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Paul B. Fisher
Researcher at Virginia Commonwealth University
Publications - 486
Citations - 35304
Paul B. Fisher is an academic researcher from Virginia Commonwealth University. The author has contributed to research in topics: Cancer & Cancer cell. The author has an hindex of 80, co-authored 449 publications receiving 31149 citations. Previous affiliations of Paul B. Fisher include Discovery Institute & Columbia University Medical Center.
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Patent
Suppressor of ap-1
TL;DR: In this paper, methods, compositions, and therapeutic products for use in the field of oncology and specifically, for the treatment of cancer and other diseases in which SARI is ameliorative or therapeutic and/or small molecule screening for anti-cancer drugs are provided.
Book ChapterDOI
Cloning differentially expressed genes using rapid subtraction hybridization (RaSH).
TL;DR: Based on its simplicity of performance and high frequency of genuine differential gene identification, the rapid subtraction hybridization (RaSH) approach will allow wide applications in diverse systems and biological contexts.
Book ChapterDOI
Surface-epitope masking (SEM): an immunological subtraction approach for developing monoclonal antibodies targeting surface-expressed molecules.
Neil I. Goldstein,Paul B. Fisher +1 more
TL;DR: An immunological subtraction approach, surface-epitope masking (SEM), is described that permits the efficient and selective production of monoclonal antibodies (MAbs) reacting with both known and unknown molecules expressed on the cell surface.
Journal ArticleDOI
Non-BRAF targeted therapies for melanoma: protein kinase inhibitors in Phase II clinical trials
Shilpa Bhatia,Luni Emdad,Swadesh K. Das,Hossein A. Hamed,Paul Dent,Devanand Sarkar,Paul B. Fisher +6 more
TL;DR: In light of several preclinical and clinical studies, it is clear that targeting single-gene mutations may not provide a desired therapeutic gain in the context of melanoma and research will need to focus on rational combinations of novel therapeutic agents targeting multiple genetic aberrations or deregulated pathways to achieve a desired maximum clinical benefit.
Journal ArticleDOI
Cnsc-01. gabaergic neuron-to-glioma synapses in diffuse midline gliomas
Tara Barron,Belgin Yalçın,Aaron Mochizuki,Evan Cantor,Kiarash Shamardani,Dana Tlais,Andrea Franson,Samantha Lyons,V. Mehta,Samina Jahan,Kathryn R. Taylor,Michael B. Keough,Haojun Xu,Minhui Su,Michael Quezada,Pamelyn Woo,Paul B. Fisher,Cynthia J. Campen,Sonia Partap,Carl Koschmann,Michelle Monje +20 more
TL;DR: In this paper , the authors identify functional, tumor-promoting GABAergic neuron-to-glioma synapses mediated by GABAA receptors in DMGs, and uncover GABAergic synaptic communication between GABAergic interneurons and diffuse midline glioma cells.