HIV Infections
|
0.300 |
Biomarker
|
group |
CTD_human |
Host cell gene expression during human immunodeficiency virus type 1 latency and reactivation and effects of targeting genes that are differentially expressed in viral latency.
|
15308739 |
2004 |
HIV Coinfection
|
0.300 |
Biomarker
|
disease |
CTD_human |
Host cell gene expression during human immunodeficiency virus type 1 latency and reactivation and effects of targeting genes that are differentially expressed in viral latency.
|
15308739 |
2004 |
Malignant tumor of cervix
|
0.010 |
Biomarker
|
disease |
BEFREE |
The purposes of this study were to explore the role of miR-802 in cervical cancer and to clarify the regulation of serine/arginine-rich splicing factor 9 (SRSF9) by miR-802.
|
30565744 |
2019 |
Cervix carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
The purposes of this study were to explore the role of miR-802 in cervical cancer and to clarify the regulation of serine/arginine-rich splicing factor 9 (SRSF9) by miR-802.
|
30565744 |
2019 |
cervical cancer
|
0.010 |
Biomarker
|
disease |
BEFREE |
The purposes of this study were to explore the role of miR-802 in cervical cancer and to clarify the regulation of serine/arginine-rich splicing factor 9 (SRSF9) by miR-802.
|
30565744 |
2019 |
Cervical Squamous Cell Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Thus, CHCHD1, SRSF9 and TMBIM6 seem to be suitable reference genes for studying hypoxia-related gene expression in squamous cervical cancer samples by RT-qPCR.
|
27244197 |
2016 |
Azoospermia, Nonobstructive
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Rs17431717 near SFRS9 and rs12046213 near SFRS4 were significantly associated with a decreased risk of NOA, whereas rs10849753 near SFRS9 and rs6103330 in SFRS6 were associated with an increased risk of NOA.
|
24661730 |
2014 |
Carcinogenesis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
SRSF1 and SRSF9 RNA binding proteins promote Wnt signalling-mediated tumorigenesis by enhancing β-catenin biosynthesis.
|
23592547 |
2013 |
Malignant neoplasm of urinary bladder
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In this study, we focused on splicing factor serine/arginine-rich 9 (SRSF9/SRp30c) on the basis of our previous genome-wide gene expression analysis using miR-1-transfected BC cell lines because putative target sites of miR-1 are existed in 3'-untranslated region (UTR) of SRSF9 mRNA.
|
22178073 |
2012 |
Bladder Neoplasm
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In this study, we focused on splicing factor serine/arginine-rich 9 (SRSF9/SRp30c) on the basis of our previous genome-wide gene expression analysis using miR-1-transfected BC cell lines because putative target sites of miR-1 are existed in 3'-untranslated region (UTR) of SRSF9 mRNA.
|
22178073 |
2012 |
Carcinoma of bladder
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In this study, we focused on splicing factor serine/arginine-rich 9 (SRSF9/SRp30c) on the basis of our previous genome-wide gene expression analysis using miR-1-transfected BC cell lines because putative target sites of miR-1 are existed in 3'-untranslated region (UTR) of SRSF9 mRNA.
|
22178073 |
2012 |
Tumor Cell Invasion
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Loss-of-function assays demonstrated that significant inhibitions of cell proliferation, migration, and invasion were observed in the si-SRSF9 transfectants.
|
22178073 |
2012 |
Glucocorticoid Receptor Deficiency
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We found that suppression of SRp30c expression by siRNA specifically antagonized bombesin's effect on glucocorticoid-mediated inhibition of PC cells, suggesting that bombesin-induced expression of SRp30c affects GR pre-mRNA splicing, leading to increased GR beta expression and contributing to glucocorticoid resistance in PC cells.
|
17540466 |
2007 |
Pick Disease of the Brain
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Increased exon 10 inclusion in FTDP mutant ENH (N279K) may arise from abolishing SRp30c binding.
|
15695522 |
2005 |
Frontotemporal dementia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Increased exon 10 inclusion in FTDP mutant ENH (N279K) may arise from abolishing SRp30c binding.
|
15695522 |
2005 |