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Search results 201 to 214 out of 214 for Crbn

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0.019s
Type Details Score
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Publication
First Author: Nguyen TV
Year: 2017
Journal: Proc Natl Acad Sci U S A
Title: p97/VCP promotes degradation of CRBN substrate glutamine synthetase and neosubstrates.
Volume: 114
Issue: 14
Pages: 3565-3571
Allele
Name: cereblon; endonuclease-mediated mutation 2, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Not Specified
Allele
Name: cereblon; endonuclease-mediated mutation 3, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Not Specified
Allele
Name: cereblon; endonuclease-mediated mutation 1, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Not Specified
Interaction Experiment
Description: Crbn modulates calcium influx by regulating Orai1 during efferocytosis.
Allele
Name: transgene insertion 123, P Leif Bergsagel
Allele Type: Transgenic
Attribute String: Inserted expressed sequence
Strain
Attribute String: coisogenic, endonuclease-mediated mutation, mutant strain
Publication
First Author: Nguyen TV
Year: 2016
Journal: Mol Cell
Title: Glutamine Triggers Acetylation-Dependent Degradation of Glutamine Synthetase via the Thalidomide Receptor Cereblon.
Volume: 61
Issue: 6
Pages: 809-20
Publication
First Author: Hirose Y
Year: 2020
Journal: Proc Natl Acad Sci U S A
Title: Hypnotic effect of thalidomide is independent of teratogenic ubiquitin/proteasome pathway.
Volume: 117
Issue: 37
Pages: 23106-23112
Publication
First Author: Basel-Vanagaite L
Year: 2006
Journal: J Med Genet
Title: The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation.
Volume: 43
Issue: 3
Pages: 203-10
Publication
First Author: Zhang S
Year: 2022
Journal: Theranostics
Title: The PROTAC selectively degrading Bcl-x(L) represents a novel Hedgehog pathway inhibitor with capacity of combating resistance to Smoothened inhibitors while sparing bone growth.
Volume: 12
Issue: 17
Pages: 7476-7490