Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Julia Gilden"'
Autor:
Jamison Grailer, Julia Gilden, Pete Stecha, Jim Hartnett, Vanessa Ott, Michael Slater, Dan Lazar, Zhijie Jey Cheng
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 8, Iss Suppl 3 (2020)
Externí odkaz:
https://doaj.org/article/e7a26181ad7e4ce1a8140cb45ef98a4e
Autor:
Jun Wang, Julia Gilden, Denise Garvin, Pete Stecha, Jim Hartnett, Frank Fan, Mei Cong, Jamison Grailer
Publikováno v:
Cancer Research. 83:3274-3274
Programmed cell death protein 1 (PD-1) is an immune checkpoint (IC) receptor that negatively regulates T cell function. Blocking the interaction of PD-1 with its ligands PD-L1 or PD-L2 unleashes the immune system and enhances anti-tumor responses. Im
Autor:
Maggie Bach, Natasha Karassina, Julia Gilden, Donna Leippe, Mike Valley, Kayla Sylvester, Jolanta Vidugiriene
Publikováno v:
Cancer Research. 83:4162-4162
Cellular energy metabolism is crucial for cell survival and the balance of metabolic pathways determines the health of the cell. Determining and understanding metabolic profiles of cells can aid in overall insight of cell health and improvement of ce
Autor:
Jun Wang, Julia Gilden, Denise Garvin, Zhi-jie Jey Cheng, Jim Hartnett, Pete Stecha, Jamison Grailer, Mei Cong, Frank Fan
Publikováno v:
Current Protocols. 1
Antibody Fc effector function is one of the main mechanisms of action (MoA) for therapeutic monoclonal antibodies. Measurement of antibody-dependent cellular cytotoxicity (ADCC) is critical for understanding the Fc effector function during monoclonal
Autor:
Pete Stecha, Jun Wang, Denise Garvin, Julia Gilden, Jamison Grailer, Jim Hartnett, Frank Fan, Mei Cong, Zhi-jie Jey Cheng
Publikováno v:
Cancer Research. 82:4249-4249
Fc effector function is one of the main mechanisms of action (MoA) for therapeutic monoclonal antibodies (mAbs). Quantitative measurement of antibody-dependent cellular cytotoxicity (ADCC) is critically required for understanding the Fc function in m
Autor:
Jamison Grailer, Julia Gilden, Jun Wang, Denise Garvin, Pete Stecha, Jim Hartnett, Steven Edenson, Frank Fan, Mei Cong, Zhi-jie Jey Cheng
Publikováno v:
Cancer Research. 82:1875-1875
Programmed death 1 (PD-1) is an immune checkpoint (IC) receptor that negatively regulates T-cell immune function. Blocking the interaction of PD-1 with its ligand PD-L1 unleashes the immune system and enhances anti-tumor responses. Immunotherapy usin
Autor:
Julia Gilden, Jamison Grailer, Michael Slater, Pete Stecha, Jim Hartnett, Dan Lazar, Gopal Krishnan, Frank Fan, Mei Cong, Zhijie Jey Cheng
Publikováno v:
Cancer Research. 82:2750-2750
Redirected T cell therapies represent a new paradigm for cancer treatment. Two main approaches for T-cell-based therapies involve molecular T cell redirection by CD3 bispecific molecules such as bispecific T-cell engagers (BiTE) and cellular T cell r
Autor:
Denise Garvin, Pete Stecha, Mei Cong, Jamison Grailer, Jim Hartnett, Michael Beck, Jun Wang, Gopal Krishnan, Zhi-Jie Cheng, Frank Fan, Julia Gilden
Publikováno v:
Late-breaking abstracts.
Background The human immune system is comprised of a complex network of immune checkpoint receptors that are promising new immunotherapy targets for the treatment of a variety of cancers and autoimmune disorders. The Nobel prize for Medicine in 2018
Autor:
Mei Cong, Pete Stecha, Jim Hartnett, Vanessa Ott, Jamison Grailer, Dan Lazar, Michael R. Slater, Frank Fan, Julia Gilden, Zhi-jie Jey Cheng
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 8, Iss Suppl 3 (2020)
Background Two main approaches for T cell-based therapies involve molecular T cell redirection by CD3 bispecific molecules such as bispecific T-cell engagers (BiTE) and cellular T cell redirection by genetic modification of T cells with chimeric anti
Autor:
Mei Cong, Frank Fan, Jim Hartnett, Jamison Grailer, Julia Gilden, Zhi-jie Jey Cheng, Jun Wang, Denise Garvin, Pete Stecha, Michael Beck
Publikováno v:
Cancer Research. 81:1650-1650
Immune checkpoint (IC) receptors play critical roles in maintaining immune homeostasis and are emerged as promising drug targets for the treatment of various cancers and autoimmune disorders. Monoclonal antibodies designed to block immune inhibitory