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The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies
The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies
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The monoclonal antibody combination REGEN-COV protects against SARS-CoV-2 mutational escape in preclinical and human studies

Copin, Richard ; Baum, Alina ; Wloga, Elzbieta ; Pascal, Kristen E. ; Giordano, Stephanie ; Fulton, Benjamin O. ; Zhou, Anbo ; Negron, Nicole ; Lanza, Kathryn ; Chan, Newton ; Coppola, Angel ; Chiu, Joyce ; Ni, Min ; Wei, Yi ; Atwal, Gurinder S. ; Hernandez, Annabel Romero ; Saotome, Kei ; Zhou, Yi ; Franklin, Matthew C. ; Hooper, Andrea T. ; McCarthy, Shane ; Hamon, Sara ; Hamilton, Jennifer D. ; Staples, Hilary M. ; Alfson, Kendra ; Carrion, Ricardo ; Ali, Shazia ; Norton, Thomas ; Somersan-Karakaya, Selin ; Sivapalasingam, Sumathi ; Herman, Gary A. ; Weinreich, David M. ; Lipsich, Leah ; Stahl, Neil ; Murphy, Andrew J. ; Yancopoulos, George D. ; Kyratsous, Christos A.

Cell, 2021-07, Vol.184 (15), p.3949-3961.e11 [Periódico revisado por pares]

United States: Elsevier Inc

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2
Transthyretin: a review from a structural perspective
Transthyretin: a review from a structural perspective
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Transthyretin: a review from a structural perspective

Hamilton, J A ; Benson, M D

Cellular and molecular life sciences : CMLS, 2001-09, Vol.58 (10), p.1491-1521 [Periódico revisado por pares]

Switzerland: Springer Nature B.V

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3
Farnesyltransferase and geranylgeranyltransferase I inhibitors and cancer therapy: lessons from mechanism and bench-to-bedside translational studies
Farnesyltransferase and geranylgeranyltransferase I inhibitors and cancer therapy: lessons from mechanism and bench-to-bedside translational studies
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Farnesyltransferase and geranylgeranyltransferase I inhibitors and cancer therapy: lessons from mechanism and bench-to-bedside translational studies

Sebti, S M ; Hamilton, A D

Oncogene, 2000-12, Vol.19 (56), p.6584-6593 [Periódico revisado por pares]

England: Nature Publishing Group

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4
Functional characterization of retromer in GLUT4 storage vesicle formation and adipocyte differentiation
Functional characterization of retromer in GLUT4 storage vesicle formation and adipocyte differentiation
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Functional characterization of retromer in GLUT4 storage vesicle formation and adipocyte differentiation

Yang, Zhe ; Hong, Lee Kian ; Follett, Jordan ; Wabitsch, Martin ; Hamilton, Nicholas A. ; Collins, Brett M. ; Bugarcic, Andrea ; Teasdale, Rohan D.

The FASEB journal, 2016-03, Vol.30 (3), p.1037-1050 [Periódico revisado por pares]

Bethesda, MD, USA: Federation of American Societies for Experimental Biology

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5
The embryonic transcription factor Brachyury blocks cell cycle progression and mediates tumor resistance to conventional antitumor therapies
The embryonic transcription factor Brachyury blocks cell cycle progression and mediates tumor resistance to conventional antitumor therapies
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The embryonic transcription factor Brachyury blocks cell cycle progression and mediates tumor resistance to conventional antitumor therapies

Huang, B ; Cohen, J R ; Fernando, R I ; Hamilton, D H ; Litzinger, M T ; Hodge, J W ; Palena, C

Cell death & disease, 2013-06, Vol.4 (6), p.e682-e682 [Periódico revisado por pares]

England: Springer Nature B.V

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6
“Gap guidance” of fibroblasts and epithelial cells by discontinuous edged surfaces
“Gap guidance” of fibroblasts and epithelial cells by discontinuous edged surfaces
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“Gap guidance” of fibroblasts and epithelial cells by discontinuous edged surfaces

Hamilton, D.W. ; Brunette, D.M.

Experimental cell research, 2005-10, Vol.309 (2), p.429-437 [Periódico revisado por pares]

United States: Elsevier Inc

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7
Inhibition of influenza virus infection and hemagglutinin cleavage by the protease inhibitor HAI-2
Inhibition of influenza virus infection and hemagglutinin cleavage by the protease inhibitor HAI-2
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Inhibition of influenza virus infection and hemagglutinin cleavage by the protease inhibitor HAI-2

Hamilton, Brian S. ; Chung, Changik ; Cyphers, Soreen Y. ; Rinaldi, Vera D. ; Marcano, Valerie C. ; Whittaker, Gary R.

Biochemical and biophysical research communications, 2014-07, Vol.450 (2), p.1070-1075 [Periódico revisado por pares]

United States: Elsevier Inc

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8
Geranylgeranyltransferase I Inhibitors Target RalB To Inhibit Anchorage-Dependent Growth and Induce Apoptosis and RalA To Inhibit Anchorage-Independent Growth
Geranylgeranyltransferase I Inhibitors Target RalB To Inhibit Anchorage-Dependent Growth and Induce Apoptosis and RalA To Inhibit Anchorage-Independent Growth
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Geranylgeranyltransferase I Inhibitors Target RalB To Inhibit Anchorage-Dependent Growth and Induce Apoptosis and RalA To Inhibit Anchorage-Independent Growth

Falsetti, Samuel C. ; Wang, De-an ; Peng, Hairuo ; Carrico, Dora ; Cox, Adrienne D. ; Der, Channing J. ; Hamilton, Andrew D. ; Sebti, Saïd M.

Molecular and Cellular Biology, 2007-11, Vol.27 (22), p.8003-8014 [Periódico revisado por pares]

United States: American Society for Microbiology

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9
Microinjection Technique for Assessment of Gap Junction Function
Microinjection Technique for Assessment of Gap Junction Function
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Microinjection Technique for Assessment of Gap Junction Function

Fridman, Michael D. ; Liu, Jun ; Sun, Yu ; Hamilton, Robert M. Vinken, Mathieu ; Johnstone, Scott R.

Gap Junction Protocols, 2016-01, Vol.1437, p.145-154

New York, NY: Springer New York

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10
The farnesyltransferase inhibitor, FTI-2153, inhibits bipolar spindle formation during mitosis independently of transformation and Ras and p53 mutation status
The farnesyltransferase inhibitor, FTI-2153, inhibits bipolar spindle formation during mitosis independently of transformation and Ras and p53 mutation status
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The farnesyltransferase inhibitor, FTI-2153, inhibits bipolar spindle formation during mitosis independently of transformation and Ras and p53 mutation status

Crespo, N C ; Delarue, F ; Ohkanda, J ; Carrico, D ; Hamilton, A D ; Sebti, S M

Cell death and differentiation, 2002-07, Vol.9 (7), p.702-709 [Periódico revisado por pares]

England: Nature Publishing Group

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