Santa Cruz Biotechnology

ERK 2 (D-2)

#sc-1647 · western blot

128
Citing papers
3.6k
Combined citations
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Research areas

Ubiquitin and proteasome pathways7Protein Degradation and Inhibitors6Cancer-related Molecular Pathways5Cytokine Signaling Pathways and Interactions4Prostate Cancer Treatment and Research4Histone Deacetylase Inhibitors Research3Melanoma and MAPK Pathways3Cell Adhesion Molecules Research3

Papers citing this product

1
Senescent cells develop a PARP-1 and nuclear factor-κB-associated secretome (PNAS)
Genes & Development·2011·259 cit.·DOI
2
Fast regulation of AP-1 activity through interaction of lamin A/C, ERK1/2, and c-Fos at the nuclear envelope
The Journal of Cell Biology·2008·173 cit.·DOI
3
Targeting chromatin binding regulation of constitutively active AR variants to overcome prostate cancer resistance to endocrine-based therapies
Nucleic Acids Research·2015·151 cit.·DOI
4
NF‐κB/Egr‐1/Gadd45 are sequentially activated upon UVB irradiation to mediate epidermal cell death
The EMBO Journal·2004·149 cit.·DOI
5
BRAF and RAS oncogenes regulate Rho GTPase pathways to mediate migration and invasion properties in human colon cancer cells: a comparative study
Molecular Cancer·2011·142 cit.·DOI
6
Quercetin mediates preferential degradation of oncogenic Ras and causes autophagy in Ha- RAS -transformed human colon cells
Carcinogenesis·2006·118 cit.·DOI
7
Pivotal role of NAMPT in the switch of melanoma cells toward an invasive and drug-resistant phenotype
Genes & Development·2018·98 cit.·DOI
8
Cobra CRISP Functions as an Inflammatory Modulator via a Novel Zn2+- and Heparan Sulfate-dependent Transcriptional Regulation of Endothelial Cell Adhesion Molecules
Journal of Biological Chemistry·2010·96 cit.·DOI
9
A noncanonical AR addiction drives enzalutamide resistance in prostate cancer
Nature Communications·2021·89 cit.·DOI
10
Involvement of formyl peptide receptors in receptor for advanced glycation end products (RAGE) - and amyloid beta 1-42-induced signal transduction in glial cells
Molecular Neurodegeneration·2012·87 cit.·DOI

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