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Showing results (81-90 of 97) with videos related to

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Endocrinology|December 6, 2003
Tyrosine agonists reverse the molecular defects associated with dominant-negative mutations in human peroxisome proliferator-activated receptor gammaMaura Agostini, Mark Gurnell, David B Savage, et al.
Cell Reports|February 27, 2020
Mechanism of Crosstalk between the LSD1 Demethylase and HDAC1 Deacetylase in the CoREST ComplexYun Song, Lisbeth Dagil, Louise Fairall, et al.
Molecular and Cellular Biology|December 6, 2021
Structure-Guided Approach to Relieving Transcriptional Repression in Resistance to Thyroid Hormone αBeatriz Romartinez-Alonso, Maura Agostini, Heulyn Jones, et al.
Journal of the American Chemical Society|February 17, 2022
Histone H2B Deacylation Selectivity: Exploring Chromatin's Dark Matter with an Engineered SortaseZhipeng A Wang, Samuel D Whedon, Mingxuan Wu, et al.
Nature Communications|June 28, 2020
The MiDAC histone deacetylase complex is essential for embryonic development and has a unique multivalent structureRobert E Turnbull, Louise Fairall, Almutasem Saleh, et al.
Diabetes|April 7, 2018
A Pharmacogenetic Approach to the Treatment of Patients With <i>PPARG</i> MutationsMaura Agostini, Erik Schoenmakers, Junaid Beig, et al.
Journal of Medical Genetics|January 16, 2016
A specific mutation in TBL1XR1 causes Pierpont syndromeCharlotte A Heinen, Aldo Jongejan, Peter J Watson, et al.
Journal of the American Chemical Society|November 25, 2024
Circular Engineered Sortase for Interrogating Histone H3 in ChromatinSamuel D Whedon, Kwangwoon Lee, Zhipeng A Wang, et al.
Biorxiv : the Preprint Server for Biology|October 7, 2024
A circular engineered sortase for interrogating histone H3 in chromatinSamuel D Whedon, Kwangwoon Lee, Zhipeng A Wang, et al.
Human Molecular Genetics|May 9, 2019
A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosisJacqueline A C Goos, Walter K Vogel, Hana Mlcochova, et al.
Pageof 10

Showing results (81-90 of 97) with videos related to

Sort By:
Pageof 10
Endocrinology|December 6, 2003
Tyrosine agonists reverse the molecular defects associated with dominant-negative mutations in human peroxisome proliferator-activated receptor gammaMaura Agostini, Mark Gurnell, David B Savage, et al.
Cell Reports|February 27, 2020
Mechanism of Crosstalk between the LSD1 Demethylase and HDAC1 Deacetylase in the CoREST ComplexYun Song, Lisbeth Dagil, Louise Fairall, et al.
Molecular and Cellular Biology|December 6, 2021
Structure-Guided Approach to Relieving Transcriptional Repression in Resistance to Thyroid Hormone αBeatriz Romartinez-Alonso, Maura Agostini, Heulyn Jones, et al.
Journal of the American Chemical Society|February 17, 2022
Histone H2B Deacylation Selectivity: Exploring Chromatin's Dark Matter with an Engineered SortaseZhipeng A Wang, Samuel D Whedon, Mingxuan Wu, et al.
Nature Communications|June 28, 2020
The MiDAC histone deacetylase complex is essential for embryonic development and has a unique multivalent structureRobert E Turnbull, Louise Fairall, Almutasem Saleh, et al.
Diabetes|April 7, 2018
A Pharmacogenetic Approach to the Treatment of Patients With <i>PPARG</i> MutationsMaura Agostini, Erik Schoenmakers, Junaid Beig, et al.
Journal of Medical Genetics|January 16, 2016
A specific mutation in TBL1XR1 causes Pierpont syndromeCharlotte A Heinen, Aldo Jongejan, Peter J Watson, et al.
Journal of the American Chemical Society|November 25, 2024
Circular Engineered Sortase for Interrogating Histone H3 in ChromatinSamuel D Whedon, Kwangwoon Lee, Zhipeng A Wang, et al.
Biorxiv : the Preprint Server for Biology|October 7, 2024
A circular engineered sortase for interrogating histone H3 in chromatinSamuel D Whedon, Kwangwoon Lee, Zhipeng A Wang, et al.
Human Molecular Genetics|May 9, 2019
A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosisJacqueline A C Goos, Walter K Vogel, Hana Mlcochova, et al.
Pageof 10