source DB |
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 |
15970799 |
Functional characterization of SLCO1B1 (OATP-C) variants, SLCO1B1*5, SLCO1B1*15 and SLCO1B1*15+C1007 |
1.97 KB |
2015-11-22 |
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7 |
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13 |
2021-12-23
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PubMed |
16001362 |
An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nuc |
2.06 KB |
2015-11-19 |
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11 |
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3 |
2021-12-23
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PubMed |
16321363 |
Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation.
We describ |
925 Bytes |
2015-11-23 |
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15 |
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7 |
2021-12-23
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PubMed |
16330669 |
Array-based comparative genomic hybridization analysis reveals recurrent chromosomal alterations and |
2 KB |
2015-11-19 |
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11 |
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0 |
2021-12-23
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PubMed |
16419642 |
A novel missense mutation, F826Y, in the mineralocorticoid receptor gene in Japanese hypertensives: |
1.78 KB |
2015-11-20 |
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12 |
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3 |
2021-12-23
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PubMed |
16629641 |
Definition and management of anemia in patients infected with hepatitis C virus.
Chronic infection w |
1.32 KB |
2015-11-23 |
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7 |
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9 |
2021-12-23
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PubMed |
16731636 |
Enhanced isoproterenol-induced cardiac hypertrophy in transgenic rats with low brain angiotensinogen |
1.47 KB |
2015-11-23 |
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7 |
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13 |
2021-12-23
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PubMed |
16737910 |
Identification of the nuclear localization motif in the ETV6 (TEL) protein.
ETV6, or Translocation-E |
1.04 KB |
2015-11-23 |
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7 |
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3 |
2021-12-23
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PubMed |
16755009 |
Pharmacological evidence for the potential of Daucus carota in the management of cognitive dysfuncti |
1.79 KB |
2021-12-23 |
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7 |
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18 |
2021-12-23
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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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8 |
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7 |
2021-12-23
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