Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: SLC7A8[original query] |
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Genetic polymorphisms in the amino acid transporters LAT1 and LAT2 in relation to the pharmacokinetics and side effects of melphalan. Pharmacogenetics and genomics 2007 Jul 17 (7): 505-17. Kühne Annett, Kaiser Rolf, Schirmer Markus, Heider Ulrike, Muhlke Sabine, Niere Wiebke, Overbeck Tobias, Hohloch Karin, Trümper Lorenz, Sezer Orhan, Brockmöller Jürg |
Effect of genetic variants GSTA1 and CYP39A1 and age on busulfan clearance in pediatric patients undergoing hematopoietic stem cell transplantation. Pharmacogenomics 2013 Nov 14 (14): 1683-90. ten Brink Marloes H, van Bavel Tom, Swen Jesse J, van der Straaten Tahar, Bredius Robbert G M, Lankester Arjan C, Zwaveling Juliëtte, Guchelaar Henk-J |
A single nucleotide polymorphism in SLC7A5 is associated with gastrointestinal toxicity after high-dose melphalan and autologous stem cell transplantation for multiple myeloma. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2014 Jul 20 (7): 1014-20. Giglia Jennifer L, White Marquitta J, Hart Andrew J, Toro Juan J, Freytes César O, Holt Cherish C, Cai Ying, Williams Scott M, Brandt Stephen |
A germline predictive signature of response to platinum chemotherapy in esophageal cancer. Translational research : the journal of laboratory and clinical medicine 2015 Dec . Rumiato Enrica, Boldrin Elisa, Malacrida Sandro, Battaglia Giorgio, Bocus Paolo, Castoro Carlo, Cagol Matteo, Chiarion-Sileni Vanna, Ruol Alberto, Amadori Alberto, Saggioro Danie |
Physical decline and survival in the elderly are affected by the genetic variability of amino acid transporter genes. Aging 2018 Apr . Crocco Paolina, Hoxha Eneida, Dato Serena, De Rango Francesco, Montesanto Alberto, Rose Giuseppina, Passarino Giusep |
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 |
Exome-wide association study of treatment-resistant depression suggests novel treatment targets. Scientific reports 2023 8 13 (1): 12467. Shrey B Shah, Teja N Peddada, Christopher Song, Maame Mensah, Heejong Sung, Mani Yavi, Peixiong Yuan, Carlos A Zarate, Brian J Mickey, Margit Burmeister, Nirmala Akula, Francis J McMah |
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