[1] |
BHANDARI J, THADA PK, YADAV D. Crigler Najjar syndrome[M]. Treasure Island (FL): StatPearls Publishing, 2022.
|
[2] |
CRIGLER JF Jr, NAJJAR VA. Congenital familial nonhemolytic jaundice with kernicterus[J]. Pediatrics, 1952, 10(2): 169-180.
|
[3] |
ARIAS IM. Chronic unconjugated hyperbilirubinemia without overt signs of hemolysis in adolescents and adults[J]. J Clin Invest, 1962, 41(12): 2233-2245. DOI: 10.1172/JCI104682.
|
[4] |
GAILITE L, VALENZUELA-PALOMO A, SANOGUERA-MIRALLES L, et al. UGT1A1 variants c. 864+5G > T and c. 996+2_996+5del of a Crigler-Najjar patient induce aberrant splicing in minigene assays[J]. Front Genet, 2020, 11: 169. DOI: 10.3389/fgene.2020.00169.
|
[5] |
MEMON N, WEINBERGER BI, HEGYI T, et al. Inherited disorders of bilirubin clearance[J]. Pediatr Res, 2016, 79(3): 378-386. DOI: 10.1038/pr.2015.247.
|
[6] |
TCACIUC E, PODUREAN M, TCACIUC A. Management of Crigler-Najjar syndrome[J]. Med Pharm Rep, 2021, 94(Suppl 1): S64-S67. DOI: 10.15386/mpr-2234.
|
[7] |
CANU G, MINUCCI A, ZUPPI C, et al. Gilbert and Crigler Najjar syndromes: an update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database[J]. Blood Cells Mol Dis, 2013, 50(4): 273-280. DOI: 10.1016/j.bcmd.2013.01.003.
|
[8] |
LEE WS, MCKIERNAN PJ, BEATH SV, et al. Bile bilirubin pigment analysis in disorders of bilirubin metabolism in early infancy[J]. Arch Dis Child, 2001, 85(1): 38-42. DOI: 10.1136/adc.85.1.38.
|
[9] |
LUND HT, JACOBSEN J. Influence of phototherapy on the biliary bilirubin excretion pattern in newborn infants with hyperbilirubinemia[J]. J Pediatr, 1974, 85(2): 262-267. DOI: 10.1016/s0022-3476(74)80408-7.
|
[10] |
YOHANNAN MD, TERRY HJ, LITTLEWOOD JM. Long term phototherapy in Crigler-Najjar syndrome[J]. Arch Dis Child, 1983, 58(6): 460-462. DOI: 10.1136/adc.58.6.460.
|
[11] |
STRAUSS KA, ROBINSON DL, VREMAN HJ, et al. Management of hyperbilirubinemia and prevention of kernicterus in 20 patients with Crigler-Najjar disease[J]. Eur J Pediatr, 2006, 165(5): 306-319. DOI: 10.1007/s00431-005-0055-2.
|
[12] |
EBRAHIMI A, RAHIM F. Crigler-Najjar syndrome: Current perspectives and the application of clinical genetics[J]. Endocr Metab Immune Disord Drug Targets, 2018, 18(3): 201-211. DOI: 10.2174/1871530318666171213153130.
|
[13] |
DHAWAN A, LAWLOR MW, MAZARIEGOS GV, et al. Disease burden of Crigler-Najjar syndrome: Systematic review and future perspectives[J]. J Gastroenterol Hepatol, 2020, 35(4): 530-543. DOI: 10.1111/jgh.14853.
|
[14] |
AHMED P, PRATT A, LAND VJ, et al. Multiple plasma exchanges successfully maintain a young adult patient with Crigler-Najjar syndrome type Ⅰ[J]. J Clin Apher, 1989, 5(1): 17-20. DOI: 10.1002/jca.2920050107.
|
[15] |
DUAN ZJ, LI LL, JU J, et al. Treatment of hyperbilirubinemia with blood purification in China[J]. World J Gastroenterol, 2006, 12(46): 7467-7471. DOI: 10.3748/wjg.v12.i46.7467.
|
[16] |
SUGATANI J, KOJIMA H, UEDA A, et al. The phenobarbital response enhancer module in the human bilirubin UDP-glucuronosyltransferase UGT1A1 gene and regulation by the nuclear receptor CAR[J]. Hepatology, 2001, 33(5): 1232-1238. DOI: 10.1053/jhep.2001.24172.
