Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Kevin Barr"'
Autor:
Rafael E. Sanchez‐Pupo, Garth A. Finch, Danielle E. Johnston, Heather Craig, Rober Abdo, Kevin Barr, Steven Kerfoot, Lina Dagnino, Silvia Penuela
Publikováno v:
Molecular Oncology, Vol 18, Iss 4, Pp 969-987 (2024)
Immunotherapies for malignant melanoma seek to boost the anti‐tumoral response of CD8+ T cells, but have a limited patient response rate, in part due to limited tumoral immune cell infiltration. Genetic or pharmacological inhibition of the pannexin
Externí odkaz:
https://doaj.org/article/b28427d0e04740b4a538b40b328ea249
Publikováno v:
Bio-Protocol, Vol 13, Iss 17 (2023)
In this article, we provide a method to isolate embryonic melanoblasts from reporter mouse strains. The mice from which these cells are isolated are bred into the ROSA26mT/mG reporter background, which results in green fluorescent protein (GFP) expre
Externí odkaz:
https://doaj.org/article/ac677553f4f6454e9644a8523748a618
Publikováno v:
Disease Models & Mechanisms, Vol 14, Iss 1 (2021)
Connexin 30 (Cx30; also known as Gjb6 when referring to the mouse gene) is expressed in ependymal cells of the brain ventricles, in leptomeningeal cells and in astrocytes rich in connexin 43 (Cx43), leading us to question whether patients harboring G
Externí odkaz:
https://doaj.org/article/121be252cf8e4df59e7baeee4bcc6659
Autor:
Akina Au, Qing Shao, Kyra K. White, Sergiu A. Lucaciu, Jessica L. Esseltine, Kevin Barr, Dale W. Laird
Publikováno v:
Biomolecules, Vol 10, Iss 10, p 1443 (2020)
When considering connexin expression and regulation, the epidermis of the skin is one of the most complex tissues found in mammals even though it largely contains a single cell type, the keratinocyte. In the rodent epidermis, up to 9 connexin family
Externí odkaz:
https://doaj.org/article/7bfec1a2523344e28e9a65d35467aae5
Publikováno v:
Developmental Dynamics.
Background: We previously determined a nonlinear relationship between connexin 43 (Cx43) function and craniofacial phenotypic variation in the mutant mouse model G60S/+, and that this variation was driven by nasal bone deviation. While nonlinearities
Autor:
Brooke L. O’Donnell, Rafael E. Sanchez-Pupo, Samar Sayedyahossein, Mehdi Karimi, Mehrnoosh Bahmani, Christopher Zhang, Danielle Johnston, John J. Kelly, C. Brent Wakefield, Kevin Barr, Lina Dagnino, Silvia Penuela
Publikováno v:
Journal of Investigative Dermatology.
Autor:
Brooke L. O’Donnell, Rafael E. Sanchez-Pupo, Samar Sayedyahossein, Mehdi Karimi, Mehrnoosh Bahmani, Christopher Zhang, Danielle Johnston, John J. Kelly, C. Brent Wakefield, Kevin Barr, Lina Dagnino, Silvia Penuela
The channel-forming glycoprotein Pannexin 3 (PANX3) functions in cutaneous wound healing and keratinocyte differentiation, but its role in skin homeostasis through aging is not yet understood. We found that PANX3 is absent in newborn skin but becomes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::059c67cd5c92d2a30b8e8afc53c8a5cf
https://doi.org/10.1101/2022.07.13.499920
https://doi.org/10.1101/2022.07.13.499920
Autor:
Abigail G. Wolpe, Melissa A. Luse, Scott R. Johnstone, Jianxiang Xue, Vikram Sabapathy, Brent Wakefield, Rahul Sharma, Kevin Barr, Frank Beier, Dale Laird, Stefanie Redemann, Linda Columbus, Silvia Penuela, Brant E. Isakson
Publikováno v:
Paediatrics Publications
Pannexin channel isoforms (Panx1-3) are thought to release nucleotides into the extracellular milieu and have been shown to effect vascular hemodynamics. For this reason, we examined their mRNA and protein expression in hypertensive humans and geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35de790385b481a395b6d6aecddd2669
https://ir.lib.uwo.ca/paedpub/762
https://ir.lib.uwo.ca/paedpub/762
Publikováno v:
The FASEB Journal. 36
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 486
International Journal of Molecular Sciences, Vol 23, Iss 486, p 486 (2022)
International Journal of Molecular Sciences
Neuroscience Institute Publications
International Journal of Molecular Sciences, Vol 23, Iss 486, p 486 (2022)
International Journal of Molecular Sciences
Neuroscience Institute Publications
Although inherited GJA1 (encoding Cx43) gene mutations most often lead to oculodentodigital dysplasia and related disorders, four variants have been linked to erythrokeratodermia variabilis et progressiva (EKVP), a skin disorder characterized by eryt