Prune Belly Syndrome
|
0.650 |
Biomarker
|
disease |
BEFREE |
T2DM mouse model was induced by high-fat-diet, and the mice were treated with fenofibrate (100 mg/kg) (DIO-FENO) or PBS (DIO-PBS) for 4 weeks.
|
29029615 |
2017 |
Prune Belly Syndrome
|
0.650 |
Biomarker
|
disease |
BEFREE |
Animals received four weekly injections of either PBS (G1), ConvitVax (200 μg cell homogenate, 0.0625 mg BCG, 0.02% formalin) (G2), 50 μg anti-PD-1 (G3), or ConvitVax plus anti-PD-1 (200 μg cell homogenate, 0.0625 mg BCG, 0.02% formalin, 50 μg anti-PD-1) (G4).
|
31762937 |
2019 |
Prune Belly Syndrome
|
0.650 |
Biomarker
|
disease |
BEFREE |
Here, we employed BALB/c ByJ mice inflected with SP, IAV, IAV followed by SP (IAV+SP) and PBS (Control) as models to survey the global gene expression using digital gene expression (DGE) profiling.
|
29348862 |
2017 |
Prune Belly Syndrome
|
0.650 |
GeneticVariation
|
disease |
BEFREE |
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome.
|
22077972 |
2011 |
Prune Belly Syndrome
|
0.650 |
GeneticVariation
|
disease |
BEFREE |
Finally, in a murine model of type 1 diabetes, NTA-modified complex micelles loading an insulin (NTA-CM-INS) group exhibited a long hypoglycemic effect which is superior to that of free insulin in the PBS (PBS-INS) group and insulin-loaded complex micelles without an NTA modification (CM-INS) group.
|
30212220 |
2018 |
Major Depressive Disorder
|
0.410 |
AlteredExpression
|
disease |
BEFREE |
We used this assay to measure CHRM3 protein levels in the frontal pole, obtained post-mortem from subjects with bipolar disorder (n = 15), major depressive disorder (n = 15) and matched controls (n = 20) and showed that [(3)H]4-DAMP binding was not altered in either bipolar disorder or major depressive disorder.
|
23962466 |
2013 |
Urinary Bladder Diseases
|
0.320 |
GeneticVariation
|
group |
BEFREE |
This is the first independent report of biallelic variants in CHRM3 in a family with a rare serious bladder disorder associated with mydriasis and provides important evidence of this association.
|
31441039 |
2019 |
Urinary Bladder Diseases
|
0.320 |
GeneticVariation
|
group |
BEFREE |
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome.
|
22077972 |
2011 |
Bipolar Disorder
|
0.310 |
AlteredExpression
|
disease |
BEFREE |
We used this assay to measure CHRM3 protein levels in the frontal pole, obtained post-mortem from subjects with bipolar disorder (n = 15), major depressive disorder (n = 15) and matched controls (n = 20) and showed that [(3)H]4-DAMP binding was not altered in either bipolar disorder or major depressive disorder.
|
23962466 |
2013 |
Unipolar Depression
|
0.310 |
AlteredExpression
|
disease |
BEFREE |
We used this assay to measure CHRM3 protein levels in the frontal pole, obtained post-mortem from subjects with bipolar disorder (n = 15), major depressive disorder (n = 15) and matched controls (n = 20) and showed that [(3)H]4-DAMP binding was not altered in either bipolar disorder or major depressive disorder.
|
23962466 |
2013 |
Mood Disorders
|
0.310 |
AlteredExpression
|
group |
BEFREE |
The use of a modified [3H]4-DAMP radioligand binding assay with increased selectivity for muscarinic M3 receptor shows that cortical CHRM3 levels are not altered in mood disorders.
|
23962466 |
2013 |
Chronic Obstructive Airway Disease
|
0.140 |
Biomarker
|
disease |
BEFREE |
After successful construction of COPD mouse model by CS, HE staining illustrated that the structure of airway wall of lung tissue in mice from PBS group was irregular.
|
29630123 |
2018 |
Chronic Obstructive Airway Disease
|
0.140 |
Biomarker
|
disease |
BEFREE |
We highlight targets for drugs and compounds in development for COPD and asthma (genes in the inositol phosphate metabolism pathway and CHRM3) and describe targets for potential drug repositioning from other clinical indications.
