PubMed (GeneRIF) for id: 54658

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Results by year

Year	Number of Results
2000	2
2001	3
2002	16
2003	19
2004	27
2005	27
2006	32
2007	51
2008	52
2009	60
2010	72
2011	33
2012	36
2013	52
2014	53
2015	42
2016	40
2017	33
2018	32
2019	18
2020	21
2021	11
2022	21
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2024	2

666 results

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[UGT1A1 gene mutation spectrum with indirect hyperbilirubinemia in children].

Shen Y, Guo HM, Zheng YC, Zheng BX, Yan KL, Kong GP, Lin Q, Jin Y, Liu ZF, Li M. Shen Y, et al. Zhonghua Gan Zang Bing Za Zhi. 2024 Feb 20;32(2):119-124. doi: 10.3760/cma.j.cn501113-20230115-00030.. Zhonghua Gan Zang Bing Za Zhi. 2024. PMID: 38514260 Chinese.

Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population.

Fan J, He HY, Li HH, Wu PL, Tang L, Deng BY, Dong WH, Wang JH. Fan J, et al. BMC Pediatr. 2024 Jan 26;24(1):82. doi: 10.1186/s12887-024-04537-0. BMC Pediatr. 2024. PMID: 38279097 Free PMC article.

Gene Therapy in Patients with the Crigler-Najjar Syndrome.

D'Antiga L, Beuers U, Ronzitti G, Brunetti-Pierri N, Baumann U, Di Giorgio A, Aronson S, Hubert A, Romano R, Junge N, Bosma P, Bortolussi G, Muro AF, Soumoudronga RF, Veron P, Collaud F, Knuchel-Legendre N, Labrune P, Mingozzi F. D'Antiga L, et al. N Engl J Med. 2023 Aug 17;389(7):620-631. doi: 10.1056/NEJMoa2214084. N Engl J Med. 2023. PMID: 37585628 Clinical Trial.

Association of Low Serum Bilirubin Concentrations and Promoter Variations in the UGT1A1 and HMOX1 Genes with Type 2 Diabetes Mellitus in the Czech Population.

Jirásková A, Škrha J, Vítek L. Jirásková A, et al. Int J Mol Sci. 2023 Jun 25;24(13):10614. doi: 10.3390/ijms241310614. Int J Mol Sci. 2023. PMID: 37445792 Free PMC article.

[Factors influencing bilirubin elevation and its correlation with UGT1A1 gene polymorphism in the early postoperative period of transjugular intrahepatic portosystemic shunt].

Zhang BF, Fang J, Zhang ZQ, Ao XL, Xia L, Wu HC, Zhang SA, Wu ZX, Li DL. Zhang BF, et al. Zhonghua Gan Zang Bing Za Zhi. 2023 May 20;31(5):524-531. doi: 10.3760/cma.j.cn501113-20220527-00285. Zhonghua Gan Zang Bing Za Zhi. 2023. PMID: 37365030 Chinese.

New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE Syndrome.

Arlabosse T, Materna M, Riccio O, Schnider C, Angelini F, Perreau M, Rochat I, Superti-Furga A, Campos-Xavier B, Héritier S, Pereira A, Deswarte C, Lévy R, Distefano M, Bustamante J, Roelens M, Borie R, Le Brun M, Crestani B, Casanova JL, Puel A, Hofer M, Fieschi C, Theodoropoulou K, Béziat V, Candotti F. Arlabosse T, et al. J Clin Immunol. 2023 Oct;43(7):1566-1580. doi: 10.1007/s10875-023-01517-4. Epub 2023 Jun 5. J Clin Immunol. 2023. PMID: 37273120 Free PMC article.

Il-6 and UGT1A1 variations may related to furosemide resistance in heart failure patients.

Koprululu Kucuk G, Guney AI, Sunbul M, Guctekin T, Koç G, Kirac D. Koprululu Kucuk G, et al. IUBMB Life. 2023 Oct;75(10):830-843. doi: 10.1002/iub.2732. Epub 2023 Jun 1. IUBMB Life. 2023. PMID: 37260062

[A family study of the compound heterozygous mutation of the UGT1A1 gene causing Crigler-Najjar syndrome type II].

Luo L, Yao XB, Zheng SJ, Yang WL. Luo L, et al. Zhonghua Gan Zang Bing Za Zhi. 2023 Feb 20;31(2):168-173. doi: 10.3760/cma.j.cn501113-20211124-00580. Zhonghua Gan Zang Bing Za Zhi. 2023. PMID: 37137832 Chinese.

The association between UGT1A1 polymorphisms and treatment toxicities of liposomal irinotecan.

Su YY, Chiang NJ, Chang JS, Wang YW, Shen BN, Li YJ, Hwang DY, Shan YS, Chen LT. Su YY, et al. ESMO Open. 2023 Feb;8(1):100746. doi: 10.1016/j.esmoop.2022.100746. Epub 2022 Dec 15. ESMO Open. 2023. PMID: 36527823 Free PMC article.

UGT1A1 variants in Chinese Uighur and Han newborns and its correlation with neonatal hyperbilirubinemia.

Yang H, Li H, Xia Q, Dai W, Li X, Liu Y, Nie J, Yang F, Sun Y, Feng L, Yang L. Yang H, et al. PLoS One. 2022 Dec 15;17(12):e0279059. doi: 10.1371/journal.pone.0279059. eCollection 2022. PLoS One. 2022. PMID: 36520959 Free PMC article.

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