Cell Signaling Technology

Phospho-GRB10 (Ser476) (D4E6) Rabbit Monoclonal Antibody

#11817 · western blot · $176,415

60

Evidence Score · Well-Established

Used by 88 independent labs across 101 papers. How we score this →

100

Citing papers

3.3k

Combined citations

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Research areas

interferon and immune responses17 Adipose Tissue and Metabolism6 RNA modifications and cancer6 NF-κB Signaling Pathways5 Curcumin's Biomedical Applications5 RNA Interference and Gene Delivery5 Cytomegalovirus and herpesvirus research5 RNA regulation and disease5

Papers citing this product

1

Phosphorylation of eucaryotic translation initiation factor 4B Ser422 is modulated by S6 kinases

The EMBO Journal·2004·461 cit.·DOI

2

Control of TANK-binding Kinase 1-mediated Signaling by the γ134.5 Protein of Herpes Simplex Virus 1

Journal of Biological Chemistry·2008·190 cit.·DOI

3

A DHX9-lncRNA-MDM2 interaction regulates cell invasion and angiogenesis of cervical cancer

Cell Death and Differentiation·2018·168 cit.·DOI

4

PLP2, a potent deubiquitinase from murine hepatitis virus, strongly inhibits cellular type I interferon production

Cell Research·2008·139 cit.·DOI

5

RIG-I-mediated Activation of p38 MAPK Is Essential for Viral Induction of Interferon and Activation of Dendritic Cells

Journal of Biological Chemistry·2009·119 cit.·DOI

6

TRAF Family Member-associated NF-κB Activator (TANK) Inhibits Genotoxic Nuclear Factor κB Activation by Facilitating Deubiquitinase USP10-dependent Deubiquitination of TRAF6 Ligase

Journal of Biological Chemistry·2015·107 cit.·DOI

7

Solitary fibrous tumors: loss of chimeric protein expression and genomic instability mark dedifferentiation

Modern Pathology·2015·95 cit.·DOI

8

A selective inhibitor of mitofusin 1-βIIPKC association improves heart failure outcome in rats

Nature Communications·2019·94 cit.·DOI

9

MicroRNA-31 negatively regulates peripherally derived regulatory T-cell generation by repressing retinoic acid-inducible protein 3

Nature Communications·2015·93 cit.·DOI

10

Caspase‐8 mutations in head and neck cancer confer resistance to death receptor‐mediated apoptosis and enhance migration, invasion, and tumor growth

Molecular Oncology·2014·84 cit.·DOI

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