Cul3 Roc1

Novel CUL3 Variant Causing Familial Hyperkalemic Hypertension Impairs

ACLY forms a complex with CUL3 Cullin3KLHL25 Kelchlike family

Double Mutants for cul3 Testis and roc1b Block Caspase Activation

Frontiers Current trends of highrisk gene Cul3 in neurodevelopmental

Regulation of the CUL3 Ubiquitin Ligase by a CalciumDependent Co

Cul3 binds to multiple BTB domainsa BTB domains from various

Double Mutants for cul3 Testis and roc1b Block Caspase Activation

Frontiers Current trends of highrisk gene Cul3 in neurodevelopmental

CUL3 E3 ligases in plant development and environmental response

Cul3 disruption causes sustained proximal tubule injury and

CUL3 functions in mitotic entry A A schematic protocol for cell

CUL3 functions in mitotic progression A Asynchronous HeLa and U2OS

Characterization of RhoBTBdependent Cul3 ubiquitin ligase complexes

CUL3 induces mitochondrial dysfunction via MRPL12 ubiquitination in

Brain regionspecific Cul3 deficiency induces largescale changes of

Full article CUL3 cullin 3mediated ubiquitination and degradation

Transcriptional activation of Cul3 rescues the cell migration defects

CUL3 Alchetron The Free Social Encyclopedia

CUL3 induces mitochondrial dysfunction via MRPL12 ubiquitination in

Coadaptor driven assembly of a CUL3 E3 ligase complex Molecular Cell

Structural Basis for Cul3 Protein Assembly with the BTBKelch Family of

CUL3 overexpression enhances the ubiquitination of RhoGDI1 HEK293T

Cul3 disruption causes progression into renal fibrosis and persistent

Novel CUL3 Variant Causing Familial Hyperkalemic Hypertension Impairs

ROC1 and ROC2 form active ubiquitin ligases with all cullins A and C

Tissuespecific actions of CUL3 and CUL39 a CUL3 employs different

CUL3 and BPM1 overlap in the cytoplasm but not in the nucleolus AD

Frontiers Current trends of highrisk gene Cul3 in neurodevelopmental

GCL and CUL3 Control the Switch between Cell Lineages by Mediating

Cul3 and Rbx1 WT AREs and not mutant AREs are inducible by

De Novo CUL3 Variant in a Child Presenting With Hypertension and Kidney

The C terminus of CUL1 interacts with ROC1 in a region that includes

Mapping the ROC1 binding region in CUL1 293T cells transiently

Insights into the diverse mechanisms and effects of variant CUL3

Novel CUL3 Variant Causing Familial Hyperkalemic Hypertension Impairs

LabelFree Interactome Analysis Revealed an Essential Role of CUL3

Figure 1 from Prospect of divergent roles for the CUL3 system in

3 CUL3 mutations tend to be mutually exclusive with KEAP1NRF2

Double Mutants for cul3 Testis and roc1b Block Caspase Activation

CUL3 antibodies Antibody search engine CiteAb

Cul3 loss leads to migration deficits in vivo and in vitro a Scheme

of the functions and substrates of three Cul3 complexes in cancer

The cul3 mds15 Alleles Contain Mutations in a New Exon of the cullin3

Weaker interaction of Keap1 with Cul3 compared with other receptors

Low Cul3 expression changes normal cell cycle profiles A The cell

Interaction Studies of WRI1 with BPM and CUL3 Proteins Download

Novel CUL3 Variant Causing Familial Hyperkalemic Hypertension Impairs

A B Representative immunohistochemistry expression patterns of Cul3

Regulation of the CUL3 Ubiquitin Ligase by a CalciumDependent Co

Frontiers Autism risk gene Cul3 alters neuronal morphology via

The Cul3 ubiquitin ligase engages Insomniac as an adaptor to impact

Translocation of Cul3 and NAC1 by bicuculline into dendrites a

Frontiers Autism risk gene Cul3 alters neuronal morphology via

CUL3 mediates STAT3 phosphorylation and IL10 production via a

CUL3 induces mitochondrial dysfunction via MRPL12 ubiquitination in

CUL3 E3 ligases in plant development and environmental response PMC

Low Cul3 expression changes normal cell cycle profiles A The cell

CUL3 expression is dysregulated in AKICKD mouse models and human

Poor elaboration of dendrites in Cul3 mutant neurons Closeup views of

