Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Daniel A. Kuppers"'
Autor:
Daniel A. Kuppers, Sonali Arora, Yiting Lim, Andrea R. Lim, Lucas M. Carter, Philip D. Corrin, Christopher L. Plaisier, Ryan Basom, Jeffrey J. Delrow, Shiyan Wang, Housheng Hansen He, Beverly Torok-Storb, Andrew C. Hsieh, Patrick J. Paddison
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-17 (2019)
Erythropoiesis can be regulated by transcriptional, epigenetic, and post-transcriptional mechanisms. Here the authors report that N6-methyladenosine mRNA methyltransferase complex stimulates erythropoiesis by promoting translation of specific mRNAs.
Externí odkaz:
https://doaj.org/article/47ac3c50e65642a7995551b19d63d3ca
Autor:
Daniel A Kuppers, Jonathan Linton, Sergio Ortiz Espinosa, Kelly M McKenna, Anthony Rongvaux, Patrick J Paddison
Publikováno v:
PLoS ONE, Vol 18, Iss 6, p e0287052 (2023)
Human CD34+ hematopoietic stem and progenitor cells (HSPCs) are a standard source of cells for clinical HSC transplantations as well as experimental xenotransplantation to generate "humanized mice". To further extend the range of applications of thes
Externí odkaz:
https://doaj.org/article/c40eaaf9412747dea3045397d9b776a9
Autor:
Daniel A Kuppers
Human CD34+ hematopoietic stem and progenitor cells (HSPCs) are a standard source of cells for clinical HSC transplantations as well as experimental xenotransplantation to generate “humanized mice”. To further extend the range of applications of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b029a0b79b33a0c273b55e2b277f143
https://doi.org/10.17504/protocols.io.q26g7y541gwz/v2
https://doi.org/10.17504/protocols.io.q26g7y541gwz/v2
Autor:
Pia Hoellerbauer, Matt C. Biery, Sonali Arora, Yiyun Rao, Emily J. Girard, Kelly Mitchell, Pratiksha Dighe, Megan Kufeld, Daniel A. Kuppers, Jacob A. Herman, Eric C. Holland, Liliana Soroceanu, Nicholas A. Vitanza, James M. Olson, Justin R. Pritchard, Patrick J. Paddison
BackgroundAdult and pediatric tumors display stark differences in their mutation spectra and chromosome alterations. Here, we attempted to identify common and unique gene dependencies and their associated biomarkers among adult and pediatric tumor is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e88e907c9043c2c5a83a45d6372a7f63
https://doi.org/10.1101/2023.01.05.522885
https://doi.org/10.1101/2023.01.05.522885
Autor:
Daniel A. Kuppers, Jonathan Linton, Sergio Ortiz Espinosa, Kelly M. McKenna, Anthony Rongvaux, Patrick J. Paddison
Human CD34+hematopoietic stem and progenitor cells (HSPCs) are a standard source of cells for clinical HSC transplantations as well as experimental xenotransplantation to generate “humanized mice”. To further extend the range of applications of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4a5481ae0e613dd87cd6777d32ad446
https://doi.org/10.1101/2022.10.06.511235
https://doi.org/10.1101/2022.10.06.511235
Autor:
Yiting Lim, Patrick J. Paddison, Housheng Hansen He, Lucas Carter, Andrea R. Lim, Ryan Basom, Jeffrey J. Delrow, Philip Corrin, Shiyan Wang, Christopher L. Plaisier, Daniel A. Kuppers, Beverly Torok-Storb, Andrew C. Hsieh, Sonali Arora
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-17 (2019)
Nature Communications
Nature Communications
Many of the regulatory features governing erythrocyte specification, maturation, and associated disorders remain enigmatic. To identify new regulators of erythropoiesis, we utilize a functional genomic screen for genes affecting expression of the ery
Autor:
Daniel A Kuppers, Harry C Hwang, Aimee L Jackson, Peter S Linsley, Bruce E Clurman, Matthew L Fero
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e14758 (2011)
Mice lacking the p27(Kip1) Cdk inhibitor (Cdkn1b) exhibit increased susceptibility to lymphomas from the Maloney murine leukemia virus (M-MuLV), and exhibit a high frequency of viral integrations at Xpcl1 (Kis2), a locus on the X-chromosome. Xpcl1 en
Externí odkaz:
https://doaj.org/article/d72def821bff4b12b228cd374b202ed2
Autor:
Harry C. Hwang, Daniel A. Kuppers, Lavanya Samraj, Matthew L. Fero, Thomas M. Schmitt, Bruce E. Clurman
Publikováno v:
Oncotarget
// Daniel A. Kuppers 1 , Thomas M. Schmitt 1 , Harry C. Hwang 2 , Lavanya Samraj 3 , Bruce E. Clurman 1 and Matthew L. Fero 4 1 Fred Hutchinson Cancer Research Center, Seattle, Washington, USA 2 Phenopath Laboratories, Seattle, Washington, USA 3 Univ
Autor:
Michael D. Nyquist, Alexandra Corella, Arja Kaipainen, Patrick J. Paddison, Osama Mohamad, Daniel A. Kuppers, Peter S. Nelson, Jared M. Lucas, Ilsa Coleman, Stephen R. Plymate, Elahe A. Mostaghel
Publikováno v:
JCI Insight. 4
Clinical trials of high-dose androgen (HDA) therapy for prostate cancer (PC) have shown promising efficacy but are limited by lack of criteria to identify likely responders. To elucidate factors that govern the growth-repressive effects of HDAs, we a
Autor:
Julie Mathieu, Logeshwaran Somasundaram, Hannele Ruohola-Baker, Sonia B. Sidhu, Aaron M. Robitaille, A. McAlister, T. Bottorff, Damien Detraux, Randall T. Moon, Filippo Artoni, R. D. Hawkins, Daniel A. Kuppers, Patrick J. Paddison, Amy Ferreccio, Carol B. Ware, Christopher Cavanaugh, Shiri Levy, Yuliang Wang, Stephanie L. Battle
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-13 (2019)
Mathieu, J, Detraux, D, Kuppers, D, Wang, Y, Cavanaugh, C, Sidhu, S, Levy, S, Robitaille, A M, Ferreccio, A, Bottorff, T, McAlister, A, Somasundaram, L, Artoni, F, Battle, S, Hawkins, R D, Moon, R T, Ware, C B, Paddison, P J & Ruohola-Baker, H 2019, ' Folliculin regulates mTORC1/2 and WNT pathways in early human pluripotency ', Nature Communications, vol. 10, no. 1, 632, pp. 632 . https://doi.org/10.1038/s41467-018-08020-0
Nature Communications
Mathieu, J, Detraux, D, Kuppers, D, Wang, Y, Cavanaugh, C, Sidhu, S, Levy, S, Robitaille, A M, Ferreccio, A, Bottorff, T, McAlister, A, Somasundaram, L, Artoni, F, Battle, S, Hawkins, R D, Moon, R T, Ware, C B, Paddison, P J & Ruohola-Baker, H 2019, ' Folliculin regulates mTORC1/2 and WNT pathways in early human pluripotency ', Nature Communications, vol. 10, no. 1, 632, pp. 632 . https://doi.org/10.1038/s41467-018-08020-0
Nature Communications
To reveal how cells exit human pluripotency, we designed a CRISPR-Cas9 screen exploiting the metabolic and epigenetic differences between naïve and primed pluripotent cells. We identify the tumor suppressor, Folliculin(FLCN) as a critical gene requi