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source ID
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text
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size
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updated at |
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# proj.
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# Ann.
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updated_at |
| PubMed |
19218574 |
Phosphatidylinositol 3-kinase p85alpha regulatory subunit gene Met326Ile polymorphism in women with |
1.83 KB |
2015-11-24 |
|
11 |
|
17 |
2021-12-23
|
| PubMed |
15623763 |
TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients.
PURPOSE: T |
1.89 KB |
2015-11-18 |
|
13 |
|
14 |
2021-12-23
|
| PubMed |
17495183 |
Tenomodulin is associated with obesity and diabetes risk: the Finnish diabetes prevention study.
We |
1.48 KB |
2015-11-23 |
|
13 |
|
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 |
2.11 KB |
2015-11-23 |
|
14 |
|
12 |
2021-12-23
|
| PubMed |
18991055 |
Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFS1, CDKAL1, KCNQ1 and |
1.55 KB |
2015-11-24 |
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11 |
|
12 |
2021-12-23
|
| PubMed |
16419642 |
A novel missense mutation, F826Y, in the mineralocorticoid receptor gene in Japanese hypertensives: |
1.78 KB |
2015-11-20 |
|
13 |
|
11 |
2021-12-23
|
| PubMed |
15970799 |
Functional characterization of SLCO1B1 (OATP-C) variants, SLCO1B1*5, SLCO1B1*15 and SLCO1B1*15+C1007 |
1.97 KB |
2015-11-22 |
|
8 |
|
10 |
2021-12-23
|
| PubMed |
16822828 |
Genotyping of five chinese patients with 17alpha-hydroxylase deficiency diagnosed through high-perfo |
1.89 KB |
2015-11-23 |
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9 |
|
9 |
2021-12-23
|
| PubMed |
17391797 |
The phosphatidylethanolamine N-methyltransferase gene V175M single nucleotide polymorphism confers t |
1.48 KB |
2015-11-23 |
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13 |
|
8 |
2021-12-23
|
| PubMed |
19592582 |
Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into |
1.38 KB |
2015-11-25 |
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11 |
|
6 |
2021-12-23
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