Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 112 Records) |
Query Trace: Syndrome and UGT1A1[original query] |
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Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution. BioMed research international 2019 8 2019 6272174. Mi Xiao-Xiao, Yan Jian, Ma Xiao-Jie, Zhu Ge-Li, Gao Yi-Dan, Yang Wen-Jun, Kong Xiao-Wen, Chen Gong-Ying, Shi Jun-Ping, Gong Li |
Study of Gilbert's Syndrome-Associated UGT1A1 Polymorphism in Jaundiced Neonates of ABO Incompatibility Hemolysis Disease. American journal of perinatology 2019 May . Yu Yingfang, Du Lizhong, Chen An, Chen Lih |
Significance of UGT1A1*28 Genotype in Patients with Advanced Liver Injury Caused By Chronic Hepatitis C. Journal of medical biochemistry 2019 3 38 (1): 45-52. Jordovic Jelena, Bojovic Ksenija, Simonovic-Babic Jasmina, Gasic Vladimir, Kotur Nikola, Zukic Branka, Vukovic Marija, Pavlovic Sonja, Lazarevic Ivana, Bekic Ivana, Nikolic Natasa, Uroševic Aleksandar, Mitrovic Nikola, Delic Drag |
[Analysis of genes related to hypothyroidism during pregnancy]. Zhonghua yi xue za zhi 2019 11 99 (42): 3350-3354. Liang L, Mao Y, Zhang J R, Zhang S C, Yang H |
Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana. PloS one 2020 9 15 (9): e0238691. Elenga Narcisse, Cuadro-Alvarez Emma, Martin Elise, Njuieyon Falucar, Defo Antoine, Maniassom Chimè |
Gilbert syndrome with systemic lupus erythematosus presenting with persistent unconjugated hyperbilirubinemia: A case report. Experimental and therapeutic medicine 2020 9 20 (5): 91. Ye Naifang, Zhou Zhuochao, Gong Huiyun, Teng Jialing, Han Yue, Yang Chengde, Ye Jun |
Relevance of Pharmacogenomics and Multidisciplinary Management in a Young-Elderly Patient With KRAS Mutant Colorectal Cancer Treated With First-Line Aflibercept-Containing Chemotherapy. Frontiers in oncology 2020 8 10 1155. Bruera Gemma, D'Andrilli Antonio, Simmaco Maurizio, Guadagni Stefano, Rendina Erino Angelo, Ricevuto Enri |
A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent ?-thalassemia. Annals of hematology 2020 7 99 (9): 2019-2026. Shrestha Oshan, Khadwal Alka Rani, Singhal Manphool, Trehan Amita, Bansal Deepak, Jain Richa, Pal Arnab, Hira Jasbir Kaur, Chhabra Sanjeev, Malhotra Pankaj, Das Reena, Sharma Prasha |
Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia. Pediatrics and neonatology 2020 6 61 (5): 506-512. Huang May-Jen, Lin Yu-Cheng, Liu Kevin, Chang Pi-Feng, Huang Ching-Sh |
The correlation between UDP-glucuronosyltransferase polymorphisms and environmental endocrine disruptors levels in polycystic ovary syndrome patients. Medicine 2020 3 99 (11): e19444. Luo Yunyao, Nie Ying, Tang Lu, Xu Charles C, Xu Liangz |
Carbon monoxide breath test assessment of mild hemolysis in Gilbert's syndrome. Medicine 2020 2 99 (7): e19109. Kang Ling-Ling, Ma Yong-Jian, Zhang Hou- |
Multimorbidity, polypharmacy, and drug-drug-gene interactions following a non-ST elevation acute coronary syndrome: analysis of a multicentre observational study. BMC medicine 2020 11 18 (1): 367. Turner R M, de Koning E M, Fontana V, Thompson A, Pirmohamed |
[Analysis of diagnostic value of UGT1A1 gene detection in Gilbert syndrome]. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2021 3 29 (2): 143-149. Zhang M, Li W N, Chen G, Xu X, Qi J |
Compound heterozygous UGT1A1*28 and UGT1A1*6 or single homozygous UGT1A1*28 are major genotypes associated with Gilbert's syndrome in Chinese Han people. Gene 2021 2 781 145526. Zhang Meng, Wang Hongwu, Huang Yuancheng, Xu Xin, Liu Wei, Ning Qin, Chen Tao, Qi Junyi |
Influence of UGT1A1 promoter polymorphism, ?-thalassemia and ? haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort. Annals of hematology 2021 Feb . Batista Jéssica V G F, Arcanjo Gabriela S, Batista Thais H C, Sobreira Marcondes J, Santana Rodrigo M, Domingos Igor F, Hatzlhofer Betânia L, Falcão Diego A, Pereira-Martins Diego A, Oliveira Jéssica M, Araujo Amanda S, Laranjeira Luana P M, Medeiros Fernanda S, Albuquerque Flávia P, Albuquerque Dulcinéia M, Santos Magnun N, Hazin Manuela F, Dos Anjos Ana C, Costa Fernando F, Araujo Aderson S, Lucena-Araujo Antonio R, Bezerra Marcos |
