Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Disease and SLC5A1[original query] |
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A family-based genome-wide association study of chronic rhinosinusitis with nasal polyps implicates several genes in the disease pathogenesis.
PloS one 2017 12 (12): e0185244. Bohman Anton, Juodakis Julius, Oscarsson Martin, Bacelis Jonas, Bende Mats, Torinsson Naluai Å |
| SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population. Human genetics 2021 11 141 (1): 81-99. Mir Ali, Almudhry Montaha, Alghamdi Fouad, Albaradie Raidah, Ibrahim Mona, Aldurayhim Fatimah, Alhedaithy Abdullah, Alamr Mushari, Bawazir Maryam, Mohammad Sahar, Abdelhay Salma, Bashir Shahid, Housawi Yous |
| Polymorphisms in glucose homeostasis genes are associated with cardiovascular and renal parameters in patients with diabetic nephropathy. Annals of medicine 2022 10 54 (1): 3039-3051. Mota-Zamorano Sonia, González Luz M, Robles Nicolás R, Valdivielso José M, Arévalo-Lorido José C, López-Gómez Juan, Gervasini Guiller |
| Genetic Variants in Carbohydrate Digestive Enzyme and Transport Genes Associated with Risk of Irritable Bowel Syndrome. medRxiv : the preprint server for health sciences 2023 10 . Hyejeong Hong, Katharina V Schulze, Ian E Copeland, Manasa Atyam, Kendra Kamp, Neil A Hanchard, John Belmont, Tamar Ringel-Kulka, Margaret Heitkemper, Robert J Shulm |
| The effect of rs2910686 on ERAP2 expression in IBD and epithelial inflammatory response. Journal of translational medicine 2024 8 22 (1): 750. Siri Sæterstad, Ann Elisabeth Østvik, Marianne Doré Hansen, Torunn Bruland, Atle van Beelen Granlu |
| Sodium-glucose cotransporter 1/2 inhibition and risk of neurodegenerative disorders: A Mendelian randomization study. Brain and behavior 2024 7 14 (7): e3624. Jinxin Liu, Xinxiu Shi, Yankun Sh |
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