[1] |
Maisels MJ. Neonatal jaundice[J]. Pediatr Rev, 2006, 27(12): 443-454.
doi: 10.1542/pir.27.12.443
|
[2] |
林佳媛. 胆红素代谢及其调节的研究进展[J]. 复旦学报(医学版), 2014, 41(3): 405-411.
|
[3] |
卜爱林, 李贵南. UGT1A1基因多态性与新生儿不明原因高胆红素血症的相关性[J]. 中国医师杂志, 2020, 22(11): 1736-1738.
|
[4] |
American Academy of Pediatrics Subcommittee on Hyperbilirubinemia. Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation[J]. Pediatrics, 2004, 114(1): 297-316.
doi: 10.1542/peds.114.1.297
|
[5] |
Mehrad-Majd H, Haerian MS, Akhtari J, et al. Effects of Gly71Arg mutation in UGT1A1 gene on neonatal hyperbilirubinemia: a systematic review and meta-analysis[J]. J Matern Fetal Neonatal Med, 2019, 32(10): 1575-1585.
doi: 10.1080/14767058.2017.1410789
pmid: 29179591
|
[6] |
Yueh MF, Chen S, Nguyen N, et al. Developmental, genetic, dietary, and xenobiotic influences on neonatal hyperbilirubinemia[J]. Mol Pharmacol, 2017, 91(5): 545-553.
doi: 10.1124/mol.116.107524
|
[7] |
Li H, Zhang P. UGT1A1*28 gene polymorphism was not associated with the risk of neonatal hyperbilirubinemia: a meta-analysis[J]. J Matern Fetal Neonatal Med, 2021, 34(24): 4064-4071.
doi: 10.1080/14767058.2019.1702962
|
[8] |
Amandito R, Rohsiswatmo R, Carolina E, et al. Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 polymorphisms in Indonesian neonates with hyperbilirubinemia using multiplex PCR sequencing[J]. Front Pediatr, 2019, 7: 328.
doi: 10.3389/fped.2019.00328
pmid: 31440488
|
[9] |
尹迪, 魏珊珊, 许无恨, 等. UGT1A1基因多态性与新生儿不明原因重度高胆红素血症的关系[J]. 中华新生儿科杂志, 2021, 36(6): 55-58.
|
[10] |
陈虹, 钟丹妮. 尿苷二磷酸葡萄糖醛酸转移酶1A1基因多态性的表达研究进展[J]. 中华实用儿科临床杂志, 2019, 5: 388-391.
|
[11] |
肖奇志, 郭洪创, 李恋湘, 等. G6PD活性、UGT1A1、SLCO1B1、ABCC2基因多态性和新生儿高胆红素血症的关系研究[J]. 分子诊断与治疗杂志, 2018, 10(3): 163-168.
|
[12] |
Sticova E, Lodererova A, van de Steeg E, et al. Down-regulation of OATP1B proteins correlates with hyper-bilirubinemia in advanced cholestasis[J]. Int J Clin Exp Pathol, 2015, 8(5): 5252-5262.
|
[13] |
Hoekstra LT, de Graaf W, Nibourg GA, et al. Physiological and biochemical basis of clinical liver function tests: a review[J]. Ann Surg, 2013, 257(1): 27-36.
doi: 10.1097/SLA.0b013e31825d5d47
pmid: 22836216
|
[14] |
van de Steeg E, Stránecký V, Hartmannová H, et al. Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver[J]. J Clin Invest, 2012, 122(2): 519-528.
doi: 10.1172/JCI59526
|
[15] |
D’Silva S, Colah RB, Ghosh K, et al. Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates[J]. Gene, 2014, 547: 18-22.
doi: 10.1016/j.gene.2014.05.047
|
[16] |
王朝, 赵玉平. 葡萄糖-6-磷酸脱氢酶缺乏症的发病机制及诊疗现状[J]. 国际输血及血液学杂志, 2017, 40(2): 178-181.
|
[17] |
Olusanya BO, Emokpae AA, Zamora TG, et al. Addressing the burden of neonatal hyperbilirubinaemia in countries with significant glucose-6-phosphate dehydrogenase deficiency[J]. Acta Paediatr, 2014, 103: 1102-1109.
doi: 10.1111/apa.12735
|
[18] |
Hu R, Lin M, Ye J, et al. Molecular epidemiological investigation of G6PD deficiency by a gene chip among Chinese Hakka of southern Jiangxi province[J]. Int J Clin Exp Pathol, 2015, 8(11): 15013-15018.
|
[19] |
奎莉越, 王明英, 周百灵, 等. 云南省婴儿期不同民族高非结合性胆红素血症UGT1A1基因多态性研究[J]. 分子诊断与治疗杂志, 2020, 12(3): 386-390.
|
[20] |
钟勇, 蒋晓梅, 冯于玲, 等. UGT1A1基因多态性与不同民族间新生儿高胆红素血症的关系[J]. 临床儿科杂志, 2013, 31(4): 324-327.
|
[21] |
何翠红, 屈艺. 新生儿高胆红素血症与基因多态性研究进展[J]. 中国当代儿科杂志, 2020, 22(3): 280-284.
|
[22] |
Huang MJ, Chen YC, Huang YY, et al. Effect of UDP-glucuronosyltransferase 1A1 activity on risk for developing Gilbert's syndrome[J]. Kaohsiung J Med Sci, 2019, 35(7): 432-439.
|
[23] |
MiXX, Yan J, Ma XJ, et al. Analysis of the UGT1A1 genotype in hyperbilirubinemia patients: differences in allele frequency and distribution[J]. Biomed Res Int, 2019, 2019:6272174.
|
[24] |
蒋榆辉, 刘玲, 奚敏, 等. SLCO1B1基因多态性与新生儿高胆红素血症的相关性[J]. 临床儿科杂志, 2018, 36(9): 7-10.
|
[25] |
Riskin A, Gery N, Kugelman A, et al. Glucose-6-phosphate dehydrogenase deficiency and borderline deficiency: association with neonatal hyperbilirubinemia[J]. J Pediatr, 2012, 161(2): 191-196.
doi: 10.1016/j.jpeds.2012.02.018
|
[26] |
Liu Z, Yu C, Li Q, et al. Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017[J]. Hum Mutat, 2020, 41(1): 212-221.
doi: 10.1002/humu.23911
|
[27] |
许冰莹, 黄尤光, 程振江, 等. 云南籍葡萄糖-6-磷酸脱氢酶缺乏症基因突变研究[J]. 昆明医学院学报, 2007, 28(4): 6-12.
|