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Epigenetics
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January 28, 2015
Studies on the catalytic domains of multiple JmjC oxygenases using peptide substrates
Sophie T Williams, Louise J Walport, Richard J Hopkinson, et al.
FEBS Letters
|
August 30, 2018
Mechanistic and structural studies of KDM-catalysed demethylation of histone 1 isotype 4 at lysine 26
Louise J Walport, Richard J Hopkinson, Rasheduzzaman Chowdhury, et al.
The Journal of Biological Chemistry
|
May 7, 2014
Human UTY(KDM6C) is a male-specific Nϵ-methyl lysyl demethylase
Louise J Walport, Richard J Hopkinson, Melanie Vollmar, et al.
Chembiochem : a European Journal of Chemical Biology
|
November 30, 2022
Biochemical and Structural Insights into FIH-Catalysed Hydroxylation of Transient Receptor Potential Ankyrin Repeat Domains
Benjamin G Saward, Thomas M Leissing, Ian J Clifton, et al.
Bioorganic & Medicinal Chemistry
|
May 17, 2018
Investigations on small molecule inhibitors targeting the histone H3K4 tri-methyllysine binding PHD-finger of JmjC histone demethylases
Bhaskar Bhushan, Alexandre Erdmann, Yijia Zhang, et al.
Nature Communications
|
April 25, 2018
Publisher Correction: JMJD5 is a human arginyl C-3 hydroxylase
Sarah E Wilkins, Md Saiful Islam, Joan M Gannon, et al.
The Biochemical Journal
|
October 25, 2012
Investigations on the oxygen dependence of a 2-oxoglutarate histone demethylase
Elena M Sánchez-Fernández, Hanna Tarhonskaya, Khalid Al-Qahtani, et al.
Journal of Proteome Research
|
June 30, 2010
Small-molecule-based inhibition of histone demethylation in cells assessed by quantitative mass spectrometry
Mukram M Mackeen, Holger B Kramer, Kai-Hsuan Chang, et al.
Organic & Biomolecular Chemistry
|
January 17, 2017
Selective recognition of the di/trimethylammonium motif by an artificial carboxycalixarene receptor
Thomas Hanauer, Richard J Hopkinson, Kamal Patel, et al.
Nature Communications
|
March 23, 2018
JMJD5 is a human arginyl C-3 hydroxylase
Sarah E Wilkins, Md Saiful Islam, Joan M Gannon, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 50) with videos related to
Sort By:
Page
of 5
Epigenetics
|
January 28, 2015
Studies on the catalytic domains of multiple JmjC oxygenases using peptide substrates
Sophie T Williams, Louise J Walport, Richard J Hopkinson, et al.
FEBS Letters
|
August 30, 2018
Mechanistic and structural studies of KDM-catalysed demethylation of histone 1 isotype 4 at lysine 26
Louise J Walport, Richard J Hopkinson, Rasheduzzaman Chowdhury, et al.
The Journal of Biological Chemistry
|
May 7, 2014
Human UTY(KDM6C) is a male-specific Nϵ-methyl lysyl demethylase
Louise J Walport, Richard J Hopkinson, Melanie Vollmar, et al.
Chembiochem : a European Journal of Chemical Biology
|
November 30, 2022
Biochemical and Structural Insights into FIH-Catalysed Hydroxylation of Transient Receptor Potential Ankyrin Repeat Domains
Benjamin G Saward, Thomas M Leissing, Ian J Clifton, et al.
Bioorganic & Medicinal Chemistry
|
May 17, 2018
Investigations on small molecule inhibitors targeting the histone H3K4 tri-methyllysine binding PHD-finger of JmjC histone demethylases
Bhaskar Bhushan, Alexandre Erdmann, Yijia Zhang, et al.
Nature Communications
|
April 25, 2018
Publisher Correction: JMJD5 is a human arginyl C-3 hydroxylase
Sarah E Wilkins, Md Saiful Islam, Joan M Gannon, et al.
The Biochemical Journal
|
October 25, 2012
Investigations on the oxygen dependence of a 2-oxoglutarate histone demethylase
Elena M Sánchez-Fernández, Hanna Tarhonskaya, Khalid Al-Qahtani, et al.
Journal of Proteome Research
|
June 30, 2010
Small-molecule-based inhibition of histone demethylation in cells assessed by quantitative mass spectrometry
Mukram M Mackeen, Holger B Kramer, Kai-Hsuan Chang, et al.
Organic & Biomolecular Chemistry
|
January 17, 2017
Selective recognition of the di/trimethylammonium motif by an artificial carboxycalixarene receptor
Thomas Hanauer, Richard J Hopkinson, Kamal Patel, et al.
Nature Communications
|
March 23, 2018
JMJD5 is a human arginyl C-3 hydroxylase
Sarah E Wilkins, Md Saiful Islam, Joan M Gannon, et al.
Page
of 5