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LitCoin_Mondo_095
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LitCoin_Mondo_095
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# proj.
# Ann.
updated_at
PubMed
19508969
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).
1.96 KB
2015-11-25
27
32
2021-12-22
PubMed
11773892
End-stage renal disease (ESRD) after orthotopic liver transplantation (OLTX) using calcineurin-based
2.71 KB
2015-11-21
23
29
2021-12-22
PubMed
20415560
Vitamin E reduces cardiovascular disease in individuals with diabetes mellitus and the haptoglobin 2
1.74 KB
2015-11-25
27
28
2021-12-22
PubMed
18366737
The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (H
2.43 KB
2015-11-24
26
26
2021-12-22
PubMed
20431083
Antithrombotic drug use, cerebral microbleeds, and intracerebral hemorrhage: a systematic review of
2.08 KB
2016-01-03
25
24
2021-12-22
PubMed
20682662
Lack of association of C-C chemokine receptor 5 Δ32 deletion status with rheumatoid arthritis, syste
1.69 KB
2015-11-25
29
24
2021-12-22
PubMed
28151486
Star-PAP, a poly(A) polymerase, functions as a tumor suppressor in an orthotopic human breast cancer
1.25 KB
2017-08-30
24
23
2021-12-22
PubMed
20540798
Sex-differential genetic effect of phosphodiesterase 4D (PDE4D) on carotid atherosclerosis. BACKGROU
2.22 KB
2016-01-06
25
21
2021-12-22
PubMed
15754732
Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with cli
1.92 KB
2015-11-19
27
20
2021-12-22
PubMed
15200408
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for diseas
2.45 KB
2015-11-19
27
20
2021-12-22
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