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# proj.
# Ann.
updated_at
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
26
2021-12-23
PubMed
17286451
Retinoblastoma in India : microsatellite analysis and its application in genetic counseling. OBJECTI
1.73 KB
2015-12-24
10
26
2021-12-23
PubMed
24126708
Association of common genetic variants of HOMER1 gene with levodopa adverse effects in Parkinson's d
1.13 KB
2016-01-15
12
26
2021-12-23
PubMed
17033974
Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy
1.16 KB
2015-11-23
19
26
2021-12-23
PubMed
15041272
A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation. Clinical, l
1.53 KB
2015-11-18
19
27
2021-12-23
PubMed
20520283
Efficacy and safety of asenapine in a placebo- and haloperidol-controlled trial in patients with acu
1.86 KB
2015-12-31
10
27
2021-12-23
PubMed
25983002
Inhibition of LDHA suppresses tumor progression in prostate cancer. A key hallmark of cancer cells i
1.11 KB
2016-01-23
11
27
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
27
2021-12-23
PubMed
19521089
Serotonin transporter gene polymorphic element 5-HTTLPR increases the risk of sporadic Parkinson's d
978 Bytes
2015-08-06
9
28
2021-12-23
PubMed
15824163
No Evidence for BRAF as a melanoma/nevus susceptibility gene. Somatic mutations of BRAF have been id
1.75 KB
2015-11-19
12
28
2021-12-23
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