Gilbert's Syndrome, Bilirubin Level and UGT1A1?28 Genotype in Men of North-West Region of Russia. Journal of clinical and experimental hepatology 2021 12 11 (6): 691-699. Ivanov Andrei, Semenova Ele |
Association of Serum Bilirubin and Functional Variants of Heme Oxygenase 1 and Bilirubin UDP-Glucuronosyl Transferase Genes in Czech Adult Patients with Non-Alcoholic Fatty Liver Disease. Antioxidants (Basel, Switzerland) 2021 12 10 (12): . Petrtýl Jaromír, Dvo?ák Karel, St?íteský Jan, Lení?ek Martin, Jirásková Alena, Šmíd Václav, Haluzík Martin, Br?ha Radan, Vítek Lib |
[Gilbert's syndrome: hyperbilirubinemia enemy or friend]. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2021 11 29 (10): 1024-1027. Xiang G Q, Sun F R, Wang B |
Bilirubin metabolism and UDP-glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response. The Kaohsiung journal of medical sciences 2022 8 38 (8): 729-738. Huang May-Jen, Chen Pei-Lain, Huang Ching-Sh |
Gilbert Syndrome and Genetic Findings in Children: A Tertiary-Center Experience from Turkey. Turkish archives of pediatrics 2022 7 57 (3): 295-299. Ça?an Appak Yeliz, Aksoy Betül, Özy?lmaz Berk, Özdemir Taha Re?id, Baran Ma?all |
Serum Bilirubin Concentrations and the Prevalence of Gilbert Syndrome in Elite Athletes. Sports medicine - open 2022 Jun 8 (1): 84. Woronyczová Jana, Nováková Miroslava, Lení?ek Martin, Bátovský Miloš, Bolek Emil, Cífková Renata, Vítek Lib |
Novel combined UGT1A1 mutations in Crigler Najjar Syndrome type I. Journal of clinical laboratory analysis 2022 Jun 36 (6): e24482. Abdellaoui Nawel, Abdelmoula Balkiss, Abdelhedi Rania, Kharrat Najla, Tabebi Mouna, Rebai Ahmed, Bouayed Abdelmoula Nou |
Gilbert or Crigler-Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity. Italian journal of pediatrics 2022 4 48 (1): 59. Cozzi Laura, Nuti Federica, Degrassi Irene, Civeriati Daniela, Paolella Giulia, Nebbia Gabriel |
Genetic testing of UGT1A1 in the diagnosis of Gilbert syndrome: The discovery of seven novel variants in the Chinese population. Molecular genetics & genomic medicine 2022 4 10 (7): e1958. Gu Leilei, Han Yue, Zhang Donghua, Gong Qiming, Zhang Xinx |
Dependence of blood biochemical parameters on various genotypes of the UGT1A1 gene associated with gilbert's syndrome. Klinicheskaia laboratornaia diagnostika 2022 2 67 (2): 69-75. Sidorenko Dar'ja Vladimirovna, Nazarov V D, Volnikova E G, Kondrasheva E A, Peshkova N G, Kovaleva I S, Kokorina O S, Svatkovskaya I B, Lapin S |
Investigation of high gamma-glutamyltransferase syndrome in California Thoroughbred racehorses. Journal of veterinary internal medicine 2022 11 36 (6): 2203-2212. Peng Sichong, Magdesian K Gary, Dowd Joseph, Blea Jeffrey, Carpenter Ryan, Ho Wayne, Finno Carrie |
The Mutation Hotspots at UGT1A Locus May Be Associated with Gilbert's Syndrome Affecting the Taiwanese Population. International journal of molecular sciences 2022 10 23 (20): . Hsu Paul Wei-Che, Liao Po-Cheng, Kao Yu-Hsiang, Lin Xin-Yu, Chien Rong-Nan, Yeh Chau-Ting, Lai Chi-Chun, Shyu Yu-Chiau, Lin Chih-La |
Association of Low Serum Bilirubin Concentrations and Promoter Variations in the UGT1A1 and HMOX1 Genes with Type 2 Diabetes Mellitus in the Czech Population. International journal of molecular sciences 2023 7 24 (13): . Alena Jirásková, Jan Škrha, Libor Vít |
[A family study of the compound heterozygous mutation of the UGT1A1 gene causing Crigler-Najjar syndrome type II]. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2023 5 31 (2): 168-173. L Luo, X B Yao, S J Zheng, W L Ya |
Chemotherapy-related hyperbilirubinemia in pediatric acute lymphoblastic leukemia: a genome-wide association study from the AIEOP-BFM ALL study group. Journal of experimental & clinical cancer research : CR 2023 1 42 (1): 21. Junk Stefanie V, Schaeffeler Elke, Zimmermann Martin, Möricke Anja, Beier Rita, Schütte Peter, Fedders Birthe, Alten Julia, Hinze Laura, Klein Norman, Kulozik Andreas, Muckenthaler Martina U, Koehler Rolf, Borkhardt Arndt, Vijayakrishnan Jayaram, Ellinghaus David, Forster Michael, Franke Andre, Wintering Astrid, Kratz Christian P, Schrappe Martin, Schwab Matthias, Houlston Richard S, Cario Gunnar, Stanulla Mart |
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- Page last updated:Apr 22, 2024
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