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VDR complex with Aromatic-D-Ring Analog[TRANSCRIPTION]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
VDR complex with aromatic D-ring analog[TRANSCRIPTION]
VDR complex with BXL-62[TRANSCRIPTION]
VDR complex of a side-chain hydroxylated derivatives of lithocholic acid[TRANSCRIPTION]
VDR complex with a side-chain hydroxylated derivative of lithocholic acid[TRANSCRIPTION]
Allene-Based Design of a Noncalcemic Vitamin D Receptor Agonist[GENE REGULATION]
VDR complex with LCA derivative[TRANSCRIPTION]
Structure of zVDR LBD-Calcitriol in complex with chimera 18[GENE REGULATION]
Structure of zVDR LBD-Calcitriol in complex with chimera 13[GENE REGULATION]
Structure of zVDR LBD-Calcitriol in complex with chimera 12[GENE REGULATION]
Structure of zVDR LBD-calcitriol in complex with chimera 11[GENE REGULATION]
Structure of zVDR LBD-Calcitriol in complex with chimera 10[GENE REGULATION]
VDR-ZK168281 complex[TRANSCRIPTION]
Optimization and biological evaluation of thiazole-bis-amide inverse agonists of RORgt[NUCLEAR PROTEIN]
RORCVAR2 (RORGT, 264-499) IN COMPLEX WITH COMPOUND 9 AT 2.3A: Identification of N-aryl imidazoles as potent and selective RORgt inhibitors[TRANSCRIPTION]
RORCVAR2 (RORGT, 264-499) IN COMPLEX WITH COMPOUND 4 AT 2.2A: Identification of N-aryl imidazoles as potent and selective RORgt inhibitors[TRANSCRIPTION]
RORCVAR2 (RORGT, 264-499) IN COMPLEX WITH COMPOUND 2 AT 2.3A: Identification of N-aryl imidazoles as potent and selective RORgt inhibitors[TRANSCRIPTION]
RORCVAR2 (RORGT, 264-499) IN COMPLEX WITH COMPOUND 1: Identification of N-aryl imidazoles as potent and selective RORgt inhibitors[TRANSCRIPTION]
Structure of RORgt in complex with a novel inverse agonist[nuclear protein/agonist]
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