Asai Lab

Publications

Asai, A; Wu, JF; Wang, KS; Yamataka, A; Nio, M; Su, DJ; Short, C; Tsuboi, K; Ochi, T; Sasaki, H; et al. The Outcome of Patients With Cystic Biliary Atresia With Intact Proximal Hepatic Ducts Following Hepatic-Cyst-Jejunostomy. Journal of Pediatric Gastroenterology and Nutrition. 2022; 75:131-137.

Li, CZ; Ogawa, H; Ng, SS; Chen, X; Kishimoto, E; Sakabe, K; Fukami, A; Hu, YC; Mayhew, CN; Hellmann, J; et al. Human iPSC-derived hepatocyte system models cholestasis with tight junction protein 2 deficiency. JHEP Reports. 2022; 4:100446.

Bezerra, JA; Asai, A; Tiao, G; Mullapudi, B; Balistreri, WF. Biliary Atresia and Other Disorders of the Extrahepatic Bile Ducts. Liver Disease in Children. : Cambridge University Press (CUP); Cambridge University Press (CUP); 2021.

Hayashi, H; Osaka, S; Sakabe, K; Fukami, A; Kishimoto, E; Aihara, E; Sabu, Y; Mizutani, A; Kusuhara, H; Naritaka, N; et al. Modeling Human Bile Acid Transport and Synthesis in Stem Cell-Derived Hepatocytes with a Patient-Specific Mutation. Stem Cell Reports. 2021; 16:309-323.

Asai, A; Miethke, A; Bezerra, JA. Pathogenesis of biliary atresia: defining biology to understand clinical phenotypes. Nature Reviews: Gastroenterology and Hepatology. 2015; 12:342-352.

Teckman, J; Rosenthal, P; Ignacio, RV; Spino, C; Bass, LM; Horslen, S; Wang, K; Magee, JC; Karpen, S; Asai, A; et al. Neonatal cholestasis in children with Alpha-1-AT deficiency is a risk for earlier severe liver disease with male predominance. Hepatology Communications. 2023; 7:e0345.

Peters, AL; Kim, S; Mourya, R; Asai, A; Taylor, A; Rogers, M; Campbell, K; Fei, L; Miethke, A; Balistreri, WF; et al. Recent Increase in Incidence of Severe Acute Hepatitis of Unknown Etiology in Children is Associated with Infection with Adenovirus and Other Nonhepatotropic Viruses. The Journal of Pediatrics. 2023; 259:113439.

Pandurangi, S; Kim, S; Asai, A; Bondoc, A; Balistreri, W; Campbell, K; Miethke, A; Peters, A; Rogers, M; Taylor, A; et al. Customized Postoperative Therapy Improves Bile Drainage in Biliary Atresia: A Single Center Preliminary Report. Journal of Pediatric Surgery. 2023; 58:1483-1488.

Uchida, H; Tiao, GM; Shivakumar, P; Wong, KK Y; Asai, A; Amano, H. Editorial: Infants with cholestasis. Frontiers in Pediatrics. 2023; 11:1175231.

Koch, RL; Soler-Alfonso, C; Kiely, BT; Asai, A; Smith, AL; Bali, DS; Kang, PB; Landstrom, AP; Akman, HO; Burrow, TA; et al. Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource. Molecular Genetics and Metabolism. 2023; 138:107525.

Koch, R; Soler-Alfonso, C; Kiely, B; Asai, A; Smith, A; Bali, D; Kang, P; Landstrom, A; Akman, HO; Burrow, TA; et al. O18: A path forward for patients with glycogen branching enzyme deficiency: Consensus on diagnosing and managing glycogen storage disease type IV*. 2023; 1:100114.

Tominaga, K; Haslam, D; Asai, A. Gas Leak in the Port: Portal Venous Gas Associated With Congenital Cytomegalovirus Colitis. 2022; 3:e267.

Asai, A; Wu, JF; Wang, KS; Yamataka, A; Nio, M; Su, DJ; Short, C; Tsuboi, K; Ochi, T; Sasaki, H; et al. The Outcome of Patients With Cystic Biliary Atresia With Intact Proximal Hepatic Ducts Following Hepatic-Cyst-Jejunostomy. Journal of Pediatric Gastroenterology and Nutrition. 2022; 75:131-137.

Hishida, T; Yamamoto, M; Hishida-Nozaki, Y; Shao, C; Huang, L; Wang, C; Shojima, K; Xue, Y; Hang, Y; Shokhirev, M; et al. In vivo partial cellular reprogramming enhances liver plasticity and regeneration. Cell Reports. 2022; 39:110730.

Li, CZ; Ogawa, H; Ng, SS; Chen, X; Kishimoto, E; Sakabe, K; Fukami, A; Hu, YC; Mayhew, CN; Hellmann, J; et al. Human iPSC-derived hepatocyte system models cholestasis with tight junction protein 2 deficiency. JHEP Reports. 2022; 4:100446.

Bezerra, JA; Asai, A; Tiao, G; Mullapudi, B; Balistreri, WF. Biliary Atresia and Other Disorders of the Extrahepatic Bile Ducts. Liver Disease in Children. : Cambridge University Press (CUP); Cambridge University Press (CUP); 2021.

Clarkston, K; Lee, J; Donoghue, S; Peters, H; Eiroa, H; Shah, AA; Loomes, K; Wen, J; Oliver, M; Hardikar, W; et al. Acute liver dysfunction with delayed peak of serum aminotransferase levels as a presentation of ornithine transcarbamylase deficiency in females. American Journal of Medical Genetics, Part A. 2021; 185:909-915.

Hayashi, H; Osaka, S; Sakabe, K; Fukami, A; Kishimoto, E; Aihara, E; Sabu, Y; Mizutani, A; Kusuhara, H; Naritaka, N; et al. Modeling Human Bile Acid Transport and Synthesis in Stem Cell-Derived Hepatocytes with a Patient-Specific Mutation. Stem Cell Reports. 2021; 16:309-323.

Shinozawa, T; Kimura, M; Cai, Y; Saiki, N; Yoneyama, Y; Ouchi, R; Koike, H; Maezawa, M; Zhang, RR; Dunn, A; et al. High-Fidelity Drug-Induced Liver Injury Screen Using Human Pluripotent Stem Cell-Derived Organoids. Gastroenterology. 2021; 160:831-846.e10.

Sakabe, K; Takebe, T; Asai, A. Organoid Medicine in Hepatology. Clinical Liver Disease. 2020; 15:3-8.

Dillman, JR; DiPaola, FW; Smith, SJ; Barth, RA; Asai, A; Lam, S; Campbell, KM; Bezerra, JA; Tiao, GM; Trout, AT. Prospective Assessment of Ultrasound Shear Wave Elastography for Discriminating Biliary Atresia from other Causes of Neonatal Cholestasis. The Journal of Pediatrics. 2019; 212:60-65.e3.