The Role of the Body in Pandemic Geographies of Encounter: Anti-Restriction Protesters Between Collective Action and Political Violence

Autor: Sabine Knierbein, Richard Pfeifer

Publikováno v: Urban Planning, Vol 8, Iss 4, Pp 107-118 (2023)

This article looks at public anti-restriction protests by framing public space as a vital component of urban life. It argues that the body is rarely introduced as a scale of spatial analysis and usually plays a more prominent role in the subfields of

Externí odkaz: https://doaj.org/article/337186b469084d15bad7671eb8da7b2e

Correction of pathology in mice displaying Gaucher disease type 1 by a clinically-applicable lentiviral vector

Autor: Maria Dahl, Emma M.K. Smith, Sarah Warsi, Michael Rothe, Maria J. Ferraz, Johannes M.F.G. Aerts, Azadeh Golipour, Claudia Harper, Richard Pfeifer, Daniella Pizzurro, Axel Schambach, Chris Mason, Stefan Karlsson

Publikováno v: Molecular Therapy: Methods & Clinical Development, Vol 20, Iss , Pp 312-323 (2021)

Gaucher disease type 1 (GD1) is an inherited lysosomal disorder with multisystemic effects in patients. Hallmark symptoms include hepatosplenomegaly, cytopenias, and bone disease with varying degrees of severity. Mutations in a single gene, glucosida

Externí odkaz: https://doaj.org/article/07372d5f46f04d9c947be435687180aa

Screening of Chimeric GAA Variants in a Preclinical Study of Pompe Disease Results in Candidate Vector for Hematopoietic Stem Cell Gene Therapy

Autor: Yildirim Dogan, Cecilia N. Barese, Jeffrey W. Schindler, John K. Yoon, Zeenath Unnisa, Swaroopa Guda, Mary E. Jacobs, Christine Oborski, Diana L. Clarke, Axel Schambach, Richard Pfeifer, Claudia Harper, Chris Mason, Niek P. van Til

Pompe disease is a rare genetic neuromuscular disorder caused by acid alpha-glucosidase (GAA) deficiency resulting in lysosomal glycogen accumulation and progressive myopathy. Enzyme replacement therapy (ERT) is the current standard of care, which pr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::89f466bcec75e33a143d065b6b9e12b3
https://doi.org/10.1101/2021.12.28.474352

Correction of pathology in mice displaying Gaucher disease type 1 by a clinically-applicable lentiviral vector

Autor: Christopher E. Mason, Daniella Pizzurro, Stefan Karlsson, Claudia Harper, Maria J. Ferraz, Emma Smith, Axel Schambach, Maria Dahl, Richard Pfeifer, Johannes M. F. G. Aerts, Michael Rothe, Azadeh Golipour, Sarah Warsi

Publikováno v: Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 20, Iss, Pp 312-323 (2021)
Molecular Therapy-Methods and Clinical Development, 20, 312-323. CELL PRESS

Gaucher disease type 1 (GD1) is an inherited lysosomal disorder with multisystemic effects in patients. Hallmark symptoms include hepatosplenomegaly, cytopenias, and bone disease with varying degrees of severity. Mutations in a single gene, glucosida

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da4bd4a9904b2a1ab5b7ccdca1589910
https://pubmed.ncbi.nlm.nih.gov/33511245

Long-term hematopoietic stem cell gene therapy corrects neuromuscular manifestations in preclinical study of Pompe mice

Autor: Abhishek Chiyyeadu, Maurine Braun, Claudia Harper, Christopher E. Mason, Christine Oborski, Daniella Pizzurro, Axel Schambach, Niek P. van Til, Bianling Liu, John K. Yoon, Yildirim Dogan, Richard Pfeifer, Swaroopa Guda, Cecilia Barese, Zeenath Unnisa, Mary Jacobs, Rena Schindler

Publikováno v: Molecular Genetics and Metabolism. 132:S107

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1b5fb46096fd0af34b7066e480ee2072
https://doi.org/10.1016/j.ymgme.2020.12.263