Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: SLC7A5[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 |
Examination of association of genes in the serotonin system to autism. Neurogenetics 2009 Jul 10 (3): 209-16. Anderson B M, Schnetz-Boutaud N C, Bartlett J, Wotawa A M, Wright H H, Abramson R K, Cuccaro M L, Gilbert J R, Pericak-Vance M A, Haines J |
Polymorphisms in genes encoding potential mercury transporters and urine mercury concentrations in populations exposed to mercury vapor from gold mining. Environmental health perspectives 2013 Jan 121 (1): 85-91. Engström Karin, Ameer Shegufta, Bernaudat Ludovic, Drasch Gustav, Baeuml Jennifer, Skerfving Staffan, Bose-O'Reilly Stephan, Broberg Kar |
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 |
Pharmacogenomic Study Reveals New Variants of Drug Metabolizing Enzyme and Transporter Genes Associated with Steady-State Plasma Concentrations of Risperidone and 9-Hydroxyrisperidone in Thai Autism Spectrum Disorder Patients. Frontiers in pharmacology 2016 12 7 475. Medhasi Sadeep, Pinthong Darawan, Pasomsub Ekawat, Vanwong Natchaya, Ngamsamut Nattawat, Puangpetch Apichaya, Chamnanphon Monpat, Hongkaew Yaowaluck, Pratoomwun Jirawat, Limsila Penkhae, Sukasem Chonlaph |
Associations of High-Dose Melphalan Pharmacokinetics and Outcomes in the Setting of a Randomized Cryotherapy Trial. Clinical pharmacology and therapeutics 2017 Sep 102 (3): 511-519. Cho Y K, Sborov D W, Lamprecht M, Li J, Wang J, Hade E M, Gao Y, Tackett K, Williams N, Benson D M, Efebera Y A, Rosko A E, Devine S M, Poi M, Hofmeister C C, Phelps M |
Genetic and Functional Study of L-Type Amino Acid Transporter 1 in Schizophrenia. Neuropsychobiology 2017 Feb 74 (2): 96-103. Comasco Erika, Vumma Ravi, Toffoletto Simone, Johansson Jessica, Flyckt Lena, Lewander Tommy, Oreland Lars, Bjerkenstedt Lars, Andreou Dimitrios, Söderman Erik, Terenius Lars, Agartz Ingrid, Jönsson Erik G, Venizelos Nikola |
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 |
A Single Nucleotide Polymorphism in SLC7A5 Was Associated With Clinical Response in Multiple Myeloma Patients. Anticancer research 2019 Jan 39 (1): 67-72. Poi Ming J, Li Junan, Johnson Jasmine A, Cho Yu Kyoung, Sborov Douglas W, Phelps Mitch A, Hofmeister Craig |
Upregulation of the solute carrier family 7 genes is indicative of poor prognosis in papillary thyroid carcinoma. World journal of surgical oncology 2018 12 16 (1): 235. Shen Lei, Qian Chunhua, Cao Huimin, Wang Zhongrui, Luo Tingxian, Liang Chun |
Role of Glutamine Metabolism in Host Defense Against Mycobacterium tuberculosis Infection. The Journal of infectious diseases 2019 Apr 219 (10): 1662-1670. Koeken Valerie A C M, Lachmandas Ekta, Riza Anca, Matzaraki Vasiliki, Li Yang, Kumar Vinod, Oosting Marije, Joosten Leo A B, Netea Mihai G, van Crevel Reino |
Genome-Wide Association Study to Identify a New Susceptibility Locus for Central Serous Chorioretinopathy in the Japanese Population.
Investigative ophthalmology & visual science 2018 11 59 (13): 5542-5547. Miki Akiko, Sakurada Yoichi, Tanaka Koji, Semba Kentaro, Mitamura Yoshinori, Yuzawa Mitsuko, Tajima Atsushi, Nakatochi Masahiro, Yamamoto Ken, Matsuo Keitaro, Imoto Issei, Honda Shige |
Carriership of the rs113883650/rs2287120 haplotype of the SLC7A5 (LAT1) gene increases the risk of obesity in infants with phenylketonuria. Molecular genetics and metabolism reports 2020 9 25 100640. Bik-Multanowski Miroslaw, Madetko-Talowska Anna, Betka Iwona, Swieczka Elzbieta, Didycz Bozena, Orchel-Szastak Karolina, Bik-Multanowska Kinga, Starostecka Ewa, Jaglowska Joanna, Mozrzymas Renata, Zolkowska Joanna, Chyz Katarzyna, Korycinska-Chaaban Doro |
Regulation of kynurenine metabolism by blood donor genetics and biology impacts red cell hemolysis in vitro and in vivo. Blood 2023 11 . Travis Nemkov, Daniel Stephenson, Christopher Erickson, Monika Dzieciatkowska, Alicia Key, Amy Moore, Eric J Earley, Grier P Page, Ian S Lacroix, Mars Stone, Xutao Deng, Thomas J Raife, Steven H Kleinman, James C Zimring, Nareg H Roubinian, Kirk C Hansen, Michael P Busch, Philip J Norris, Angelo D'Alessand |
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- Page last updated:Apr 22, 2024
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