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# proj.
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# Ann.
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@dpavot |
26626801 |
The 21 genes comprised 8 tumor suppressor candidates (ATM, MSH2, PIK3R1, PTCH1, PTEN, TET2, TP53, an |
229 Bytes |
2020-02-26 |
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@dpavot |
26715604 |
Here we discuss 'congenital disorders of autophagy' as an emerging subclass of inborn errors of meta |
509 Bytes |
2020-02-26 |
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@dpavot |
26944031 |
Mosaicism was identified for autosomal dominant (JAG1, COL3A1), autosomal recessive (PYGM), and X-li |
147 Bytes |
2020-02-26 |
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@dpavot |
27193597 |
Mining GWAS databases revealed association of cis-eSNPs for more than 50 genes with T2D (e.g. PIK3C2 |
213 Bytes |
2020-02-26 |
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7 |
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@dpavot |
27585752 |
In the present study, we first analyzed two expression quantitative trait loci (eQTL) datasets in he |
219 Bytes |
2020-02-26 |
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@dpavot |
27693232 |
Although overlapping features with Bohring-Opitz and Bainbridge-Ropers syndromes exist, features tha |
298 Bytes |
2020-02-21 |
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5 |
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@dpavot |
27807832 |
TNFAIP8 mRNA is induced by NF-kB, and overexpression of TNFAIP8 has been correlated with poor progno |
488 Bytes |
2020-02-26 |
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@dpavot |
27827380 |
While examining pedigrees of JEB patients with LAMA3 mutations, we observed that heterozygous carrie |
219 Bytes |
2020-02-26 |
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@dpavot |
27840944 |
As poor differentiation and low apoptosis are closely associated with poor survival rates and a poor |
337 Bytes |
2020-02-26 |
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@dpavot |
28409271 |
Metabolic cutis laxa results from Menkes syndrome, caused by a defect in the ATPase copper transport |
1.31 KB |
2020-02-26 |
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