Human Genome Epidemiology Literature Finder
|
Records 1 - 14 (of 14 Records) |
| Query Trace: Disease and UGT2B17[original query] |
|---|
| Association between polymorphisms in HSD3B1 and UGT2B17 and prostate cancer risk. Urology 2007 Aug 70 (2): 374-9. Park Jong Y, Tanner Jean-Paul, Sellers Thomas A, Huang Yifan, Stevens Colleen K, Dossett Nicole, Shankar Ravi A, Zachariah Babu, Heysek Randy, Pow-Sang Jul |
| Role of minor histocompatibility antigens in renal transplantation. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2008 Jan 8 (1): 95-102. Heinold A, Opelz G, Scherer S, Ruhenstroth A, Laux G, Doehler B, Tran T |
| Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis. American journal of human genetics 2008 Dec 83 (6): 663-74. Yang Tie-Lin, Chen Xiang-Ding, Guo Yan, Lei Shu-Feng, Wang Jin-Tang, Zhou Qi, Pan Feng, Chen Yuan, Zhang Zhi-Xin, Dong Shan-Shan, Xu Xiang-Hong, Yan Han, Liu Xiaogang, Qiu Chuan, Zhu Xue-Zhen, Chen Teng, Li Meng, Zhang Hong, Zhang Liang, Drees Betty M, Hamilton James J, Papasian Christopher J, Recker Robert R, Song Xiao-Ping, Cheng Jing, Deng Hong-W |
| Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease. Nature genetics 2009 Dec 41 (12): 1341-4. McCarroll Steven A, Bradner James E, Turpeinen Hannu, Volin Liisa, Martin Paul J, Chilewski Shannon D, Antin Joseph H, Lee Stephanie J, Ruutu Tapani, Storer Barry, Warren Edus H, Zhang Bo, Zhao Lue Ping, Ginsburg David, Soiffer Robert J, Partanen Jukka, Hansen John A, Ritz Jerome, Palotie Aarno, Altshuler Dav |
| Genetic variation of genes involved in dihydrotestosterone metabolism and the risk of prostate cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2010 Jan 19 (1): 1. Setlur Sunita R, Chen Chen X, Hossain Ruhella R, Ha Jung Sook, Van Doren Vanessa E, Stenzel Birgit, Steiner Eberhard, Oldridge Derek, Kitabayashi Naoki, Banerjee Samprit, Chen Jin Yun, Schäfer Georg, Horninger Wolfgang, Lee Charles, Rubin Mark A, Klocker Helmut, Demichelis Frances |
| Impact of UDP-gluconoryltransferase 2B17 genotype on vorinostat metabolism and clinical outcomes in Asian women with breast cancer. Pharmacogenetics and genomics 2011 Nov 21 (11): 760-8. Wong Nan-Soon, Seah Elaine Zh, Wang Ling-Zhi, Yeo Wee-Lee, Yap Hui-Ling, Chuah Benjamin, Lim Yi-Wan, Ang Peter Cs, Tai Bee-Choo, Lim Robert, Goh Boon-Cher, Lee Soo-Ch |
| A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals. Journal of human genetics 2011 Jul 56 (7): 524-33. Teo Shu-Mei, Ku Chee-Seng, Naidoo Nasheen, Hall Per, Chia Kee-Seng, Salim Agus, Pawitan Yu |
| Increased severity of acute graft versus host disease as a result of differential expression following a homozygous gene deletion. International journal of immunogenetics 2013 Apr 40 (2): 116-9. Jervis S, Collins P, Tate D, Foster L, Bowman V, Adhern C, Bloor A, Yin J, Wynn R, Poulton |
| Copy Number Variation of UGT 2B Genes in Indian Families Using Whole Genome Scans. Journal of nucleic acids 2016 2016 1648527. Veerappa Avinash M, Padakannaya Prakash, Ramachandra Nallur |
| Effect of UGT2B17 deletion polymorphism on prognosis in pediatric cancer. Pediatrics international : official journal of the Japan Pediatric Society 2016 Nov . Ishimaru Sae, Yuza Yuki, Kaneko Takashi, Urashima Mitsuyos |
| Copy number variations exploration of multiple genes in Graves' disease. Medicine 2017 Jan 96 (4): e5866. Song Rong-Hua, Shao Xiao-Qing, Li Ling, Wang Wen, Zhang Jin- |
Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent.
Molecular psychiatry 2020 Mar . Buchwald Jadwiga, Chenoweth Meghan J, Palviainen Teemu, Zhu Gu, Benner Christian, Gordon Scott, Korhonen Tellervo, Ripatti Samuli, Madden Pamela A F, Lehtimäki Terho, Raitakari Olli T, Salomaa Veikko, Rose Richard J, George Tony P, Lerman Caryn, Pirinen Matti, Martin Nicholas G, Kaprio Jaakko, Loukola Anu, Tyndale Rachel |
| Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia. PloS one 2021 16 (1): e0245362. Boujemaa Maroua, Hamdi Yosr, Mejri Nesrine, Romdhane Lilia, Ghedira Kais, Bouaziz Hanen, El Benna Houda, Labidi Soumaya, Dallali Hamza, Jaidane Olfa, Ben Nasr Sonia, Haddaoui Abderrazek, Rahal Khaled, Abdelhak Sonia, Boussen Hamouda, Boubaker Mohamed Sam |
| High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis. Journal of personalized medicine 2022 10 12 (10): . Tesolin Paola, Bertinetto Francesca Eleonora, Sonaglia Arianna, Cappellani Stefania, Concas Maria Pina, Morgan Anna, Ferrero Norma Maria, Zabotti Alen, Gasparini Paolo, Amoroso Antonio, Quartuccio Luca, Girotto Giorg |
- Page last reviewed:Feb 1, 2024
- Content source: