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Transcription factor that acts during endoplasmic reticulum stress by activating unfolded protein response target genes. Additionally we are shipping CAMP Responsive Element Binding Protein 3-Like 1 Antibodies (73) and many more products for this protein.
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The results suggest that CREB3L1 is required for decidualization in mice and humans and may be linked to the pathogenesis of endometriosis in a progesterone-dependent manner.
Our data further strengthens the role for CREB3L1 as a metastasis suppressor in breast cancer and demonstrates that epigenetic silencing is a major regulator of the loss of CREB3L1 expression
CREB3L1 was expressed in 19% of RCC, which is generally resistant to doxorubicin, but in 70% of diffuse (show XRCC1 Proteins) large B-cell lymphoma that is sensitive to doxorubicin.
CREB3L1 mRNA expression is downregulated in human bladder cancer.CREB3L1 is epigenetically silenced in human bladder cancer facilitating tumor cell spreading and migration in vitro.
Cleavage of CREB3L1 releases its NH2-terminal domain from membranes, allowing it to enter the nucleus where it binds to Smad4 (show SMAD4 Proteins) to activate transcription of genes encoding proteins required for assembly of collagen-containing extracellular matrix.
CREB3L1 expression may be a useful biomarker in identifying cancer cells sensitive to doxorubicin.
Case Reports: genetically confirmed primary renal sclerosing epithelioid fibrosarcoma with EWSR1 (show EWSR1 Proteins)-CREB3L1 gene fusion.
Case Report: low-grade fibromyxoid sarcoma of the kidney found to harbor the EWSR1 (show EWSR1 Proteins)-CREB3L1 gene fusion.
EWSR1 (show EWSR1 Proteins)-CREB3L1 gene fusions are predominant over FUS (show FUS Proteins) and CREB3L2 (show CREB3L2 Proteins) rearrangements in pure sclerosing epithelioid fibrosarcoma.
CREB3L1 plays an important role in suppressing tumorigenesis and that loss of expression is required for the development of a metastatic phenotype.
OASIS affects the expression of HIF-1alpha (show HIF1A Proteins) target genes through the protein interaction with HIF-1alpha (show HIF1A Proteins), and that OASIS-HIF-1alpha (show HIF1A Proteins) complexes may play essential roles in angiogenesis during bone development.
Higher levels of CREB3L1 protein are correlated with increased doxorubicin sensitivity of xenograft RCC (show XRCC1 Proteins) tumors
Increased susceptibility to dextran sulfate sodium-induced colitis in the endoplasmic reticulum stress transducer OASIS deficient mice.
We conclude that OASIS functions as an anti-regenerative transcription factor by establishing a non-permissive microenvironment to regenerating axons
Fbxw7 (show FBXW7 Proteins) controls osteogenesis and chondrogenesis by targeting OASIS and BBF2H7 (show CREB3L2 Proteins), respectively, for degradation.
Gliosis-specific transcription factor OASIS coincides with proteoglycan core protein (show EPYC Proteins) genes in the glial scar and inhibits neurite outgrowth.
Findings demonstrate a novel mechanism by which OASIS and its associated family members are modulated by the unfolded protein response to finely control astrocyte differentiation.
OASIS plays crucial roles in promoting the differentiation of early goblet cells to mature goblet cells in the large intestine.
OASIS may play a role in bone formation through the expression of type I collagen and the secretion of bone matrix proteins in fracture healing.
Transcription factor that acts during endoplasmic reticulum stress by activating unfolded protein response target genes. Specifically involved in ER-stress response in astrocytes in the central nervous system. May play a role in gliosis. In vitro, binds to box-B element, cAMP response element (CRE) and CRE-like sequences, and activates transcription through box-B element but not through CRE (By similarity).
cAMP responsive element binding protein 3-like 1
, cyclic AMP-responsive element-binding protein 3-like protein 1-like
, BBF-2 homolog
, cAMP-responsive element-binding protein 3-like protein 1
, cyclic AMP-responsive element-binding protein 3-like protein 1
, old astrocyte specifically-induced substance
, old astrocyte specifically induced substance