Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 82 Records) |
Query Trace: SLC22A4[original query] |
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Haplotype in the IBD5 region is associated with refractory Crohn's disease in Slovenian patients and modulates expression of the SLC22A5 gene. Journal of gastroenterology 2011 Jun . Repnik K, Poto?nik U |
Pathway analysis of a genome-wide association study of ileal Crohn's disease. DNA and cell biology 2012 Oct 31 (10): 1549-54. Lee Young Ho, Song Gwan G |
Contribution of higher risk genes and European admixture to Crohn's disease in African Americans. Inflammatory bowel diseases 2012 Dec 18 (12): 2277-87. Wang Ming-Hsi, Okazaki Toshihiko, Kugathasan Subra, Cho Judy H, Isaacs Kim L, Lewis James D, Smoot Duane T, Valentine John F, Kader Howard A, Ford Jean G, Harris Mary L, Oliva-Hemker Maria, Cuffari Carmen, Torbenson Michael S, Duerr Richard H, Silverberg Mark S, Rioux John D, Taylor Kent D, Nguyen Geoffrey C, Wu Yuqiong, Datta Lisa W, Hooker Stanley, Dassopoulos Themistocles, Kittles Rick A, Kao Linda W H, Brant Steven |
Polymorphisms in OCTN1 and OCTN2 transporters genes are associated with prolonged time to progression in unresectable gastrointestinal stromal tumours treated with imatinib therapy. Pharmacological research : the official journal of the Italian Pharmacological Society 2012 Nov . Angelini S, Pantaleo MA, Ravegnini G, Zenesini C, Cavrini G, Nannini M, Fumagalli E, Palassini E, Saponara M, Di Battista M, Casali PG, Hrelia P, Cantelli-Forti G, Biasco G |
Genetic variants in the JAK1 gene confer higher risk of Behcet's disease with ocular involvement in Han Chinese. Human genetics 2013 Sep 132 (9): 1049-58. Hou Shengping, Qi Jian, Zhang Qi, Liao Dan, Li Qi, Hu Ke, Zhou Yan, Kijlstra Aize, Yang Peize |
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 |
Human candidate polymorphisms in sympatric ethnic groups differing in malaria susceptibility in Mali. PloS one 2013 8 (10): e75675. Maiga Bakary, Dolo Amagana, Touré Ousmane, Dara Victor, Tapily Amadou, Campino Susana, Sepulveda Nuno, Risley Paul, Silva Nilupa, Silva Nipula, Corran Patrick, Rockett Kirk A, Kwiatkowski Dominic, , Clark Taane G, Troye-Blomberg Marita, Doumbo Ogobara |
Meta-analysis of SLC22A4 and RUNX1 polymorphisms : Associations with rheumatoid arthritis susceptibility. Zeitschrift für Rheumatologie 2015 May 74 (4): 351-8. Lee Y H, Bae S-C, Kim J-H, Seo Y H, Choi S J, Ji J D, Song G |
Metabolic heritability at birth: implications for chronic disease research. Human genetics 2014 Aug 133 (8): 1049-57. Ryckman Kelli K, Smith Caitlin J, Jelliffe-Pawlowski Laura L, Momany Allison M, Berberich Stanton L, Murray Jeffrey |
Association of SLC22A4 gene polymorphism with Rheumatoid arthritis in the Chinese population. Journal of biochemical and molecular toxicology 2014 May 28 (5): 206-10. Ren Tian-li, Han Zhi-jun, Yang Cheng-jian, Hang Yuan-xing, Fang De-yu, Wang Ke, Zhu Xue, Ji Xiao-Jing, Zhou Fan-f |
The effect of turmeric (Curcuma longa) extract on the functionality of the solute carrier protein 22 A4 (SLC22A4) and interleukin-10 (IL-10) variants associated with inflammatory bowel disease. Nutrients 2014 Oct 6 (10): 4178-90. McCann Mark J, Johnston Sarah, Reilly Kerri, Men Xuejing, Burgess Elaine J, Perry Nigel B, Roy Nicole |
