Are Rodent Models Fit for Investigation of Human Obesity and Related Diseases?
	Tác giả: Robert K Semple, Gilles Fromentin, Nicholas M Morton, Patrick C Even, Sam Virtue
	Xuất bản: Frontiers Media SA , 2018
	Bộ sưu tập: Tài liệu truy cập mở
	eBook (pdf) ddc:   Thêm vào giỏ

Discovery of Potent Myeloid Cell Leukemia-1 (Mcl-1) Inhibitors That Demonstrate in Vivo Activity in Mouse Xenograft Models of Human Cancer [electronic resource]
	Tác giả:
	Xuất bản: Washington, D.C. : Oak Ridge, Tenn: United States. Dept. of Energy. Office of Science ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy , 2019
	Bộ sưu tập: Metadata
	ddc:  616.9945  Thêm vào giỏ

Discovery of AG-270, a First-in-Class Oral MAT2A Inhibitor for the Treatment of Tumors with Homozygous MTAP Deletion [el...
	Tác giả:
	Xuất bản: Washington, D.C. : Oak Ridge, Tenn: United States. Dept. of Energy. Office of Science ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy , 2021
	Bộ sưu tập: Metadata
	ddc:  615.7  Thêm vào giỏ

Complexity of Blocking Bivalent Protein?Protein Interactions [electronic resource] : Development of a Highly Potent Inhi...
	Tác giả:
	Xuất bản: Bethesda, Md. : Oak Ridge, Tenn: National Institutes of Health (U.S.) ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy , 2018
	Bộ sưu tập: Metadata
	ddc:  616.07  Thêm vào giỏ

Discovery of LSZ102, a Potent, Orally Bioavailable Selective Estrogen Receptor Degrader (SERD) for the Treatment of Estr...
	Tác giả:
	Xuất bản: Argonne, Ill. : Oak Ridge, Tenn: Argonne National Laboratory ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy , 2018
	Bộ sưu tập: Metadata
	ddc:  616.9945  Thêm vào giỏ

Discovery of Isonicotinamides as Highly Selective, Brain Penetrable, and Orally Active Glycogen Synthase Kinase-3 Inhibi...
	Tác giả:
	Xuất bản: Argonne, Ill. : Oak Ridge, Tenn: Argonne National Laboratory ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy , 2016
	Bộ sưu tập: Metadata
	ddc:  577.13  Thêm vào giỏ

Crystal Structures of mPGES-1 Inhibitor Complexes Form a Basis for the Rational Design of Potent Analgesic and Anti-Infl...
	Tác giả:
	Xuất bản: Washington, D.C. : Oak Ridge, Tenn: United States. Dept. of Energy. Office of Science ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy , 2015
	Bộ sưu tập: Metadata
	ddc:  572.4  Thêm vào giỏ

Design and Synthesis of Selective Phosphodiesterase 4D (PDE4D) Allosteric Inhibitors for the Treatment of Fragile X Synd...
	Tác giả:
	Xuất bản: Bethesda, Md. : Oak Ridge, Tenn: National Institutes of Health (U.S.) ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy , 2019
	Bộ sưu tập: Metadata
	ddc:  619.45  Thêm vào giỏ

Discovery of QCA570 as an Exceptionally Potent and Efficacious Proteolysis Targeting Chimera (PROTAC) Degrader of the Br...
	Tác giả:
	Xuất bản: Argonne, Ill. : Oak Ridge, Tenn: Argonne National Laboratory ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy , 2018
	Bộ sưu tập: Metadata
	ddc:  616.079  Thêm vào giỏ

Structure-Based Discovery of CF53 as a Potent and Orally Bioavailable Bromodomain and Extra-Terminal (BET) Bromodomain I...
	Tác giả:
	Xuất bản: Washington, D.C. : Oak Ridge, Tenn: United States. Dept. of Energy. Office of Science ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy , 2018
	Bộ sưu tập: Metadata
	ddc:  547.7  Thêm vào giỏ