Rnf8 Rnf168

Figure 1 from The ubiquitin ligases RNF8 and RNF168 display rapid but

The RNF8 and RNF168 Ubiquitin Ligases Regulate Pro and AntiResection

RNF8 and RNF168 promote the accumulation of 53BP1 and RAP80 at DSB

RNF8 and RNF168 have epistatic NHEJ functions A Western blot of

The RNF8 and RNF168 Ubiquitin Ligases Regulate Pro and AntiResection

RNF8 and RNF168 promote the accumulation of 53BP1 and RAP80 at DSB

A viral E3 ligase targets RNF8 and RNF168 to control histone

RNF8 and RNF168 promote the accumulation of 53BP1 and RAP80 at DSB

The RNF8 and RNF168 Ubiquitin Ligases Regulate Pro and AntiResection

A viral E3 ligase targets RNF8 and RNF168 to control histone

ZNF451 collaborates with RNF8 to regulate RNF168 localization and

RNF8 binds to FOXM1 and is required for the recruitment of RNF168 and

The RNF8 and RNF168 Ubiquitin Ligases Regulate Pro and AntiResection

BLM is ubiquitylated by RNF8 and RNF168 in vivo A Loss of RNF8 leads

Frontiers Put a RING on it regulation and inhibition of RNF8 and

RNF168 Ubiquitinates K1315 on H2AH2AX to Drive DNA Damage Signaling Cell

Frontiers Put a RING on it regulation and inhibition of RNF8 and

RNF168 Ubiquitinates K1315 on H2AH2AX to Drive DNA Damage Signaling Cell

Calling RNF168 to action

Frontiers Put a RING on it regulation and inhibition of RNF8 and

Model of RNF8RNF168mediated ubiquitylation at DSBs RNF8 is recruited

Structure of the RING domains of E3 ligases RNF8 and RNF168 a Ribbon

New answers to the old RIDDLE RNF168 and the DNA damage response

RNF168 Binds and Amplifies Ubiquitin Conjugates on Damaged Chromosomes

Ubiquitination of chromatin regulates DSB repair A Following RNF8

Pin1promoted SUMOylation of RNF168 restrains its chromatin

Frontiers Put a RING on it regulation and inhibition of RNF8 and

E3 ligase activity of RNF168 at stake on ring domain mutation Journal

RNF168 Binds and Amplifies Ubiquitin Conjugates on Damaged Chromosomes

Structural basis for role of ring finger protein RNF168 RING domain PMC

RNF168 Ubiquitinates K1315 on H2AH2AX to Drive DNA Damage Signaling Cell

PCNAbinding activity separates RNF168 functions in DNA replication and

RNF168 Binds and Amplifies Ubiquitin Conjugates on Damaged Chromosomes

RNF168 Ubiquitinates K1315 on H2AH2AX to Drive DNA Damage Signaling Cell

RNF168 forms a functional complex with RAD6 during the DNA damage

RNF168 Binds and Amplifies Ubiquitin Conjugates on Damaged Chromosomes

RNF8 promotes cell survival upon replication stress a Western blot

53BP1 degradation upon irradiation is regulated by RNF8 and RNF168 A

Complex formation and ubiquitylation activity of RNF168 1113 and

RNF168 RING domain interacts with the target through a charged region

RNF8 stimulates the formation of K48linked ubiquitin chains on JMJD2A

RNF126 Quenches RNF168 Function in the DNA Damage Response Abstract

RNF8 interacts with Ubc13 through its ZnFs A alignment of the RNF8

RNF168 in Tumor Progression Encyclopedia MDPI

RNF168 forms a functional complex with RAD6 during the DNA damage

a Representative results of immunohistochemical staining for RNF168

New answers to the old RIDDLE RNF168 and the DNA damage response

Structural basis for role of ring finger protein RNF168 RING domain PMC

The Functions of DNA Damage Factor RNF8 in the Pathogenesis and

RNF168 is expressed at high levels in LN renal tissues and podocytes a

53BP1 IRIF can be restored in RNF8 depleted cells by expression of

The expression of RNF168 and the activation of NF-κB signaling pathway ...

