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The Biochemical Journal
|
September 26, 2018
Inhibitor potency varies widely among tumor-relevant human isocitrate dehydrogenase 1 mutants
Diego Avellaneda Matteo, Grace A Wells, Lucas A Luna, et al.
The Journal of Cell Biology
|
September 2, 2022
Origin of cytoplasmic GDP-fucose determines its contribution to glycosylation reactions
Paulina Sosicka, Bobby G Ng, Lauren E Pepi, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 16, 2011
In vitro and in vivo evaluation of 6-aminopyrazolyl-pyridine-3-carbonitriles as JAK2 kinase inhibitors
Tao Wang, Stephanos Ioannidis, Lynsie Almeida, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 8, 2011
3-amido-4-anilinocinnolines as a novel class of CSF-1R inhibitor
David A Scott, Les A Dakin, David J Del Valle, et al.
Science (New York, N.Y.)
|
December 8, 2018
Functionally diverse type V CRISPR-Cas systems
Winston X Yan, Pratyusha Hunnewell, Lauren E Alfonse, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 13, 2008
Pyridyl and thiazolyl bisamide CSF-1R inhibitors for the treatment of cancer
David A Scott, Brian M Aquila, Geraldine A Bebernitz, et al.
Advances in Therapy
|
December 9, 2021
Treatments for Chronic Kidney Disease: A Systematic Literature Review of Randomized Controlled Trials
Juan Jose Garcia Sanchez, Juliette Thompson, David A Scott, et al.
British Journal of Cancer
|
May 13, 2021
Porphyromonas gingivalis infection exacerbates oesophageal cancer and promotes resistance to neoadjuvant chemotherapy
Shegan Gao, Yiwen Liu, Xiaoxian Duan, et al.
Nature
|
April 2, 2015
In vivo genome editing using Staphylococcus aureus Cas9
F Ann Ran, Le Cong, Winston X Yan, et al.
Nature Biotechnology
|
April 23, 2014
Genome-wide binding of the CRISPR endonuclease Cas9 in mammalian cells
Xuebing Wu, David A Scott, Andrea J Kriz, et al.
Page
of 33
Search research articles
Search
Showing results (251-260 of 327) with videos related to
Sort By:
Page
of 33
The Biochemical Journal
|
September 26, 2018
Inhibitor potency varies widely among tumor-relevant human isocitrate dehydrogenase 1 mutants
Diego Avellaneda Matteo, Grace A Wells, Lucas A Luna, et al.
The Journal of Cell Biology
|
September 2, 2022
Origin of cytoplasmic GDP-fucose determines its contribution to glycosylation reactions
Paulina Sosicka, Bobby G Ng, Lauren E Pepi, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 16, 2011
In vitro and in vivo evaluation of 6-aminopyrazolyl-pyridine-3-carbonitriles as JAK2 kinase inhibitors
Tao Wang, Stephanos Ioannidis, Lynsie Almeida, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 8, 2011
3-amido-4-anilinocinnolines as a novel class of CSF-1R inhibitor
David A Scott, Les A Dakin, David J Del Valle, et al.
Science (New York, N.Y.)
|
December 8, 2018
Functionally diverse type V CRISPR-Cas systems
Winston X Yan, Pratyusha Hunnewell, Lauren E Alfonse, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 13, 2008
Pyridyl and thiazolyl bisamide CSF-1R inhibitors for the treatment of cancer
David A Scott, Brian M Aquila, Geraldine A Bebernitz, et al.
Advances in Therapy
|
December 9, 2021
Treatments for Chronic Kidney Disease: A Systematic Literature Review of Randomized Controlled Trials
Juan Jose Garcia Sanchez, Juliette Thompson, David A Scott, et al.
British Journal of Cancer
|
May 13, 2021
Porphyromonas gingivalis infection exacerbates oesophageal cancer and promotes resistance to neoadjuvant chemotherapy
Shegan Gao, Yiwen Liu, Xiaoxian Duan, et al.
Nature
|
April 2, 2015
In vivo genome editing using Staphylococcus aureus Cas9
F Ann Ran, Le Cong, Winston X Yan, et al.
Nature Biotechnology
|
April 23, 2014
Genome-wide binding of the CRISPR endonuclease Cas9 in mammalian cells
Xuebing Wu, David A Scott, Andrea J Kriz, et al.
Page
of 33