Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Alexandra T. Star"'
Autor:
Anna Jezierski, Jez Huang, Arsalan S. Haqqani, Julie Haukenfrers, Ziying Liu, Ewa Baumann, Caroline Sodja, Claudie Charlebois, Christie E. Delaney, Alexandra T. Star, Qing Liu, Danica B. Stanimirovic
Publikováno v:
Fluids and Barriers of the CNS, Vol 20, Iss 1, Pp 1-20 (2023)
Abstract Blood brain barrier (BBB) models in vitro are an important tool to aid in the pre-clinical evaluation and selection of BBB-crossing therapeutics. Stem cell derived BBB models have recently demonstrated a substantial advantage over primary an
Externí odkaz:
https://doaj.org/article/80fa25998cc847f2a3c4935dc2ccbd5b
Autor:
Arsalan S. Haqqani, Zainab Mianoor, Alexandra T. Star, Flavie E. Detcheverry, Christie E. Delaney, Danica B. Stanimirovic, Edith Hamel, AmanPreet Badhwar
Publikováno v:
Biology, Vol 12, Iss 12, p 1500 (2023)
Cerebrovascular pathology that involves altered protein levels (or signaling) of the transforming growth factor beta (TGFβ) family has been associated with various forms of age-related dementias, including Alzheimer disease (AD) and vascular cogniti
Externí odkaz:
https://doaj.org/article/cf0d6b392e1244ee84500453668f48fd
Autor:
Wandong Zhang, Qing Yan Liu, Arsalan S. Haqqani, Sonia Leclerc, Ziying Liu, François Fauteux, Ewa Baumann, Christie E. Delaney, Dao Ly, Alexandra T. Star, Eric Brunette, Caroline Sodja, Melissa Hewitt, Jagdeep K. Sandhu, Danica B. Stanimirovic
Publikováno v:
Fluids and Barriers of the CNS, Vol 17, Iss 1, Pp 1-17 (2020)
Abstract Receptor-mediated transcytosis (RMT) is a principal pathway for transport of macromolecules essential for brain function across the blood–brain barrier (BBB). Antibodies or peptide ligands which bind RMT receptors are often co-opted for br
Externí odkaz:
https://doaj.org/article/0b303c3f54f44cd1a6df157f40dd7f54
Autor:
Aline Do Minh, Alexandra T. Star, Jacek Stupak, Kelly M. Fulton, Arsalan S. Haqqani, Jean-François Gélinas, Jianjun Li, Susan M. Twine, Amine A. Kamen
Publikováno v:
Viruses, Vol 13, Iss 5, p 797 (2021)
Lentiviral vectors (LVs) are a powerful tool for gene and cell therapy and human embryonic kidney cells (HEK293) have been extensively used as a platform for production of these vectors. Like most cells and cellular tissues, HEK293 cells release extr
Externí odkaz:
https://doaj.org/article/ae60cfc5f989402bb956d971cc196cd8
Autor:
Amine Kamen, Susan M. Twine, Jean-François Gélinas, Alexandra T. Star, Jacek Stupak, Arsalan S. Haqqani, Aline Do Minh, Kelly M. Fulton, Jianjun Li
Publikováno v:
Viruses, Vol 13, Iss 797, p 797 (2021)
Viruses
Volume 13
Issue 5
Viruses
Volume 13
Issue 5
Lentiviral vectors (LVs) are a powerful tool for gene and cell therapy and human embryonic kidney cells (HEK293) have been extensively used as a platform for production of these vectors. Like most cells and cellular tissues, HEK293 cells release extr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b424fef9e647a0f708a91048f3f86c5e
https://www.mdpi.com/1999-4915/13/5/797
https://www.mdpi.com/1999-4915/13/5/797
Autor:
Alexandra T. Star, Jacek Stupak, Amine Kamen, Susan M. Twine, Aline Do Minh, Jianjun Li, Jean-François Gélinas
Lentiviral vectors (LVs) are a powerful tool for gene and cell therapy and human embryonic kidney cells (HEK293) have been extensively used as a platform for production of these vectors. Like most cells and cellular tissues, HEK293 cells release extr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67191f754e503b3f44dc6621e102d0a4
