Downregulation of organic cation transporters OCT1 (<it>SLC22A1</it>) and OCT3 (<it>SLC22A3</it>) in human hepatocellular carcinoma and their prognostic significance by Heise Michael, Lautem Anja, Knapstein Johanna, Schattenberg Jörn M, Hoppe-Lotichius Maria, Foltys Daniel, Weiler Nina, Zimmermann Anca, Schad Arno, Gründemann Dirk, Otto Gerd, Galle Peter R, Schuchmann Marcus, Zimmermann Tim

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Expression and Its Clinical Significance of SLC22A18 in Non-small Cell Lung Cancer by Ming LEI, Qingshu CHENG, Yachao ZHAO, Tao LIU, Xuejiao WANG, Yingchun DENG, Jing YANG, Zhipei ZHANG

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SLC22A5 polymorphism associated with risk of extra-articular manifestations in rheumatoid arthritis patients by Andrzej Pawlik, Agnieszka Paradowska-Gorycka, Krzysztof Safranow, Violetta Dziedziejko, Grażyna Dutkiewicz, Sylwia Słucznowska-Głabowska, Zygmunt Juzyszyn, Marek Drozdzik

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Polymorphisms of ABCG2 and SLC22A12 Genes Associated with Gout Risk in Vietnamese Population by Nguyen Thuy Duong, Nguyen Thy Ngoc, Nguyen Tran Minh Thang, Bach Thi Hoai Phuong, Nguyen Thanh Nga, Nguyen Doan Tinh, Do Hai Quynh, Nguyen Dang Ton, Nong Van Hai

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SLC22A3 rs2048327 Polymorphism Is Associated with Diabetic Retinopathy in Caucasians with Type 2 Diabetes Mellitus by Emin Grbić, Mojca Globočnik Petrovič, Ines Cilenšek, Danijel Petrovič

Subjects: “…SLC22A3…”
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Investigation of the SLC22A23 gene in laryngeal squamous cell carcinoma by Seda Ekizoglu, Didem Seven, Turgut Ulutin, Jalal Guliyev, Nur Buyru

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Dual actions on gout flare and acute kidney injury along with enhanced renal transporter activities by Yokuininto, a Kampo medicine by Seung Hoon Lee, Ho-Sung Lee, Gunhyuk Park, Sung-Man Oh, Dal-Seok Oh

Subjects: “…SLC22A8…”
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Association of the Reduced Function Met420del Polymorphism of SLC22A1 with Metformin-Induced Gastrointestinal Intolerance in Ethiopian Patients with Type 2 Diabetes Mellitus by Degaga A, Sirgu S, Huri HZ, Sim MS, Loganadan NK, Kebede T, Tegene B, Engidawork E, Shibeshi W

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Genetic Variation in <i>CYP2D6</i> and <i>SLC22A1</i> Affects Amlodipine Pharmacokinetics and Safety by Paula Soria-Chacartegui, Pablo Zubiaur, Dolores Ochoa, Gonzalo Villapalos-García, Manuel Román, Miriam Matas, Laura Figueiredo-Tor, Gina Mejía-Abril, Sofía Calleja, Alejandro de Miguel, Marcos Navares-Gómez, Samuel Martín-Vilchez, Francisco Abad-Santos

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A heterozygous variant in the SLC22A12 gene in a Sri Lanka family associated with mild renal hypouricemia by Dinesha Maduri Vidanapathirana, Subashinie Jayasena, Eresha Jasinge, Blanka Stiburkova

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A Syndrome of Variable Allergy, Short Stature, and Fatty Liver by Jing Qiao, Yue Chen, Ying Lu, Tiejun Wang, Xiaoli Li, Wei Qin, Aifen Li, Guangquan Chen

Subjects: “…SLC22A18…”
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Residual OCTN2 transporter activity, carnitine levels and symptoms correlate in patients with primary carnitine deficiency by Jan Rasmussen, Allan M. Lund, Lotte Risom, Flemming Wibrand, Hannes Gislason, Olav W. Nielsen, Lars Køber, Morten Duno

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A report of a pedigree with compound heterozygous mutations in the SLC22A5 gene by Yunguo Zhou, Yunguo Zhou, Yunguo Zhou, Yucai Liu, Yang Shen, Fang Xu, Fang Xu, Fei Xu, Fei Xu, Hui Huang, Junkai Duan, Junkai Duan

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The Value of Neutrophil Gelatinase-Associated Lipocalin Receptor as a Novel Partner of CD38 in Chronic Lymphocytic Leukemia: From an Adverse Prognostic Factor to a Potential Pharma... by Brigitte Bauvois, Elise Chapiro, Claire Quiney, Karim Maloum, Santos A. Susin, Florence Nguyen-Khac

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An exploratory pharmacogenetic screening of SLC22A6, SLC22A8, ABCC4 and ABCC10 genes in a cohort of Ghanaian HBV patients by Nicholas Ekow Thomford, Faustina Adu, Cyril Gavor-Kwashi, Samuel Badu Nyarko, Paul Nsiah, Richard Dadzie Ephraim, George Adjei, Akwasi Anyanful

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Evaluation of combination gene therapy with SLC22A18 upregulation and sequence binding protein 1 downregulation for glioma U251 cells in vitro and in vivo by Shenghua Chu, Yanbin Ma

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Pharmacogenetic Aspects of Type 2 Diabetes Treatment by N. O. Pozdnyakov, I. N. Kagarmanyan, A. E. Miroshnikov, E. S. Emelyanov, A. A. Gruzdeva, A. M. Sirotkina, I. A. Dukhanina, A. A. Milkina, A. A. Khokhlov, S. O. Pozdnyakov

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The Influence of SLC22A3 Genetic Polymorphisms on Susceptibility to Type 2 Diabetes Mellitus in Chinese Population by Li Z, Yuan X, Liu X, Yang Y, Huang L, Tan Q, Li C

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Lipocalin 2 receptors: facts, fictions, and myths by Sarah K. Schröder, Natalie Gasterich, Sabine Weiskirchen, Ralf Weiskirchen

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A case of atypical systemic primary carnitine deficiency in Saudi Arabia by Abdulrahman Alghamdi, Hani Almalki, Aiman Shawli, Rahaf Waggass, Fahad Hakami

Subjects: “…Systemic Primary Carnitine Deficiency, SLC22A5, Dilated Cardiomyopathy, OCTN2.…”
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