Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and AANAT[original query] |
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| Association study of tryptophan hydroxylase 1 and arylalkylamine N-acetyltransferase polymorphisms with adolescent idiopathic scoliosis in Han Chinese. Spine 2008 Sep 33 (20): 2199-203. Wang Hai, Wu Zhihong, Zhuang Qianyu, Fei Qi, Zhang Jianguo, Liu Yong, Wang Yipeng, Ding Yaozhong, Qiu Guixi |
| Melatonin pathway genes are associated with progressive subtypes and disability status in multiple sclerosis among Finnish patients. Journal of neuroimmunology 2012 Sep 250 (1-2): 106-10. Natarajan Renuka, Einarsdottir Elisabet, Riutta Asko, Hagman Sanna, Raunio Minna, Mononen Nina, Lehtimäki Terho, Elovaara Iri |
| [Association of polymorphic variants of DDC (AADC), AANAT and ASMT genes encoding enzymes for melatonin synthesis with the higher risk of neuropsychiatric disorders]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2021 121 (5): 151-157. Moskaleva P V, Shnayder N A, Nasyrova R |
| Gender-specific associations between polymorphisms of the circadian gene RORA and cutaneous melanoma susceptibility. Journal of translational medicine 2021 2 19 (1): 57. Benna Clara, Rajendran Senthilkumar, Spiro Giovanna, Menin Chiara, Dall'Olmo Luigi, Rossi Carlo Riccardo, Mocellin Simo |
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