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Items: 1 to 20 of 214

1.
UGT1A1 and BLVRA allele and genotype variants in neonatal patients with hyperbilirubinemia in southern China
XiuJu Liu, Chao Zhang, LiWen Chen, ShuYan Liu, ZhenWen Zhou
Sci Rep. 2024; 14: 25744. Published online 2024 Oct 28. doi: 10.1038/s41598-024-77499-z
PMCID:
PMC11519535
AbstractArticlePDF–1.5M
2.
ASSOCIATION OF UGT1A1 GLY71ARG WITH URINE UROBILINOGEN
RYUJI KATAOKA, AKIKO KIMATA, KANAMI YAMAMOTO, NAOKO HIROSAWA, JUN UEYAMA, TAKAAKI KONDO, RIEKO OKADA, SAYO KAWAI, ASAHI HISHIDA, MARIKO NAITO, EMI MORITA, KENJI WAKAI, NOBUYUKI HAMAJIMA
Nagoya J Med Sci. 2011 Feb; 73(1-2): 33–40.
PMCID:
PMC11254357
AbstractArticlePDF–1.1M
3.
Role of UGT1A1*6, UGT1A1*28 and ABCG2 c.421C>A polymorphisms in irinotecan‐induced neutropenia in Asian cancer patients
Srinivasa Rao Jada, Robert Lim, Chiung Ing Wong, Xiaochen Shu, Soo Chin Lee, Qingyu Zhou, Boon Cher Goh, Balram Chowbay
Cancer Sci. 2007 Sep; 98(9): 1461–1467. Published online 2007 Jul 11. doi: 10.1111/j.1349-7006.2007.00541.x
PMCID:
PMC11159294
AbstractArticlePDF–138K
4.
Phase I study of irinotecan and doxifluridine for metastatic colorectal cancer focusing on the UGT1A1*28 polymorphism
Shoichi Hazama, Atsushi Nagashima, Hiroshi Kondo, Shin Yoshida, Ryoichi Shimizu, Atsuhiro Araki, Shigefumi Yoshino, Naoko Okayama, Yuji Hinoda, Masaaki Oka
Cancer Sci. 2010 Mar; 101(3): 722–727. Published online 2009 Nov 7. doi: 10.1111/j.1349-7006.2009.01428.x
PMCID:
PMC11159193
AbstractArticlePDF–156K
5.
Pharmacogenetic impact of polymorphisms in the coding region of the UGT1A1 gene on SN‐38 glucuronidation in Japanese patients with cancer
Kazuhiro Araki, Ken‐ichi Fujita, Yuichi Ando, Fumio Nagashima, Wataru Yamamoto, Hisashi Endo, Toshimichi Miya, Keiji Kodama, Masaru Narabayashi, Yasutsuna Sasaki
Cancer Sci. 2006 Nov; 97(11): 1255–1259. Published online 2006 Sep 12. doi: 10.1111/j.1349-7006.2006.00321.x
PMCID:
PMC11158602
AbstractArticlePDF–179K
6.
Uridine diphosphate glucuronosyltransferase 1A1 prevents the progression of liver injury
Jin-Lian Jiang, Yi-Yang Zhou, Wei-Wei Zhong, Lin-Yan Luo, Si-Ying Liu, Xiao-Yu Xie, Mao-Yuan Mu, Zhi-Gang Jiang, Yuan Xue, Jian Zhang, Yi-Huai He
World J Gastroenterol. 2024 Mar 7; 30(9): 1189–1212. Published online 2024 Mar 7. doi: 10.3748/wjg.v30.i9.1189
PMCID:
PMC10989491
AbstractArticlePDF–19M
7.
Identification of novel F2-isoprostane metabolites by specific UDP-glucuronosyltransferases
Ginger L. Milne, Marina S. Nogueira, Benlian Gao, Stephanie C. Sanchez, Warda Amin, Sarah Thomas, Camille Oger, Jean-Marie Galano, Harvey J. Murff, Gong Yang, Thierry Durand
Redox Biol. 2024 Apr; 70: 103020. Published online 2024 Jan 4. doi: 10.1016/j.redox.2023.103020
PMCID:
PMC10821610
AbstractArticlePDF–4.1M
8.
Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population
Juan Fan, Hua-Yun He, Huan-Huan Li, Pi-Liu Wu, Lei Tang, Bo-Yin Deng, Wen-Hui Dong, Jian-Hui Wang
BMC Pediatr. 2024; 24: 82. Published online 2024 Jan 26. doi: 10.1186/s12887-024-04537-0
PMCID:
PMC10811893
AbstractArticlePDF–1.2M
9.
New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE Syndrome
Tiphaine Arlabosse, Marie Materna, Orbicia Riccio, Caroline Schnider, Federica Angelini, Matthieu Perreau, Isabelle Rochat, Andrea Superti-Furga, Belinda Campos-Xavier, Sébastien Héritier, Anaïs Pereira, Caroline Deswarte, Romain Lévy, Marco Distefano, Jacinta Bustamante, Marie Roelens, Raphaël Borie, Mathilde Le Brun, Bruno Crestani, Jean-Laurent Casanova, Anne Puel, Michaël Hofer, Claire Fieschi, Katerina Theodoropoulou, Vivien Béziat, Fabio Candotti
J Clin Immunol. 2023; 43(7): 1566–1580. Published online 2023 Jun 5. doi: 10.1007/s10875-023-01517-4
Correction in:
J Clin Immunol. 2023; 43(7): 1674.
PMCID:
PMC10499999
AbstractArticlePDF–2.0M
10.