|
[17] |
ABDUL RAFFAY E, LIAQAT A, KHAN M, et al. A rare case report of Crigler Najjar syndrome type Ⅱ[J]. Cureus, 2021, 13(1): e12669. DOI: 10.7759/cureus.12669.
|
[18] |
GUERCIOLINI R. Mode of action of orlistat[J]. Int J Obes Relat Metab Disord, 1997, 21(Suppl 3): S12-S23.
|
[19] |
KOTAL P, van der VEERE CN, SINAASAPPEL M, et al. Intestinal excretion of unconjugated bilirubin in man and rats with inherited unconjugated hyperbilirubinemia[J]. Pediatr Res, 1997, 42(2): 195-200. DOI: 10.1203/00006450-199708000-00011.
|
[20] |
CLARENBURG R, KAO CC. Shared and separate pathways for biliary excretion of bilirubin and BSP in rats[J]. Am J Physiol, 1973, 225(1): 192-200. DOI: 10.1152/ajplegacy.1973.225.1.192.
|
[21] |
HAFKAMP AM, HAVINGA R, OSTROW JD, et al. Novel kinetic insights into treatment of unconjugated hyperbilirubinemia: phototherapy and orlistat treatment in Gunn rats[J]. Pediatr Res, 2006, 59(4 Pt 1): 506-512. DOI: 10.1203/01.pdr.0000203180.79636.98.
|
[22] |
HAFKAMP AM, HAVINGA R, SINAASAPPEL M, et al. Effective oral treatment of unconjugated hyperbilirubinemia in Gunn rats[J]. Hepatology, 2005, 41(3): 526-534. DOI: 10.1002/hep.20589.
|
[23] |
HAFKAMP AM, NELISSE-HAAK R, SINAASAPPEL M, et al. Orlistat treatment of unconjugated hyperbilirubinemia in Crigler-Najjar disease: a randomized controlled trial[J]. Pediatr Res, 2007, 62(6): 725-730. DOI: 10.1203/PDR.0b013e3181598cc5.
|
[24] |
van der VEERE CN, SCHOEMAKER B, van der MEER R, et al. Rapid association of unconjugated bilirubin with amorphous calcium phosphate[J]. J Lipid Res, 1995, 36(8): 1697-1707.
|
[25] |
van der VEERE CN, JANSEN PL, SINAASAPPEL M, et al. Oral calcium phosphate: a new therapy for Crigler-Najjar disease?[J]. Gastroenterology, 1997, 112(2): 455-462. DOI: 10.1053/gast.1997.v112.pm9024299.
|
[26] |
SHANMUGAM NP, PERUMALLA R, GOPINATH R, et al. Auxiliary liver transplantation: a form of gene therapy in selective metabolic disorders[J]. J Clin Exp Hepatol, 2011, 1(2): 118-120. DOI: 10.1016/S0973-6883(11)60132-1.
|
[27] |
WOLFF H, OTTO G, GIEST H. Liver transplantation in Crigler-Najjar syndrome. A case report[J]. Transplantation, 1986, 42(1): 84. DOI: 10.1097/00007890-198607000-00018.
|
[28] |
OZÇAY F, ALEHAN F, SEVMIŞ S, et al. Living related liver transplantation in Crigler-Najjar syndrome type 1[J]. Transplant Proc, 2009, 41(7): 2875-2877. DOI: 10.1016/j.transproceed.2009.07.025.
|
[29] |
RIBES-KONINCKX C, IBARS EP, CALZADO AMÁ, et al. Clinical outcome of hepatocyte transplantation in four pediatric patients with inherited metabolic diseases[J]. Cell Transplant, 2012, 21(10): 2267-2282. DOI: 10.3727/096368912X637505.
|
[30] |
ANDERSON TN, ZARRINPAR A. Hepatocyte transplantation: past efforts, current technology, and future expansion of therapeutic potential[J]. J Surg Res, 2018, 226: 48-55. DOI: 10.1016/j.jss.2018.01.031.
|
[31] |
AMBROSINO G, VAROTTO S, STROM SC, et al. Isolated hepatocyte transplantation for Crigler-Najjar syndrome type 1[J]. Cell Transplant, 2005, 14(2-3): 151-157. DOI: 10.3727/000000005783983250.
