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LitCoin-GeneOrGeneProduct-v3
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# proj.
# Ann.
updated_at
PubMed
16005363
Identification of a novel WFS1 mutation (AFF344-345ins) in Japanese patients with Wolfram syndrome.
909 Bytes
2015-11-19
33
4
2021-12-22
PubMed
16046395
Allelic expression imbalance of human mu opioid receptor (OPRM1) caused by variant A118G. As a prima
1.52 KB
2015-11-19
49
12
2021-12-22
PubMed
16112787
In vivo evidences suggesting the role of oxidative stress in pathogenesis of vancomycin-induced neph
1.68 KB
2015-11-22
23
5
2021-12-22
PubMed
16116131
rTMS of supplementary motor area modulates therapy-induced dyskinesias in Parkinson disease. The neu
630 Bytes
2015-11-22
24
2
2021-12-22
PubMed
16152606
Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients
1.76 KB
2015-11-19
29
8
2021-12-22
PubMed
16157158
A Cys 23-Ser 23 substitution in the 5-HT(2C) receptor gene influences body weight regulation in fema
1.54 KB
2015-11-19
30
5
2021-12-22
PubMed
16181814
Mono-allelic POLG expression resulting from nonsense-mediated decay and alternative splicing in a pa
1.73 KB
2015-11-19
26
9
2021-12-22
PubMed
16186368
Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutations. PURPOSE: Mutations
1.8 KB
2015-11-19
26
7
2021-12-22
PubMed
16200390
A genetic analysis of serotonergic biosynthetic and metabolic enzymes in migraine using a DNA poolin
1.39 KB
2015-11-19
26
9
2021-12-22
PubMed
16225977
Amisulpride related tic-like symptoms in an adolescent schizophrenic. Tic disorders can be effective
1.13 KB
2017-09-04
26
5
2021-12-22
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