These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
134 related articles for article (PubMed ID: 18466997)
1. Hepatic repopulation with stably transduced conditionally immortalized hepatocytes in the Gunn rat. Kawashita Y; Guha C; Moitra R; Wang X; Fox IJ; Roy-Chowdhury J; Roy-Chowdhury N J Hepatol; 2008 Jul; 49(1):99-106. PubMed ID: 18466997 [TBL] [Abstract][Full Text] [Related]
2. Normal hepatocytes correct serum bilirubin after repopulation of Gunn rat liver subjected to irradiation/partial resection. Guha C; Parashar B; Deb NJ; Garg M; Gorla GR; Singh A; Roy-Chowdhury N; Vikram B; Roy-Chowdhury J Hepatology; 2002 Aug; 36(2):354-62. PubMed ID: 12143043 [TBL] [Abstract][Full Text] [Related]
3. Gunn Rats as a Surrogate Model for Evaluation of Hepatocyte Transplantation-Based Therapies of Crigler-Najjar Syndrome Type 1. Polgar Z; Li Y; Li Wang X; Guha C; Roy-Chowdhury N; Roy-Chowdhury J Methods Mol Biol; 2017; 1506():131-147. PubMed ID: 27830550 [TBL] [Abstract][Full Text] [Related]
4. A novel strategy for in vivo expansion of transplanted hepatocytes using preparative hepatic irradiation and FasL-induced hepatocellular apoptosis. Takahashi M; Deb NJ; Kawashita Y; Lee SW; Furgueil J; Okuyama T; Roy-Chowdhury N; Vikram B; Roy-Chowdhury J; Guha C Gene Ther; 2003 Feb; 10(4):304-13. PubMed ID: 12595889 [TBL] [Abstract][Full Text] [Related]
6. Strong, long-term transgene expression in rat liver using chicken beta-actin promoter associated with cytomegalovirus immediate-early enhancer (CAG promoter). Kosuga M; Enosawa S; Li XK; Suzuki S; Matsuo N; Yamada M; Roy-Chowdhury J; Koiwai O; Okuyama T Cell Transplant; 2000; 9(5):675-80. PubMed ID: 11144964 [TBL] [Abstract][Full Text] [Related]
7. Human neonatal hepatocyte transplantation induces long-term rescue of unconjugated hyperbilirubinemia in the Gunn rat. Tolosa L; López S; Pareja E; Donato MT; Myara A; Nguyen TH; Castell JV; Gómez-Lechón MJ Liver Transpl; 2015 Jun; 21(6):801-11. PubMed ID: 25821167 [TBL] [Abstract][Full Text] [Related]
8. Single hepatic venous injection of liver-specific naked plasmid vector expressing human UGT1A1 leads to long-term correction of hyperbilirubinemia and prevention of chronic bilirubin toxicity in Gunn rats. Jia Z; Dankó I Hum Gene Ther; 2005 Aug; 16(8):985-95. PubMed ID: 16076256 [TBL] [Abstract][Full Text] [Related]
9. Nonviral gene transfer into liver and muscle for treatment of hyperbilirubinemia in the gunn rat. Dankó I; Jia Z; Zhang G Hum Gene Ther; 2004 Dec; 15(12):1279-86. PubMed ID: 15684703 [TBL] [Abstract][Full Text] [Related]
10. Amelioration of Hyperbilirubinemia in Gunn Rats after Transplantation of Human Induced Pluripotent Stem Cell-Derived Hepatocytes. Chen Y; Li Y; Wang X; Zhang W; Sauer V; Chang CJ; Han B; Tchaikovskaya T; Avsar Y; Tafaleng E; Madhusudana Girija S; Tar K; Polgar Z; Strom S; Bouhassira EE; Guha C; Fox IJ; Roy-Chowdhury J; Roy-Chowdhury N Stem Cell Reports; 2015 Jul; 5(1):22-30. PubMed ID: 26074313 [TBL] [Abstract][Full Text] [Related]
11. Complete correction of hyperbilirubinemia in the Gunn rat model of Crigler-Najjar syndrome type I following transient in vivo adenovirus-mediated expression of human bilirubin UDP-glucuronosyltransferase. Askari FK; Hitomi Y; Mao M; Wilson JM Gene Ther; 1996 May; 3(5):381-8. PubMed ID: 9156798 [TBL] [Abstract][Full Text] [Related]
12. Long-term amelioration of bilirubin glucuronidation defect in Gunn rats by transplanting genetically modified immortalized autologous hepatocytes. Tada K; Roy-Chowdhury N; Prasad V; Kim BH; Manchikalapudi P; Fox IJ; van Duijvendijk P; Bosma PJ; Roy-Chowdhury J Cell Transplant; 1998; 7(6):607-16. PubMed ID: 9853589 [TBL] [Abstract][Full Text] [Related]
13. Transplantation of Gunn rats with autologous fibroblasts expressing bilirubin UDP-glucuronosyltransferase: correction of genetic deficiency and tumor formation. Seppen J; Tada K; Ottenhoff R; Sengupta K; Chowdhury NR; Chowdhury JR; Bosma PJ; Oude Elferink RP Hum Gene Ther; 1997 Jan; 8(1):27-36. PubMed ID: 8989992 [TBL] [Abstract][Full Text] [Related]
14. A step toward liver gene therapy: efficient correction of the genetic defect of hepatocytes isolated from a patient with Crigler-Najjar syndrome type 1 with lentiviral vectors. Birraux J; Menzel O; Wildhaber B; Jond C; Nguyen TH; Chardot C Transplantation; 2009 Apr; 87(7):1006-12. PubMed ID: 19352119 [TBL] [Abstract][Full Text] [Related]