Crohn Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
We assess the frequency of the CARD15 SNPs and of the R30Q mutation in DLG5 and their contribution to the development of CD in a cohort of unrelated IBD patients (151 CD, 325 ulcerative colitis (UC)) and healthy controls (236) from South-east Norway (IBSEN cohort).
|
16493449 |
2006 |
Crohn Disease
|
0.100 |
GeneticVariation
|
disease |
LHGDN |
Polymorphisms 3020insC in CARD15 and SNP rs2165047 in DLG5 were associated with specific phenotypes in this pediatric-onset CD cohort.
|
17476680 |
2007 |
Crohn Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
DLG5 variants contribute to Crohn disease risk in a Canadian population.
|
16450402 |
2006 |
Crohn Disease
|
0.100 |
GeneticVariation
|
disease |
LHGDN |
Further investigation of the observed TRD may contribute towards enlightening the role of DLG5 in physiological processes influencing transmission of chromosomes to the surviving offspring, which, in turn, may help in understanding its implication in the development of CD among men.
|
16446977 |
2006 |
Crohn Disease
|
0.100 |
GeneticVariation
|
disease |
LHGDN |
Polymorphisms of CARD15 and OCTN genes, but not DLG5 are associated with pediatric onset of CD.
|
17451203 |
2007 |
Crohn Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Furthermore, we evaluated whether DLG5 variants alter gastrointestinal permeability in Crohn's disease (CD).
|
16494592 |
2006 |
Ulcerative Colitis
|
0.080 |
GeneticVariation
|
disease |
BEFREE |
We assess the frequency of the CARD15 SNPs and of the R30Q mutation in DLG5 and their contribution to the development of CD in a cohort of unrelated IBD patients (151 CD, 325 ulcerative colitis (UC)) and healthy controls (236) from South-east Norway (IBSEN cohort).
|
16493449 |
2006 |
Ulcerative Colitis
|
0.080 |
Biomarker
|
disease |
BEFREE |
DLG5 and OCTN do not play a role in the susceptibility to IBD, CD, or ulcerative colitis in the Flemish population but play a role in the phenotypic expression of the disease.
|
16344053 |
2005 |
Ulcerative Colitis
|
0.080 |
GeneticVariation
|
disease |
BEFREE |
We have now examined the association of the R30Q polymorphism in a large cohort of British IBD cases, tested for interaction between the DLG5 and CARD15 genes and assessed possible association of DLG5 with clinical features of Crohn's disease (CD) and ulcerative colitis (UC).
|
16944184 |
2007 |
Ulcerative Colitis
|
0.080 |
GeneticVariation
|
disease |
BEFREE |
Recently, Stoll and colleagues reported a novel finding of genetic variation in the DLG5 gene that is associated with IBD (CD and UC combined).
|
15841097 |
2005 |
Ulcerative Colitis
|
0.080 |
GeneticVariation
|
disease |
BEFREE |
No significant association of DLG5 polymorphisms with CD or UC was observed.
|
15955786 |
2005 |
Ulcerative Colitis
|
0.080 |
GeneticVariation
|
disease |
BEFREE |
Six DLG5 variants (p.R30Q, p.P1371Q, p.G1066G, rs2289308, DLG_e26, p.D1507D) were genotyped in two study populations: (1) German IBD patients (CD n = 250; ulcerative colitis (UC) n = 150) and German healthy controls (n = 422); (2) Hungarian IBD patients (CD n = 144; UC n = 124) and Hungarian healthy controls (n = 205).
|
16494592 |
2006 |
Ulcerative Colitis
|
0.080 |
Biomarker
|
disease |
BEFREE |
No associations between DLG5 and UC were observed.
|
15843420 |
2005 |
Ulcerative Colitis
|
0.080 |
GeneticVariation
|
disease |
BEFREE |
In this study we genotyped a cohort of 402 Canadian CD and 179 ulcerative colitis (UC) patients and 537 healthy controls for three IBD/CD-associated DLG5 variants.
|
16450402 |
2006 |
Malignant neoplasm of breast
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Taken together, our data indicate that down-regulated DLG5 expression increases the stemness of breast cancer cells by enhancing TAZ expression, contributing to TAM resistance in breast cancer.
|
30450766 |
2019 |
Malignant neoplasm of breast
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
In summary, loss of DLG5 expression promoted breast cancer malignancy by inactivating the Hippo signaling pathway and increasing nuclear YAP.
|
28169360 |
2017 |
Celiac Disease
|
0.020 |
Biomarker
|
disease |
LHGDN |
Association of DLG5 variants with gluten-sensitive enteropathy.
|
18559397 |
2008 |
Celiac Disease
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Our study does not support the effect of the R30Q DLG5 variant in CeD or IBD predisposition in the Spanish population.
|
20796250 |
2011 |
Irritable Bowel Syndrome
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
DLG5 R30Q is not associated with IBD in Hungarian IBD patients but predicts clinical response to steroids in Crohn's disease.
|
16670524 |
2006 |
Irritable Bowel Syndrome
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
We studied the incidence of DLG5 alleles in a population of IBD patients from Pennsylvania.
|
20037206 |
2009 |
Breast Carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
In summary, loss of DLG5 expression promoted breast cancer malignancy by inactivating the Hippo signaling pathway and increasing nuclear YAP.
|
28169360 |
2017 |
Breast Carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Taken together, our data indicate that down-regulated DLG5 expression increases the stemness of breast cancer cells by enhancing TAZ expression, contributing to TAM resistance in breast cancer.
|
30450766 |
2019 |
Liver carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Lower Dlg5 expression was associated with advanced stages of HCC, and poor overall and disease-free survival of HCC patients.
|
28390157 |
2017 |
Liver carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
The effect of Dlg5 on HCC tumor growth in vivo was studied in a tumor xenograft model in mice.
|
31787846 |
2019 |
Pediatric Crohn's disease
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms 3020insC in CARD15 and SNP rs2165047 in DLG5 were associated with specific phenotypes in this pediatric-onset CD cohort.
|
17476680 |
2007 |