|
source DB |
source ID
|
text
|
size
|
updated at |
|
# proj.
|
|
# Ann.
|
updated_at |
| PubMed |
15623763 |
TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients.
PURPOSE: To identify mutations in the TGFBI gene in Indian patients with lattice corneal dystrophy (LCD) or gr |
1.89 KB |
2015-11-18 |
|
12 |
|
14 |
2021-12-23
|
| PubMed |
19918264 |
FGFR4 Gly388Arg polymorphism and prostate cancer risk in Scottish men.
Fibroblast growth factor receptor 4 (FGFR4), a member of the fibroblast growth receptor family, was recently reported to be more |
1.34 KB |
2015-11-25 |
|
13 |
|
1 |
2021-12-23
|
| PubMed |
20806042 |
A novel mutation in GJA8 causing congenital cataract-microcornea syndrome in a Chinese pedigree.
PURPOSE: To identify the underlying genetic defect in a four-generation family of Chinese origin with a |
1.31 KB |
2015-11-25 |
|
13 |
|
3 |
2021-12-23
|
| PubMed |
18991055 |
Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFS1, CDKAL1, KCNQ1 and type 2 diabetes in the Korean population.
According to recent genome-wide association studies, a num |
1.55 KB |
2025-10-02 |
|
13 |
|
12 |
2021-12-23
|
| PubMed |
22729903 |
Contribution of STAT4 gene single-nucleotide polymorphism to systemic lupus erythematosus in the Polish population.
The STAT4 has been found to be a susceptible gene in the development of systemic lup |
1.54 KB |
2015-11-26 |
|
13 |
|
2 |
2021-12-23
|
| PubMed |
18408250 |
A single nucleotide polymorphism in the IRF5 promoter region is associated with susceptibility to rheumatoid arthritis in the Japanese population.
OBJECTIVES: Interferon regulatory factor 5 (IRF5) is |
1.87 KB |
2025-10-02 |
|
14 |
|
3 |
2021-12-23
|
| PubMed |
24126708 |
Association of common genetic variants of HOMER1 gene with levodopa adverse effects in Parkinson's disease patients.
Levodopa is the most effective symptomatic therapy for Parkinson's disease, but its |
1.13 KB |
2025-10-02 |
|
14 |
|
5 |
2021-12-23
|
| PubMed |
15824163 |
No Evidence for BRAF as a melanoma/nevus susceptibility gene.
Somatic mutations of BRAF have been identified in both melanoma tumors and benign nevi. Germ line mutations in BRAF have not been identifi |
1.75 KB |
2025-10-02 |
|
14 |
|
1 |
2021-12-23
|
| PubMed |
17495183 |
Tenomodulin is associated with obesity and diabetes risk: the Finnish diabetes prevention study.
We recently showed that long-term weight reduction changes the gene expression profile of adipose tissu |
1.48 KB |
2025-10-02 |
|
15 |
|
13 |
2021-12-23
|
| PubMed |
17000021 |
No independent role of the -1123 G>C and+2740 A>G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations.
INTRODUCTION: The PTPN22 is |
2.11 KB |
2025-10-02 |
|
15 |
|
12 |
2021-12-23
|