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Publications by Molly Broache
Nuclear Receptor Co-Repressors Are Required for the Histone-Deacetylase Activity of HDAC3 in Vivo
Nature Structural and Molecular Biology
Structural Biology
Molecular Biology
Related publications
The Nuclear Envelope Protein Emerin Binds Directly to Histone Deacetylase 3 (HDAC3) and Activates HDAC3 Activity
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Frataxin (FXN); Histone Deacetylase 3 (HDAC3)
Science-Business eXchange
Deacetylase Activity of Histone Deacetylase 3 Is Required for productiveVDJrecombination and B-Cell Development
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Histone Deacetylase Activity Is Required for Botrylloides Leachii Whole Body Regeneration
Journal of Experimental Biology
Evolution
Ecology
Insect Science
Molecular Biology
Systematics
Animal Science
Medicine
Aquatic Science
Behavior
Zoology
Physiology
Engineered Repressors Are Potent Inhibitors of Androgen Receptor Activity
Oncotarget
Oncology
Holocarboxylase Synthetase Interacts Physically With Nuclear Receptor Co-Repressor, Histone Deacetylase 1 and a Novel Splicing Variant of Histone Deacetylase 1 to Repress Repeats
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Sds3 (Suppressor of Defective Silencing 3) Is an Integral Component of the Yeast Sin3·Rpd3 Histone Deacetylase Complex and Is Required for Histone Deacetylase Activity
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
HDAC3 and HDAC8 Are Required for Cilia Assembly and Elongation
Biology Open
Biochemistry
Agricultural
Genetics
Molecular Biology
Biological Sciences
Histone Deacetylase 10 Relieves Repression on the Melanogenic Program by Maintaining the Deacetylation Status of Repressors
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
