Li J, Bessho K, Shivakumar P, Mourya R, Mohanty SK, Dos Santos JL, Miura IK, Porta G, Bezerra JA. Th2 signals induce epithelial injury in mice and are compatible with the biliary atresia phenotype. J Clin Invest 2011 Nov;121(11):4244-56. Epub 2011 Oct 17. |
Leyva-Vega M, Gerfen J, Thiel BD, Jurkiewicz D, Rand EB, Pawlowska J, Kaminska D, Russo P, Gai X, Krantz ID, Kamath BM, Hakonarson H, Haber BA, Spinner NB. Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3. Am J Med Genet A 2010 Apr;152A(4):886-95. |
Leung DH, Ye W, Molleston JP, Weymann A, Ling S, Paranjape SM, Romero R, Schwarzenberg SJ, Palermo J, Alonso EM, Murray KF, Marshall BC, Sherker AH, Siegel MJ, Krishnamurthy R, Harned R, Karmazyn B, Magee JC, Narkewicz MR, Cystic Fibrosis Liver Disease Network (CFLD NET). Baseline Ultrasound and Clinical Correlates in Children with Cystic Fibrosis. J Pediatr 2015 Oct;167(4):862-868.e2. Epub 2015 Aug 5. |
Lee WS, Sokol RJ. Liver disease in mitochondrial disorders. Semin Liver Dis 2007 Aug;27(3):259-73. |
Karjoo S, Wells RG. Isolation of neonatal extrahepatic cholangiocytes. J Vis Exp 2014 Jun 5;(88). |
Karjoo S, Pack M, Porter JR, Wells R. A toxin that induces biliary atresia causes disruption of microtubules and loss of primary cilia. Proceedings of American Association for the Study of Liver Diseases (AASLD) 63rd Annual Meeting; November 9-13, 2012; Boston, MA. 2012 Nov. |
Karjoo S, Hand NJ, Russo P, Friedman J, Wells R. Primary cilia are absent in human biliary remnants and in extra-hepatic ducts of RRV mice. Proceedings of American Association for the Study of Liver Diseases (AASLD) 63rd Annual Meeting; November 9-13, 2012; Boston, MA. 2012 Nov. |
Karjoo S, Hand NJ, Loarca L, Russo PA, Friedman JR, Wells RG. Extrahepatic cholangiocyte cilia are abnormal in biliary atresia. J Pediatr Gastroenterol Nutr 2013 Jul;57(1):96-101. |
Kamath BM, Piccoli DA, Magee JC, Sokol RJ, Childhood Liver Disease Research and Education Network. Pancreatic insufficiency is not a prevalent problem in Alagille syndrome. J Pediatr Gastroenterol Nutr 2012 Nov;55(5):612-4. |
Kamath BM, Chen Z, Romero R, Fredericks EM, Alonso EM, Arnon R, Heubi J, Hertel PM, Karpen SJ, Loomes KM, Murray KF, Rosenthal P, Schwarz KB, Subbarao G, Teckman JH, Turmelle YP, Wang KS, Sherker AH, Sokol RJ, Magee JC, Childhood Liver Disease Research Network (ChiLDReN). Quality of Life and Its Determinants in a Multicenter Cohort of Children with Alagille Syndrome. J Pediatr 2015 Aug;167(2):390-6.e3. Epub 2015 Jun 6. |
Kamath BM, Chen Z, Romero R, Fredericks E and Magee J, Childhood Liver Disease Research and Education Network. Quality of Life in Alagille syndrome is associated with growth failure and cardiac defects. Proceedings of American Association for the Study of Liver Diseases (AASLD) 63rd Annual Meeting; November 9-13, 2012; Boston, MA. 2012 Nov. |
Kamath BM, Bauer RC, Loomes KM, Chao G, Gerfen J, Hutchinson A, Hardikar W, Hirschfield G, Jara P, Krantz ID, Lapunzina P, Leonard L, Ling S, Ng VL, Hoang PL, Piccoli DA, Spinner NB. NOTCH2 mutations in Alagille syndrome. J Med Genet 2012 Feb;49(2):138-44. Epub 2011 Dec 29. |
Jericho H, Westfall E, Knisely A, Verkade H, Whitington P. Bile salt kinetics in children with genetic cholestasis and bile diversion therapy. Proceedings of American Association for the Study of Liver Diseases (AASLD) 63rd Annual Meeting; November 9-13, 2012; Boston, MA. |
