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<identifier identifierType="DOI">10.15151/ESRF-ES-2113990035</identifier>
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<creatorName nameType="Personal">Vladimir ARINKIN</creatorName>
<givenName>Vladimir</givenName>
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<creatorName nameType="Personal">Vladimir ARINKIN</creatorName>
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<creatorName nameType="Personal">Ege CIGIRGAN</creatorName>
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<creatorName nameType="Personal">Ege CIGIRGAN</creatorName>
<givenName>Ege</givenName>
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<creator>
<creatorName nameType="Personal">Max NANAO</creatorName>
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<creatorName nameType="Personal">Jirka PESCHEK</creatorName>
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<creator>
<creatorName nameType="Personal">Jirka PESCHEK</creatorName>
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<familyName>Peschek</familyName>
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<title>Heidelberg BAG (HeidelBAG)</title>
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<publisher>Example Institute</publisher>
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<resourceType resourceTypeGeneral="Collection">Data from large facility measurement</resourceType>
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<date dateType="Collected">2025-06-01T07:30:00Z/2025-06-02T06:00:00Z</date>
<date dateType="Accepted">2025-06-02T06:00:00Z</date>
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<description descriptionType="Abstract">The HeidelBAG unifies structural efforts of EMBL Heidelberg inclusive former PIs and the Heidelberg University Biochemistry Center (BZH). Central to all projects are large assemblies involved in chromosome organization and transcription control, in nuclear and cytoplasmic RNA regulation, in translational control by ribosome associated factors, in protein targeting and membrane protein insertion, or in post-translational and RNA modification and processing. Nearly all projects make use of integrated structural biology techniques (MX, SAXS/SANS, NMR, cryo-EM) combined with complementary biophysical approaches. MX remains the essential and invariant tool for high resolution information of challenging functional modules.</description>
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