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TEST-DiseaseOrPhenotypicFeature
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# proj.
# Ann.
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
8
1
2021-12-23
PubMed
16001362
An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nuc
2.06 KB
2015-11-19
12
8
2021-12-23
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
16
2
2021-12-23
PubMed
16330669
Array-based comparative genomic hybridization analysis reveals recurrent chromosomal alterations and
2 KB
2015-11-19
12
7
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
5
2021-12-23
PubMed
16629641
Definition and management of anemia in patients infected with hepatitis C virus. Chronic infection w
1.32 KB
2015-11-23
8
17
2021-12-23
PubMed
16731636
Enhanced isoproterenol-induced cardiac hypertrophy in transgenic rats with low brain angiotensinogen
1.47 KB
2015-11-23
8
4
2021-12-23
PubMed
16737910
Identification of the nuclear localization motif in the ETV6 (TEL) protein. ETV6, or Translocation-E
1.04 KB
2015-11-23
8
2
2021-12-23
PubMed
16755009
Pharmacological evidence for the potential of Daucus carota in the management of cognitive dysfuncti
1.79 KB
2021-12-23
8
4
2021-12-23
PubMed
16822828
Genotyping of five chinese patients with 17alpha-hydroxylase deficiency diagnosed through high-perfo
1.89 KB
2015-11-23
9
7
2021-12-23
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