Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Hyperbilirubinemia and SLCO1B3[original query] |
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Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.
Human molecular genetics 2009 Jul 18 (14): 2711-8. Sanna Serena, Busonero Fabio, Maschio Andrea, McArdle Patrick F, Usala Gianluca, Dei Mariano, Lai Sandra, Mulas Antonella, Piras Maria Grazia, Perseu Lucia, Masala Marco, Marongiu Mara, Crisponi Laura, Naitza Silvia, Galanello Renzo, Abecasis Gonçalo R, Shuldiner Alan R, Schlessinger David, Cao Antonio, Uda Manue |
UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association? Pediatric research 2012 Aug 72 (2): 169-73. Alencastro de Azevedo Laura, Reverbel da Silveira Themis, Carvalho Clarissa Gutierrez, Martins de Castro Simone, Giugliani Roberto, Matte Ursu |
Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms. Journal of human genetics 2015 Jan 60 (1): 35-40. Sato Hiroko, Uchida Toshihiko, Toyota Kentaro, Nakamura Tomohiro, Tamiya Gen, Kanno Miyako, Hashimoto Taeko, Watanabe Masashi, Aoki Kuraaki, Hayasaka Kiyos |
Multiple Genetic Modifiers of Bilirubin Metabolism Involvement in Significant Neonatal Hyperbilirubinemia in Patients of Chinese Descent. PloS one 2015 10 (7): e0132034. Yang Hui, Wang Qian, Zheng Lei, Lin Min, Zheng Xiang-bin, Lin Fen, Yang Li- |
Polymorphisms in SLCO1B1 and UGT1A1 are associated with sorafenib-induced toxicity. Pharmacogenomics 2016 09 17 (14): 1483-90. Bins Sander, Lenting Anne, El Bouazzaoui Samira, van Doorn Leni, Oomen-de Hoop Esther, Eskens Ferry Alm, van Schaik Ron Hn, Mathijssen Ron |
Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population. BMC pediatrics 2024 1 24 (1): 82. Juan Fan, Hua-Yun He, Huan-Huan Li, Pi-Liu Wu, Lei Tang, Bo-Yin Deng, Wen-Hui Dong, Jian-Hui Wa |
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- Page last updated:Apr 16, 2024
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