Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and SLC7A8[original query] |
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| Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss. eLife 2018 01 7 . Espino Guarch Meritxell, Font-Llitjós Mariona, Murillo-Cuesta Silvia, Errasti-Murugarren Ekaitz, Celaya Adelaida M, Girotto Giorgia, Vuckovic Dragana, Mezzavilla Massimo, Vilches Clara, Bodoy Susanna, Sahún Ignasi, González Laura, Prat Esther, Zorzano Antonio, Dierssen Mara, Varela-Nieto Isabel, Gasparini Paolo, Palacín Manuel, Nunes Virgin |
| SLC7A8 coding for LAT2 is associated with early disease progression in osteosarcoma and transports doxorubicin. Frontiers in pharmacology 2022 11 13 1042989. Hurkmans Evelien G E, Koenderink Jan B, van den Heuvel Jeroen J M W, Versleijen-Jonkers Yvonne M H, Hillebrandt-Roeffen Melissa H S, Groothuismink Johanne M, Vos Hanneke I, van der Graaf Winette T A, Flucke Uta, Muradjan Grigor, Schreuder Hendrik W B, Hagleitner Melanie M, Brunner Han G, Gelderblom Hans, Cleton-Jansen Anne-Marie, Guchelaar Henk-Jan, de Bont Eveline S J M, Touw Daan J, Nijhoff G Jan, Kremer Leontien C M, Caron Huib, Windsor Rachael, Patiño-García Ana, González-Neira Anna, Saletta Federica, McCowage Geoff, Nagabushan Sumanth, Catchpoole Daniel, Te Loo D Maroeska W M, Coenen Marieke J |
| The Genetic Variability of Members of the SLC38 Family of Amino Acid Transporters (SLC38A3, SLC38A7 and SLC38A9) Affects Susceptibility to Type 2 Diabetes and Vascular Complications. Nutrients 2022 11 14 (21): . Crocco Paolina, Dato Serena, Montesanto Alberto, Bonfigli Anna Rita, Testa Roberto, Olivieri Fabiola, Passarino Giuseppe, Rose Giuseppi |
| Evidence for a relationship between genetic polymorphisms of the L-DOPA transporter LAT2/4F2hc and risk of hypertension in the context of chronic kidney disease. BMC medical genomics 2024 6 17 (1): 163. Paolina Crocco, Serena Dato, Rossella La Grotta, Giuseppe Passarino, Giuseppina Ro |
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