Asako Tajima Institute of Cellular Therapeutics Allegheny Health Network Biography Publications Institution JoVE Articles Asako Tajima has not added a biography. If you are Asako Tajima and would like to personalize this page please email our Author Liaison for assistance. Publications Bioengineering Thymus Organoids to Restore Thymic Function and Induce Donor-Specific Immune Tolerance to Allografts Molecular Therapy : the Journal of the American Society of Gene Therapy. Jul, 2015 | Pubmed ID: 25903472 Bioengineering Mini Functional Thymic Units with EAK16-II/EAKIIH6 Self-assembling Hydrogel Clinical Immunology (Orlando, Fla.). Sep, 2015 | Pubmed ID: 25805654 Evolution of Hepatic Steatosis to Fibrosis and Adenoma Formation in Liver-specific Growth Hormone Receptor Knockout Mice Frontiers in Endocrinology. 2014 | Pubmed ID: 25566190 Compromised Central Tolerance of ICA69 Induces Multiple Organ Autoimmunity Journal of Autoimmunity. Sep, 2014 | Pubmed ID: 25088457 Mutational Analyses of the ATP6V1B1 and ATP6V0A4 Genes in Patients with Primary Distal Renal Tubular Acidosis Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. Aug, 2013 | Pubmed ID: 23729491 Diagnostic Usefulness of 3 Tesla MRI of the Brain for Cushing Disease in a Child Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology. Oct, 2011 | Pubmed ID: 23926401 Gaucher Disease Patient with Myoclonus Epilepsy and a Novel Mutation Pediatric Neurology. Jan, 2010 | Pubmed ID: 20004867 Clinical and Genetic Study of Japanese Patients with Type 3 Gaucher Disease Molecular Genetics and Metabolism. Aug, 2009 | Pubmed ID: 19481486 Roles of Specific Cytokines in Bone Remodeling and Hematopoiesis in Gaucher Disease Pediatrics International : Official Journal of the Japan Pediatric Society. Dec, 2007 | Pubmed ID: 18045304 Successful Intrauterine Therapy for Fetal Goitrous Hypothyroidism During Late Gestation Endocrine Journal. Dec, 2007 | Pubmed ID: 17917306 Identification and Functional Analysis of the Novel S179R POU1F1 Mutation Associated with Combined Pituitary Hormone Deficiency The Journal of Clinical Endocrinology and Metabolism. Dec, 2006 | Pubmed ID: 16968807 A Novel Mutation of the Arginine Vasopressin Receptor 2 Gene in a Patient with Congenital Nephrogenic Diabetes Insipidus Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology. 2005 | Pubmed ID: 24790307 促进FACS纯化的胸腺上皮细胞的3-D聚合，EAK 16-II / EAKIIH6自组装凝胶 Asako Tajima1, Wen Liu2, Isha Pradhan1, Suzanne Bertera1, Robert A. Lakomy1, William A. Rudert1, Massimo Trucco1,3, Wilson S. Meng2, Yong Fan1,3 1Institute of Cellular Therapeutics, Allegheny Health Network, 2Division of Pharmaceutical Sciences, Mylan School of Pharmacy, Duquesne University, 3Department of Biological Sciences, Carnegie Mellon University Immunology and Infection
促进FACS纯化的胸腺上皮细胞的3-D聚合，EAK 16-II / EAKIIH6自组装凝胶 Asako Tajima1, Wen Liu2, Isha Pradhan1, Suzanne Bertera1, Robert A. Lakomy1, William A. Rudert1, Massimo Trucco1,3, Wilson S. Meng2, Yong Fan1,3 1Institute of Cellular Therapeutics, Allegheny Health Network, 2Division of Pharmaceutical Sciences, Mylan School of Pharmacy, Duquesne University, 3Department of Biological Sciences, Carnegie Mellon University Immunology and Infection
