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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 polycystic ovary syndrome.
BACKGROUND: Insulin resistance is a core feature of polycystic ovary synd |
1.83 KB |
2015-11-24 |
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10 |
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17 |
2021-12-23
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| 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 |
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12 |
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14 |
2021-12-23
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| 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 |
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15 |
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13 |
2021-12-23
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| 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 |
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15 |
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12 |
2021-12-23
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| 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
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| PubMed |
16419642 |
A novel missense mutation, F826Y, in the mineralocorticoid receptor gene in Japanese hypertensives: its implications for clinical phenotypes.
A gain-of-function mutation resulting in the S810L amino a |
1.78 KB |
2015-11-20 |
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28 |
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11 |
2021-12-23
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| PubMed |
15970799 |
Functional characterization of SLCO1B1 (OATP-C) variants, SLCO1B1*5, SLCO1B1*15 and SLCO1B1*15+C1007G, by using transient expression systems of HeLa and HEK293 cells.
OBJECTIVES: SLCO1B1*5 and SLCO1B1 |
1.97 KB |
2015-11-22 |
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7 |
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10 |
2021-12-23
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| PubMed |
16822828 |
Genotyping of five chinese patients with 17alpha-hydroxylase deficiency diagnosed through high-performance liquid chromatography serum adrenal profile: identification of two novel CYP17 mutations.
CON |
1.89 KB |
2015-11-23 |
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8 |
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9 |
2021-12-23
|
| PubMed |
17391797 |
The phosphatidylethanolamine N-methyltransferase gene V175M single nucleotide polymorphism confers the susceptibility to NASH in Japanese population.
BACKGROUND/AIMS: The genetic predisposition on the |
1.48 KB |
2015-11-23 |
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12 |
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8 |
2021-12-23
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| PubMed |
19592582 |
Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into protease activation mechanisms.
Mutations leading to abrogation of matriptase-2 proteolytic activity |
1.38 KB |
2015-11-25 |
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10 |
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6 |
2021-12-23
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