Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: XYLT1[original query] |
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Xylosyltransferase I variants and their impact on abdominal aortic aneurysms. Clinica chimica acta; international journal of clinical chemistry 2008 May 391 (1-2): 41-5. Götting Christian, Prante Christian, Schillinger Martin, Exner Markus, Domanovits Hans, Raith Marianne, Kuhn Joachim, Kleesiek Kn |
The xylosyltransferase Iota gene polymorphism c.343G>T (p.A115S) is associated with decreased serum glycosaminoglycan levels. Clinical biochemistry 2009 Jan 42 (1-2): 1-4. Ambrosius Michael, Kleesiek Knut, Götting Christi |
Xylosyltransferase gene variants and their role in essential hypertension. American journal of hypertension 2009 Apr 22 (4): 432-6. Pönighaus Claudia, Speirs Helen J L, Morris Brian J, Kuhn Joachim, Kleesiek Knut, Götting Christi |
Mutations in DZIP1 and XYLT1 are associated with nonsyndromic early onset high myopia in the Korean population. Ophthalmic genetics 2017 1 38 (4): 395-397. Lee Jong-Keuk, Kim Hyuna, Park Young-Mi, Kim Dae Hee, Lim Hyun Ta |
Genetic diagnosis of acute aortic dissection in South China Han population using next-generation sequencing. International journal of legal medicine 2018 7 132 (5): 1273-1280. Zheng Jinxiang, Guo Jian, Huang Lei, Wu Qiuping, Yin Kun, Wang Lin, Zhang Tongda, Quan Li, Zhao Qianhao, Cheng Jiandi |
The genetic map of diabetic nephropathy: evidence from a systematic review and meta-analysis of genetic association studies. Clinical kidney journal 2020 10 13 (5): 768-781. Tziastoudi Maria, Stefanidis Ioannis, Zintzaras Eli |
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease. NPJ Parkinson's disease 2023 8 9 (1): 128. Alejandro Martinez-Carrasco, Raquel Real, Michael Lawton, Hirotaka Iwaki, Manuela M X Tan, Lesley Wu, Nigel M Williams, Camille Carroll, Michele T M Hu, Donald G Grosset, John Hardy, Mina Ryten, Tom Foltynie, Yoav Ben-Shlomo, Maryam Shoai, Huw R Morr |
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease. medRxiv : the preprint server for health sciences 2023 7 . Alejandro Martinez-Carrasco, Raquel Real, Michael Lawton, Hirotaka Iwaki, Manuela M X Tan, Lesley Wu, Nigel M Williams, Camille Carroll, Michele T M Hu, Donald G Grosset, John Hardy, Mina Ryten, Tom Foltynie, Yoav Ben-Shlomo, Maryam Shoai, Huw R Morr |
Mutational investigation of 17 causative genes in a cohort of 113 families with nonsyndromic early-onset high myopia in northwestern China. Molecular genetics and genomics : MGG 2023 3 . Ye Min, Ma Ya, Qin Yi-Xuan, Cai Bo, Ma Li-Mei, Ma Zhen, Liu Yang, Jin Zi-Bing, Zhuang Wen-Ju |
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- Page last updated:Apr 22, 2024
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