Hoofnagle JH. Biliary Atresia Research Consortium (BARC). Hepatology 2004 Apr;39(4):891. |
Heubi JE, Setchell KD, Rosenthal P, Shah S, Buckley D, Jha P, Zhang W, Potter CJ, Suskind D, Bull LN. Oral glycocholic acid treatment of patients with Bile acid Amidation Defects improves growth and fat-soluble vitamin absorption. Proceedings of American Association for the Study of Liver Diseases (AASLD) 60th Annual Meeting; October 30-November 3, 2009; Boston, MA. 2009 Oct. |
Heubi JE, Setchell KD, Jha P, Buckley D, Zhang W, Rosenthal P, Potter C, Horslen S, Suskind D. Treatment of bile acid amidation defects with glycocholic acid. Hepatology 2015 Jan;61(1):268-74. Epub 2014 Dec 23. |
Heubi JE, Setchell KD, Bove KE. Inborn errors of bile acid metabolism. Semin Liver Dis 2007 Aug;27(3):282-94. |
He M, Vockley J. New acyl-coA dehydrogenases: redefining long chain fatty acid catabolism in human. Proceedings of Society for Inherited Metabolic Disorders (SIMD); March 5-9, 2005; Pacific Grove, CA. 2005 Mar. |
He M, Rutledge SL, Kelly DR, Palmer CA, Murdoch G, Majumder N, Nicholls RD, Pei Z, Watkins PA, Vockley J. A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency. Proceedings of International Congress on Inborn Errors of Metabolism; 2005; 2005. |
He M, Rutledge SL, Kelly DR, Palmer CA, Murdoch G, Majumder N, Nicholls RD, Pei Z, Watkins PA, Vockley J. A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency. Am J Hum Genet 2007 Jul;81(1):87-103. Epub 2007 Jun 4. |
He M, Rutledge SL, Kelly D, Goetzman E, Vockley J. A new defect in beta-oxidation presenting as sudden liver failure. Proceedings of American Society of Human Genetics (ASHG) 55th Annual Meeting; October 25-29, 2005; Salt Lake City, UT. 2005 Oct. |
He M, Pei Z, Mohsen AW, Watkins P, Murdoch G, Van Veldhoven PP, Ensenauer R, Vockley J. Identification and characterization of new long chain acyl-CoA dehydrogenases. Mol Genet Metab 2011 Apr;102(4):418-29. Epub 2010 Dec 17. |
Hahn CL, Sokol RJ, Hines JM, CLiC Patient Advocacy Group Committee. The Patient Advocacy Group Committee of the Cholestatic Liver Disease Consortium: giving families, parents and patients a partnership with researchers. Proceedings of Presented at National Institutes of Health (NIH) Conference “Advancing Rare Diseases Research through Networks and Collaboration”; July 16, 2009; Bethesda, MD. 2009 Jul. |
Haber BA, Brown M, Shneider B, Sokol R, Whitington P, DeRusso P, Squires Jr R, Bezerra J, Shepherd R, Rosenthal P, Robuck P, BARC. Patient demographics and clinical practices in a US multi-center study of biliary atresia. Proceedings of American Association for the Study of Liver Diseases (AASLD) 55th Annual Meeting; October 29-November 2, 2004; Boston, MA. 2004 Oct. |
Haber B, Fredericks EM, Magee J, Bezerra JA, Karpen SJ, Kerkar N, Rosenthal P, Schwarz KB, Shepherd RW, Shneider BL, Whitington PF, Robuck PR, Sokol RJ, BARC. Predictors of neurodevelopmental outcome in non-transplanted children with biliary atresia at one year of age. Proceedings of American Association for the Study of Liver Diseases (AASLD) 59th Annual Meeting; October 31-November 4, 2008; San Francisco, CA. 2008 Oct. |