lin, Cui Peng, Qiu Zhipeng, Wang Min, Yu Yingchao, Wang Jing, Sun Qian, Zhao Hairo |
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 |
Ancient mitochondrial DNA pathogenic variants putatively associated with mitochondrial disease. PloS one 2020 9 15 (9): e0233666. Toncheva Draga, Serbezov Dimitar, Karachanak-Yankova Sena, Nesheva Desisla |
Expanding and validating the biomarkers for mitochondrial diseases. Journal of molecular medicine (Berlin, Germany) 2020 8 98 (10): 1467-1478. Maresca Alessandra, Del Dotto Valentina, Romagnoli Martina, La Morgia Chiara, Di Vito Lidia, Capristo Mariantonietta, Valentino Maria Lucia, Carelli Valerio, |
Seasonal and residential clustering at disease onset of anti-MDA5-associated interstitial lung disease. RMD open 2020 6 6 (2): . Nishina Naoshi, Sato Shinji, Masui Kenichi, Gono Takahisa, Kuwana Masata |
Association of mitochondrial variants A4336G of the tRNAGln gene and 8701G/A of the MT-ATP6 gene in Mexicans Mestizos with Parkinson disease. Folia neuropathologica 2020 4 57 (4): 335-339. García Silvia, López-Hernández Luz, Dávila-Maldonado Luis, Cuevas-García Carlos, Gallegos-Arreola Martha, Alcaraz-Estrada Sofía, Cortes-Espinosa Leticia, Flores Carlos, Canto Patricia, Vázquez Ram |
Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease. Applied biochemistry and biotechnology 2020 Feb . Heidari Mohammad Mehdi, Mirfakhradini Fatemeh Sadat, Tayefi Fahime, Ghorbani Saghar, Khatami Mehri, Hadadzadeh Meh |
Profiling of mitochondrial genomes in SCA3/MJD patients from mainland China. Gene 2020 2 738 144487. Yuan Hongyu, Yang Huihua, Peng Linliu, Peng Yun, Chen Zhao, Wan Linlin, Wang Chunrong, Shi Yuting, Zhang Victor Wei, Tang Beisha, Qiu Rong, Jiang Ho |
Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy. Human mutation 2020 Dec . Campbell Teresa, Lou Xiaoting, Slone Jesse, Brown Jenice, Bromwell Meghan, Liu Jie, Bai Renkui, Haude Katrina, Balog Amanda, Cui Hong, Zou Weiwei, Yang Li, Al-Beshri Ali, Huang Taoshe |
Detecting Rare Variants and Heteroplasmy of Mitochondrial DNA from High-Throughput Sequencing in Patients with Coronary Artery Disease. Medical science monitor : international medical journal of experimental and clinical research 2020 11 26 e925401. Jia Qian, Xu Lu, Shen Juan, Wei Yanping, Xu Huaiqian, Shi Jinlong, Jia Zhilong, Zhao Xiaojing, Liu Chunlei, Zhong Qin, Tian Yaping, He Kunl |
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 |
Lack of PTRHD1 mutation in patients with young-onset and familial Parkinson's disease in a Taiwanese population. Neurobiology of aging 2020 10 100 118.e15-118.e16. Chen Szu-Ju, Ho Chang-Han, Lin Hang-Yi, Lin Chin-Hsien, Wu Ruey-Me |
Assessment of the Changes in Mitochondrial Gene Polymorphism in Ulcerative Colitis and the Etiology of Ulcerative Colitis-associated Colorectal Cancer. Anticancer research 2020 Jan 40 (1): 101-107. Tanaka Toshiaki, Kobunai Takashi, Yamamoto Yoko, Murono Koji, Emoto Shigenbu, Hiyoshi Masaya, Kaneko Manabu, Sasaki Kazuhito, Shuno Yasutaka, Nishikawa Takeshi, Hata Keisuke, Kawai Kazushige, Nozawa Hiroaki, Ishihara Soichi |
Novel Alanyl-tRNA Synthetase 2 Pathogenic Variants in Leukodystrophies. Frontiers in neurology 2019 10 1321. Wang Xingao, Wang Qun, Tang Hefei, Chen Bin, Dong Xiang, Niu Songtao, Li Shaowu, Shi Yuzhi, Shan Wei, Zhang Zaiqia |
Evaluation of D-loop hypervariable region I variations, haplogroups and copy number of mitochondrial DNA in Bangladeshi population with type 2 diabetes. Heliyon 2021 Jul 7 (7): e07573. Saha Sajoy Kanti, Saba Abdullah Al, Hasib Md, Rimon Razoan Al, Hasan Imrul, Alam Md Sohrab, Mahmud Ishtiaq, Nabi A H M Nur |
