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Bioorganic & Medicinal Chemistry
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January 24, 2007
The efficacy and cardiac evaluation of aminomethyl tetrahydronaphthalene ketopiperazines: a novel class of potent MCH-R1 antagonists
José L Méndez-Andino, Anny-Odile Colson, Kenneth M Meyers, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
September 29, 2017
A High-Throughput Dose-Response Cellular Thermal Shift Assay for Rapid Screening of Drug Target Engagement in Living Cells, Exemplified Using SMYD3 and IDO1
Dean E McNulty, William G Bonnette, Hongwei Qi, et al.
Journal of Medical Genetics
|
October 4, 2005
Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate
F Laumonnier, S Holbert, N Ronce, et al.
Journal of Pediatric Nursing
|
May 18, 2024
Barriers and co-designed strategies for the implementation of negative pressure wound therapy in acute pediatric burn care in Australia: A mixed method study
Maleea D Holbert, Jed Duff, Fiona Wood, et al.
Chemistry & Biology
|
June 11, 2010
Virtual ligand screening of the p300/CBP histone acetyltransferase: identification of a selective small molecule inhibitor
Erin M Bowers, Gai Yan, Chandrani Mukherjee, et al.
Plos One
|
December 10, 2024
Implementation of negative pressure for acute pediatric burns (INPREP): A stepped-wedge cluster randomized controlled trial protocol
Maleea D Holbert, Fiona Wood, Andrew J A Holland, et al.
Journal of the American Chemical Society
|
February 19, 2014
An Fc domain protein-small molecule conjugate as an enhanced immunomodulator
Meng-Jung Chiang, Marc A Holbert, Jay H Kalin, et al.
Human Molecular Genetics
|
July 1, 1996
Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders
C Néri, V Albanèse, A S Lebre, et al.
Scientific Reports
|
February 27, 2026
Development and characterization of an inducible Tensin1 deficient transgenic murine model
Ksenija Bernau, Kelsey Holbert, Ivy S McDermott, et al.
American Journal of Human Genetics
|
August 9, 2011
KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2
Jean-Baptiste Rivière, Siriram Ramalingam, Valérie Lavastre, et al.
Page
of 37
Search research articles
Search
Showing results (351-360 of 365) with videos related to
Sort By:
Page
of 37
Bioorganic & Medicinal Chemistry
|
January 24, 2007
The efficacy and cardiac evaluation of aminomethyl tetrahydronaphthalene ketopiperazines: a novel class of potent MCH-R1 antagonists
José L Méndez-Andino, Anny-Odile Colson, Kenneth M Meyers, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
September 29, 2017
A High-Throughput Dose-Response Cellular Thermal Shift Assay for Rapid Screening of Drug Target Engagement in Living Cells, Exemplified Using SMYD3 and IDO1
Dean E McNulty, William G Bonnette, Hongwei Qi, et al.
Journal of Medical Genetics
|
October 4, 2005
Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate
F Laumonnier, S Holbert, N Ronce, et al.
Journal of Pediatric Nursing
|
May 18, 2024
Barriers and co-designed strategies for the implementation of negative pressure wound therapy in acute pediatric burn care in Australia: A mixed method study
Maleea D Holbert, Jed Duff, Fiona Wood, et al.
Chemistry & Biology
|
June 11, 2010
Virtual ligand screening of the p300/CBP histone acetyltransferase: identification of a selective small molecule inhibitor
Erin M Bowers, Gai Yan, Chandrani Mukherjee, et al.
Plos One
|
December 10, 2024
Implementation of negative pressure for acute pediatric burns (INPREP): A stepped-wedge cluster randomized controlled trial protocol
Maleea D Holbert, Fiona Wood, Andrew J A Holland, et al.
Journal of the American Chemical Society
|
February 19, 2014
An Fc domain protein-small molecule conjugate as an enhanced immunomodulator
Meng-Jung Chiang, Marc A Holbert, Jay H Kalin, et al.
Human Molecular Genetics
|
July 1, 1996
Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders
C Néri, V Albanèse, A S Lebre, et al.
Scientific Reports
|
February 27, 2026
Development and characterization of an inducible Tensin1 deficient transgenic murine model
Ksenija Bernau, Kelsey Holbert, Ivy S McDermott, et al.
American Journal of Human Genetics
|
August 9, 2011
KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2
Jean-Baptiste Rivière, Siriram Ramalingam, Valérie Lavastre, et al.
Page
of 37