https://doi.org/10.20944/preprints202103.0696.v1
https://doi.org/10.20944/preprints202103.0696.v1
Autor:
Sonia Leclerc, Alexandra T. Star, Ziying Liu, Dao Ly, Arsalan S. Haqqani, Caroline Sodja, Qing Yan Liu, Wandong Zhang, Jagdeep K. Sandhu, Eric Brunette, Ewa Baumann, François Fauteux, Danica Stanimirovic, Christie Delaney, Melissa Hewitt
Publikováno v:
Fluids and Barriers of the CNS, Vol 17, Iss 1, Pp 1-17 (2020)
Fluids and Barriers of the CNS
Fluids and Barriers of the CNS
Receptor-mediated transcytosis (RMT) is a principal pathway for transport of macromolecules essential for brain function across the blood-brain barrier (BBB). Antibodies or peptide ligands which bind RMT receptors are often co-opted for brain deliver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9198f63fc7d8f4add55f721bfce74185
https://doi.org/10.1186/s12987-020-00209-0
https://doi.org/10.1186/s12987-020-00209-0
Autor:
Wandong Zhang, Qing Yan Liu, Arsalan S. Haqqani, Sonia Leclerc, Joy Lei, Francois Fauteux, Ewa Baumann, Christie E. Delaney, Dao Ly, Alexandra T. Star, Eric Brunette, Caroline Sodja, Melissa Hewitt, Jagdeep K. Sandhu, Danica B. Stanimirovic
Receptor-mediated transcytosis (RMT) is a principal pathway for transport of macromolecules essential for brain function across the blood-brain barrier (BBB). Antibodies or peptide ligands which bind RMT receptors are often co-opted for brain deliver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fce762c0283940349487f07665063c20
https://doi.org/10.21203/rs.3.rs-16449/v1
https://doi.org/10.21203/rs.3.rs-16449/v1
Autor:
Alexandra T. Star, Heidi M. McBride, Thomas M. Durcan, Elizabeth M. Meiering, Myriam Gagné, Janice Robertson, Christine Vande Velde, Jean-François Trempe, Sabrina Semmler, Neil R. Cashman, Pranav Garg, Elise Caron, Andrew N. Bayne, Nathalie Grandvaux, Steven S. Plotkin, Laurie Destroismaisons, Yousra Khalfallah, Sarah Pickles, Charlotte Baudouin, Mathilde Chaineau, Arsalan S. Haqqani, Emeline Hamon-Keromen
Publikováno v:
J Biol Chem
Amyotrophic lateral sclerosis (ALS) is a fatal disease, characterized by the selective loss of motor neurons leading to paralysis. Mutations in the gene encoding superoxide dismutase 1 (SOD1) are the second most common cause of familial ALS, and cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e140f4f50d7b9cd9106484395b1381a
https://nrc-publications.canada.ca/eng/view/object/?id=a04144de-e1cd-4b3e-a9fd-85a9f8650044
https://nrc-publications.canada.ca/eng/view/object/?id=a04144de-e1cd-4b3e-a9fd-85a9f8650044
Autor:
Steven S. Plotkin, Neil R. Cashman, Elise Caron, Laurie Destroismaisons, Alexandra T. Star, Mathilde Chaineau, Andrew N. Bayne, Charlotte Baudouin, Christine Vande Velde, Thomas M. Durcan, Yousra Khalfallah, Elizabeth M. Meiering, Heidi M. McBride, Myriam Gagné, Pranav Garg, Janice Robertson, Sabrina Semmler, Sarah Pickles, Arsalan S. Haqqani, Nathalie Grandvaux, Jean-François Trempe, Emeline Hamon-Keromen
Amyotrophic lateral sclerosis (ALS) is a fatal disease, characterized by the selective loss of motor neurons leading to paralysis. Mutations in the gene encoding superoxide dismutase1(SOD1) are the second most common cause of familial ALS, and consid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::231767bf007cffe9a8e0311f65929bfb