POROKERATOSIS 9, MULTIPLE TYPES
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
POROKERATOSIS 9, MULTIPLE TYPES
|
0.700 |
Biomarker
|
disease |
CTD_human |
|
|
|
Porokeratosis
|
0.110 |
Biomarker
|
disease |
HPO |
|
|
|
Squamous cell carcinoma
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Pruritus
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Photosensitivity of skin
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Neoplasms
|
0.060 |
AlteredExpression
|
group |
BEFREE |
The incomplete penetrance of the neoplastic phenotype and the monoclonality of lymphoid tumors suggest that tumor formation in v-fps mice requires genetic or epigenetic events in addition to expression of the P130gag-fps protein-tyrosine kinase.
|
2555699 |
1989 |
Anaplastic thyroid carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Semi-quantitative RT-PCR experiments carried out for some genes that had shown altered expression on the microarray verified frequent over-expression of destrin, HSPA8, stathmin, LDH-A, ATP5A1, PSMB6, B23, HDP-1 and LDH-B, and frequent under-expression of thyroglobulin, PBP and c-FES/FPS genes among the cell lines and also among ten primary ATCs.
|
15613457 |
2004 |
Colonic Neoplasms
|
0.010 |
AlteredExpression
|
group |
LHGDN |
Higher farnesyl diphosphate synthase activity in human colorectal cancer inhibition of cellular apoptosis.
|
15713990 |
2004 |
Enzyme inhibition disorder
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
The target of all of the most active bisphosphonates appears to be the isoprene biosynthesis pathway enzyme farnesyl pyrophosphate synthase (FPPS), as indicated by the correlations between T. gondii growth inhibition and FPPS (human and Leishmania major) enzyme inhibition and by the fact that a T. gondii strain engineered to overexpress FPPS required considerably higher levels of bisphosphonates to achieve 50% growth inhibition, while the IC(50) for atovaquone (which does not inhibit FPPS) remained the same in the overexpressing strain.
|
15857119 |
2005 |
Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
FPS-1 cells showed the same morphological and immunophenotypical characteristics as the primary tumor.
|
17094458 |
2006 |
Malignant Fibrous Histiocytoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
FPS-1 cells might be useful for investigating biological behavior and developing new molecular targeting antitumor drugs for UPS with EGFR or COX-2 expression.
|
17094458 |
2006 |
Alzheimer's Disease
|
0.030 |
GeneticVariation
|
disease |
BEFREE |
Replication trials in five independent European samples detected associations of variants within HMGCS2, FDPS, NPC2, or ABCG1 with AD in some samples (P = 0.05 to P = 0.005).
|
17387528 |
2007 |
Osteosarcoma
|
0.010 |
Biomarker
|
disease |
LHGDN |
Farnesyl diphosphate synthase is involved in the resistance to zoledronic acid of osteosarcoma cells.
|
18494934 |
2008 |
Accessory spleen
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Of the 21 TR13 subjects, 12 had intrapancreatic splenic tissue (IPST) and 17 had fusion of the pancreatic tail and splenic hilus and/or accessory spleen (FPS/FPAS).All 21 had IPST and/or FPS/FPAS.
|
19261091 |
2009 |
Glioblastoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
The present results suggest that FPPS plays an important role in apoptotic cell death of cancer cells by blocking the JNK signaling cascade and activating mevalonate metabolism in paclitaxel-treated glioblastoma cells.
|
20298756 |
2010 |
Adult Glioblastoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
The present results suggest that FPPS plays an important role in apoptotic cell death of cancer cells by blocking the JNK signaling cascade and activating mevalonate metabolism in paclitaxel-treated glioblastoma cells.
|
20298756 |
2010 |
Childhood Glioblastoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
The present results suggest that FPPS plays an important role in apoptotic cell death of cancer cells by blocking the JNK signaling cascade and activating mevalonate metabolism in paclitaxel-treated glioblastoma cells.
|
20298756 |
2010 |
Glioblastoma Multiforme
|
0.030 |
Biomarker
|
disease |
BEFREE |
The present results suggest that FPPS plays an important role in apoptotic cell death of cancer cells by blocking the JNK signaling cascade and activating mevalonate metabolism in paclitaxel-treated glioblastoma cells.
|
20298756 |
2010 |
Malignant neoplasm of prostate
|
0.030 |
GeneticVariation
|
disease |
BEFREE |
To determine if a higher sensitivity to bisphosphonates could in part explain the development of ONJ, the segregation of A/C rs2297480 polymorphism of gene encoding for the farnesyl pyrophosphate synthase (FDPS) with ONJ was evaluated in a cohort of 68 Caucasian patients treated with zoledronic acid for multiple myeloma and metastatic mammary and prostate cancer.
|
21196316 |
2011 |
Prostate carcinoma
|
0.030 |
GeneticVariation
|
disease |
BEFREE |
To determine if a higher sensitivity to bisphosphonates could in part explain the development of ONJ, the segregation of A/C rs2297480 polymorphism of gene encoding for the farnesyl pyrophosphate synthase (FDPS) with ONJ was evaluated in a cohort of 68 Caucasian patients treated with zoledronic acid for multiple myeloma and metastatic mammary and prostate cancer.
|
21196316 |
2011 |
Multiple Myeloma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
To determine if a higher sensitivity to bisphosphonates could in part explain the development of ONJ, the segregation of A/C rs2297480 polymorphism of gene encoding for the farnesyl pyrophosphate synthase (FDPS) with ONJ was evaluated in a cohort of 68 Caucasian patients treated with zoledronic acid for multiple myeloma and metastatic mammary and prostate cancer.
|
21196316 |
2011 |
Alzheimer's Disease
|
0.030 |
Biomarker
|
disease |
BEFREE |
Our data suggest that FPS-ZM1 is a potent multimodal RAGE blocker that effectively controls progression of Aβ-mediated brain disorder and that it may have the potential to be a disease-modifying agent for AD.
|
22406537 |
2012 |
Brain Diseases
|
0.010 |
Biomarker
|
group |
BEFREE |
Our data suggest that FPS-ZM1 is a potent multimodal RAGE blocker that effectively controls progression of Aβ-mediated brain disorder and that it may have the potential to be a disease-modifying agent for AD.
|
22406537 |
2012 |
Heart failure
|
0.010 |
Biomarker
|
disease |
BEFREE |
Here, we further investigate the role of FPPS in cardiac hypertrophy and heart failure (HF) using a transgenic (Tg) model, and its mechanisms.
|
23180723 |
2013 |