Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Fumiko, TAKADA"'
Autor:
Qiang Liu, Emily Sever, Sreenivasan Paruthiyil, Ana G Lujan Hernandez, Aaron K. Sato, Fumiko Takada Axelrod, Joyce Lai, Tom Z. Yuan, Greg Szot, Burcu Hasdemir, Pankaj Garg, Linya Wang, Emily Tuscano, Eric Kwan, Erica Keane
Publikováno v:
mAbs
article-version (VoR) Version of Record
article-version (VoR) Version of Record
G protein-coupled receptors (GPCRs) are a group of seven-transmembrane receptor proteins that have proven to be successful drug targets. Antibodies are becoming an increasingly promising modality to target these receptors due to their unique properti
Autor:
Tom Z. Yuan, Mohammad Javad Aman, Fumiko Takada Axelrod, Erica Keane, Aaron K. Sato, Yasmina N Abdiche, Madeleine Noonan-Shueh, Qiang Liu, Shweta Kailasan, Ana G Lujan Hernandez
Publikováno v:
Antibody Therapeutics
Background Development of successful neutralizing antibodies is dependent upon broad epitope coverage to increase the likelihood of achieving therapeutic function. Recent advances in synthetic biology have allowed us to conduct an epitope binning stu
Autor:
Fumiko, TAKADA
Publikováno v:
研究年報. 24:21
Autor:
Kellie Pickell, Andrew Lam, Lucas Donigan, Marcus Fischer, Satyajit Sujit Kumar Mitra, Fumiko Takada Axelrod, Hoang Tran, Aurélie Chaudhari, In-Kyung Park, Christopher J. Bond, Austin L. Gurney, Timothy Hoey, Sanjeev Satyal, Aaron K. Sato, John Lewicki, Jennifer Cain, Cecile Chartier, Michelle Stroud, Sasha Lazetic, Ann M. Kapoun, May Ji, Wan-Ching Yen, Shirley Ma
Publikováno v:
Proceedings of the National Academy of Sciences. 109:11717-11722
The Wnt/β-catenin pathway, which signals through the Frizzled (Fzd) receptor family and several coreceptors, has long been implicated in cancer. Here we demonstrate a therapeutic approach to targeting the Wnt pathway with a monoclonal antibody, OMP-
Autor:
Jenny Pokorny, Austin L. Gurney, Fumiko Takada Axelrod, Janice Yu, Rui Yun, Minu K. Srivastava, Angie Inkyung Park
Publikováno v:
Cancer Research. 78:70-70
Mouse tumor models have been successfully used to generate preclinical data for numerous clinical programs including immunotherapy. Preclinical in vivo studies are typically carried out using young mice (often less than 2 months old) to generate effi
Autor:
Ming-Hong Xie, Fumiko Takada Axelrod, Belinda Cancilla, Ann M. Kapoun, Reyhaneh Lahmy, Alayne Brunner, Jorge Monteon, Gilbert O'Young, Rose Harris, Pete Yeung, Austin L. Gurney, Andrew Lam, Fiore Cattaruzza, Earth Light Lowe, Gretchen Argast, Jennifer Elechko, Min Wang, Erwan Le Scolan
Publikováno v:
Cancer Research. 78:3826-3826
Activation of the co-stimulatory receptor GITR (Glucocorticoid-Induced Tumor Necrosis Factor Receptor) by GITR-Ligand (GITRL) promotes proliferation and activation of effector T cells (T eff) and inhibits suppressive activity of regulatory T cells (T
Autor:
Fumiko Takada Axelrod, Rose Harris, Austin L. Gurney, Ming-Hong Xie, Pete Yeung, Ann M. Kapoun, Alayne Brunner, Reyhaneh Lahmy, Fiore Cattaruzza, Erwan Le Scolan, John Lewicki, Gilbert O'Young, Jorge Monteon, Andrew Lam, Belinda Cancilla, Min Wang, Earth Light Lowe, Gretchen Argast, Jennifer Elechko
Publikováno v:
Cancer Research. 78:5627-5627
The immune checkpoint co-inhibitory receptor TIGIT (T cell immunoreceptor with Ig ITIM domain) is expressed on regulatory T cells (Tregs) and on activated CD4+ T, CD8+ T, and NK cells. We have reported that by blocking TIGIT activity with an IgG2a an
Autor:
Fumiko Takada Axelrod, Andrew Lam, Angie I. Park, Austin L. Gurney, Ivan H. Chan, Ming-Hong Xie, Jennifer Elechko
Publikováno v:
Cancer Research. 78:2726-2726
Glucocorticoid-induced TNFR-related protein (GITR) is a member of the TNF receptor superfamily. GITR, a co-stimulatory surface receptor, is activated upon binding to GITR Ligand (GITRL) and mediates co-stimulation of T-cell and NK responses and inhib
Autor:
Fumiko Takada Axelrod, Austin L. Gurney, Christopher Murriel, Ann M. Kapoun, Hyun-Bae Jie, Rui Yun, Minu K. Srivastava, Trevor Bentley, Raymond Tam, Ming-Hong Xie, John Lewicki, Belinda Cancilla, Tim Hoey, Park Angie Inkyung, Erin Mayes, Gilbert O'Young
Publikováno v:
Journal for Immunotherapy of Cancer
Meeting abstracts Blocking DLL4, a Notch ligand, effectively inhibits tumor growth by increasing non-functional angiogenesis and decreasing the cancer stem cell (CSC) population. Preclinical studies have demonstrated inhibition of tumor growth by ant
Autor:
John Lewicki, Andrew Lam, Michelle Stroud, Janak Raval, May Ji, Belinda Cancilla, Jie Wei, Fumiko Takada Axelrod, Gilbert O'Young, Wan-Ching Yen, Min Wang, Timothy Hoey, Ann M. Kapoun, Cecile Chartier, Cristina Dee-Hoskins, Austin L. Gurney, Pete Yeung, Shirley Ma, Christopher J. Bond, Jalpa Shah, Jennifer Cain, Marcus Fischer
Publikováno v:
Cancer research. 76(3)
Deregulation of the β-catenin signaling has long been associated with cancer. Intracellular components of this pathway, including axin, APC, and β-catenin, are frequently mutated in a range of human tumors, but the contribution of specific extracel