Abnormality of cardiovascular system morphology
|
0.010 |
Biomarker
|
disease |
BEFREE |
The LIM homeodomain transcriptor factor ISL1 is a marker for undifferentiated cardiac progenitor cells that give rise to both the right ventricle and the inflow and outflow tracts, which are affected by several cardiovascular malformations.
|
23229290 |
2013 |
Acute lymphocytic leukemia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Our data implicate TES methylation in ALL and provide additional evidence for the involvement of LIM domain proteins in leukaemogenesis.
|
20573277 |
2010 |
Adult Fibrosarcoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
In this study, we have determined the effect of ribozymes specific for LIM kinase-2 on metastatic and proliferative phenotypes of human fibrosarcoma cells.
|
15026997 |
2004 |
Adult Glioblastoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Suppression of LIM Kinase 1 and LIM Kinase 2 Limits Glioblastoma Invasion.
|
31641031 |
2020 |
Adult Pre-B Acute Lymphoblastic Leukemia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
A novel chromosomal translocation t(1;14)(q25;q32) in pre-B acute lymphoblastic leukemia involves the LIM homeodomain protein gene, Lhx4.
|
12118377 |
2002 |
Adult Rhabdomyosarcoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Wild-type and mutant IGFBP-6, as well as IGF-II, induced cell migration in RD rhabdomyosarcoma and LIM 1215 colon cancer cells.
|
17519236 |
2007 |
Adult T-Cell Lymphoma/Leukemia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Specific in vivo association between the bHLH and LIM proteins implicated in human T cell leukemia.
|
7957052 |
1994 |
Alcoholic Intoxication, Chronic
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms in PDLIM5 gene are associated with alcohol dependence, type 2 diabetes, and hypertension.
|
27693979 |
2017 |
Anemia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In the mouse, Lhx2, which encodes a member of the LIM (Lin-11, Isl-1, and Mec-3) class of homeodomain proteins, was shown to be expressed during early development in the posterior pituitary, eye, and liver, and its expression persists in adulthood in the central nervous system Lhx2(-/-) mice display absence of posterior pituitary and intermediate lobes, malformation of the anterior lobe, anophthalmia, and they die from anemia.
|
22535646 |
2012 |
Arteriosclerosis
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The four and a half LIM domain protein 2 (FHL2) is a member of the four and a half LIM domain (FHL) gene family, and it is associated with cholesterol-enriched diet-promoted atherosclerosis.
|
31714683 |
2020 |
Arthritis, Psoriatic
|
0.010 |
Biomarker
|
disease |
BEFREE |
The LIM-Only Protein Four and a Half LIM Domain Protein 2 Attenuates Development of Psoriatic Arthritis by Blocking Adam17-Mediated Tumor Necrosis Factor Release.
|
28823868 |
2017 |
Atherosclerosis
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The four and a half LIM domain protein 2 (FHL2) is a member of the four and a half LIM domain (FHL) gene family, and it is associated with cholesterol-enriched diet-promoted atherosclerosis.
|
31714683 |
2020 |
B-Cell Lymphomas
|
0.010 |
Biomarker
|
group |
BEFREE |
We evaluated MEF2B expression, in comparison with additional GC markers, LIM domain-only transcription factor 2 (LMO2), and human GC-associated lymphoma (HGAL), in a variety of B-cell lymphomas, with particular emphasis on their utility in differentiating FL from MZL.
|
29309299 |
2018 |
Bipolar Disorder
|
0.390 |
GeneticVariation
|
disease |
BEFREE |
Our genetic association study only offered evidence for susceptibility of PDLIM5 to bipolar disorder, but the positive SNP rs2433322 could not indicate a direct cause of this complicated brain disorder.
|
19448850 |
2009 |
Bipolar Disorder
|
0.390 |
Biomarker
|
disease |
PSYGENET |
Nonsynonymous polymorphisms of the PDLIM5 gene association with the occurrence of both bipolar disorder and schizophrenia.
|
24064681 |
2013 |
Bipolar Disorder
|
0.390 |
AlteredExpression
|
disease |
BEFREE |
The PDLIM5 gene and lithium prophylaxis: an association and gene expression analysis in Sardinian patients with bipolar disorder.
|
18456508 |
2008 |
Bipolar Disorder
|
0.390 |
AlteredExpression
|
disease |
BEFREE |
Peripheral PDLIM5 expression in bipolar disorder and the effect of olanzapine administration.
|
23031404 |
2012 |
Bipolar Disorder
|
0.390 |
Biomarker
|
disease |
BEFREE |
PDLIM5 may have a minor effect on susceptibility to BP in Caucasians.
|
18496208 |
2008 |
Bipolar Disorder
|
0.390 |
AlteredExpression
|
disease |
LHGDN |
In addition, we found the altered expression of LIM and HSPF1 both in the brains and lymphoblastoid cells in bipolar disorder.
|
14743183 |
2004 |
Bipolar Disorder
|
0.390 |
Biomarker
|
disease |
BEFREE |
These findings suggested the role of LIM in the pathophysiology of bipolar disorder and schizophrenia.
|
16044170 |
2005 |
Bipolar Disorder
|
0.390 |
GeneticVariation
|
disease |
LHGDN |
Although the findings presented in this paper do not provide strong evidence that the PDLIM5 gene significantly affects the pathophysiology of BD, they suggest that rare variants within the promoter region of the gene may have a marginal effect on the disorder.
|
18496210 |
2008 |
Bipolar Disorder
|
0.390 |
AlteredExpression
|
disease |
BEFREE |
Expression of HSPF1 and LIM in the lymphoblastoid cells derived from patients with bipolar disorder and schizophrenia.
|
15362566 |
2004 |
Bipolar Disorder
|
0.390 |
Biomarker
|
disease |
PSYGENET |
Our genetic association study only offered evidence for susceptibility of PDLIM5 to bipolar disorder, but the positive SNP rs2433322 could not indicate a direct cause of this complicated brain disorder.
|
19448850 |
2009 |
Bipolar Disorder
|
0.390 |
GeneticVariation
|
disease |
BEFREE |
Nonsynonymous polymorphisms of the PDLIM5 gene association with the occurrence of both bipolar disorder and schizophrenia.
|
24064681 |
2013 |
Bipolar Disorder
|
0.390 |
GeneticVariation
|
disease |
BEFREE |
Although the findings presented in this paper do not provide strong evidence that the PDLIM5 gene significantly affects the pathophysiology of BD, they suggest that rare variants within the promoter region of the gene may have a marginal effect on the disorder.
|
18496210 |
2008 |