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GADD45GIP1 encodes a nuclear-localized protein that may be induced by p53 and regulates the cell cycle by inhibiting G1 to S phase progression. Additionally we are shipping Growth Arrest and DNA-Damage-Inducible, gamma Interacting Protein 1 Antibodies (30) and many more products for this protein.
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SNF5 (show SMARCB1 Proteins) is indispensable for CRIF1-enhanced p53 (show TP53 Proteins) activity and its function in the suppression of cell cycle arrest in human cancer cells.
Study shows that Lck (show LCK Proteins) interacts with CRIF1 in the mitochondria and negatively regulates CRIF1-mediated translation of mitochondrion-encoded proteins.
our results support a novel function of nuclear Lck (show LCK Proteins) in promoting human leukemic T cell survival through interaction with a tumor suppressor, CRIF1
Crif1 is an indispensable regulator of PKAalpha cat that modulates the PKA/CREB (show CREB1 Proteins) signaling pathway to promote adipogenic differentiation of bone marrow mesenchymal stem cells after irradiation
The results identify the ROS (show ROS1 Proteins)-Sp1 (show PSG1 Proteins)-Crif1 pathway to be a new mechanism underlying Abeta (show APP Proteins)-induced mitochondrial dysfunction and suggest that ROS (show ROS1 Proteins)-mediated downregulation of Crif1 is a crucial event in AD pathology.
CRIF1 knockdown partially induces endothelial activation via increased ROS (show ROS1 Proteins) production and phosphorylation of p66shc (show SHC1 Proteins)
CRIF1 may play a regulatory role in the BM microenvironment-induced leukemia cell cycle arrest possibly through interacting with CDK2 (show CDK2 Proteins) and acting as a cyclin-dependent kinase (show CDK1 Proteins) inhibitor.
CKbetaBP2/CRIF1 is expressed with STAT3 (show STAT3 Proteins) in prostate cancer where STAT3 (show STAT3 Proteins) may help to offset the AR repressor effect of CKbetaBP2/CRIF1.
results indicated cell cycle arrest of Jurkat cells in the G0/G1 phase to be induced by primary cultured leukemic BMSCs associated with increased expression of CRIF1 by leukemic cells
CRIF1, unlike KEAP1 (show KEAP1 Proteins) (which only interacts with N-terminal region of NRF2 (show GABPA Proteins)), physically interacts with both N- and C-terminal regions of NRF2 (show GABPA Proteins) and promotes NRF2 (show GABPA Proteins) ubiquitination and subsequent proteasome-mediated NRF2 (show GABPA Proteins) protein degradation
Crif1(beta-/-) mouse is a useful model for the study of beta cell failure caused by mitochondrial OxPhos dysfunction.
The results identify the ROS (show ROS1 Proteins)-Sp1 (show SP1 Proteins)-Crif1 pathway to be a new mechanism underlying Abeta (show APP Proteins)-induced mitochondrial dysfunction and suggest that ROS (show ROS1 Proteins)-mediated downregulation of Crif1 is a crucial event in AD pathology.
Study showed that loss of Crif1 impairs mitochondrial oxidative phosphorylation and adipocyte differentiation in vitro and in vivo.
Crif1 plays a critical role in the maintenance of both mitochondrial structure and respiration in cardiac muscles.
Although adipose-specific Crif1-haploinsufficient mice showed normal growth and development, they became insulin (show INS Proteins)-resistant.
CRIF1 is essential for the synthesis and insertion of oxidative phosphorylation polypeptides in the mammalian mitochondrial membrane.
Results reveal that Crif1 is a novel and essential transcriptional coactivator of Elf3 (show EFNB3 Proteins) for the terminal differentiation of absorptive enterocytes.
Crif1 is a novel and essential transcriptional coactivator of STAT3 (show STAT3 Proteins) that modulates its DNA binding ability.
This gene encodes a nuclear-localized protein that may be induced by p53 and regulates the cell cycle by inhibiting G1 to S phase progression. The encoded protein may interact with other cell cycle regulators.
CKII beta binding protein 2
, CKII beta-associating protein
, CR6 interacting factor 1
, growth arrest and DNA damage-inducible proteins-interacting protein 1
, growth arrest- and DNA damage-inducible GADD45G-interacting protein
, p53-responsive gene 6 protein
, papillomavirus L2 interacting nuclear protein 1
, growth arrest and DNA-damage-inducible proteins-interacting protein 1