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lhgdn:association:23051
action of clioquinol on several age-dependent neurodegenerative diseases with distinct etiologies might result from a slowing down of the aging process through action of the drug on CLK-1.
lhgdn:association:58848
The fat-1 gene expression inhibited prostate cancer cell proliferation via reduction of GSK-3beta phosphorylation and subsequent down-regulation of both beta-catenin and cyclin D1.
lhgdn:association:53914
Nir2, a human homolog of Drosophila melanogaster retinal degeneration B protein, is essential for cytokinesis.
lhgdn:association:13585
Data demonstrate that the Drosophila homologs of mixed-lineage leukemia protein and host cell factor 1, called Trithorax and dHCF, are both cleaved by Drosophila taspase 1.
lhgdn:association:3522
These results demonstrate that scl is an important mediator of the ability of AML1-ETO to reprogram hematopoietic cell fate decisions, suggesting that scl may be an important contributor to AML1-ETO-associated leukemia.
lhgdn:association:35932
The spectrum of disorders generated by morpholino inhibition and the more severe defects (microphthalmia and anophthalmia) observed at higher doses illustrate the key role of GDF6 in ocular development.
lhgdn:association:406
A significant increase of stromal cell-derived factor-1alpha and CXCR4 was observed in protein extracts of idiopathic inflammatory myopathies in comparison with normal controls.
lhgdn:association:62588
Chk1 appears to help defend genomic integrity through effects on several other pathways, including Fanconi anemia proteins, the mitotic spindle, and transcription of cell cycle-related genes [review]
lhgdn:association:61936
Immunity to CD30 could play a role in Marek disease lymphoma regression.
lhgdn:association:61960
Immunity to CD30 could play a role in Marek disease lymphoma regression.
lhgdn:association:62603
26 new mutations in RP2 and RPGR patients with X-linked Retinitis Pigmentosa.
lhgdn:association:8868
Primary role for IL-1beta and TNF-alpha in the triggering of preterm labor associated with inflammation or infection.
lhgdn:association:9009
Primary role for IL-1beta and TNF-alpha in the triggering of preterm labor associated with inflammation or infection.
lhgdn:association:9034
Primary role for IL-1beta and TNF-alpha in the triggering of preterm labor associated with inflammation or infection.
lhgdn:association:47906
Primary role for IL-1beta and TNF-alpha in the triggering of preterm labor associated with inflammation or infection.
lhgdn:association:48078
Primary role for IL-1beta and TNF-alpha in the triggering of preterm labor associated with inflammation or infection.
lhgdn:association:48117
Primary role for IL-1beta and TNF-alpha in the triggering of preterm labor associated with inflammation or infection.
lhgdn:association:42734
Characterizes the hamster ortholog and suggests that it may modulate the ability of the proteasome to degrade retroviral cores upon cellular infection.
lhgdn:association:63161
A2M-D allele played a weak Alzheimer disease protective role, and APOE-E4 and A2M-G alleles might act synergistically in Alzheimer disease risk for mainland Han Chinese.
lhgdn:association:63150
The risk of symptomatic thromboembolism was significantly increased with elevated alpha2MG levels.
lhgdn:association:63125
paclitaxel affected human leukemia HL-60 cells arylamine N-acetyltransferase (NAT) activity and DNA-2-aminofluorene adduct formation.
lhgdn:association:55122
It is unlikely that the NAT1*10 or NAT2 rapid/intermediate genotypes are related to stomach cancer risk.
lhgdn:association:63105
It is unlikely that the NAT1*10 or NAT2 rapid/intermediate genotypes are related to stomach cancer risk.
lhgdn:association:55135
genetic polymorphisms of NAT1 and NAT2 have no independent effect on breast cancer risk, but they modulate breast cancer risk in the presence of GSTM1 and GSTT1 null genotypes.
lhgdn:association:55177
genetic polymorphisms of NAT1 and NAT2 have no independent effect on breast cancer risk, but they modulate breast cancer risk in the presence of GSTM1 and GSTT1 null genotypes.
lhgdn:association:57729
genetic polymorphisms of NAT1 and NAT2 have no independent effect on breast cancer risk, but they modulate breast cancer risk in the presence of GSTM1 and GSTT1 null genotypes.
lhgdn:association:57827
genetic polymorphisms of NAT1 and NAT2 have no independent effect on breast cancer risk, but they modulate breast cancer risk in the presence of GSTM1 and GSTT1 null genotypes.
