Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: SPTLC2[original query] |
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Investigating the influence of mtDNA and nuclear encoded mitochondrial variants on high intensity interval training outcomes. Scientific reports 2020 7 10 (1): 11089. Harvey N R, Voisin S, Lea R A, Yan X, Benton M C, Papadimitriou I D, Jacques M, Haupt L M, Ashton K J, Eynon N, Griffiths L |
Increased expression of serine palmitoyl transferase and ORMDL3 polymorphism are associated with eosinophilic inflammation and airflow limitation in aspirin-exacerbated respiratory disease. PloS one 2020 15 (10): e0240334. Ban Ga-Young, Youn Dong-Ye, Ye Young-Min, Park Hae-S |
Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohort. Journal of the neurological sciences 2021 6 427 117498. Cintra Vivian Pedigone, Dohrn Maike F, Tomaselli Pedro José, Figueiredo Fernanda Barbosa, Marques Sandra Elisabete, Camargos Sarah Teixeira, Barbosa Luiz Sergio Mageste, P Rebelo Adriana, Abreu Lisa, Danzi Matt, Marques Wilson, Züchner Steph |
Genetic Variants Associated with Elevated Plasma Ceramides in Individuals with Metabolic Syndrome. Genes 2022 8 13 (8): . Lee Sanghoo, Kim Seol-A, Kim Yejin, Kim Juhoon, Hong Gayeon, Hong Jeonghoon, Choi Kyeonghwan, Eom Chun-Sick, Baik Saeyun, Lee Mi-Kyeong, Lee Kyoung-Ry |
Mutation screening of SPTLC1 and SPTLC2 in amyotrophic lateral sclerosis. Human genomics 2023 3 17 (1): 28. Li Chunyu, Hou Yanbing, Wei Qianqian, Lin Junyu, Jiang Zheng, Jiang Qirui, Yang Tianmi, Xiao Yi, Huang Jingxuan, Cheng Yangfan, Ou Ruwei, Liu Kuncheng, Chen Xueping, Song Wei, Zhao Bi, Wu Ying, Cao Bei, Chen Yongping, Shang Huifa |
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- Page last updated:May 13, 2024
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