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# proj.
# Ann.
PubMed
30413633
PCNT point mutations and familial intracranial aneurysms. OBJECTIVE: To identify novel genes involve
1.63 KB
2023-12-21
1
3
PubMed
1901346
Structural and functional properties of reconstituted high density lipoprotein discs prepared with s
2.46 KB
2015-12-07
3
-2
PubMed
21913903
Allelic and phenotypic heterogeneity in 49 Italian patients with the muscle form of CPT-II deficienc
1.49 KB
2017-01-27
2
-1
PubMed
1307610
[Detection of the mutation responsible for adenine phosphoribosyltransferase deficiency among Japane
1.39 KB
2015-11-22
2
-2
PubMed
1301939
Human hepatic lipase mutations and polymorphisms. Human hepatic lipase (HL) is a 477 residue glycopr
1.12 KB
2015-11-22
2
-2
PubMed
8882882
The origin of the most common mutation of adenine phosphoribosyltransferase among Japanese goes back
1.53 KB
2015-12-06
2
-1
PubMed
12475768
Searching for type 2 diabetes genes on chromosome 20. Genome scans in families with type 2 diabetes
1.21 KB
2015-11-22
1
1
PubMed
16048944
Quantifying mixed populations of drug-resistant human immunodeficiency virus type 1. In order to sur
1.39 KB
2015-11-22
2
-1
PubMed
28479318
Identification of Somatic Mutations in Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type by
1.5 KB
2017-08-29
2
-1
PubMed
12827501
Mutations in the yeast cyclin-dependent kinase Cdc28 reveal a role in the spindle assembly checkpoin
1.43 KB
2015-11-22
1
1
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