Cullin 3 and Blood Pressure Regulation Insights From Familial

A Proposed structural organization of SCFROC1 and interactions

SpringerLink Header Hypertension and the Kidney Robert M Carey

The Cul3Roc1bKlhl10 Complex Promotes Protein Ubiquitination during

CRL3 mediates TNFAIP1 ubiquitination and degradation a b The

BTB Protein Keap1 Targets Antioxidant Transcription Factor Nrf2 for

PDF Cullin 3 Exon 9 Deletion in Familial Hyperkalemic Hypertension

MEL26Cul3Roc1 promotes MEI1 ubiquitination in vitroa The BTB

Cullin 3 and Blood Pressure Regulation Insights From Familial

Cullin 3 mutant causing familial hyperkalemic hypertension lacks normal

Cul3 structure is illustrated CRL3 contains three primary components

Protein Degradation CUL3 and BTB Partners in Proteolysis Current

Cullin 3 and Blood Pressure Regulation Insights From Familial

Nature子刊 | E3泛素连接酶如何组装成完整有活性二聚化六元复合物？尹玉新团队给出答案医药新闻-ByDrug-一站式医药资源共享中心-医药魔方

Nature E3ByDrug

BTB domain of KIAA1309 binds to an Nterminal sequence of Cul3a A

Activation of UBC5 Ubiquitinconjugating Enzyme by the RING Finger of

Full article Cullin3 and the endocytic system

RAC1 activity is increased in CUL3KD cells and inhibited by the

JCI Insight Mutant Cullin 3 causes familial hyperkalemic hypertension

Structural model of E3 ubiquitin ligase complex CUL4DDBROC1 Protein

Cullin 3 CUL3 is essential for vascular endothelial VEcadherin

1 Assembly of CullinRING E3 ubiquitin ligases CRLs Download

Regulation of TIP60 by ATF2 Modulates ATM Activation Journal of

Cullin 3 and Blood Pressure Regulation Insights From Familial

Role of Nrf2 and Its Activators in Cardiocerebral Vascular Disease PMC

Disruption of CUL3mediated ubiquitination causes proximal tubule

The E3 Ligase CUL3RDX Controls Centromere Maintenance by

Unbiased interrogation of functional lysine residues in human proteome

JCI Insight Cullin3 regulates the renal baroreceptor machinery that

Active Treatment Treatment Spotlight on Anemia

Mechanisms and controversies in mutant Cul3mediated familial

Ubiquitin Ligase Activity of Cul3KLHL7 Protein Is Attenuated by

Recruitment of a ROC1CUL1 Ubiquitin Ligase by Skp1 and HOS to Catalyze

A Cul3Based E3 Ligase Removes Aurora B from Mitotic Chromosomes

Cullin 3 mutant causing familial hyperkalemic hypertension lacks normal

CUL3 migrates to nuclei in response to RA A MCF7 cells treated

Neddylation and Its Target Cullin 3 Are Essential for Adipocyte

The Cullin3Rbx1KLHL9 E3 ubiquitin ligase complex ubiquitinates Rheb

Cullin3 CUL3 and KCTD10 regulate cell proliferation in SKBR3 cells

A Cul3Based E3 Ligase Removes Aurora B from Mitotic Chromosomes

Figure 4 from The SCFROC1 E3 Ubiquitin Ligase Utilizes Two Distinct

The CRL3BTBD9 E3 ubiquitin ligase complex targets TNFAIP1 for

Structure of the Cand1Cul1Roc1 Complex Reveals Regulatory Mechanisms

The E3 UbiquitinProtein Ligase Cullin 3 Regulates HIV1 Transcription

JCI Insight Mutant Cullin 3 causes familial hyperkalemic hypertension

Human Genetics and Genomics Advances Human Genetics and Genomics Advances

Cullin 3 mutant causing familial hyperkalemic hypertension lacks normal

Identification of the regions of interaction in ARMC5 CUL3 and RPB1

Disruption of CUL3mediated ubiquitination causes proximal tubule

SPOPCul3Rbx1 ubiquitin ligase complex targets SRC3 protein for

KEAP1CUL3RBX1 E3ligase protein complex In the absence of ROS a

ROC1 a Homolog of APC11 Represents a Family of Cullin Partners with

Generation and characterization of Cul3 mouse model a Download

Cullin 3 CUL3 required for endothelial barrier function a

Identification of the regions of interaction in ARMC5 CUL3 and RPB1

CUL1 Antibody Cell Signaling Technology

CUL3KLHL25 ubiquitinates and degrades ACLY A The downregulation of

Behavioral circuitry and molecular aberrations by regionspecific

Recruitment of a ROC1CUL1 Ubiquitin Ligase by Skp1 and HOS to Catalyze

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