Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Yet, none of these T-ALLs had a clonal chromosome t(12;14) translocation that deleted Bcl11b indicating that Tcrδ translocations that inactivate a copy of Bcl11b promote transformation of Atm-deficient thymocytes.
|
25486566 |
2014 |
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
Within the standard risk group of thymic T-ALL (n = 102), low BCL11b expression identified patients with an unexpected poor outcome compared to those with high expression (5-year OS: 20%, n = 18 versus 62%, n = 84, P < 0.01).
|
25023966 |
2014 |
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
When highly efficient and specific BCL11B-935-siRNA was used to analyze the inhibition of BCL11B mRNA level in primary T-cell acute lymphoblastic leukemia (T-ALL) cells, similar result was obtained.
|
21756541 |
2011 |
Chronic Lymphocytic Leukemia
|
0.080 |
Biomarker
|
disease |
BEFREE |
We recently found that a unique subset of innate-like γδ T cells develops from the DN2a stage of the fetal thymus independently of the zinc-finger transcription factor B cell leukemia/lymphoma 11b (Bcl11b).
|
29091759 |
2017 |
Leukemia, B-Cell
|
0.040 |
Biomarker
|
disease |
BEFREE |
We recently found that a unique subset of innate-like γδ T cells develops from the DN2a stage of the fetal thymus independently of the zinc-finger transcription factor B cell leukemia/lymphoma 11b (Bcl11b).
|
29091759 |
2017 |
Huntington Disease
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
We propose that sequestration and/or decreased expression of Bcl11b in HD is responsible, at least in part, for the dysregulation of striatal gene expression observed in HD and may contribute to the specificity of pathology observed in this disease.
|
18595722 |
2008 |
Asthma
|
0.020 |
Biomarker
|
disease |
BEFREE |
We found significantly decreased Bcl11b but increased IL-17A and TGF-β1 expression in patients with asthma and a strongly negative correlation between Bcl11b and these 2 cytokines in SA patients.
|
30088373 |
2018 |
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
0.400 |
Biomarker
|
disease |
BEFREE |
We describe a novel variant t(5;14) whereby NKX2-5, a related (NK-like family) homeobox gene located approximately 2 Mb telomeric of TLX3, juxtaposes BCL11B in a subset of T-cell ALL cell lines.
|
14500364 |
2003 |
Alopecia
|
0.010 |
Biomarker
|
disease |
BEFREE |
We demonstrated that keratinocytic ablation of Ctip2 leads to atopic dermatitis (AD)-like skin inflammation, characterized by alopecia, pruritus and scaling, as well as extensive infiltration of immune cells including T lymphocytes, mast cells, and eosinophils.
|
23284675 |
2012 |
Inflammatory dermatosis
|
0.110 |
Biomarker
|
disease |
BEFREE |
We demonstrated that keratinocytic ablation of Ctip2 leads to atopic dermatitis (AD)-like skin inflammation, characterized by alopecia, pruritus and scaling, as well as extensive infiltration of immune cells including T lymphocytes, mast cells, and eosinophils.
|
23284675 |
2012 |
Dermatitis
|
0.010 |
Biomarker
|
disease |
BEFREE |
We demonstrated that keratinocytic ablation of Ctip2 leads to atopic dermatitis (AD)-like skin inflammation, characterized by alopecia, pruritus and scaling, as well as extensive infiltration of immune cells including T lymphocytes, mast cells, and eosinophils.
|
23284675 |
2012 |
Dermatitis, Atopic
|
0.010 |
Biomarker
|
disease |
BEFREE |
We demonstrated that keratinocytic ablation of Ctip2 leads to atopic dermatitis (AD)-like skin inflammation, characterized by alopecia, pruritus and scaling, as well as extensive infiltration of immune cells including T lymphocytes, mast cells, and eosinophils.
|
23284675 |
2012 |
Eczema
|
0.010 |
Biomarker
|
disease |
BEFREE |
We demonstrated that keratinocytic ablation of Ctip2 leads to atopic dermatitis (AD)-like skin inflammation, characterized by alopecia, pruritus and scaling, as well as extensive infiltration of immune cells including T lymphocytes, mast cells, and eosinophils.
