Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 65018
Gene Symbol: PINK1
PINK1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker LHGDN PINK1-associated Parkinson's disease is caused by neuronal vulnerability to calcium-induced cell death. 19285945

2009

Entrez Id: 1401
Gene Symbol: CRP
CRP
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.100 Biomarker LHGDN As the integrated changes of those indices are summarized by oxygen extraction tension (PaO2x), the objective of this study was to explore the association between C-reactive protein (CRP) blood levels and either PaO2x or each of its determinants, in stable COPD. 19281089

2008

Entrez Id: 2252
Gene Symbol: FGF7
FGF7
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.040 AlteredExpression LHGDN To this end, we compared the levels of HGF and KGF, measured by enzyme-linked immunosorbent assay (ELISA), in bronchoalveolar lavage (BAL) fluid and in serum in 18 patients with COPD (62 +/- 9 yrs, forced expiratory volume in one second [FEV1] 57 +/- 12% ref, X +/- standard deviation of mean), 18 smokers with normal lung function (58 +/- 8 yrs, FEV1 90 +/- 6% ref) and 8 never smokers (67 +/- 9 yrs, 94 +/- 14% ref). 19281086

2008

Entrez Id: 3082
Gene Symbol: HGF
HGF
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.020 AlteredExpression LHGDN For this study, we investigated potential abnormalities of hepatocyte growth factor (HGF) and keratinocyte growth factor (KGF) in patients with COPD. 19281086

2008

Entrez Id: 7052
Gene Symbol: TGM2
TGM2
CUI: C0029172
Disease: Oral Submucous Fibrosis
Oral Submucous Fibrosis
0.010 AlteredExpression LHGDN Transglutaminase-2 regulation by arecoline in gingival fibroblasts. 19278990

2009

Entrez Id: 5743
Gene Symbol: PTGS2
PTGS2
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.400 Biomarker LHGDN Multicolor immunohistofluorescence staining confirmed the COX-expression profiles in organotypic 3D cultures and the COX-2 dominance in OSCC tumors. 19278989

2009

Entrez Id: 10002
Gene Symbol: NR2E3
NR2E3
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
0.050 GeneticVariation LHGDN Moreover, patients who are homozygous for the same NR2E3 mutation have variable expression of retinal disease, suggesting the involvement of modifier genes. 19273793

2009

Entrez Id: 4879
Gene Symbol: NPPB
NPPB
CUI: C0242698
Disease: Ventricular Dysfunction, Left
Ventricular Dysfunction, Left
0.580 Biomarker LHGDN Accuracy of N-terminal pro-brain natriuretic peptide in the identification of left ventricular dysfunction in high-risk asymptomatic patients. 19262210

2009

Entrez Id: 348
Gene Symbol: APOE
APOE
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 GeneticVariation LHGDN Surprisingly, both APOE4 (OR = 4.6, 95% CI = 1.3-16.5) and APOE2 (OR = 7.8, 95% CI = 1.5-40.2) carriers were more likely to meet neuropathologic criteria for AD than those with APOE3/3 genotype. 19255410

2009

Entrez Id: 348
Gene Symbol: APOE
APOE
CUI: C0497327
Disease: Dementia
Dementia
0.200 GeneticVariation LHGDN Compared to those with an APOE epsilon3/epsilon3 genotype (APOE3/3), APOE4 carriers were more likely to be diagnosed with dementia (odds ratio [OR] = 12.2, 95% confidence interval [CI] = 1.5-102.0), whereas APOE2 carriers were not (OR = 0.3, 95% CI = 0.1-1.3). 19255410

2009

Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
0.700 GeneticVariation LHGDN Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. 19251628

2009

Entrez Id: 2521
Gene Symbol: FUS
FUS
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
0.700 GeneticVariation LHGDN In contrast, the mutant forms of FUS/TLS accumulated in the cytoplasm of neurons, a pathology that is similar to that of the gene TAR DNA-binding protein 43 (TDP43), whose mutations also cause ALS. 19251627

2009

Entrez Id: 1958
Gene Symbol: EGR1
EGR1
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal
0.020 AlteredExpression LHGDN The present study demonstrates the differential up-regulation of Egr-1 in the thrombus-covered wall of human AAA and also suggests its possible contribution to the thrombogenic and inflammatory pathogenesis in human AAA. 19245972

2009

Entrez Id: 1233
Gene Symbol: CCR4
CCR4
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.020 AlteredExpression LHGDN This study sheds new light on Treg physiology and validates CCR4/CCL22 and ICOS as therapeutic targets in breast tumors, which represent a major health problem. 19244125

2009

Entrez Id: 6367
Gene Symbol: CCL22
CCL22
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.010 AlteredExpression LHGDN This study sheds new light on Treg physiology and validates CCR4/CCL22 and ICOS as therapeutic targets in breast tumors, which represent a major health problem. 19244125

2009

Entrez Id: 1385
Gene Symbol: CREB1
CREB1
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
0.020 AlteredExpression LHGDN RGS17, an overexpressed gene in human lung and prostate cancer, induces tumor cell proliferation through the cyclic AMP-PKA-CREB pathway. 19244110

2009

Entrez Id: 26575
Gene Symbol: RGS17
RGS17
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
0.010 AlteredExpression LHGDN Through microarray and gene expression analysis, we show that expression of RGS17 is up-regulated in 80% of lung tumors, and also up-regulated in prostate tumors. 19244110

2009

Entrez Id: 1956
Gene Symbol: EGFR
EGFR
CUI: C0024121
Disease: Lung Neoplasms
Lung Neoplasms
0.600 GeneticVariation LHGDN Comparison of EGFR and K-RAS gene status between primary tumours and corresponding metastases in NSCLC. 19238633

2008

Entrez Id: 1956
Gene Symbol: EGFR
EGFR
CUI: C0024121
Disease: Lung Neoplasms
Lung Neoplasms
0.600 GeneticVariation LHGDN Dual MET-EGFR combinatorial inhibition against T790M-EGFR-mediated erlotinib-resistant lung cancer. 19238632

2008

Entrez Id: 2099
Gene Symbol: ESR1
ESR1
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.500 AlteredExpression LHGDN Wnt-5a signaling restores tamoxifen sensitivity in estrogen receptor-negative breast cancer cells. 19237581

2009

Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.060 AlteredExpression LHGDN Wnt-5a signaling restores tamoxifen sensitivity in estrogen receptor-negative breast cancer cells. 19237581

2009

Entrez Id: 3934
Gene Symbol: LCN2
LCN2
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.060 Biomarker LHGDN Finally, orthotopic studies demonstrated that Lcn2-expressing breast tumors displayed a poorly differentiated phenotype and showed increased local tumor invasion and lymph node metastasis. 19237579

2009

Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.040 GeneticVariation LHGDN Glycogen synthase kinase 3beta missplicing contributes to leukemia stem cell generation. 19237556

2009

Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0005699
Disease: Blast Phase
Blast Phase
0.010 GeneticVariation LHGDN Glycogen synthase kinase 3beta missplicing contributes to leukemia stem cell generation. 19237556

2009

Entrez Id: 3458
Gene Symbol: IFNG
IFNG
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.100 Biomarker LHGDN The adrenal steroid response during tuberculosis and its effects on the mycobacterial-driven IFN-gamma production of patients and their household contacts. 19236347

2009