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C Reid

Showing results (931-940 of 983) with videos related to

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Bioorganic & Medicinal Chemistry Letters|March 15, 2018
Indole acids as a novel PDE2 inhibitor chemotype that demonstrate pro-cognitive activity in multiple speciesShawn J Stachel, Melissa S Egbertson, Jenny Wai, et al.
Cell Reports. Medicine|July 11, 2023
Leukemic progenitor compartment serves as a prognostic measure of cancer stemness in patients with acute myeloid leukemiaAllison L Boyd, Justin Lu, Cameron G Hollands, et al.
Journal of Medicinal Chemistry|May 9, 1997
Improved P1/P1' substituents for cyclic urea based HIV-1 protease inhibitors: synthesis, structure-activity relationship, and X-ray crystal structure analysisD A Nugiel, K Jacobs, L Cornelius, et al.
World Neurosurgery|June 22, 2018
Rod Fracture After Apparently Solid Radiographic Fusion in Adult Spinal Deformity PatientsAlan H Daniels, J Mason DePasse, Wesley Durand, et al.
Bioorganic & Medicinal Chemistry Letters|December 14, 2023
Exploration of macrocyclic peptide binders to the extracellular CRD domain of human receptor tyrosine kinase-like orphan receptor 1 (ROR1)Jennifer X Qiao, Mark R Witmer, Ving Lee, et al.
Cell Reports. Medicine|April 6, 2024
Identification of cells of leukemic stem cell origin with non-canonical regenerative propertiesCameron G Hollands, Allison L Boyd, Xueli Zhao, et al.
Cell Chemical Biology|June 28, 2023
Chemical genomics reveals targetable programs of human cancers rooted in pluripotencyLuca Orlando, Yannick D Benoit, Jennifer C Reid, et al.
Journal of Neurosurgery. Spine|December 21, 2019
Upper-thoracic versus lower-thoracic upper instrumented vertebra in adult spinal deformity patients undergoing fusion to the pelvis: surgical decision-making and patient outcomesAlan H Daniels, Daniel B C Reid, Wesley M Durand, et al.
Journal of Virology|May 21, 2010
Structural basis for the inhibition of RNase H activity of HIV-1 reverse transcriptase by RNase H active site-directed inhibitorsHua-Poo Su, Youwei Yan, G Sridhar Prasad, et al.
Chemistry & Biology|November 18, 1998
Design and selection of DMP 850 and DMP 851: the next generation of cyclic urea HIV protease inhibitorsJ D Rodgers, P Y Lam, B L Johnson, et al.
Pageof 99

Showing results (931-940 of 983) with videos related to

Sort By:
Pageof 99
Bioorganic & Medicinal Chemistry Letters|March 15, 2018
Indole acids as a novel PDE2 inhibitor chemotype that demonstrate pro-cognitive activity in multiple speciesShawn J Stachel, Melissa S Egbertson, Jenny Wai, et al.
Cell Reports. Medicine|July 11, 2023
Leukemic progenitor compartment serves as a prognostic measure of cancer stemness in patients with acute myeloid leukemiaAllison L Boyd, Justin Lu, Cameron G Hollands, et al.
Journal of Medicinal Chemistry|May 9, 1997
Improved P1/P1' substituents for cyclic urea based HIV-1 protease inhibitors: synthesis, structure-activity relationship, and X-ray crystal structure analysisD A Nugiel, K Jacobs, L Cornelius, et al.
World Neurosurgery|June 22, 2018
Rod Fracture After Apparently Solid Radiographic Fusion in Adult Spinal Deformity PatientsAlan H Daniels, J Mason DePasse, Wesley Durand, et al.
Bioorganic & Medicinal Chemistry Letters|December 14, 2023
Exploration of macrocyclic peptide binders to the extracellular CRD domain of human receptor tyrosine kinase-like orphan receptor 1 (ROR1)Jennifer X Qiao, Mark R Witmer, Ving Lee, et al.
Cell Reports. Medicine|April 6, 2024
Identification of cells of leukemic stem cell origin with non-canonical regenerative propertiesCameron G Hollands, Allison L Boyd, Xueli Zhao, et al.
Cell Chemical Biology|June 28, 2023
Chemical genomics reveals targetable programs of human cancers rooted in pluripotencyLuca Orlando, Yannick D Benoit, Jennifer C Reid, et al.
Journal of Neurosurgery. Spine|December 21, 2019
Upper-thoracic versus lower-thoracic upper instrumented vertebra in adult spinal deformity patients undergoing fusion to the pelvis: surgical decision-making and patient outcomesAlan H Daniels, Daniel B C Reid, Wesley M Durand, et al.
Journal of Virology|May 21, 2010
Structural basis for the inhibition of RNase H activity of HIV-1 reverse transcriptase by RNase H active site-directed inhibitorsHua-Poo Su, Youwei Yan, G Sridhar Prasad, et al.
Chemistry & Biology|November 18, 1998
Design and selection of DMP 850 and DMP 851: the next generation of cyclic urea HIV protease inhibitorsJ D Rodgers, P Y Lam, B L Johnson, et al.
Pageof 99