Susceptibility to ulcerative colitis in Hungarian patients determined by gene-gene interactions. World journal of gastroenterology : WJG 2014 Jan 20 (1): 219-27. Sarlos Patricia, Varszegi Dalma, Csongei Veronika, Magyari Lili, Jaromi Luca, Nagy Lajos, Melegh Be |
Association of single nucleotide polymorphism rs3792876 in SLC22A4 gene with autoimmune thyroid disease in a Chinese Han population. BMC medical genetics 2015 16 (1): 76. Hou Xin, Mao Jinyuan, Li Yushu, Li Jia, Wang Weiwei, Fan Chenling, Wang Hong, Zhang Hongmei, Shan Zhongyan, Teng Weipi |
Association of joint erosion with SLC22A4 gene polymorphisms inconsistently associated with rheumatoid arthritis susceptibility. Autoimmunity 2015 48 (5): 313-7. Han Tae-Un, Lee Hye-Soon, Kang Changwon, Bae Sang-Che |
Polymorphisms Associated with Age at Onset in Patients with Moderate-to-Severe Plaque Psoriasis. Journal of immunology research 2015 2015 101879. Prieto-Pérez Rocío, Solano-López Guillermo, Cabaleiro Teresa, Román Manuel, Ochoa Dolores, Talegón María, Baniandrés Ofelia, López-Estebaranz José Luis, de la Cueva Pablo, Daudén Esteban, Abad-Santos Francis |
Single Nucleotide Polymorphisms in MORC4, CD14, and TLR4 Are Related to Outcome of Allogeneic Stem Cell Transplantation. Annals of transplantation : quarterly of the Polish Transplantation Society 2016 21 56-67. Norén Elisabeth, Verma Deepti, Söderkvist Peter, Weisselberg Tilman, Söderman Jan, Lotfi Kourosh, Almer Sv |
Pharmacogenetics of ustekinumab in patients with moderate-to-severe plaque psoriasis. Pharmacogenomics 2016 Dec . Prieto-Pérez Rocío, Llamas-Velasco Mar, Cabaleiro Teresa, Solano-López Guillermo, Márquez Beatriz, Román Manuel, Ochoa Dolores, Talegón María, Daudén Esteban, Abad-Santos Francis |
Genotypes of SLC22A4 and SLC22A5 regulatory loci are predictive of the response of chronic myeloid leukemia patients to imatinib treatment. Journal of experimental & clinical cancer research : CR 2017 Apr 36 (1): 55. Jaruskova Monika, Curik Nikola, Hercog Rajna, Polivkova Vaclava, Motlova Eliska, Benes Vladimir, Klamova Hana, Pecherkova Pavla, Belohlavkova Petra, Vrbacky Filip, Machova Polakova Kateri |
Pharmacogenetics-based population pharmacokinetic analysis of gabapentin in patients with chronic pain: Effect of OCT2 and OCTN1 gene polymorphisms. Basic & clinical pharmacology & toxicology 2019 Mar 124 (3): 266-272. Yamamoto Priscila A, Benzi Jhohann R L, Azeredo Francine J, Dach Fabíola, Ianhez Júnior Edgar, Zanelli Cleslei F, de Moraes Natália |
Relationship Between SLC22A1 and SLC22A4 Gene Polymorphisms and Risk of Type 2 Diabetes in Chinese Han Population. Clinical laboratory 2018 Sep 64 (9): 1357-1361. Long Guanghui, Zhang Guangtao, Zhang Fangting, Ye Dongshuo, Yang Dengke, Yang Yin |
SLC22A5 polymorphism associated with risk of extra-articular manifestations in rheumatoid arthritis patients. Reumatologia 2019 57 (1): 3-7. Pawlik Andrzej, Paradowska-Gorycka Agnieszka, Safranow Krzysztof, Dziedziejko Violetta, Dutkiewicz Gra?yna, S?ucznowska-G?abowska Sylwia, Juzyszyn Zygmunt, Drozdzik Mar |
Tooth loss and adiposity: possible role of carnitine transporter (OCTN1/2) polymorphisms in women but not in men. Clinical oral investigations 2020 9 25 (2): 701-709. Meisel Peter, Pagels Stefanie, Grube Markus, Jedlitschky Gabriele, Völzke Henry, Kocher Thom |