Analysis of PTRHD1 common and rare variants in European patients with Parkinson's disease. Neurobiology of aging 2021 7 107 178-180. Sosero Yuri L, Bandres-Ciga Sara, Gan-Or Ziv, Krohn Lynne, |
Single Nucleotide Polymorphism in the IL17A Gene Is Associated with Interstitial Lung Disease Positive to Anti-Jo1 Antisynthetase Autoantibodies. Life (Basel, Switzerland) 2021 3 11 (2): . Ponce-Gallegos Marco Antonio, González-Pérez Montserrat I, Mejía Mayra, Nava-Quiroz Karol J, Pérez-Rubio Gloria, Buendía-Roldán Ivette, Ramos-Martínez Espiridión, Rojas-Serrano Jorge, Falfán-Valencia Ramc |
Variants of aminoacyl-tRNA synthetase genes in Charcot-Marie-Tooth disease: A Korean cohort study. Journal of the peripheral nervous system : JPNS 2021 Nov . Nam Da Eun, Park Jin Hee, Park Cho Eun, Jung Na Young, Nam Soo Hyun, Kwon Hye Mi, Kim Hyun Su, Kim Sang Beom, Son Won Seok, Choi Byung-Ok, Chung Ki W |
Alanyl-tRNA Synthetase 1 Gene Variants in Hereditary Neuropathy: Genotype and Phenotype Overview. Neurology. Genetics 2022 9 8 (5): e200019. Setlere Signe, Jurcenko Marija, Gailite Linda, Rots Dmitrijs, Kenina Viktori |
Systems biology approach delineates critical pathways associated with disease progression in rheumatoid arthritis. Journal of biomolecular structure & dynamics 2022 9 1-22. Srimadh Bhagavatham Sai Krishna, Pulukool Sujith Kumar, Pradhan Sai Sanwid, R Saiswaroop, Ashok Naik Ashwin, V M Datta Darshan, Sivaramakrishnan Venkete |
Association of CDKAL1 gene polymorphism (rs10946398) with gestational diabetes mellitus in Pakistani population. Molecular biology reports 2022 10 50 (1): 57-64. Asghar Aleesha, Firasat Sabika, Afshan Kiran, Naz Shaguf |
Screening for Mitochondrial tRNA Mutations in 318 Patients with Dilated Cardiomyopathy. Human heredity 2022 1 . Qi Yujuan, Wu Zhenhua, Bai Yaobang, Jiao Yan, Li Peij |
Mitochondrial DNA Variants at Low-Level Heteroplasmy and Decreased Copy Numbers in Chronic Kidney Disease (CKD) Tissues with Kidney Cancer. International journal of molecular sciences 2023 12 24 (24): . Yuki Kanazashi, Kazuhiro Maejima, Todd A Johnson, Shota Sasagawa, Ryosuke Jikuya, Hisashi Hasumi, Naomichi Matsumoto, Shigekatsu Maekawa, Wataru Obara, Hidewaki Nakaga |
Identification of hepatoblastoma susceptibility loci in the TRMT6 gene from a seven-center case-control study. Journal of cellular and molecular medicine 2023 10 . Lin Ma, Jinhong Zhu, Jiao Zhang, Wenli Zhang, Yong Li, Zhonghua Yang, Suhong Li, Jiwen Cheng, Li Li, Jing He, Peng L |
Assessment of tRNA and tRNA Variants and Mitochondrial Functionality in Parkinson's Disease (PD) Patients of Tamil Nadu Population. Journal of molecular neuroscience : MN 2023 10 . Dhivya Venkatesan, Mahalaxmi Iyer, Neethu Raj, Abilash Valsala Gopalakrishnan, Arul Narayanasamy, Nachimuthu Senthil Kumar, Balachandar Vellingi |
TRMT10C gene polymorphisms confer hepatoblastoma susceptibility: evidence from a seven-center case-control study. Journal of Cancer 2024 9 15 (16): 5396-5402. Yanfei Liu, Jinhong Zhu, Xianqiang Wang, Wenli Zhang, Yong Li, Zhonghua Yang, Jiao Zhang, Jiwen Cheng, Li Li, Suhong Li, Jing He, Jun Bi |
Novel Cases of Non-Syndromic Hearing Impairment Caused by Pathogenic Variants in Genes Encoding Mitochondrial Aminoacyl-tRNA Synthetases. Genes 2024 7 15 (7): . María Domínguez-Ruiz, Margarita Olarte, Esther Onecha, Irene García-Vaquero, Nancy Gelvez, Greizy López, Manuela Villamar, Matías Morín, Miguel A Moreno-Pelayo, Carmelo Morales-Angulo, Rubén Polo, Martha L Tamayo, Ignacio Del Castil |
Complete mitochondrial genomes of patients from Thailand with cardiovascular diseases. PloS one 2024 7 19 (7): e0307036. Wipada Woravatin, Rattanasak Wongkomonched, Wichittra Tassaneeyakul, Mark Stoneking, Pattarapong Makarawate, Wibhu Kutan |
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