Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: PLAGL1[original query] |
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Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes: a comparative genomic and tagging single nucleotide polymorphism approach. Diabetes 2006 Aug 55 (8): 2272-6. Gloyn Anna L, Mackay Deborah J G, Weedon Michael N, McCarthy Mark I, Walker Mark, Hitman Graham, Knight Bridget A, Owen Katharine R, Hattersley Andrew T, Frayling Timothy |
Study of the genetic variability of ZAC1 (PLAGL1) in French population-based samples. Journal of hypertension 2009 Feb 27 (2): 314-21. Goumidi Louisa, Spengler Dietmar, Cottel Dominique, Wagner Aline, Ducimetière Pierre, Ruidavets Jean-Bernard, Legry Vanessa, Arveiler Dominique, Bingham Annie, Ferrières Jean, Amouyel Philippe, Meirhaeghe Ali |
A novel variation of PLAGL1 in Chinese patients with isolated ventricular septal defect. Genetic testing and molecular biomarkers 2012 Aug 16 (8): 984-7. Xuan Chao, Wang Bin-Bin, Gao Ge, Bai Xiao-Yan, Yang Qin, Liu Xiao-Cheng, Jing Wen-Bin, Ma Xu, He Guo-W |
Both gene deletion and promoter hyper-methylation contribute to the down-regulation of ZAC/PLAGL1 gene in gastric adenocarcinomas: a case control study. Clinics and research in hepatology and gastroenterology 2014 Dec 38 (6): 744-50. Li Zhi, Ding Yi, Zhu Yunliang, Yin Mingxing, Le Xiaoping, Wang Luo, Yang Yang, Zhang Qinxi |
High-dose folic acid supplementation alters the human sperm methylome and is influenced by the MTHFR C677T polymorphism. Human molecular genetics 2015 Aug . Aarabi Mahmoud, San Gabriel Maria C, Chan Donovan, Behan Nathalie A, Caron Maxime, Pastinen Tomi, Bourque Guillaume, MacFarlane Amanda J, Zini Armand, Trasler Jacquet |
Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57. BMC medical genetics 2016 17 (1): 29. Bak Mads, Boonen Susanne E, Dahl Christina, Hahnemann Johanne M D, Mackay Deborah J D G, Tümer Zeynep, Grønskov Karen, Temple I Karen, Guldberg Per, Tommerup Nie |
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients. Clinical epigenetics 2020 6 12 (1): 86. Inoue Takanobu, Nakamura Akie, Iwahashi-Odano Megumi, Tanase-Nakao Kanako, Matsubara Keiko, Nishioka Junko, Maruo Yoshihiro, Hasegawa Yukihiro, Suzumura Hiroshi, Sato Seiji, Kobayashi Yoshiyuki, Murakami Nobuyuki, Nakabayashi Kazuhiko, Yamazawa Kazuki, Fuke Tomoko, Narumi Satoshi, Oka Akira, Ogata Tsutomu, Fukami Maki, Kagami Masa |
Polymorphism rs368234815 of interferon lambda 4 gene and spontaneous clearance of hepatitis C virus in haemodialysis patients: a case-control study. BMC infectious diseases 2021 Jan 21 (1): 102. Grzegorzewska Alicja E, Mostowska Adrianna, ?widerska Monika K, Marcinkowski Wojciech, Stolarek Ireneusz, Figlerowicz Marek, Jagodzi?ski Pawe? |
Ultra-low-coverage genome-wide association study-insights into gestational age using 17,844 embryo samples with preimplantation genetic testing.
Genome medicine 2023 2 15 (1): 10. Li Shumin, Yan Bin, Li Thomas K T, Lu Jianliang, Gu Yifan, Tan Yueqiu, Gong Fei, Lam Tak-Wah, Xie Pingyuan, Wang Yuexuan, Lin Ge, Luo Ruiba |
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- Page last updated:Apr 16, 2024
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