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TEST-DiseaseOrPhenotypicFeature
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# proj.
# Ann.
updated_at
PubMed
16970763
Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and
1.89 KB
2015-11-20
12
26
2021-12-23
PubMed
19728177
Prolonged hypothermia as a bridge to recovery for cerebral edema and intracranial hypertension assoc
1.51 KB
2017-09-04
11
23
2021-12-23
PubMed
1711760
Delayed institution of hypertension during focal cerebral ischemia: effect on brain edema. The effec
1.61 KB
2015-12-23
10
21
2021-12-23
PubMed
21911891
Plasminogen activator inhibitor type 1 serum levels and 4G/5G gene polymorphism in morbidly obese Hi
2 KB
2015-11-26
12
21
2021-12-23
PubMed
27384305
Male 11β-HSD1 Knockout Mice Fed Trans-Fats and Fructose Are Not Protected From Metabolic Syndrome or
1.89 KB
2017-09-04
11
21
2021-12-23
PubMed
29045486
Thiamine deficiency activates hypoxia inducible factor-1α to facilitate pro-apoptotic responses in m
1.74 KB
2021-12-23
9
20
2021-12-23
PubMed
20195852
Risk of nephropathy after consumption of nonionic contrast media by children undergoing cardiac angi
2.15 KB
2016-01-01
10
19
2021-12-23
PubMed
17495183
Tenomodulin is associated with obesity and diabetes risk: the Finnish diabetes prevention study. We
1.48 KB
2015-11-23
13
18
2021-12-23
PubMed
21699520
PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and
1.54 KB
2016-01-03
13
17
2021-12-23
PubMed
19353688
Pure monosomy and pure trisomy of 13q21.2-31.1 consequent to a familial insertional translocation: e
1.81 KB
2015-11-25
13
17
2021-12-23
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