Association of Low Serum Bilirubin Concentrations and Promoter Variations in the UGT1A1 and HMOX1 Genes with Type 2 Diabetes Mellitus in the Czech Population
Alena Jirásková, Jan Škrha, Libor Vítek
Int J Mol Sci. 2023 Jul; 24(13): 10614. Published online 2023 Jun 25. doi: 10.3390/ijms241310614
PMCID:
PMC10342136
AbstractArticlePDF–272K
11.
The association between UGT1A1 polymorphisms and treatment toxicities of liposomal irinotecan
Y.-Y. Su, N.-J. Chiang, J.S. Chang, Y.-W. Wang, B.-N. Shen, Y.-J. Li, D.-Y. Hwang, Y.-S. Shan, L.-T. Chen
ESMO Open. 2023 Feb; 8(1): 100746. Published online 2022 Dec 15. doi: 10.1016/j.esmoop.2022.100746
PMCID:
PMC10024091
AbstractArticlePDF–405K
12.
Concurrence of novel mutations causing Gilbert’s and Dubin–Johnson syndrome with poor clinical outcomes in a Han Chinese family
Tai-Cheng Zhou, Xiao Li, Hui Li, Feng-Wei Liu, Si-Hang Zhang, Jing-Hua Fan, Wen-Xiu Yang, Ya-Li Yang, Liang Zhang, Jia Wei
J Hum Genet. 2023; 68(1): 17–23. Published online 2022 Oct 24. doi: 10.1038/s10038-022-01086-1
PMCID:
PMC9812767
AbstractArticlePDF–1.8M
13.
UGT1A1 variants in Chinese Uighur and Han newborns and its correlation with neonatal hyperbilirubinemia
Hui Yang, Huijun Li, Qingyao Xia, Wencheng Dai, Xin Li, Yan Liu, Jie Nie, Fei Yang, Yunfeng Sun, Lei Feng, Liye Yang
PLoS One. 2022; 17(12): e0279059. Published online 2022 Dec 15. doi: 10.1371/journal.pone.0279059
PMCID:
PMC9754166
AbstractArticlePDF–1.2M
14.
The Mutation Hotspots at UGT1A Locus May Be Associated with Gilbert’s Syndrome Affecting the Taiwanese Population
Paul Wei-Che Hsu, Po-Cheng Liao, Yu-Hsiang Kao, Xin-Yu Lin, Rong-Nan Chien, Chau-Ting Yeh, Chi-Chun Lai, Yu-Chiau Shyu, Chih-Lang Lin
Int J Mol Sci. 2022 Oct; 23(20): 12709. Published online 2022 Oct 21. doi: 10.3390/ijms232012709
PMCID:
PMC9603874
AbstractArticlePDF–1.3M
15.
Influence of UGT1A1 Genetic Variants on Free Bilirubin Levels in Japanese Newborns: A Preliminary Study
Hiroaki Hanafusa, Shinya Abe, Shohei Ohyama, Yuki Kyono, Takumi Kido, Ruka Nakasone, Mariko Ashina, Kenji Tanimura, Kandai Nozu, Kazumichi Fujioka
Int J Environ Res Public Health. 2022 Oct; 19(20): 13090. Published online 2022 Oct 12. doi: 10.3390/ijerph192013090
PMCID:
PMC9603041
AbstractArticlePDF–498K
16.
广西三江县侗族新生儿UGT1A1基因变异分析
姚 璇, 钟 丹妮, 彭 运聪
Zhongguo Dang Dai Er Ke Za Zhi. 2022 Jul 15; 24(7): 792–796. Chinese. doi: 10.7499/j.issn.1008-8830.2202127
PMCID:
PMC9336619
AbstractArticlePDF–712K
17.
Association of UGT1A1*6, UGT1A1*28, or ABCC2 c.3972C>T genetic polymorphisms with irinotecan‐induced toxicity in Asian cancer patients: Meta‐analysis
Chalirmporn Atasilp, Mohitosh Biswas, Pimonpan Jinda, Nutthan Nuntharadthanaphong, Jiratha Rachanakul, Yaowaluck Hongkaew, Natchaya Vanwong, Surasak Saokaew, Chonlaphat Sukasem
Clin Transl Sci. 2022 Jul; 15(7): 1613–1633. Published online 2022 May 31. doi: 10.1111/cts.13277
PMCID:
PMC9283744
AbstractArticlePDF–3.8M
18.
UGT1A1 and UGT1A9 Are Responsible for Phase II Metabolism of Tectorigenin and Irigenin In Vitro
Ji Li, Zhangyao Xu, Jifeng Gu
Molecules. 2022 Jul; 27(13): 4104. Published online 2022 Jun 26. doi: 10.3390/molecules27134104
PMCID:
PMC9268515
AbstractArticlePDF–2.5M
19.
Genetic testing of UGT1A1 in the diagnosis of Gilbert syndrome: The discovery of seven novel variants in the Chinese population
Leilei Gu, Yue Han, Donghua Zhang, Qiming Gong, Xinxin Zhang
Mol Genet Genomic Med. 2022 Jul; 10(7): e1958. Published online 2022 Apr 14. doi: 10.1002/mgg3.1958
PMCID:
PMC9266601
AbstractArticlePDF–453K
20.
Novel combined UGT1A1 mutations in Crigler Najjar Syndrome type I
Nawel Abdellaoui, Balkiss Abdelmoula, Rania Abdelhedi, Najla Kharrat, Mouna Tabebi, Ahmed Rebai, Nouha Bouayed Abdelmoula
J Clin Lab Anal. 2022 Jun; 36(6): e24482. Published online 2022 May 9. doi: 10.1002/jcla.24482
PMCID:
PMC9169181
AbstractArticlePDF–309K

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