The expression of RNF168 and the activation of NFB signaling pathway

JCI Ubiquitin ligase RNF8 suppresses Notch signaling to regulate

The nucleosomal acidic patch is critical for RNF168 reaction a The

Structure of the RING domains of E3 ligases RNF8 and RNF168 a Ribbon

RNF168 regulates the growth and survival of the human growth factor

BRD7 recruits RNF168 to the DSB site AB BRD7 interacts with RNF168

Critical Roles of Ring Finger Protein RNF8 in Replication Stress

RNF8 and H2AX function epistatically in class switching and

RNF168 Ubiquitinates K1315 on H2AH2AX to Drive DNA Damage Signaling Cell

The Functions of DNA Damage Factor RNF8 in the Pathogenesis and

Recruitment of BLM to the sites of stalled replication depends on RNF8

The RNF168 paralog RNF169 defines a new class of ubiquitylated histone

Figure 2 from PCNAbinding activity separates RNF168 functions in DNA

RNF168 Binds and Amplifies Ubiquitin Conjugates on Damaged Chromosomes

Conjugation of NEDD8 regulates RNF168 E3 ligase activity A RNF168 is

Model of RNF8RNF168mediated ubiquitylation at DSBs RNF8 is recruited

RNF168 ubiquitylates 53BP1 and controls its response to DNA double

Emerging Roles of RNF168 in Tumor Progression

Roles of PIAS4mediated SUMOylation of HERC2 and RNF168 in cellular DSB

Complex formation and ubiquitylation activity of RNF168 1113 and

Ectopic RNF168 promotes DNA synthesis in the presence of HU A GFP or

RNF168 Recombinant Rabbit Monoclonal Antibody PSH0737 Invitrogen

RNF168 facilitates proliferation and invasion of esophageal carcinoma

Modulation of RNF8RNF168 signaling through deubiquitylation

Assembly of checkpoint and repair machineries at DNA damage sites PMC

Figure 1 from RING Domain Mutation Hinders the E3 Ligase Activity of

RNF8 and RNF168mediated repair of RAG or AIDinduced DSBs A DSBs

Tandem Protein Interaction Modules Organize the UbiquitinDependent

UVinduced H1 ubiquitylation is mediated by HUWE1 and stimulates the

The RIDDLE Syndrome Protein Mediates a UbiquitinDependent Signaling

Figure 2 from The RNF8RNF168 ubiquitin ligase cascade facilitates

RNF169 accumulates in DSB repair foci in an RNF8RNF168dependent

RNF8and RNF168mediated repair of RAGor AIDinduced DSBs A DSBs

Lack of recruitment of the ubiquitin E3 ligases RNF8 RNF168 and BRCA1

Ring Finger Protein RNF169 Antagonizes the Ubiquitindependent

Assembly of checkpoint and repair machineries at DNA damage sites

UDM1 is required for RNF168mediated 53BP1 recruitment a Schematic

The RNF8RNF168 ubiquitin ligase cascade facilitates class switch

Figure 1 from The Deubiquitylating Enzyme USP44 Counteracts the DNA

The RIDDLE Syndrome Protein Mediates a UbiquitinDependent Signaling

RNF168mediated ubiquitin signaling inhibits the viability of BRCA1

RNF169 accumulates in DSB repair foci in an RNF8RNF168dependent

Full article SET8 localization to chromatin flanking DNA damage is

SUMOylation of HERC2 promotes its interaction with RNF8 A

RNF8ubiquitinated KMT5A is required for RNF168induced H2A

Figure 1 from The Deubiquitylating Enzyme USP44 Counteracts the DNA

SUMO accumulation at sites associated with incoming viral genomes is

RNF8ubiquitinated KMT5A is required for RNF168induced H2A

Overexpression of RNF168 but not RNF4 and RNF8 effectively repressed

VGLL3 modulates chemosensitivity through promoting DNA doublestrand

Overexpression of RNF168 but not RNF4 and RNF8 effectively repressed

Proposed model for the accumulation of BRCA1 complexes at DSB sites

Overexpression of RNF168 but not RNF4 and RNF8 effectively repressed

Defective DNA repair and sustained DNAdamage signaling in

The RNF8RNF168 ubiquitin ligase cascade facilitates class switch

Figure 3 from The Deubiquitylating Enzyme USP44 Counteracts the DNA

Conjugated ubiquitin accumulation at sites associated with incoming

RNF126 168 and CUL1 The Potential Utilization of MultiFunctional E3

PDF Opposing roles of RNF8RNF168 and deubiquitinating enzymes in

A PRMT5RNF168SMURF2 Axis Controls H2AX ProteostasisCell Reports XMOL

53BP1 accumulation at sites associated with incoming HSV1 genomes is

Chromatin Remodeling Complex

Cell Signaling Pathway

Histone H1

Ubiquitin Staining

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