Rubinstein-Taybi Syndrome
|
0.100 |
Biomarker
|
disease |
BEFREE |
Here, we investigate mechanisms of CBP function during brain development in order to elucidate morphological and functional mechanisms underlying the development of RSTS.
|
31806049 |
2019 |
Intellectual Disability
|
0.030 |
GeneticVariation
|
group |
BEFREE |
Germline mutations within the CBP gene are known to cause Rubinstein-Taybi syndrome (RSTS), a developmental disorder characterized by intellectual disability, specific facial features and physical anomalies.
|
31806049 |
2019 |
Developmental Disabilities
|
0.020 |
GeneticVariation
|
group |
BEFREE |
Germline mutations within the CBP gene are known to cause Rubinstein-Taybi syndrome (RSTS), a developmental disorder characterized by intellectual disability, specific facial features and physical anomalies.
|
31806049 |
2019 |
Osteosarcoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Ras-ERK1/2 Signaling Promotes The Development Of Osteosarcoma By Regulating H2BK12ac Through CBP.
|
31695502 |
2019 |
Osteosarcoma of bone
|
0.010 |
Biomarker
|
disease |
BEFREE |
Ras-ERK1/2 Signaling Promotes The Development Of Osteosarcoma By Regulating H2BK12ac Through CBP.
|
31695502 |
2019 |
Childhood Osteosarcoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Ras-ERK1/2 Signaling Promotes The Development Of Osteosarcoma By Regulating H2BK12ac Through CBP.
|
31695502 |
2019 |
Malignant neoplasm of prostate
|
0.100 |
Biomarker
|
disease |
BEFREE |
The novel BET-CBP/p300 dual inhibitor NEO2734 is active in SPOP mutant and wild-type prostate cancer.
|
31559706 |
2019 |
Prostate carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
The novel BET-CBP/p300 dual inhibitor NEO2734 is active in SPOP mutant and wild-type prostate cancer.
|
31559706 |
2019 |
Muscular Dystrophy, Facioscapulohumeral
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Facioscapulohumeral muscular dystrophy (FSHD) results from mutations causing overexpression of the transcription factor, DUX4, which interacts with the histone acetyltransferases, EP300 and CBP.
|
31535023 |
2019 |
Triple Negative Breast Neoplasms
|
0.020 |
Biomarker
|
disease |
BEFREE |
In addition, these copper complexes decrease the stemness of triple-negative breast cancer cells and have synergistic effects with CBP on TNBC cells, indicating their great potential as a novel therapy for triple-negative breast cancer.
|
31531205 |
2019 |
Triple-Negative Breast Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
In addition, these copper complexes decrease the stemness of triple-negative breast cancer cells and have synergistic effects with CBP on TNBC cells, indicating their great potential as a novel therapy for triple-negative breast cancer.
|
31531205 |
2019 |
Rubinstein-Taybi Syndrome
|
0.100 |
Biomarker
|
disease |
BEFREE |
We also show that complementation of CBP or p300 partially reversed RSTS cell sensitivity to DNA damage.
|
31504229 |
2019 |
Carcinogenesis
|
0.080 |
GeneticVariation
|
phenotype |
BEFREE |
This model provides a mechanistic framework for understanding how Cbp/p300 loss of function mutations impact on skin tumorigenesis and suggests potential therapeutic options in CBP/p300 mutated human cSCC.
|
31397888 |
2020 |
Squamous cell carcinoma of skin
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
This model provides a mechanistic framework for understanding how Cbp/p300 loss of function mutations impact on skin tumorigenesis and suggests potential therapeutic options in CBP/p300 mutated human cSCC.
|
31397888 |
2020 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, garcinol treatment dose-dependently decreased the protein levels of p300/CBP (transcriptional cofactors and HATs) and p-Smad2/3 expression in the nucleus, thus impeding tumor cell proliferation and metastasis.
|
31371781 |
2020 |
Neoplasm Metastasis
|
0.040 |
AlteredExpression
|
phenotype |
BEFREE |
Furthermore, garcinol treatment dose-dependently decreased the protein levels of p300/CBP (transcriptional cofactors and HATs) and p-Smad2/3 expression in the nucleus, thus impeding tumor cell proliferation and metastasis.
|
31371781 |
2020 |
Tumor Cell Invasion
|
0.070 |
AlteredExpression
|
phenotype |
BEFREE |
When overexpressed BMAL1, CBP (CREB binding protein) was recruited to enhance the activity of p65 and further activate the NF-κB signaling pathway to regulate the expression of its downstream target genes, including MMP9, TNFα, uPA and IL8, and then promote the invasion and metastasis of breast cancer cells.
|
31346317 |
2019 |
Neoplasm Metastasis
|
0.040 |
AlteredExpression
|
phenotype |
BEFREE |
When overexpressed BMAL1, CBP (CREB binding protein) was recruited to enhance the activity of p65 and further activate the NF-κB signaling pathway to regulate the expression of its downstream target genes, including MMP9, TNFα, uPA and IL8, and then promote the invasion and metastasis of breast cancer cells.
|
31346317 |
2019 |
Pulmonary Fibrosis
|
0.010 |
Biomarker
|
disease |
BEFREE |
The purpose of this study is to explore the target cells of Wnt/β-catenin inhibition in pulmonary fibrosis and to examine the antifibrotic effect of the novel inhibitor PRI-724 specifically disrupting the interaction of β-catenin and CBP.
|
31298961 |
2019 |
Tumor Cell Invasion
|
0.070 |
Biomarker
|
phenotype |
BEFREE |
The reduced invasion ability in MLLT3-knockdown cells was rescued with double knockdown of MLLT3 and CBP/p300-interacting transactivator with ED rich carboxy-terminal domain 4 (CITED4; 21.0% vs. 61.5%).
|
31273053 |
2019 |
Malignant Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Although the K-CBP could be used for cancer research, the legal and regulatory aspects of data distribution and usage need to be addressed first.
|
31261630 |
2019 |
Primary malignant neoplasm
|
0.100 |
Biomarker
|
group |
BEFREE |
Although the K-CBP could be used for cancer research, the legal and regulatory aspects of data distribution and usage need to be addressed first.
|
31261630 |
2019 |
Malignant neoplasm of urinary bladder
|
0.020 |
Biomarker
|
disease |
BEFREE |
A CRISPR Interference of CBP and p300 Selectively Induced Synthetic Lethality in Bladder Cancer Cells <i>In Vitro</i>.
|
31223286 |
2019 |
Bladder Neoplasm
|
0.020 |
Biomarker
|
disease |
BEFREE |
A CRISPR Interference of CBP and p300 Selectively Induced Synthetic Lethality in Bladder Cancer Cells <i>In Vitro</i>.
|
31223286 |
2019 |
Carcinoma of bladder
|
0.020 |
Biomarker
|
disease |
BEFREE |
A CRISPR Interference of CBP and p300 Selectively Induced Synthetic Lethality in Bladder Cancer Cells <i>In Vitro</i>.
|
31223286 |
2019 |