Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Brian Gloss"'
Autor:
Yolanda Colino-Sanguino, Laura Rodriguez de la Fuente, Brian Gloss, Andrew M.K. Law, Kristina Handler, Marina Pajic, Robert Salomon, David Gallego-Ortega, Fatima Valdes-Mora
Publikováno v:
Heliyon, Vol 10, Iss 17, Pp e37185- (2024)
Single-cell transcriptomics has emerged as the preferred tool to define cell identity through the analysis of gene expression signatures. However, there are limited studies that have comprehensively compared the performance of different scRNAseq syst
Externí odkaz:
https://doaj.org/article/d3384de68ec04f0ba843ae1f7fd84e1d
Autor:
Gaurav Sutrave, Ning Xu, Tiffany C.Y. Tang, Alla Dolnikov, Brian Gloss, David J. Gottlieb, Kenneth P. Micklethwaite, Kavitha Gowrishankar
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 25, Iss , Pp 250-263 (2022)
Chimeric antigen receptor (CAR) T cells targeting CD19 have demonstrated remarkable efficacy in the treatment of B cell malignancies. Current CAR T cell manufacturing protocols are complex and costly due to their reliance on viral vectors. Non-viral
Externí odkaz:
https://doaj.org/article/3c81a532e7eb410fa741a50dda3035f5
Autor:
Dmitrii Shek, Brian Gloss, Joey Lai, Li Ma, Hui E. Zhang, Matteo S. Carlino, Hema Mahajan, Adnan Nagrial, Bo Gao, Scott A. Read, Golo Ahlenstiel
Publikováno v:
Methods and Protocols, Vol 6, Iss 2, p 35 (2023)
Increasing evidence strongly supports the key role of the tumour microenvironment in response to systemic therapy, particularly immune checkpoint inhibitors (ICIs). The tumour microenvironment is a complex tapestry of immune cells, some of which can
Externí odkaz:
https://doaj.org/article/895c56f178b948e095da66e3a1f1eeb8
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 19, p 11125 (2022)
Rett syndrome (RTT) is a rare disorder and one of the most abundant causes of intellectual disabilities in females. Single mutations in the gene coding for methyl-CpG-binding protein 2 (MeCP2) are responsible for the disorder. MeCP2 regulates gene ex
Externí odkaz:
https://doaj.org/article/5111da5d45fc47e8a7d808a7df5f8e51
Autor:
Ya Wang, Brian Gloss, Benjamin Tang, Suat Dervish, Brigitte Santner-Nanan, Christina Whitehead, Kristy Masters, Kristen Skarratt, Sally Teoh, Stephen Schibeci, Nicole Fewings, Chrystelle Brignone, Frederic Triebel, David Booth, Anthony McLean, Marek Nalos
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Sepsis is associated with a dysregulated inflammatory response to infection. Despite the activation of inflammation, an immune suppression is often observed, predisposing patients to secondary infections. Therapies directed at restoration of immunity
Externí odkaz:
https://doaj.org/article/660d1f9b389346e5ab5b6fa59f1016a4
Autor:
David Jonathan Gottlieb, Leighton Edward Clancy, Barbara Withers, Helen Marie McGuire, Fabio Luciani, Mandeep Singh, Brendan Hughes, Brian Gloss, David Kliman, Chun Kei Kris Ma, Shyam Panicker, David Bishop, Ming‐Celine Dubosq, Ziduo Li, Selmir Avdic, Kenneth Micklethwaite, Emily Blyth
Publikováno v:
Clinical & Translational Immunology, Vol 10, Iss 3, Pp n/a-n/a (2021)
Abstract Objectives Adoptive immunotherapy using donor‐derived antigen‐specific T‐cells can prevent and treat infection after allogeneic haemopoietic stem cell transplant (HSCT). Methods We treated 11 patients with a prophylactic infusion of 2
Externí odkaz:
https://doaj.org/article/c6d93492015040e8973b59141979120a
Autor:
Yolanda Colino-Sanguino, Laura Rodriguez de la Fuente, Brian Gloss, Andrew M. K. Law, Kristina Handler, Marina Pajic, Robert Salomon, David Gallego-Ortega, Fatima Valdes-Mora
Single-cell transcriptomics has emerged as the preferred tool to define cell identity through the analysis of gene expression signatures. However, there are limited studies that have comprehensively compared the performance of different scRNAseq syst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea0f7cd54c6fe7433a22db3329d1bd14
https://doi.org/10.1101/2023.04.04.535585
https://doi.org/10.1101/2023.04.04.535585
Rett syndrome (RTT) is a rare disease and one of the most abundant causes for intellectual disa-bilities in females. Single mutations in the gene coding for methyl-CpG-binding protein 2 (MECP2), are responsible for the disease. MeCP2 regulates gene e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5f9b2230c315f9970dc4cd42fea5277
Publikováno v:
International journal of molecular sciences. 23(19)
Rett syndrome (RTT) is a rare disorder and one of the most abundant causes of intellectual disabilities in females. Single mutations in the gene coding for methyl-CpG-binding protein 2 (MeCP2) are responsible for the disorder. MeCP2 regulates gene ex
Autor:
Cristian David Peña Martinez, Mahdi Zeraati, Romain Rouet, Ohan Mazigi, Brian Gloss, Chia-Ling Chan, Tracy M. Bryan, Nicole M. Smith, Marcel E. Dinger, Sarah Kummerfeld, Daniel Christ
DNA i-motif structures are formed in the nucleus of human cells and are believed to provide critical genomic regulation. While the existence of i-motif structures in human cells has been demonstrated by immunofluorescent staining and by characterisat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b24a6e4851a8dc26d37a9913721aa66
https://doi.org/10.1101/2022.04.14.488274
https://doi.org/10.1101/2022.04.14.488274