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21-30 trong số 44 kết quả
Behavioral analyses in rodent models of tuberous sclerosis complex
Tác giả: Victor Rodrigues Santos, Lilian G Jerow, Candi L LaSarge
Xuất bản: United States: Epilepsy & behavior : E&B , 2025
Bộ sưu tập: NCBI
ddc:  616.07563
 
GDF10 promotes rodent cardiomyocyte maturation during the postnatal period
Tác giả: Maria Uscategui Calderon, Maria L Spaeth, Marissa Granitto, Brittany A Gonzalez, Matthew T Weirauch, Leah C Kottyan, Katherine E Yutzey
Xuất bản: England: Journal of molecular and cellular cardiology , 2025
Bộ sưu tập: NCBI
ddc:  352.745
 
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: Báo, Tạp chí
ddc:  577.13
 
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: Báo, Tạp chí
ddc:  572.4
 
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: Báo, Tạp chí
ddc:  615.7
 
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: Báo, Tạp chí
ddc:  619.45
 
Discovery of Potent Myeloid Cell Leukemia-1 (Mcl-1) Inhibitors That Demonstrate in Vivo Activity in Mouse Xenograft Mode...
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: Báo, Tạp chí
ddc:  616.9945
 
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: Báo, Tạp chí
ddc:  616.079
 
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: Báo, Tạp chí
ddc:  547.7
 
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: Báo, Tạp chí
ddc:  616.07
 

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