|
23284675 |
2012 |
Coronal craniosynostosis
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Using whole-genome sequencing, we identified a novel, de novo variant in BCL11B, c.7C>A, encoding an R3S substitution (p.R3S), in a male patient with coronal suture synostosis.
|
31067316 |
2019 |
Malignant Neoplasms
|
0.090 |
GeneticVariation
|
group |
BEFREE |
Two of these interstitial deletions (murine Notch1 and Bcl11b deletions) have been detected, at low frequency, in tissues from healthy mice with no evidence of malignancy, similar to the finding of chromosomal translocations in the peripheral blood or tonsils of healthy individuals.
|
22334400 |
2012 |
Primary malignant neoplasm
|
0.060 |
GeneticVariation
|
group |
BEFREE |
Two of these interstitial deletions (murine Notch1 and Bcl11b deletions) have been detected, at low frequency, in tissues from healthy mice with no evidence of malignancy, similar to the finding of chromosomal translocations in the peripheral blood or tonsils of healthy individuals.
|
22334400 |
2012 |
Leukemia, T-Cell
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Two different T-cell lines were forced to express BCL11B at levels similar to those observed in primary T-cell leukemias.
|
20824091 |
2010 |
Sepsis of the newborn
|
0.010 |
Biomarker
|
disease |
BEFREE |
TSPO, ZAP70, CEBPB targeting MAPK14, has-miR-150 targeting BCL11B might affect the pathogenesis of neonatal sepsis.
|
30497506 |
2018 |
Bacterial sepsis of newborn
|
0.010 |
Biomarker
|
disease |
BEFREE |
TSPO, ZAP70, CEBPB targeting MAPK14, has-miR-150 targeting BCL11B might affect the pathogenesis of neonatal sepsis.
|
30497506 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Together, our results argue that Bcl11b impairment promotes tumor development in mouse and human intestine at least in part through deregulation of β-catenin pathway.
|
25827435 |
2015 |
Chronic Lymphocytic Leukemia
|
0.080 |
Biomarker
|
disease |
BEFREE |
To screen the highly efficient and specific B-cell chronic lymphocytic leukemia/lymphoma 11B (BCL11B) small interfering RNA (siRNA) which are able to downregulate the BCL11B gene expression in human T-cell acute lymphoblastic leukemia, thereby inhibiting the leukemic T-cell proliferation and inducing apoptosis, four BCL11B-siRNAs and the scrambled non-silencing siRNA control (sc) were designed and obtained by chemosynthesis.
|
21756541 |
2011 |
B-CELL MALIGNANCY, LOW-GRADE
|
0.020 |
Biomarker
|
disease |
BEFREE |
To screen the highly efficient and specific B-cell chronic lymphocytic leukemia/lymphoma 11B (BCL11B) small interfering RNA (siRNA) which are able to downregulate the BCL11B gene expression in human T-cell acute lymphoblastic leukemia, thereby inhibiting the leukemic T-cell proliferation and inducing apoptosis, four BCL11B-siRNAs and the scrambled non-silencing siRNA control (sc) were designed and obtained by chemosynthesis.
|
21756541 |
2011 |
Hematologic Neoplasms
|
0.030 |
Biomarker
|
group |
BEFREE |
To our knowledge, this is the first report implicating BCL11B in hematological malignancies.
|
15104287 |
2004 |
Hematologic Neoplasms
|
0.030 |
Biomarker
|
group |
LHGDN |
To our knowledge, this is the first report implicating BCL11B in hematological malignancies.
|
15104287 |
2004 |
Malignant neoplasm of lung
|
0.020 |
Biomarker
|
disease |
BEFREE |
Thus, targeting the PDK1- and HOTAIR-mediated downstream molecule EZH2 by the combination of ATL-1 and erlotinib potentially facilitates the development of an additional novel strategy to combat lung cancer.
|
30223276 |
2018 |