Amphetamine-Related Disorders
|
0.300 |
Biomarker
|
group |
CTD_human |
Genome-wide association for methamphetamine dependence: convergent results from 2 samples.
|
18316681 |
2008 |
Amphetamine Addiction
|
0.300 |
Biomarker
|
disease |
CTD_human |
Genome-wide association for methamphetamine dependence: convergent results from 2 samples.
|
18316681 |
2008 |
Amphetamine Abuse
|
0.300 |
Biomarker
|
disease |
CTD_human |
Genome-wide association for methamphetamine dependence: convergent results from 2 samples.
|
18316681 |
2008 |
Asthma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Candidate genes for asthma and allergic diseases co-associated with sepsis including innate immunity receptors and related molecules (CD14, TLR4 and AOAH) and novel genes such as MYLK provide good examples of pleitropic effects of innate immunity genes, where variants conferring risk to specific traits (i.e. sepsis) under one set of genetic and environmental circumstances confer a reduced risk in a different (but possibly related) clinical outcome (i.e. allergic asthma), and support the 'common variant/multiple disease' hypothesis.
|
17989521 |
2007 |
Asthma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Our results indicate that polymorphisms in markers within the AOAH gene are associated with risk of asthma and associated quantitative traits (IgE and cytokine levels) among asthmatic subjects and their families in Barbados, and there is an interactive effect on tIgE and asthma concentrations between an AOAH marker and the functional CD14(-260)C >T polymorphism.
|
16815140 |
2006 |
Anxiety
|
0.010 |
Biomarker
|
disease |
BEFREE |
We previously showed that AOAH-deficient mice mimicked interstitial cystitis/bladder pain syndrome, a condition frequently associated with comorbid anxiety and depression.
|
31017816 |
2019 |
Anxiety Disorders
|
0.010 |
Biomarker
|
group |
BEFREE |
We previously showed that AOAH-deficient mice mimicked interstitial cystitis/bladder pain syndrome, a condition frequently associated with comorbid anxiety and depression.
|
31017816 |
2019 |
Mental Depression
|
0.010 |
Biomarker
|
disease |
BEFREE |
PPARγ did not affect AA-dependent <i>Crf</i> expression in vitro, and conditional <i>Ppar</i>γ knockout did not alter the AOAH-deficient depressive phenotype, despite previous studies implicating PPARγ as a therapeutic target for depression.
|
31017816 |
2019 |
Depressive disorder
|
0.010 |
Biomarker
|
disease |
BEFREE |
PPARγ did not affect AA-dependent <i>Crf</i> expression in vitro, and conditional <i>Ppar</i>γ knockout did not alter the AOAH-deficient depressive phenotype, despite previous studies implicating PPARγ as a therapeutic target for depression.
|
31017816 |
2019 |
Interstitial Cystitis
|
0.010 |
Biomarker
|
disease |
BEFREE |
We previously showed that AOAH-deficient mice mimicked interstitial cystitis/bladder pain syndrome, a condition frequently associated with comorbid anxiety and depression.
|
31017816 |
2019 |
Depressed mood
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
PPARγ did not affect AA-dependent <i>Crf</i> expression in vitro, and conditional <i>Ppar</i>γ knockout did not alter the AOAH-deficient depressive phenotype, despite previous studies implicating PPARγ as a therapeutic target for depression.
|
31017816 |
2019 |
Chronic interstitial cystitis
|
0.010 |
Biomarker
|
disease |
BEFREE |
We previously showed that AOAH-deficient mice mimicked interstitial cystitis/bladder pain syndrome, a condition frequently associated with comorbid anxiety and depression.
|
31017816 |
2019 |
Bladder pain syndrome
|
0.010 |
Biomarker
|
disease |
BEFREE |
We previously showed that AOAH-deficient mice mimicked interstitial cystitis/bladder pain syndrome, a condition frequently associated with comorbid anxiety and depression.
|
31017816 |
2019 |
Pelvic Pain
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
These findings indicate that AOAH modulates pelvic pain severity, suggesting that allelic variation in Aoah influences pelvic pain in IC.
|
29118019 |
2018 |
Allergic asthma
|
0.010 |
Biomarker
|
disease |
BEFREE |
We report here that acyloxyacyl hydrolase (AOAH), a host lipase that degrades and inactivates LPS, renders mice more susceptible to house dust mite (HDM)-induced allergic asthma.
|
30021797 |
2018 |
Chronic pelvic pain of female
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
Finally, AOAH-deficient mice had significantly higher levels of bladder vascular endothelial growth factor, an emerging marker of chronic pelvic pain in humans.
|
29118019 |
2018 |
Pelvic pain female
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
These findings indicate that AOAH modulates pelvic pain severity, suggesting that allelic variation in Aoah influences pelvic pain in IC.
|
29118019 |
2018 |
Pneumonia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Inactivation of LPS by AOAH is a previously unappreciated mechanism for promoting resolution of pulmonary inflammation/injury induced by Gram-negative bacterial infection.
|
28622363 |
2017 |
Gram-Negative Bacterial Infections
|
0.010 |
Biomarker
|
group |
BEFREE |
Inactivation of LPS by AOAH is a previously unappreciated mechanism for promoting resolution of pulmonary inflammation/injury induced by Gram-negative bacterial infection.
|
28622363 |
2017 |
Pneumonitis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Inactivation of LPS by AOAH is a previously unappreciated mechanism for promoting resolution of pulmonary inflammation/injury induced by Gram-negative bacterial infection.
|
28622363 |
2017 |
Chronic sinusitis
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms in RYBP and AOAH genes are associated with chronic rhinosinusitis in a Chinese population: a replication study.
|
22723975 |
2012 |
Craniosynostosis
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Although these studies are subject to methodologic difficulties, associations of CRS and polymorphisms in more than 30 genes have been published, with single nucleotide polymorphisms in 3 (IL1A, TNFA, AOAH) replicated.
|
21499907 |
2011 |
Septicemia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Candidate genes for asthma and allergic diseases co-associated with sepsis including innate immunity receptors and related molecules (CD14, TLR4 and AOAH) and novel genes such as MYLK provide good examples of pleitropic effects of innate immunity genes, where variants conferring risk to specific traits (i.e. sepsis) under one set of genetic and environmental circumstances confer a reduced risk in a different (but possibly related) clinical outcome (i.e. allergic asthma), and support the 'common variant/multiple disease' hypothesis.
|
17989521 |
2007 |
Sepsis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Candidate genes for asthma and allergic diseases co-associated with sepsis including innate immunity receptors and related molecules (CD14, TLR4 and AOAH) and novel genes such as MYLK provide good examples of pleitropic effects of innate immunity genes, where variants conferring risk to specific traits (i.e. sepsis) under one set of genetic and environmental circumstances confer a reduced risk in a different (but possibly related) clinical outcome (i.e. allergic asthma), and support the 'common variant/multiple disease' hypothesis.
|
17989521 |
2007 |