|
28166213 |
2017 |
Chronic Obstructive Airway Disease
|
0.140 |
AlteredExpression
|
disease |
BEFREE |
Also, CHRM3 gene expression was significantly elevated in COPD patients with BHR as compared with patients without BHR.
|
22192964 |
2012 |
Chronic Obstructive Airway Disease
|
0.140 |
GeneticVariation
|
disease |
BEFREE |
Eighty-two patients with COPD and 17 healthy smokers were recruited and screened for ADRb2 (T164I and R175R), for CHRM2 (rs1824024) and for CHRM3 (-513C/A and -492C/T).
|
26633752 |
2016 |
Constipation
|
0.130 |
GeneticVariation
|
phenotype |
BEFREE |
Generalized linear univariate model analysis performed on the opiate-induced constipation-associated SNPs and a single CHRM3 SNP revealed an association between anticholinergic symptoms and a score of 8 SNPs (adjusted P = 0.038, permuted P = 0.002).
|
29620694 |
2018 |
Constipation
|
0.130 |
Biomarker
|
phenotype |
BEFREE |
Excess risk of IC/PBS was observed in the first- and second-degree relatives in probands with myalgia and myositis/unspecified (fibromyalgia) and in probands with constipation.
|
25349937 |
2016 |
Constipation
|
0.130 |
Biomarker
|
phenotype |
BEFREE |
The control and constipation group received 1× PBS under the same pattern.
|
30122898 |
2018 |
Epilepsy
|
0.110 |
Biomarker
|
disease |
BEFREE |
Moreover, two candidate genes for therapeutic targeting came out from this analysis: SSTR1, a relevant common hub in febrile and afebrile transcriptomes, and CHRM3, due to its putative role in epilepsy susceptibility development.
|
22022585 |
2011 |
Myocardial Infarction
|
0.100 |
Biomarker
|
disease |
BEFREE |
Male C57BL/6 mice were subjected to left coronary artery ligation to induce MI and then treated with MCC950 (10 mg/kg) or PBS for 14 days.
|
31299609 |
2019 |
Myocardial Infarction
|
0.100 |
Biomarker
|
disease |
BEFREE |
Wistar rats were subjected to left anterior descending artery ligation to induce myocardial infarction (MI) and then randomly allocated to receive an intramyocardial injection of PBS (MI group) or 5-azacytidine-induced MSCs (MSCs group).
|
28929261 |
2018 |
Myocardial Infarction
|
0.100 |
Biomarker
|
disease |
BEFREE |
NOD/SCID mice were treated with hiPSC-CCND2<sup>OE</sup> CMs (i.e., the CCND2<sup>OE</sup> group), hiPSC-CCND2<sup>WT</sup> CMs (the CCND2<sup>WT</sup> group), or an equal volume of PBS immediately after experimentally-induced myocardial infarction.
|
31629738 |
2019 |
Myocardial Infarction
|
0.100 |
Biomarker
|
disease |
BEFREE |
Phosphate-buffered solution (PBS group), Dex-PCL-HEMA/PNIPAAm hydrogel (Gel group), bFGF in phosphate-buffered solution (bFGF group) or bFGF in hydrogel (Gel + bFGF group) was injected into a peri-infarcted area of cardiac tissue immediately following MI.
|
29042955 |
2017 |
Myocardial Infarction
|
0.100 |
Biomarker
|
disease |
BEFREE |
Magnetic resonance imaging (MRI) revealed that the microvascular grafts effectively preserved contractile performance 3 d and 6 wk after myocardial infarction, attenuated left ventricular dilation, and decreased infarct size as compared to infarcted rats treated with PBS injection as a control (3 d ejection fraction, + ∼7%, P < 0.001; 6 wk ejection faction, + ∼12%, P < 0.001).
|
21035182 |
2011 |
Myocardial Infarction
|
0.100 |
Biomarker
|
disease |
BEFREE |
Male Balb/C mice were subjected to MI or sham operation; the infarcted animals were subdivided to receive intramyocardial injections of PBS, GILZ overexpressing cells (GILZ) or their controls expressing the green fluorescent protein (GFP).
|
28499885 |
2017 |