Jiang, J. et al. Epidemiological characteristics and risk factors of biliary atresia: a case-control study. BMJ Open. 11, e049354 (2021).
Article PubMed PubMed Central Google Scholar
Livesey, E. et al. Epidemiology of biliary atresia in England and Wales (1999–2006). Arch. Dis. Child Fetal Neonatal Ed. 94, F451–F455 (2009).
Article CAS PubMed Google Scholar
The, N. S. et al. National Birth Defects Prevention Study. Risk factors for isolated biliary atresia, National Birth Defects Prevention Study, 1997–2002. Am. J. Med. Genet. A. 143A, 2274–2284 (2007).
Article CAS PubMed Google Scholar
Medappil, N. et al. Kasai portoenterostomy for biliary atresia - surgical precautions for better outcomes. J. Pediatr. Surg. 54, 868–869 (2019).
Davenport, M. et al. Surgical and medical aspects of the initial treatment of biliary atresia: position paper. J. Clin. Med. 11, 6601 (2022).
Article PubMed PubMed Central Google Scholar
Madadi-Sanjani, O. et al. Long-term outcome and necessity of liver transplantation in infants with biliary atresia are independent of cytokine milieu in native liver and serum. Cytokine 111, 382–388 (2018).
Article CAS PubMed Google Scholar
Leyva-Vega, M. et al. Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3. Am. J. Med. Genet A. 152A, 886–895 (2010).
Article CAS PubMed PubMed Central Google Scholar
Ningappa, M. et al. The role of ARF6 in biliary atresia. PLoS ONE 10, e0138381 (2015).
Article PubMed PubMed Central Google Scholar
Chen, Y. et al. A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1. PLoS Genet. 14, e1007532 (2018).
Article PubMed PubMed Central Google Scholar
Garcia-Barceló, M. M. et al. Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. Hum. Mol. Genet. 19, 2917–2925 (2010).
Article PubMed PubMed Central Google Scholar
Rajagopalan, R. et al. Exome sequencing in individuals with isolated biliary atresia. Sci. Rep. 10, 2709 (2020).
Article CAS PubMed PubMed Central Google Scholar
Glessner, J. T. et al. Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes. J. Hepatol. 79, 1385–1395 (2023).
Article CAS PubMed PubMed Central Google Scholar
Luo, Z., Shivakumar, P., Mourya, R., Gutta, S. & Bezerra, J. A. Gene expression signatures associated with survival times of pediatric patients with biliary atresia identify potential therapeutic agents. Gastroenterology 157, 1138–1152.e14 (2019).
Article CAS PubMed Google Scholar
Everhart, J. E. et al. Prognostic value of Ishak fibrosis stage: findings from the hepatitis C antiviral long-term treatment against cirrhosis trial. Hepatology 51, 585–594 (2010).
Kamp, J. C. et al. Fibrosis-related gene profiling in liver biopsies of PiZZ α1-antitrypsin children with different clinical courses. Int J. Mol. Sci. 24, 2485 (2023).
Article CAS PubMed PubMed Central Google Scholar
Puchtler, H., Sweat, F. & Levine, M. On the binding of congo red by amyloid. J. Histochem. Cytochem. 10, 355–364 (1962).
Schindelin, J. et al. Fiji: an open-source platform for biological-image analysis. Nat. Methods 9, 676–682 (2012).
Article CAS PubMed Google Scholar
Liu, X., Liu, Y. & Ji, S. Secretases related to amyloid precursor protein processing. Membranes 11, 983 (2021).
Article CAS PubMed PubMed Central Google Scholar
Ozdogan, E. & Arikan, C. Liver fibrosis in children: a comprehensive review of mechanisms, diagnosis, and therapy. Clin. Exp. Pediatr. 66, 110–124 (2023).
Article CAS PubMed Google Scholar
Schoen, B. T., Lee, H., Sullivan, K. & Ricketts, R. R. The Kasai portoenterostomy: when is it too late? J. Pediatr. Surg. 36, 97–99 (2001).
Article CAS PubMed Google Scholar
Davenport, M., Gonde, C., Narayanaswamy, B., Mieli-Vergani, G. & Tredger, J. M. Soluble adhesion molecule profiling in preoperative infants with biliary atresia. J. Pediatr. Surg. 40, 1464–1469 (2005).
Langenburg, S. E., Poulik, J., Goretsky, M., Klein, A. A. & Klein, M. D. Bile duct size does not predict success of portoenterostomy for biliary atresia. J. Pediatr. Surg. 35, 1006–1007 (2000).
Article CAS PubMed Google Scholar
Weerasooriya, V. S., White, F. V. & Shepherd, R. W. Hepatic fibrosis and survival in biliary atresia. J. Pediatr. 144, 123–125 (2004).
Wu, L. N., Zhu, Z. J. & Sun, L. Y. Genetic factors and their role in the pathogenesis of biliary atresia. Front. Pediatr. 10, 912154 (2022).
Article PubMed PubMed Central Google Scholar
Stone, R. C. et al. Epithelial-mesenchymal transition in tissue repair and fibrosis. Cell Tissue Res. 365, 495–506 (2016).
Article CAS PubMed PubMed Central Google Scholar
Venkat, V. et al. Childhood Liver Disease Research Network. Modeling outcomes in children with biliary atresia with native liver after 2 years of age. Hepatol. Commun. 4, 1824–1834 (2020).
Article CAS PubMed PubMed Central Google Scholar
Gunadi et al. Collagen gene cluster expression and liver fibrogenesis in patients with biliary atresia: a preliminary study. BMC Res. Notes 16, 356 (2023).
Article CAS PubMed PubMed Central Google Scholar
Kerola, A. et al. Molecular signature of active fibrogenesis prevails in biliary atresia after successful portoenterostomy. Surgery 162, 548–556 (2017).
Jonigk, D. et al. Comparative analysis of morphological and molecular motifs in bronchiolitis obliterans and alveolar fibroelastosis after lung and stem cell transplantation. J. Pathol. Clin. Res. 3, 17–28 (2016).
Article PubMed PubMed Central Google Scholar
Madadi-Sanjani, O. et al. Growth factors assessed during Kasai procedure in liver and serum are not predictive for the postoperative liver deterioration in infants with biliary atresia. J. Clin. Med. 10, 1978 (2021).
Article CAS PubMed PubMed Central Google Scholar
Anvarian, Z., Mykytyn, K., Mukhopadhyay, S., Pedersen, L. B. & Christensen, S. T. Cellular signalling by primary cilia in development, organ function and disease. Nat. Rev. Nephrol. 15, 199–219 (2019).
留言 (0)