Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ainslie Derrick-Roberts"'
Autor:
Ainslie Derrick-Roberts
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 30, Iss, Pp 100831-(2022)
Autor:
Ainslie Derrick-Roberts, Xenia Kaidonis, Matilda R. Jackson, Wan Chin Liaw, XiaoDan Ding, Chun Ong, Enzo Ranieri, Peter Sharp, Janice Fletcher, Sharon Byers
Publikováno v:
Molecular Genetics and Metabolism. 135:114
Publikováno v:
Molecular Genetics and Metabolism. 123:S84
Autor:
Ainslie Derrick Roberts, Marleesa Ly, Sharon Byers, Donald S. Anson, Xenia Kaidonis, Wan Chin Liaw
Publikováno v:
European Journal of Human Genetics. 18:194-199
Neurological pathology is characteristic of the mucopolysaccharidoses (MPSs) that store heparan sulphate (HS) glycosaminoglycan (gag) and has been proven to be refractory to systemic therapies. Substrate deprivation therapy (SDT) using general inhibi
Autor:
Matilda R. Jackson, Ellenore Martin, Stan Gronthos, Ainslie Derrick Roberts, Nathan Rout-Pitt, Sharon Byers
Mucopolysaccharidoses (MPS) are inherited metabolic disorders that arise from a complete loss or a reduction in one of eleven specific lysosomal enzymes. MPS children display pathology in multiple cell types leading to tissue and organ failure and ea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ec51b95f5bc91a226eac85d22725cb7
https://hdl.handle.net/11541.2/28170
https://hdl.handle.net/11541.2/28170
Publikováno v:
Molecular Genetics and Metabolism. 117:S72
Autor:
Sharon Byers, Ainslie Derrick Roberts, Enzo Ranieri, Peter R. Clements, Donald S. Anson, Chantelle McIntyre
Publikováno v:
Molecular genetics and metabolism. 93(4)
Mucopolysaccharidosis type IIIA (MPS IIIA) is a heritable glycosaminoglycan (GAG) storage disorder which is characterised by lysosomal accumulation of heparan sulphate, secondary to a deficiency of sulphamidase (heparan-N-sulphatase, N-sulphoglucosam