|
[32] |
KHAN AA, PARVEEN N, MAHABOOB VS, et al. Treatment of Crigler-Najjar syndrome type 1 by hepatic progenitor cell transplantation: a simple procedure for management of hyperbilirubinemia[J]. Transplant Proc, 2008, 40(4): 1148-1150. DOI: 10.1016/j.transproceed.2008.03.022.
|
[33] |
LYSY PA, NAJIMI M, STEPHENNE X, et al. Liver cell transplantation for Crigler-Najjar syndrome type Ⅰ: update and perspectives[J]. World J Gastroenterol, 2008, 14(22): 3464-3470. DOI: 10.3748/wjg.14.3464.
|
[34] |
FOLLENZI A, SANTAMBROGIO L, ANNONI A. Immune responses to lentiviral vectors[J]. Curr Gene Ther, 2007, 7(5): 306-315. DOI: 10.2174/156652307782151515.
|
[35] |
SOMANATHAN S, CALCEDO R, WILSON JM. Adenovirus-antibody complexes contributed to lethal systemic inflammation in a gene therapy trial[J]. Mol Ther, 2020, 28(3): 784-793. DOI: 10.1016/j.ymthe.2020.01.006.
|
[36] |
MAESTRO S, WEBER ND, ZABALETA N, et al. Novel vectors and approaches for gene therapy in liver diseases[J]. JHEP Rep, 2021, 3(4): 100300. DOI: 10.1016/j.jhepr.2021.100300.
|
[37] |
COLLAUD F, BORTOLUSSI G, GUIANVARC'H L, et al. Preclinical development of an AAV8-hUGT1A1 vector for the treatment of Crigler-Najjar syndrome[J]. Mol Ther Methods Clin Dev, 2019, 12: 157-174. DOI: 10.1016/j.omtm.2018.12.011.
|
[38] |
YAN Z, YAN H, OU H. Human thyroxine binding globulin (TBG) promoter directs efficient and sustaining transgene expression in liver-specific pattern[J]. Gene, 2012, 506(2): 289-294. DOI: 10.1016/j.gene.2012.07.009.
|
[39] |
de CANEVA A, PORRO F, BORTOLUSSI G, et al. Coupling AAV-mediated promoterless gene targeting to SaCas9 nuclease to efficiently correct liver metabolic diseases[J]. JCI Insight, 2019, 5(15): e128863. DOI: 10.1172/jci.insight.128863.
|
[40] |
BOMMINENI VR, CHOWDHURY NR, WU GY, et al. Depolymerization of hepatocellular microtubules after partial hepatectomy[J]. J Biol Chem, 1994, 269(40): 25200-25205. DOI: 10.1016/s0021-9258(17)31517-x.
|
[41] |
KREN BT, PARASHAR B, BANDYOPADHYAY P, et al. Correction of the UDP-glucuronosyltransferase gene defect in the Gunn rat model of Crigler-Najjar syndrome type Ⅰ with a chimeric oligonucleotide[J]. Proc Natl Acad Sci U S A, 1999, 96(18): 10349-10354. DOI: 10.1073/pnas.96.18.10349.
|
[42] |
FISCHER D, LI Y, AHLEMEYER B, et al. In vitro cytotoxicity testing of polycations: influence of polymer structure on cell viability and hemolysis[J]. Biomaterials, 2003, 24(7): 1121-1131. DOI: 10.1016/s0142-9612(02)00445-3.
|
[43] |
APGAR JF, TANG JP, SINGH P, et al. Quantitative systems pharmacology model of hUGT1A1-modRNA encoding for the UGT1A1 enzyme to treat Crigler-Najjar syndrome type 1[J]. CPT Pharmacometrics Syst Pharmacol, 2018, 7(6): 404-412. DOI: 10.1002/psp4.12301.
|
[44] |
BORTOLUSSI G, MURO AF. Advances in understanding disease mechanisms and potential treatments for Crigler-Najjar syndrome[J]. Expert Opin Orphan D, 2018, 6(7): 425-439. DOI: 10.1080/21678707.2018.1495558.
|
[45] |
AN D, SCHNELLER JL, FRASSETTO A, et al. Systemic messenger RNA therapy as a treatment for methylmalonic acidemia[J]. Cell Rep, 2017, 21(12): 3548-3558. DOI: 10.1016/j.celrep.2017.11.081.
|