Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Paul T. Toran"'
Autor:
Brian M. Barth, Weiyuan Wang, Paul T. Toran, Todd E. Fox, Charyguly Annageldiyev, Regina M. Ondrasik, Nicole R. Keasey, Timothy J. Brown, Viola G. Devine, Emily C. Sullivan, Andrea L. Cote, Vasiliki Papakotsi, Su-Fern Tan, Sriram S. Shanmugavelandy, Tye G. Deering, David B. Needle, Stephan T. Stern, Junjia Zhu, Jason Liao, Aaron D. Viny, David J. Feith, Ross L. Levine, Hong-Gang Wang, Thomas P. Loughran, Jr, Arati Sharma, Mark Kester, David F. Claxton
Publikováno v:
Blood Advances, Vol 3, Iss 17, Pp 2598-2603 (2019)
Externí odkaz:
https://doaj.org/article/c4625d35b02b4dee8bf8588d9b18b16d
Autor:
Charyguly Annageldiyev, Nicole R. Keasey, Emily Sullivan, Paul T. Toran, Hong Gang Wang, Regina M. Ondrasik, Su Fern Tan, Andrea L. Cote, Tye G. Deering, Todd E. Fox, David J. Feith, Brian M. Barth, Timothy J Brown, Stephan T. Stern, Mark Kester, David F. Claxton, Thomas P. Loughran, Vasiliki Papakotsi, Arati Sharma, Ross L. Levine, David B. Needle, Junjia Zhu, Sriram S. Shanmugavelandy, Aaron D. Viny, Viola Devine, Weiyuan Wang, Jason Liao
Publikováno v:
Blood Advances. 3:2598-2603
Key Points Distinct sphingolipid metabolism of AML with MDS-related changes defines unique sensitivity to nanoliposomal C6-ceramide. Vinblastine alters sphingolipid metabolism to enhance the sensitivity of AML to nanoliposomal C6-ceramide.
Publikováno v:
Exp Hematol
As important vectors for ectopic protein expression, gene silencing, and progenitor cell barcoding, lentiviruses continue to emerge as versatile research and clinical tools. For studies employing cell types that are relatively resistant to transducti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17eb7204bda76b455b4b333e5a6bacb2
https://europepmc.org/articles/PMC7372909/
https://europepmc.org/articles/PMC7372909/
Autor:
Paul T. Toran, Vladislav B. Bergo, Jeffrey C. Silva, Ghaith M. Hamza, M. Paola Castaldi, Camilla R. Worsfold, Don M. Wojchowski, Sergey Mamaev
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 6, p 2016 (2020)
Volume 21
Issue 6
International Journal of Molecular Sciences, Vol 21, Iss 6, p 2016 (2020)
Volume 21
Issue 6
The ability to quantitatively probe diverse panels of proteins and their post-translational modifications (PTMs) across multiple samples would aid a broad spectrum of biological, biochemical and pharmacological studies. We report a novel, microarray
Publikováno v:
International journal of biopharmaceutical sciences. 1(2)
Sphingolipids represent one of the major classes of bioactive lipids. Studies of sphingolipids have intensified in the past several years, revealing their roles in nearly all cell biological processes. In addition, epigenetic regulation has gained su
Autor:
Colin M, McGill, Timothy J, Brown, Yuan-Yin, Cheng, Lindsey N, Fisher, Sriram S, Shanmugavelandy, Sally J, Gustafson, Kriya L, Dunlap, Mary Ann, Lila, Mark, Kester, Paul T, Toran, David F, Claxton, Brian M, Barth
Publikováno v:
International journal of biopharmaceutical sciences. 1(1)
Acute myeloid leukemia (AML) is an aggressive hematological malignancy with high incidence in the aging population. In addition, AML is one of the more common pediatric malignancies. Unfortunately, both of these patient groups are quite sensitive to
Autor:
Brian M. Barth, Emily Sullivan, Thomas P. Loughran, Vasiliki Papakotsi, Sarah R. Walker, Paul T. Toran, Weiyuan Wang, Andrea L. Cote
Publikováno v:
Blood. 134:1700-1700
Myelodysplastic syndrome (MDS) is a clonal hematopoietic disorder characterized by ineffective hematopoiesis, cytopenias, and an increased risk of transformation to acute myeloid leukemia. New studies are urgently needed to understand the underlying
SummaryHemochromatosis is caused by mutations in HFE, a protein that competes with transferrin (TF) for binding to transferrin receptor 1 (TFR1). We developed mutant mouse strains to gain insight into the role of the Hfe/Tfr1 complex in regulating ir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6906444418748ce23d036ed58a3b7f8
https://resolver.caltech.edu/CaltechAUTHORS:20170327-141608645
https://resolver.caltech.edu/CaltechAUTHORS:20170327-141608645
Publikováno v:
Blood. 108:267-267
Hemochromatosis is a common genetic disease resulting from increased dietary iron absorption and tissue iron deposition. Mutations in five unrelated genes are known to cause hemochromatosis in humans and mice. These encode the classic hemochromatosis