lhgdn:association:58445
genetic polymorphisms of NAT1 and NAT2 have no independent effect on breast cancer risk, but they modulate breast cancer risk in the presence of GSTM1 and GSTT1 null genotypes.
lhgdn:association:58509
genetic polymorphisms of NAT1 and NAT2 have no independent effect on breast cancer risk, but they modulate breast cancer risk in the presence of GSTM1 and GSTT1 null genotypes.
lhgdn:association:63117
genetic polymorphisms of NAT1 and NAT2 have no independent effect on breast cancer risk, but they modulate breast cancer risk in the presence of GSTM1 and GSTT1 null genotypes.
lhgdn:association:63119
genetic polymorphisms of NAT1 and NAT2 have no independent effect on breast cancer risk, but they modulate breast cancer risk in the presence of GSTM1 and GSTT1 null genotypes.
lhgdn:association:63097
although there is little overall association between NAT genotypes and risk of developing systemic lupus erythematosus, the interaction between NAT1 and NAT2 and specific exposures such as hair dyes may be important.
lhgdn:association:63124
The genotype for the NAT1 C1095A polymorphism does not appear to be an independent risk factor for spina bifida.
lhgdn:association:63116
NAT1 variants that reduce or abolish enzyme activity appear to protect against spina bifida, and to exert their influence via both the maternal and the offspring genotypes.
lhgdn:association:63098
Evidence that NAT1 and NAT2 genotypes are associated with Non-Hodgkin Lymphoma risk.
lhgdn:association:63108
Identification of NAT1 residues that play a critical role in substrate binding reveals why human NAT1 acetylates sunscreen additive p-aminobenzoic acid and tobacco smoke carcinogen 4-aminobiphenyl but not arylamines linked to bladder cancer.
lhgdn:association:55119
Genetic variation may affect the degree of association between pre-1980 hair dye use and the risk of non-Hodgkin lymphoma.
lhgdn:association:63103
Genetic variation may affect the degree of association between pre-1980 hair dye use and the risk of non-Hodgkin lymphoma.
lhgdn:association:63109
The effect of tamoxifen on NAT1 activity in a breast tumor cell line was studied.
lhgdn:association:63106
NAT1 is significantly overexpressed in estrogen receptor-positive cancers; increasing evidence supports a biological role for NAT1 in breast cancer progression.
lhgdn:association:63096
findings indicate an association between inflammation and suppression of NAT1 in cholangiocarcinoma cells, which perhaps contributes to chemical-mediated toxicity and carcinogenesis.
lhgdn:association:63107
findings indicate an association between inflammation and suppression of NAT1 in cholangiocarcinoma cells, which perhaps contributes to chemical-mediated toxicity and carcinogenesis.
lhgdn:association:14362
The aim of the study was to investigate NAT1, NAT2, GSTM1, GSTT1, GSTP1, SULT1A1, XRCC1, XRCC3 and XPD genetic polymorphisms, coffee consumption and risk of bladder cancer (BC) through a hospital-based case-control study.
lhgdn:association:21019
The aim of the study was to investigate NAT1, NAT2, GSTM1, GSTT1, GSTP1, SULT1A1, XRCC1, XRCC3 and XPD genetic polymorphisms, coffee consumption and risk of bladder cancer (BC) through a hospital-based case-control study.
lhgdn:association:21080
The aim of the study was to investigate NAT1, NAT2, GSTM1, GSTT1, GSTP1, SULT1A1, XRCC1, XRCC3 and XPD genetic polymorphisms, coffee consumption and risk of bladder cancer (BC) through a hospital-based case-control study.
lhgdn:association:55136
The aim of the study was to investigate NAT1, NAT2, GSTM1, GSTT1, GSTP1, SULT1A1, XRCC1, XRCC3 and XPD genetic polymorphisms, coffee consumption and risk of bladder cancer (BC) through a hospital-based case-control study.
lhgdn:association:57788
The aim of the study was to investigate NAT1, NAT2, GSTM1, GSTT1, GSTP1, SULT1A1, XRCC1, XRCC3 and XPD genetic polymorphisms, coffee consumption and risk of bladder cancer (BC) through a hospital-based case-control study.
lhgdn:association:57948
The aim of the study was to investigate NAT1, NAT2, GSTM1, GSTT1, GSTP1, SULT1A1, XRCC1, XRCC3 and XPD genetic polymorphisms, coffee consumption and risk of bladder cancer (BC) through a hospital-based case-control study.
