Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Stefanos Kalomoiris"'
Autor:
Baarkullah Awan, David Turkov, Cameron Schumacher, Antonio Jacobo, Amber McEnerney, Ashley Ramsey, Gege Xu, Dayoung Park, Stefanos Kalomoiris, Wei Yao, Li-En Jao, Miguel L. Allende, Carlito B. Lebrilla, Fernando A. Fierro
Publikováno v:
Stem Cell Reports, Vol 11, Iss 2, Pp 325-333 (2018)
Summary: Since hundreds of clinical trials are investigating the use of multipotent stromal cells (MSCs) for therapeutic purposes, effective delivery of the cells to target tissues is critical. We have found an unexplored mechanism, by which basic fi
Externí odkaz:
https://doaj.org/article/ce444aabfa97499b803810207be599ce
Autor:
Kyle D. Fink Ph.D, Peter Deng, Josh Gutierrez, Joseph S. Anderson, Audrey Torrest, Anvita Komarla, Stefanos Kalomoiris, Whitney Cary, Johnathon D. Anderson, William Gruenloh, Alexandra Duffy, Teresa Tempkin, Geralyn Annett, Vicki Wheelock, David J. Segal, Jan A. Nolta
Publikováno v:
Cell Transplantation, Vol 25 (2016)
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by an abnormal expansion of CAG repeats. Although pathogenesis has been attributed to this polyglutamine expansion, the underlying mechanisms through which the hunti
Externí odkaz:
https://doaj.org/article/60ffe3d02b6247aa90a1db31550cc403
Preclinical evaluation of mesenchymal stem cells overexpressing VEGF to treat critical limb ischemia
Autor:
Julie R Beegle, Nataly Lessa Magner, Stefanos Kalomoiris, Aja Harding, Ping Zhou, Catherine Nacey, Jeannine Logan White, Karen Pepper, William Gruenloh, Geralyn Annett, Jan A Nolta, Fernando A Fierro
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 3, Iss C (2016)
Numerous clinical trials are utilizing mesenchymal stem cells (MSC) to treat critical limb ischemia, primarily for their ability to secrete signals that promote revascularization. These cells have demonstrated clinical safety, but their efficacy has
Externí odkaz:
https://doaj.org/article/f5d2146d36424c12ac8287fae4099f7b
Autor:
Li-En Jao, Miguel L. Allende, Stefanos Kalomoiris, Dayoung Park, Antonio Jacobo, Ashley Ramsey, Wei Yao, Cameron Schumacher, Carlito B. Lebrilla, David Turkov, Fernando A. Fierro, Amber McEnerney, Baarkullah Awan, Gege Xu
Publikováno v:
Stem Cell Reports, Vol 11, Iss 2, Pp 325-333 (2018)
Stem cell reports, vol 11, iss 2
Stem Cell Reports
Stem cell reports, vol 11, iss 2
Stem Cell Reports
Summary Since hundreds of clinical trials are investigating the use of multipotent stromal cells (MSCs) for therapeutic purposes, effective delivery of the cells to target tissues is critical. We have found an unexplored mechanism, by which basic fib
Publikováno v:
Journal of Cellular Biochemistry. 117:300-307
Mesenchymal stem cells (MSC) are currently being tested clinically for a plethora of conditions, with most approaches relying on the secretion of paracrine signals by MSC to modulate the immune system, promote wound healing, and induce angiogenesis.
Publikováno v:
STEM CELLS. 32:1074-1082
Multipotent mesenchymal stromal cells (MSCs) are ideal candidates for different cellular therapies due to their simple isolation, extensive expansion potential, and low immunogenicity. For various therapeutic approaches, such as bone and cartilage re
Autor:
Kyle D. Fink, Joseph S. Anderson, Anvita Komarla, Johnathon D. Anderson, Audrey Torrest, David J. Segal, Peter Deng, Stefanos Kalomoiris, Vicki L. Wheelock, Alexandra Duffy, Josh Gutierrez, Teresa Tempkin, Jan A. Nolta, William Gruenloh, Geralyn Annett, Whitney Cary
Publikováno v:
Cell transplantation, vol 25, iss 4
Cell Transplantation, Vol 25 (2016)
Fink, KD; Deng, P; Gutierrez, J; Anderson, JS; Torrest, A; Komarla, A; et al.(2016). Allele-specific reduction of the mutant huntingtin allele using transcription activator-like effectors in human huntington’s disease fibroblasts. Cell Transplantation, 25(4), 677-686. doi: 10.3727/096368916X690863. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/93x8z46g
Cell Transplantation, Vol 25 (2016)
Fink, KD; Deng, P; Gutierrez, J; Anderson, JS; Torrest, A; Komarla, A; et al.(2016). Allele-specific reduction of the mutant huntingtin allele using transcription activator-like effectors in human huntington’s disease fibroblasts. Cell Transplantation, 25(4), 677-686. doi: 10.3727/096368916X690863. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/93x8z46g
© 2016 Cognizant, LLC. Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder caused by an abnormal expansion of CAG repeats. Although pathogenesis has been attributed to this polyglutamine expansion, the underlying mechanis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46bfd6e38b90b92ff0b5eaacc1c782a0
https://escholarship.org/uc/item/93x8z46g
https://escholarship.org/uc/item/93x8z46g
Autor:
Whitney Cary, Kari Pollock, Stefanos Kalomoiris, Gaela Mitchell, Heather Stewart, Catherine Nacey, Scott D. Olson, Jan A. Nolta, Karen Pepper, Amal Kambal
Publikováno v:
Molecular and Cellular Neuroscience. 49:271-281
Huntington’s disease (HD) is a fatal, autosomal dominant neurodegenerative disorder caused by an expanded trinucleotide (CAG) repeat in exon 1 of the huntingtin gene (Htt). This expansion creates a toxic polyglutamine tract in the huntingtin protei
Autor:
Scott D. Olson, Suzanne Pontow, Yunjoon Jung, Todd E. Meyerrose, Jan A. Nolta, Geralyn Annett, Gerhard Bauer, Stefanos Kalomoiris
Publikováno v:
Advanced Drug Delivery Reviews. 62:1167-1174
Mesenchymal stem cells (MSC) are a promising tool for cell therapy, either through direct contribution to the repair of bone, tendon and cartilage or as an adjunct therapy through protein production and immune mediation. They are an attractive vehicl
Autor:
Alexandria Duffy, Haley Nelson, Joshua Gutierrez, Gerhard Bauer, Heather Dahlenburg, Jan A. Nolta, Karen Pepper, Geralyn Annett, William Gruenloh, Stefanos Kalomoiris, Vicki L. Wheelock, Audrey Torrest, Kyle Hendrix, Johnathon D. Anderson, Peter Deng, Brian Fury, Kyle D. Fink, Catherine Nacey, Whitney Cary, Theresa Tempkin, Kari Pollock, Jeannine McGee
Publikováno v:
Molecular Therapy
Molecular therapy : the journal of the American Society of Gene Therapy, vol 24, iss 5
Molecular therapy : the journal of the American Society of Gene Therapy, vol 24, iss 5
Huntington's disease (HD) is a fatal degenerative autosomal dominant neuropsychiatric disease that causes neuronal death and is characterized by progressive striatal and then widespread brain atrophy. Brain-derived neurotrophic factor (BDNF) is a lea