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LitCoin-MeSH-Disease-2
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# proj.
# Ann.
updated_at
PubMed
17035713
Chloroacetaldehyde as a sulfhydryl reagent: the role of critical thiol groups in ifosfamide nephropa
1.55 KB
2015-12-24
24
8
2021-12-22
PubMed
17059986
A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial h
1.74 KB
2015-11-23
36
23
2021-12-22
PubMed
17065198
Analysis of skin cancer risk factors in immunosuppressed renal transplant patients shows high levels
1.78 KB
2015-11-23
27
22
2021-12-22
PubMed
17074608
Valproate-induced chorea and encephalopathy in atypical nonketotic hyperglycinemia. Nonketotic hyper
781 Bytes
2015-12-28
27
15
2021-12-22
PubMed
17083016
Genetic polymorphism of the binding domain of surfactant protein-A2 increases susceptibility to meni
1.72 KB
2015-11-23
29
12
2021-12-22
PubMed
19101703
Study of a Taiwanese family with oculopharyngeal muscular dystrophy. BACKGROUND: Oculopharyngeal mus
1.2 KB
2015-11-24
26
11
2021-12-22
PubMed
19082493
Combination of polymorphisms within 5' and 3' untranslated regions of thymidylate synthase gene modu
2.15 KB
2015-08-06
25
11
2021-12-22
PubMed
19067809
Hemodynamic parameters and heart rate variability during a tilt test in relation to gene polymorphis
1.79 KB
2015-11-24
25
5
2021-12-22
PubMed
16288197
Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree. PURPOSE: C
2.59 KB
2015-11-19
29
19
2021-12-22
PubMed
16277682
Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's
1.92 KB
2015-08-06
28
13
2021-12-22
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