lhgdn:association:58386
The aim of the study was to investigate NAT1, NAT2, GSTM1, GSTT1, GSTP1, SULT1A1, XRCC1, XRCC3 and XPD genetic polymorphisms, coffee consumption and risk of bladder cancer (BC) through a hospital-based case-control study.
lhgdn:association:63120
The aim of the study was to investigate NAT1, NAT2, GSTM1, GSTT1, GSTP1, SULT1A1, XRCC1, XRCC3 and XPD genetic polymorphisms, coffee consumption and risk of bladder cancer (BC) through a hospital-based case-control study.
lhgdn:association:63110
The present study does not support a relevant impact of the NAT1 genotype on colorectal cancer risk development in the study area.
lhgdn:association:55145
Polymorphism of the N-acetyltransferase 2 gene as a susceptibility risk factor for antituberculosis drug-induced hepatitis.
lhgdn:association:55181
The combined effect of N-acetyltransferase 2 (NAT2) slow genotype and exposure to smoking is observed during the development of laryngeal cancer.
lhgdn:association:55114
NAT2 slow acetylation genotype may be a risk factor of individual susceptibility to rheumatoid arthritis.
lhgdn:association:55141
Women with the GSTT1 null genotype were found to have a significant 3.15-fold increased risk of breast cancer (95% CI = 1.7-5.8), while GSTM1 and NAT2 genotypes were not associated with breast cancer risk.
lhgdn:association:55153
Women with the GSTT1 null genotype were found to have a significant 3.15-fold increased risk of breast cancer (95% CI = 1.7-5.8), while GSTM1 and NAT2 genotypes were not associated with breast cancer risk.
lhgdn:association:57730
Women with the GSTT1 null genotype were found to have a significant 3.15-fold increased risk of breast cancer (95% CI = 1.7-5.8), while GSTM1 and NAT2 genotypes were not associated with breast cancer risk.
lhgdn:association:57740
Women with the GSTT1 null genotype were found to have a significant 3.15-fold increased risk of breast cancer (95% CI = 1.7-5.8), while GSTM1 and NAT2 genotypes were not associated with breast cancer risk.
lhgdn:association:58345
Women with the GSTT1 null genotype were found to have a significant 3.15-fold increased risk of breast cancer (95% CI = 1.7-5.8), while GSTM1 and NAT2 genotypes were not associated with breast cancer risk.
lhgdn:association:58450
Women with the GSTT1 null genotype were found to have a significant 3.15-fold increased risk of breast cancer (95% CI = 1.7-5.8), while GSTM1 and NAT2 genotypes were not associated with breast cancer risk.
lhgdn:association:55179
A slow acetylator genotype of this enzyme is associated with an increased risk of advanced cervical cancer.
lhgdn:association:55182
NAT2 slow acetylator genotype plays an important role in determining the risk of developing prostate cancer in Japanese men and is also associated with more clinically advanced and pathologically aggressive disease.
lhgdn:association:55155
The NAT2 acetylator genotype may modify esophageal cancer risk in humans from exposure to barbecued/grilled meat.
lhgdn:association:55140
NAT2 slow acetylation and GSTM1 null genotypes may increase postmenopausal breast cancer risk in long-term smoking women.
lhgdn:association:14367
We conclude that smoking increases risk of colorectal adenomas and that SULT1A1 and NAT2 only modestly modify this association.
lhgdn:association:55165
We conclude that smoking increases risk of colorectal adenomas and that SULT1A1 and NAT2 only modestly modify this association.
lhgdn:association:55167
Cigarette smoking is associated with increased risk of breast cancer in women with the NAT2 slow acetylator genotype.
lhgdn:association:55160
Only NAT2*14A fast type was associated with increased risk in patients with colorectal carcinoma (OR = 3.03; 95% CI, 1.56-5.86), when a high protein diet was considered, NAT2*7A/B fast genotype was also found to be associated with an increased risk.
lhgdn:association:55158
Risks for colorectal cancer are significantly associated with the genetic polymorphisms of GSTT1 deletion, NAT2-rapid acetylator phenotype and genotye and NAT2-rapid acetylator phenotype.
lhgdn:association:57745
Risks for colorectal cancer are significantly associated with the genetic polymorphisms of GSTT1 deletion, NAT2-rapid acetylator phenotype and genotye and NAT2-rapid acetylator phenotype.
lhgdn:association:55131
Risk of colorectal cancer decreased with the NAT2 slow phenotype, and the use of white meat or its drippings.
