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المؤلفون: Patrick Bertolino, Anton Cozijnsen, Stephen J. Turner, Mireille H. Lahoud, Daniel Fernandez-Ruiz, Benjamin J. Compton, Matthias H. Enders, Lauren E. Holz, Geoffrey I. McFadden, Kathryn J. Farrand, Kirsteen M. Tullett, Ana Maria Valencia-Hernandez, Juby Mathew, Ian F. Hermans, Taryn L. Osmond, Dale I. Godfrey, William R. Heath, David G. Bowen, Vanessa Mollard, Rose May, Thiago M. Steiner, Zhongfang Wang, Gavin F. Painter, Joshua Lange, Lynette Beattie, Catarina F. Almeida, Lukasz Kedzierski, Sarah L. Draper, Jasmine Li, Susanna T. S. Chan, Maria N. de Menezes, Yu Cheng Chua, Katherine Kedzierska, Irina Caminschi, Sonia Ghilas, Regan J. Anderson, Rebecca Seneviratna
المصدر: Science Immunology. 5
مصطلحات موضوعية: 0301 basic medicine, Synthetic vaccine, biology, medicine.medical_treatment, Immunology, General Medicine, Natural killer T cell, Major histocompatibility complex, Virology, Epitope, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Immune system, 030220 oncology & carcinogenesis, biology.protein, medicine, Cytotoxic T cell, Adjuvant, CD8
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d50a1f0e1adb3904171a8633891b9161
https://doi.org/10.1126/sciimmunol.aaz8035 -
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المؤلفون: S. Udhaya Kumar, Saravanamuthu Thiyagarajan, Meenakshi Bhat, Juby Mathew, Sudha Srinivasan, Sujatha Jagadeesh
المصدر: Molecular Genetics and Metabolism Reports, Vol 4, Iss C, Pp 53-61 (2015)
Molecular Genetics and Metabolism Reportsمصطلحات موضوعية: Mucopolysaccharidosis VI (MPS VI), Arylsulfatase B, ARSB, arylsulfatase B, Population, India, LSD, lysosomal storage disorder, GAG, glycosaminoglycan, Lysosomal storage disorder (LSD), Biology, MPS, mucopolysaccharidosis, medicine.disease_cause, HSCT, hematopoietic stem cell transplantation, Endocrinology, VUS, variants of unknown significance, Genetics, medicine, MPS - Mucopolysaccharidosis, education, Arylsulfatase B (ARSB), lcsh:QH301-705.5, Molecular Biology, Gene, GALNS, N-acetyl galactosamine 6-sulfatase, lcsh:R5-920, education.field_of_study, Mutation, Maroteaux–Lamy syndrome, Active site, Mucopolysaccharidosis VI, medicine.disease, Lysosomal enzyme, ERT, enzyme replacement therapy, lcsh:Biology (General), Inborn error of metabolism (IEM), Inborn error of metabolism, PCT, pharmacological chaperone therapy, HGMD, Human Gene Mutation Database, lcsh:Medicine (General), Mutations, Research Paper