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Plos One
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January 19, 2012
Mechanism-based screen for G1/S checkpoint activators identifies a selective activator of EIF2AK3/PERK signalling
Simon R Stockwell, Georgina Platt, S Elaine Barrie, et al.
Cancer Research
|
July 9, 2010
A useful approach to identify novel small-molecule inhibitors of Wnt-dependent transcription
Kenneth Ewan, Bozena Pajak, Mark Stubbs, et al.
Nature Communications
|
February 14, 2025
Structural insights into human brachyury DNA recognition and discovery of progressible binders for cancer therapy
Joseph A Newman, Angeline E Gavard, Nergis Imprachim, et al.
Cancer Discovery
|
March 30, 2013
Histone H3.3. mutations drive pediatric glioblastoma through upregulation of MYCN
Lynn Bjerke, Alan Mackay, Meera Nandhabalan, et al.
Plos One
|
April 15, 2009
Molecular and phenotypic characterisation of paediatric glioma cell lines as models for preclinical drug development
Dorine A Bax, Suzanne E Little, Nathalie Gaspar, et al.
NAR Cancer
|
March 16, 2026
Human DEAH-box helicase 8 regulates HSF1-mediated stress response and cancer-associated pre-mRNA splicing in tumour cells
Jennifer R Tall, Robert Te Poele, Alexandra Vasile, et al.
Molecular Cancer Therapeutics
|
April 29, 2010
AT7867 is a potent and oral inhibitor of AKT and p70 S6 kinase that induces pharmacodynamic changes and inhibits human tumor xenograft growth
Kyla M Grimshaw, Lisa-Jane K Hunter, Timothy A Yap, et al.
Journal of Medicinal Chemistry
|
December 15, 2017
Demonstrating In-Cell Target Engagement Using a Pirin Protein Degradation Probe (CCT367766)
Nicola E A Chessum, Swee Y Sharp, John J Caldwell, et al.
Nucleic Acids Research
|
November 13, 2024
canSAR 2024-an update to the public drug discovery knowledgebase
Phillip W Gingrich, Rezvan Chitsazi, Ansuman Biswas, et al.
Bioorganic & Medicinal Chemistry
|
October 11, 2011
Design, synthesis and biological evaluation of 6-pyridylmethylaminopurines as CDK inhibitors
Stuart C Wilson, Butrus Atrash, Clare Barlow, et al.
Page
of 32
Search research articles
Search
Showing results (251-260 of 315) with videos related to
Sort By:
Page
of 32
Plos One
|
January 19, 2012
Mechanism-based screen for G1/S checkpoint activators identifies a selective activator of EIF2AK3/PERK signalling
Simon R Stockwell, Georgina Platt, S Elaine Barrie, et al.
Cancer Research
|
July 9, 2010
A useful approach to identify novel small-molecule inhibitors of Wnt-dependent transcription
Kenneth Ewan, Bozena Pajak, Mark Stubbs, et al.
Nature Communications
|
February 14, 2025
Structural insights into human brachyury DNA recognition and discovery of progressible binders for cancer therapy
Joseph A Newman, Angeline E Gavard, Nergis Imprachim, et al.
Cancer Discovery
|
March 30, 2013
Histone H3.3. mutations drive pediatric glioblastoma through upregulation of MYCN
Lynn Bjerke, Alan Mackay, Meera Nandhabalan, et al.
Plos One
|
April 15, 2009
Molecular and phenotypic characterisation of paediatric glioma cell lines as models for preclinical drug development
Dorine A Bax, Suzanne E Little, Nathalie Gaspar, et al.
NAR Cancer
|
March 16, 2026
Human DEAH-box helicase 8 regulates HSF1-mediated stress response and cancer-associated pre-mRNA splicing in tumour cells
Jennifer R Tall, Robert Te Poele, Alexandra Vasile, et al.
Molecular Cancer Therapeutics
|
April 29, 2010
AT7867 is a potent and oral inhibitor of AKT and p70 S6 kinase that induces pharmacodynamic changes and inhibits human tumor xenograft growth
Kyla M Grimshaw, Lisa-Jane K Hunter, Timothy A Yap, et al.
Journal of Medicinal Chemistry
|
December 15, 2017
Demonstrating In-Cell Target Engagement Using a Pirin Protein Degradation Probe (CCT367766)
Nicola E A Chessum, Swee Y Sharp, John J Caldwell, et al.
Nucleic Acids Research
|
November 13, 2024
canSAR 2024-an update to the public drug discovery knowledgebase
Phillip W Gingrich, Rezvan Chitsazi, Ansuman Biswas, et al.
Bioorganic & Medicinal Chemistry
|
October 11, 2011
Design, synthesis and biological evaluation of 6-pyridylmethylaminopurines as CDK inhibitors
Stuart C Wilson, Butrus Atrash, Clare Barlow, et al.
Page
of 32