LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G (disorder)
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G (disorder)
|
0.700 |
Biomarker
|
disease |
CTD_human |
|
|
|
LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G (disorder)
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
Muscular Dystrophies, Limb-Girdle
|
0.450 |
Biomarker
|
group |
HPO |
|
|
|
Myopathy
|
0.110 |
Biomarker
|
group |
HPO |
|
|
|
Cataract
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Hyporeflexia
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Creatine phosphokinase serum increased
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Shoulder girdle weakness
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Pelvic girdle weakness
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Proximal lower limb amyotrophy
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Decreased movement range in interphalangeal joints
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Rimmed vacuoles on biopsy
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Slow progression
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Proximal upper limb amyotrophy
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Flexion limitation of toes
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Herpes Simplex Infections
|
0.010 |
Biomarker
|
group |
BEFREE |
2 cells with herpes simplex virus type 1 (HSV-1) leads to a reorganization of antigens associated with both the small and heterogeneous nuclear ribonucleoprotein complexes (snRNP and hnRNP).
|
2824525 |
1987 |
Lupus Erythematosus, Systemic
|
0.030 |
Biomarker
|
disease |
BEFREE |
Antibodies to other hnRNP proteins (A1, A2, and B) have been previously found in patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and mixed connective tissue disease (MCTD).
|
8843857 |
1996 |
Rheumatoid Arthritis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Antibodies to other hnRNP proteins (A1, A2, and B) have been previously found in patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and mixed connective tissue disease (MCTD).
|
8843857 |
1996 |
Mixed Connective Tissue Disease
|
0.010 |
Biomarker
|
disease |
BEFREE |
Antibodies to other hnRNP proteins (A1, A2, and B) have been previously found in patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and mixed connective tissue disease (MCTD).
|
8843857 |
1996 |
Glioma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
These data indicate that hnRNP A2 is the Glut1 AURE binding protein whose cytoplasmic expression in gliomas is associated with translational repression and mRNA instability.
|
10441480 |
1999 |
Hypoglycemia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Using this approach, we also identified the other major Glut1 3'UTR RNA binding activity as hnRNP L. Stimuli (hypoxia and hypoglycemia) which increase Glut1 mRNA stability selectively decreased polysomal levels of hnRNP A2 and L. Immunoprecipitation demonstrated that hnRNP A2 and L exist as a complex in vivo.
|
10441480 |
1999 |
MYOTONIC DYSTROPHY 1
|
0.010 |
Biomarker
|
disease |
BEFREE |
Using a combination of indirect immunofluorescence to detect endogenous proteins and overexpression of proteins with green fluorescent protein (GFP) tags we have shown that CUG-BP and hnRNP C do not co-localise with expanded repeat foci in DM1 cell lines.
|
11433021 |
2001 |
Malignant Neoplasms
|
0.090 |
Biomarker
|
group |
BEFREE |
This paper briefly reviews four topics related to mechanisms of action of tea polyphenols: (I) identification of the genes commonly affected by EGCG, as demonstrated by Clontech's Atlas cDNA Expression Array; (II) the significance of heterogeneous nuclear ribonucleoprotein B1 (hnRNP B1) as a new biomarker for early detection of lung cancer, and inhibition of its expression by EGCG; (III) the synergistic or additive effects of EGCG with the cancer preventive agents, sulindac and tamoxifen, on induction of apoptosis in PC-9 cells and on inhibition of intestinal tumor development in multiple intestinal neoplasia (Min) mice; (IV) the results of a 10 year prospective cohort study demonstrating the effectiveness of daily consumption of green tea in preventing cancer, and a prototype study for developing green tea beverage as cancer preventive.
|
11506822 |
2001 |
Primary malignant neoplasm
|
0.080 |
Biomarker
|
group |
BEFREE |
This paper briefly reviews four topics related to mechanisms of action of tea polyphenols: (I) identification of the genes commonly affected by EGCG, as demonstrated by Clontech's Atlas cDNA Expression Array; (II) the significance of heterogeneous nuclear ribonucleoprotein B1 (hnRNP B1) as a new biomarker for early detection of lung cancer, and inhibition of its expression by EGCG; (III) the synergistic or additive effects of EGCG with the cancer preventive agents, sulindac and tamoxifen, on induction of apoptosis in PC-9 cells and on inhibition of intestinal tumor development in multiple intestinal neoplasia (Min) mice; (IV) the results of a 10 year prospective cohort study demonstrating the effectiveness of daily consumption of green tea in preventing cancer, and a prototype study for developing green tea beverage as cancer preventive.
|
11506822 |
2001 |