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ncbi-valid-gpt-r-m
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# proj.
# Ann.
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PubMed
8589722
BRCA1 is secreted and exhibits properties of a granin. Germline mutations in BRCA1 are responsible f
755 Bytes
2015-11-27
25
1
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PubMed
8659549
Identification and expression of eight novel mutations among non-Jewish patients with Canavan diseas
1.77 KB
2015-11-27
27
7
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PubMed
9020847
Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice. Myotonic d
1.16 KB
2015-11-27
26
4
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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
8621452
Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gl
1.14 KB
2015-12-05
52
4
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PubMed
8828602
Gene therapy for phenylketonuria. Classical phenylketonuria (PKU) is an autosomal recessive disorder
1.12 KB
2015-11-27
26
7
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PubMed
8622978
Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von
1.4 KB
2015-11-27
26
3
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PubMed
8894695
HPRT-APRT-deficient mice are not a model for lesch-nyhan syndrome. Complete hypoxanthine-guanine pho
1.2 KB
2015-12-06
24
8
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PubMed
8637912
Tumor suppression and apoptosis of human prostate carcinoma mediated by a genetic locus within human
1.72 KB
2015-11-27
25
9
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PubMed
8651278
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma. We have searched for germ-line
1.38 KB
2015-12-05
24
3
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