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ncbi-valid-gpt-r-m
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# proj.
# Ann.
updated_at
PubMed
9272171
Adult onset globoid cell leukodystrophy (Krabbe disease): analysis of galactosylceramidase cDNA from
1.74 KB
2015-11-27
25
9
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PubMed
9271438
The von Hippel-Lindau tumor suppressor gene product interacts with Sp1 to repress vascular endotheli
1.82 KB
2015-03-12
23
10
-
PubMed
9245987
Constitutively methylated CpG dinucleotides as mutation hot spots in the retinoblastoma gene (RB1).
1.5 KB
2015-03-12
23
2
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PubMed
9241282
Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP. Myotonic
1.45 KB
2015-11-27
25
9
-
PubMed
9241281
atm and p53 cooperate in apoptosis and suppression of tumorigenesis, but not in resistance to acute
1.5 KB
2015-11-27
25
5
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PubMed
9223312
Fusion genes resulting from alternative chromosomal translocations are overexpressed by gene-specifi
1.22 KB
2015-11-27
25
5
-
PubMed
9223307
Isolation of full-length ATM cDNA and correction of the ataxia-telangiectasia cellular phenotype. A
1.09 KB
2015-11-27
25
7
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PubMed
9222760
Molecular heterogeneity of classical and Duarte galactosemia: mutation analysis by denaturing gradie
1.21 KB
2015-03-12
26
8
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PubMed
9218625
Molecular bases of C7 deficiency: three different defects. The molecular basis of C7 deficiency has
946 Bytes
2015-12-06
23
3
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PubMed
9195227
Screening for ESR mutations in breast and ovarian cancer patients. In the present study, leukocyte D
1.09 KB
2015-11-28
27
9
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