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Select item 112543571.

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

Abstract Article PDF–1.1M

Select item 111592942.

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

Abstract Article PDF–138K

Select item 111591933.

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

Abstract Article PDF–156K

Select item 111586024.

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

Abstract Article PDF–179K

Select item 109894915.

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

Abstract Article PDF–19M

Select item 108118936.

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

Abstract Article PDF–1.2M

Select item 104999997.

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

Abstract Article PDF–2.0M

Select item 103421368.

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

Abstract Article PDF–272K

Select item 100604369.

Hepatotoxicity with High-Dose Green Tea Extract: Effect of Catechol-O-Methyltransferase and Uridine 5′-Diphospho-glucuronosyltransferase 1A4 Genotypes

Laura Acosta, Laura Byham-Gray, Mindy Kurzer, Hamed Samavat

J Diet Suppl. Author manuscript; available in PMC 2024 Jan 1.

Published in final edited form as: J Diet Suppl. 2023; 20(6): 850–869. Published online 2022 Sep 30. doi: 10.1080/19390211.2022.2128501

PMCID:: PMC10060436

Abstract Article PDF–914K

Select item 1002409110.

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

Abstract Article PDF–405K

Select item 981276711.

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

Abstract Article PDF–1.8M

Select item 975416612.

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

Abstract Article PDF–1.2M

Select item 960387413.

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

Abstract Article PDF–1.3M

Select item 960304114.

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

Abstract Article PDF–498K

Select item 933661915.

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

Abstract Article PDF–712K

Select item 928374416.

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

Abstract Article PDF–3.8M

Select item 926851517.

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

Abstract Article PDF–2.5M

Select item 926660118.

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

Abstract Article PDF–453K

Select item 916918119.

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

Abstract Article PDF–309K

Select item 915139020.

UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab

Nan Lin, Amy Damask, Anita Boyapati, Jennifer D. Hamilton, Sara Hamon, Nils Ternes, Michael C. Nivens, John Penn, Alexander Lopez, Jeffrey G. Reid, John Overton, Alan R. Shuldiner, Goncalo Abecasis, Aris Baras, Charles Paulding

Pharmacogenomics J. 2022; 22(3): 160–165. Published online 2022 Feb 11. doi: 10.1038/s41397-022-00269-5

PMCID:: PMC9151390

Abstract Article PDF–1.1M

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PMC Links for GEO Profiles (Select 87768873) (282)
PMC
PREDICTED: Homo sapiens G-patch domain containing 8 (GPATCH8), transcript varian...
PREDICTED: Homo sapiens G-patch domain containing 8 (GPATCH8), transcript variant X4, mRNA
gi|2217310862|ref|XM_011524561.3|

Nucleotide
UV-stimulated scaffold protein A isoform X2 [Homo sapiens]
UV-stimulated scaffold protein A isoform X2 [Homo sapiens]
gi|2462598445|ref|XP_054206596.1|

Protein

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