Effects of Trough Concentration and Solute Carrier Polymorphisms on Imatinib Efficacy in Chinese Patients with Chronic Myeloid Leukemia. Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques 2020 23 (1): 1-9. Wang Qing, Jiang Zhi-Ping, Zeng Jing, Zhu Yan, Cai Hua-Lin, Xiang Da-Xiong, He Qun, Shi Xiao-Liu, Zhong An-Ni, Zhao Xie-Lan, Xu Pi |
Population pharmacokinetics of gabapentin in patients with neuropathic pain: Lack of effect of diabetes or glycaemic control. British journal of clinical pharmacology 2020 10 87 (4): 1981-1989. Costa Ana Carolina Conchon, de Lima Benzi Jhohann Richard, Yamamoto Priscila Akemi, de Freitas Maria Cristina Foss, de Paula Francisco José Albuquerque, Zanelli Cleslei Fernando, Lauretti Gabriela Rocha, de Moraes Natália Valadar |
Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population. Journal of advanced research 2021 7 31 13-24. Souissi Amal, Ben Said Mariem, Ben Ayed Ikhlas, Elloumi Ines, Bouzid Amal, Mosrati Mohamed Ali, Hasnaoui Mehdi, Belcadhi Malek, Idriss Nabil, Kamoun Hassen, Gharbi Nourhene, Gibriel Abdullah A, Tlili Abdelaziz, Masmoudi Sab |
SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa. Frontiers in genetics 2021 3 12 606630. Chiereghin Chiara, Robusto Michela, Mauri Lucia, Primignani Paola, Castorina Pierangela, Ambrosetti Umberto, Duga Stefano, Asselta Rosanna, Soldà Giul |
Implications of genetic variations, differential gene expression, and allele-specific expression on metformin response in drug-naïve type 2 diabetes. Journal of endocrinological investigation 2022 12 . Vohra M, Sharma A R, Mallya S, Prabhu N B, Jayaram P, Nagri S K, Umakanth S, Rai P |
Identification of clinical and pharmacogenetic factors influencing metformin response in Type 2 diabetes mellitus. Pharmacogenomics 2023 8 . Noelia Pérez-Gómez, María Dolores Fernández-Ortega, Miren Elizari-Roncal, Estefanía Santos-Mazo, Laura de la Maza-Pereg, Sara Calvo, Raquel Alcaraz, Antonio Sanz-Solas, Raquel Vinuesa, Miriam Saiz-Rodrígu |
Identification of Transporter Polymorphisms Influencing Metformin Pharmacokinetics in Healthy Volunteers. Journal of personalized medicine 2023 3 13 (3): . Saiz-Rodríguez Miriam, Ochoa Dolores, Zubiaur Pablo, Navares-Gómez Marcos, Román Manuel, Camargo-Mamani Paola, Luquero-Bueno Sergio, Villapalos-García Gonzalo, Alcaraz Raquel, Mejía-Abril Gina, Santos-Mazo Estefanía, Abad-Santos Francis |
The SNP rs460089 in the gene promoter of the drug transporter OCTN1 has prognostic value for treatment-free remission in chronic myeloid leukemia patients treated with imatinib. Leukemia 2023 12 . Katerina Machova Polakova, Ali Albeer, Vaclava Polivkova, Monika Krutska, Katerina Vlcanova, Nikola Curik, Alice Fabarius, Hana Klamova, Birgit Spiess, Cornelius F Waller, Tim H Brümmendorf, Jolanta Dengler, Volker Kunzmann, Andreas Burchert, Petra Belohlavkova, Satu Mustjoki, Edgar Faber, Jiri Mayer, Daniela Zackova, Panayiotis Panayiotidis, Johan Richter, Henrik Hjorth-Hansen, Magdalena Kami?ska, Magdalena P?onka, El?bieta Szczepanek, Monika Szarejko, Gra?yna Bober, Iwona Hus, Olga Grzybowska-Izydorczyk, Ewa Wasilewska, Edyta Paczkowska, Joanna Niesiob?dzka-Kr??el, Krzysztof Giannopoulos, Francois X Mahon, Tomasz Sacha, Susanne Saußele, Markus Pfirrma |
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- Page last updated:Apr 22, 2024
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