Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Matthew A Spear"'
Autor:
Matthew B. Spear, Kristen Miller, Craig Press, Christopher Ruzas, Jaime LaVelle, Peter M. Mourani, Tellen D. Bennett, Aline B. Maddux
Publikováno v:
The Neurohospitalist. 13(1)
Background and Purpose Long-term outcomes after pediatric neurocritical illness are poorly characterized. This study aims to characterize the frequency and risk factors for post-discharge unplanned health resource use in a pediatric neurocritical car
Autor:
Matthew A. Spear, Ahmet Dogan, Simon F. Lacey, Nikoletta Lendvai, Adam D. Cohen, Christopher E. Martin, Alfred L. Garfall, Dan T. Vogl, Alexander M. Lesokhin
Publikováno v:
Blood Advances. 3:2487-2490
Key Points Myeloma patients progressing on BCMA-targeted therapy can maintain BCMA expression and still respond to different BCMA-targeted therapy. These observations suggest this patient population could be included in ongoing BCMA-targeted therapy
Autor:
Matthew A. Spear
Publikováno v:
BioTechniques, Vol 28, Iss 4, Pp 660-668 (2000)
Described here is a selective restriction endonuclease digestion method that eliminates the electrophoresis step that is usually used during the subcloning of new DNA sequences into typical E. coli-based plasmids. The method increases yield while dec
Externí odkaz:
https://doaj.org/article/7be8b0e3b16f450582038e492312b90e
Autor:
Susan F. Slovin, Tanya B. Dorff, Gerald Steven Falchook, Xiao X. Wei, Xin Gao, Rana R. McKay, David Yoonsuk Oh, Andreas Georg Wibmer, Matthew A. Spear, Joanne McCaigue, Devon J. Shedlock, Manjima Dhar, Julia Coronella, Christopher E. Martin, Majid Ghodussi, Ann Murphy, Eric M. Ostertag
Publikováno v:
Journal of Clinical Oncology. 40:98-98
98 Background: P-PSMA-101 is an autologous CAR-T therapy targeting PSMA, with a high percentage of stem cell memory T cells (TSCM) associated with efficacy, safety, and bone homing (particularly relevant to prostate cancer). It is manufactured using
Autor:
Katherine McArthur, Abbas Abbas Ali, Tara K. Gregory, Christopher E. Martin, Bhagirathbhai Dholaria, Caitlin Costello, Ben A Derman, Rajneesh Nath, Joanne McCaigue, Majid Ghoddusi, Matthew A. Spear, Jesus G. Berdeja, David S. Siegel, Adam D. Cohen, Rajesh Belani, Eric M. Ostertag, Abhinav Deol, Krina K. Patel, Nina Shah, Mehmet Hakan Kocoglu, Hamid Namini
Publikováno v:
Blood. 138:3858-3858
P-BCMA-101 and P-BCMA-ALLO1, autologous and allogeneic BCMA targeting CAR-T cell therapies respectively, are manufactured using a novel transposon-based system called piggyBac (PB). They comprise a high percentage of desirable stem cell memory T-cell
Autor:
Adam D. Cohen, Eric M. Ostertag, Nina Shah, Jesus G. Berdeja, Sreeni Yalamanchili, Tara K. Gregory, Mehrdad Abedi, Joanne McCaigue, Hamid Namini, Matthew A. Spear, Syed S Ali, Siddhartha Ganguly, Christopher E. Martin, Caitlin Costello, Mehmet Hakan Kocoglu, Majid Ghoddussi, Krina K. Patel, Devon J. Shedlock
Publikováno v:
Blood. 136:29-30
P-BCMA-101 is an autologous chimeric antigen receptor-T cell (CAR-T) therapeutic targeting BCMA and comprised of a high percentage of desirable stem cell memory T cells. P-BCMA-101 is manufactured using a novel transposon-based system called piggyBac
Autor:
Krina K. Patel, Caitlin Costello, Matthew A. Spear, Devon J. Shedlock, Adam D. Cohen, Tara K. Gregory, Syed Abbas Ali, Jesus G. Berdeja, Majid Ghoddusi, Christopher E. Martin, Eric M. Ostertag, Robert Z. Orlowski, Nina Shah
Publikováno v:
Blood. 134:3184-3184
P-BCMA-101 is a novel chimeric antigen receptor (CAR)-T cell product targeting B Cell Maturation Antigen (BCMA). P-BCMA-101 is produced using the piggyBac® (PB) DNA Modification System instead of the viral vector that is used with most CAR-T cells,
Autor:
Saskia T. C. Neuteboom, Shawgi Sukumaran, Matthew A. Spear, G. Kenneth Lloyd, Timothy J. Price, Girish Sharma, Ana Lay, David J. McConkey, Michael A. Palladino, Christopher Sweeney, Angie M. Longenecker, Harry A. Drabkin, Amanda R. Townsend, Robert M. Gemmill, Andrew Spencer, Michael Millward, Lonnie Lee
Publikováno v:
Investigational New Drugs. 30:2303-2317
Purpose Combining proteasome and histone deacetylase (HDAC) inhibition has been seen to provide synergistic anti-tumor activity, with complementary effects on a number of signaling pathways. The novel bi-cyclic structure of marizomib with its unique
Autor:
Irene M. Ghobrial, KC Anderson, Saskia T. C. Neuteboom, E. Valashi, G. K. Lloyd, William H. McBride, Paul G. Richardson, Barbara C. M. Potts, Joya Chandra, Huib Ovaa, Michael A. Palladino, Callum M. Sloss, Michael Groll, William Fenical, Aldo M. Roccaro, Frank Pajonk, Anas Younes, Y. Oki, James C. Cusack, Paul R. Jensen, Celia R. Berkers, Claudia P. Miller, M. X. Albitar, Stavroula Baritaki, Kin S. Lam, David J. McConkey, Ben Bonavida, D Chauhan, Matthew A. Spear
Publikováno v:
Current Cancer Drug Targets. 11:254-284
The proteasome has emerged as an important clinically relevant target for the treatment of hematologic malignancies. Since the Food and Drug Administration approved the first-in-class proteasome inhibitor bortezomib (Velcade®) for the treatment of r
Autor:
Tara K. Gregory, Jesus G. Berdeja, Robert Z. Orlowski, Matthew A. Spear, Eric M. Ostertag, Krina K. Patel, Adam D. Cohen, Devon J. Shedlock, Michelle Lynn Resler, Syed Abbas Ali, Caitlin Costello, Christopher E. Martin
Publikováno v:
Blood. 132:1012-1012
P-BCMA-101 is a novel chimeric antigen receptor (CAR)-T cell therapeutic targeting BCMA, which is highly expressed on MM cells. It is designed to increase efficacy while minimizing toxicity through reduced immunogenicity, lack of tonic signaling, a s