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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Disease and IMPDH1[original query]
Retinitis pigmentosa: mutation analysis of RHO, PRPF31, RP1, and IMPDH1 genes in patients from India.
Molecular vision 2008 14 1105-13.
Gandra M, Anandula V, Authiappan V, Sundaramurthy S, Raman R, Bhattacharya S, Govindasamy K
Genetic variations in the HGPRT, ITPA, IMPDH1, IMPDH2, and GMPS genes in Japanese individuals.
Drug metabolism and pharmacokinetics 2009 24 (6): 6.
Kudo Mutsumi, Saito Yuka, Sasaki Takamitsu, Akasaki Hitomi, Yamaguchi Yuri, Uehara Moe, Fujikawa Kiyomi, Ishikawa Masaaki, Hirasawa Noriyasu, Hiratsuka Masahi
Genetic variations in the mycophenolate mofetil target enzyme are associated with acute GVHD risk after related and unrelated hematopoietic cell transplantation.
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2012 Feb 18 (2): 273-9.
Cao Weijie, Xiao Haowen, Lai Xiaoyu, Luo Yi, Shi Jimin, Tan Yamin, Zheng Weiyan, He Jingsong, Xie Wanzhuo, Li Li, Ye Xiujin, Yu Xiaohong, Lin Maofang, Cai Zhen, Huang
Prevalence of mutations in eyeGENE probands with a diagnosis of autosomal dominant retinitis pigmentosa.
Investigative ophthalmology & visual science 2013 Sep 54 (9): 6255-61.
Sullivan Lori S, Bowne Sara J, Reeves Melissa J, Blain Delphine, Goetz Kerry, Ndifor Vida, Vitez Sally, Wang Xinjing, Tumminia Santa J, Daiger Stephen
Detection of novel mutations that cause autosomal dominant retinitis pigmentosa in candidate genes by long-range PCR amplification and next-generation sequencing.
Molecular vision 2013 19 654-64.
de Sousa Dias Miguel, Hernan Imma, Pascual Beatriz, Borràs Emma, Mañé Begoña, Gamundi Maria José, Carballo Migu
Impact of Genetic Polymorphisms on 6-Thioguanine Nucleotide Levels and Toxicity in Pediatric Patients with IBD Treated with Azathioprine.
Inflammatory bowel diseases 2015 Aug .
Lee Mi-Na, Kang Ben, Choi So Yoon, Kim Mi Jin, Woo Sook Young, Kim Jong-Won, Choe Yon Ho, Lee Soo-Yo
Identification of the genetic determinants responsible for retinal degeneration in families of Mexican descent.
Ophthalmic genetics 2017 Sep 1-7.
Villanueva Adda, Biswas Pooja, Kishaba Kameron, Suk John, Tadimeti Keerti, Raghavendra Pongali B, Nadeau Karine, Lamontagne Bruno, Busque Lambert, Geoffroy Steve, Mongrain Ian, Asselin Géraldine, Provost Sylvie, Dubé Marie-Pierre, Nudleman Eric, Ayyagari Rad
Inosine Monophosphate Dehydrogenase Pharmacogenetics in Hematopoietic Cell Transplantation Patients.
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2018 4 24 (9): 1802-1807.
McCune Jeannine S, Storer Barry, Thomas Sushma, McKiernan Jožefa, Gupta Rohan, Sandmaier Brenda
Influence of SLCO1B1 521T>C, UGT2B7 802C>T and IMPDH1 -106G>A Genetic Polymorphisms on Mycophenolic Acid Levels and Adverse Reactions in Chinese Autoimmune Disease Patients.
Pharmacogenomics and personalized medicine 2021 6 14 713-722.
Shu Qing, Fan Qingqing, Hua Bingzhu, Liu Hang, Wang Shiying, Liu Yunxing, Yao Yao, Xie Han, Ge Weiho
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