lhgdn:association:55123
There is a possible relationship between the NAT2 polymorphisms and colorectal cancer in Hebei Han Chinese.
lhgdn:association:55183
NAT2 gene is one of the determinants for Crohn disease in Japanese patients.
lhgdn:association:55162
The fast NAT acetylator status, which may result in altered NAT detoxifaction capacity, is associated with preeclampsia.
lhgdn:association:55188
Polymorphism of NAT2 is associated with the risk of atopic dermatitis.
lhgdn:association:55161
NAT2 genotype might play a role of effect modifier in bladder cancer carcinogenesis.
lhgdn:association:55118
No evidence of an overall association of NAT2 gene polymorphisms to either colon or lung cancer risk.
lhgdn:association:55133
These data do not support the hypothesis that the NAT2 acetylatorship acts as a modifying factor on the age of onset in sporadic and familial, microsatellite stable colorectal cancer.
lhgdn:association:55117
These results suggest that NAT2 slow acetylator phenotype influences the susceptibility of gallbladder cancer.
lhgdn:association:55128
patients with the NAT2 fast acetylator genotype were more prone to colorectal cancer and reflected the possibility that exposure to heterocyclic amines may contribute to colorectal cancer development in Taiwan, especially in Taiwanese females.
lhgdn:association:55147
Paclitaxel inhibits NAT2 activity and gene expression in stomach neoplasms.
lhgdn:association:55148
NAT2 genotypes and phenotypes are not associated with gastric cancer risk predisposition.
lhgdn:association:55146
The researchers found an association between a NAT2 gene substitution at T341C and an increased risk of head and neck cancer in Tunisia.
lhgdn:association:55187
Opposite effects of NAT2 gene polymorphisms on the risk of lung cancer are possible.
lhgdn:association:55127
NAT2 gene polymorphisms may be associated with genetic susceptibility to pancreatic cancer.
lhgdn:association:55152
The analysis of NAT2 polymorphism does not seem to be useful in predicting the risk of PD with dementia or AD.
lhgdn:association:55134
The combination of NAT2 rapid plus other genotypes is associated with susceptibility to colorectal cancer in Japanese never-smokers.
lhgdn:association:55185
The presence of NAT2*7 allele might be a potential risk factor for the development of brain tumors in Taiwan.
lhgdn:association:55111
Lack of the NAT2*4 haplotype is strongly linked to adverse effects with sulfosalazine therapy in Japanese patients with rheumatoid arthritis.
lhgdn:association:55178
The present study indicates that bladder cancer risk due to exposure to aromatic amines is modulated by the polymorphic xenobiotic-metabolizing enzyme NAT2.
lhgdn:association:55189
polymorphic variants of genes GSTT1, GSTM1, NAT2 and MTRR can modulate the risk of childhood acute leukemia, residents of European part of Russia.
lhgdn:association:57765
polymorphic variants of genes GSTT1, GSTM1, NAT2 and MTRR can modulate the risk of childhood acute leukemia, residents of European part of Russia.
lhgdn:association:58475
polymorphic variants of genes GSTT1, GSTM1, NAT2 and MTRR can modulate the risk of childhood acute leukemia, residents of European part of Russia.
lhgdn:association:59110
polymorphic variants of genes GSTT1, GSTM1, NAT2 and MTRR can modulate the risk of childhood acute leukemia, residents of European part of Russia.
lhgdn:association:55144
These results implicate fast NAT2 acetylation as a risk factor for oral cancer.
lhgdn:association:31420
The results indicate that phenotypic differences in NAT2 alone or in combination with CYP1A2 might help explain the higher incidence rates of transitional cell bladder cancer in white cigarette smokers compared with black smokers.
lhgdn:association:55129
The results indicate that phenotypic differences in NAT2 alone or in combination with CYP1A2 might help explain the higher incidence rates of transitional cell bladder cancer in white cigarette smokers compared with black smokers.
lhgdn:association:55176
There was no association with the NAT2 gene, genital talc use and risk of ovarian cancer.
lhgdn:association:55095
Multivariate analysis showed that ACT mRNA level, but not STC2 mRNA level, in HR-positive patients, was a significant prognostic factor (P = 0.042), which was independent of tumor size and lymph node metastases.
lhgdn:association:55096
Multivariate analysis showed that ACT mRNA level, but not STC2 mRNA level, in HR-positive patients, was a significant prognostic factor (P = 0.042), which was independent of tumor size and lymph node metastases.
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