Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 52 Records) |
Query Trace: TFAM[original query] |
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Association of a polymorphism in mitochondrial transcription factor A (TFAM) with Parkinson's disease dementia but not dementia with Lewy bodies. Neuroscience letters 2013 Dec 557 Pt B 177-80. Gatt Ariana P, Jones Emma L, Francis Paul T, Ballard Clive, Bateman Joseph |
PGC-related gene variants and elite endurance athletic status in a Chinese cohort: a functional study. Scandinavian journal of medicine & science in sports 2015 Apr 25 (2): 184-95. He Z-H, Hu Y, Li Y-C, Gong L-J, Cieszczyk P, Maciejewska-Karlowska A, Leonska-Duniec A, Muniesa C A, Marín-Peiro M, Santiago C, Garatachea N, Eynon N, Lucia |
Physical-capacity-related genetic polymorphisms in children with cystic fibrosis. Pediatric exercise science 2015 Feb 27 (1): 102-12. Yvert Thomas, Santiago Catalina, Santana-Sosa Elena, Verde Zoraida, Gómez-Gallego Felix, López-Mojares Luis M, Pérez Margarita, Garatachea Nuria, Lucia Alejand |
Association of DNA sequence variation in mitochondrial DNA polymerase with mitochondrial DNA synthesis and risk of oral cancer. Gene 2015 Sep . Datta Sayantan, Ray Anindita, Roy Roshni, Roy Bidy |
Polymorphisms of CHAT but not TFAM or VR22 are Associated with Alzheimer Disease Risk. Medical science monitor : international medical journal of experimental and clinical research 2016 22 1924-35. Gao Lili, Zhang Yan, Deng Jinghua, Yu Wenbing, Yu Yunx |
Genetic variants associated with physical and mental characteristics of the elite athletes in the Polish population. Scandinavian journal of medicine & science in sports 2016 May . Peplonska B, Adamczyk J G, Siewierski M, Safranow K, Maruszak A, Sozanski H, Gajewski A K, Zekanowski |
Association of a TFAM haplotype with aggressive prostate cancer in overweight or obese Mexican Mestizo men. Urologic oncology 2016 Nov . Granados Jesús Benítez, Méndez Juan Pablo, Feria-Bernal Guillermo, García-García Eduardo, Tejeda María Elena, Rojano-Mejía David, Tapia André, Canto Patric |
Parkinson's disease-related gene variants influence pre-mRNA splicing processes. Neurobiology of aging 2016 Nov 47 127-138. Gaweda-Walerych K, Mohagheghi F, Zekanowski C, Buratti |
Lower Prevalence of Alzheimer's Disease among Tibetans: Association with Religious and Genetic Factors. Journal of Alzheimer's disease : JAD 2016 Jan . Huang Fukai, Shang Ying, Luo Yuandai, Wu Peng, Huang Xue, Tan Xiaohui, Lu Xingyi, Zhen Lifang, Hu Xian |
The mtDNA replication-related genes TFAM and POLG are associated with leprosy in Han Chinese from Southwest China. Journal of dermatological science 2017 Sep . Wang Dong, Li Guo-Dong, Fan Yu, Zhang Deng-Feng, Bi Rui, Yu Xiu-Feng, Long Heng, Li Yu-Ye, Yao Yong-Ga |
Mitochondrial transcription factor A (TFAM) rs1937 and AP endonuclease 1 (APE1) rs1130409 alleles are associated with reduced cognitive performance. Neuroscience letters 2017 Feb . Lillenes Meryl S, Støen Mari, Günther Clara-Cecilie, Selnes Per, Stenset Vidar T V, Espeseth Thomas, Reinvang Ivar, Fladby Tormod, Tønjum To |
Polymorphisms in the TFAM and PGC1-? genes and their association with polycystic ovary syndrome among South Indian women. Gene 2017 Oct . Reddy Tumu Venkat, Govatati Suresh, Deenadayal Mamata, Shivaji Sisinthy, Bhanoori Manju |
A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts.
Human genomics 2019 Jan 13 (1): 6. Guyatt Anna L, Brennan Rebecca R, Burrows Kimberley, Guthrie Philip A I, Ascione Raimondo, Ring Susan M, Gaunt Tom R, Pyle Angela, Cordell Heather J, Lawlor Debbie A, Chinnery Patrick F, Hudson Gavin, Rodriguez Santia |
The mitochondrial transcription machinery genes are upregulated in acute myeloid leukemia and associated with poor clinical outcome. Metabolism open 2020 8 2 100009. Wu Sharon, Fahmy Nicole, Alachkar Hou |
Mitochondrial GWAS and association of nuclear - mitochondrial epistasis with BMI in T1DM patients. BMC medical genomics 2020 Jul 13 (1): 97. Ludwig-S?omczy?ska Agnieszka H, Seweryn Micha? T, Kapusta Przemys?aw, Pitera Ewelina, Handelman Samuel K, Mantaj Urszula, Cyganek Katarzyna, Gutaj Pawe?, Dobrucka ?ucja, Wender-O?egowska Ewa, Ma?ecki Maciej T, Wo?kow Pawe? |
Mitochondrial DNA polymorphisms and biogenesis genes in primary and metastatic uveal melanoma cell lines. Cancer genetics 2021 6 256-257 91-99. Singh Lata, Atilano Shari R, Jager Martine J, Kenney M Cristi |
PTEN Regulates Mitochondrial Biogenesis via the AKT/GSK-3?/PGC-1? Pathway in Autism. Neuroscience 2021 4 465 85-94. Feng Chenxi, Chen Yajing, Zhang Yuyang, Yan Yinghui, Yang Mengjie, Gui Huan, Wang M |
Nuclear genome-wide associations with mitochondrial heteroplasmy.
Science advances 2021 3 7 (12): . Nandakumar Priyanka, Tian Chao, O'Connell Jared, , Hinds David, Paterson Andrew D, Sondheimer Ne |
The impact of mitochondria-related POLG and TFAM variants on breast cancer pathomorphological characteristics and patient outcomes. Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2021 Mar 1-11. Golubickaite Ieva, Ugenskiene Rasa, Korobeinikova Erika, Gudaitiene Jurgita, Vaitiekus Domas, Poskiene Lina, Juozaityte Elo |
Mitochondria-related TFAM gene variants and their effects on patients with cervical cancer. Biomedical reports 2021 11 15 (6): 106. Golubickaite Ieva, Ugenskiene Rasa, Cepaite Juste, Ziliene Egle, Inciura Arturas, Poskiene Lina, Juozaityte Elo |
A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss. Human genetics 2021 10 140 (12): 1733-1751. Ullah Farid, Rauf Waqar, Khan Kamal, Khan Sheraz, Bell Katrina M, de Oliveira Vanessa Cristina, Tariq Muhammad, Bakhshalizadeh Shabnam, Touraine Philippe, Katsanis Nicholas, Sinclair Andrew, He Sijie, Tucker Elena J, Baig Shahid M, Davis Erica |
Unique mutations in mitochondrial DNA and associated pathways involved in high altitude pulmonary edema susceptibility in Indian lowlanders. Journal of biomolecular structure & dynamics 2022 6 1-16. Sharma Swati, Sandhir Rajat, Ganju Lilly, Kumar Bhuvnesh, Singh Yami |
Mitochondrial DNA copy number as a prognostic marker is age-dependent in adult glioblastoma. Neuro-oncology advances 2022 2 4 (1): vdab191. Sourty Baptiste, Dardaud Laure-Marie, Bris Céline, Desquiret-Dumas Valérie, Boisselier Blandine, Basset Laëtitia, Figarella-Branger Dominique, Morel Alain, Sanson Marc, Procaccio Vincent, Rousseau Audr |
Metabolic Reprogramming in Response to Alterations of Mitochondrial DNA and Mitochondrial Dysfunction in Gastric Adenocarcinoma. International journal of molecular sciences 2022 2 23 (3): . Chang Tzu-Ching, Lee Hui-Ting, Pan Siao-Cian, Cho Shih-Han, Cheng Chieh, Ou Liang-Hung, Lin Chia-I, Lin Chen-Sung, Wei Yau-Hu |
Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number.
HGG advances 2022 10 4 (1): 100147. Pillalamarri Vamsee, Shi Wen, Say Conrad, Yang Stephanie, Lane John, Guallar Eliseo, Pankratz Nathan, Arking Dan |
Whole-exome sequencing of epithelial ovarian carcinomas differing in resistance to platinum therapy. Life science alliance 2022 10 5 (12): . Hlavá? Viktor, Holý Petr, Václavíková Radka, Rob Lukáš, Hruda Martin, Mrhalová Marcela, ?ernaj Petr, Bouda Ji?í, Sou?ek Pav |
Association between single nucleotide polymorphism of rs1937 in TFAM gene and longevity among the elderly Chinese population: based on the CLHLS study. BMC geriatrics 2022 1 22 (1): 16. Chen Qing, Li Zhi-Hao, Song Wei-Qi, Yao Yao, Zhang Yu-Jie, Zhong Wen-Fang, Zhang Pei-Dong, Liu Dan, Zhang Xi-Ru, Huang Qing-Mei, Zhao Xiao-Yang, Shi Xiao-Ming, Mao Ch |
Genetic Alterations in Mitochondrial DNA Are Complementary to Nuclear DNA Mutations in Pheochromocytomas. Cancers 2022 1 14 (2): . Tabebi Mouna, ?ysiak Ma?gorzata, Dutta Ravi Kumar, Lomazzi Sandra, Turkina Maria V, Brunaud Laurent, Gimm Oliver, Söderkvist Pet |
Mitochondria-Related TFAM and POLG Gene Variants and Associations with Tumor Characteristics and Patient Survival in Head and Neck Cancer. Genes 2023 2 14 (2): . Golubickaite Ieva, Ugenskiene Rasa, Bartnykaite Agne, Poskiene Lina, Vegiene Aurelija, Padervinskis Evaldas, Rudzianskas Viktoras, Juozaityte Elo |
MicroRNA-599-Regulated Susceptibility to Acute Kidney Injury in Patients with Cirrhosis is Mediated by the Sirtuin 1 (SIRT1) rs4746720 Single Nucleotide Polymorphism. Frontiers in bioscience (Landmark edition) 2023 12 28 (11): 318. Fangfang Zhou, Yixin Chen, Youjun Xu, Qun L |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
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