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# proj.
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# Ann.
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updated_at |
@dpavot |
23086420 |
Several myotubularins have been genetically linked to human diseases: MTM1 is mutated in the congeni |
317 Bytes |
2020-02-26 |
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1 |
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5 |
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@dpavot |
24357125 |
Likely haploinsufficiency of one or several of the 19 genes in the common deleted interval (ACTN1, D |
555 Bytes |
2020-02-21 |
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1 |
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22 |
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@dpavot |
24455740 |
We initially selected 6 fluoropyrimidine metabolism-related genes (DPYD, ORPT, TYMS, TYMP, TK1, and |
249 Bytes |
2020-02-26 |
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1 |
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3 |
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@dpavot |
24827421 |
Our study reports the first mutations in the VARS2 and TARS2 genes, which encode two mitochondrial a |
204 Bytes |
2020-02-26 |
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1 |
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3 |
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@dpavot |
24898506 |
These include other keratin genes for monilethrix, the HR gene for atrichia congenita, the genes CDS |
314 Bytes |
2020-02-21 |
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1 |
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3 |
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@dpavot |
25264125 |
The genes HLA complex P5 (HCP5), spermatogenesis associated 2 (SPATA2), tumour necrosis factor alpha |
327 Bytes |
2020-02-26 |
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1 |
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3 |
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@dpavot |
25343988 |
In humans, mutations in several genes involved in the Notch pathway are associated with SDV, with bo |
191 Bytes |
2020-02-26 |
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1 |
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3 |
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@dpavot |
25590583 |
Based on the generated interaction network, we examine several apoptotic markers to determine the ef |
280 Bytes |
2020-02-26 |
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1 |
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3 |
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@dpavot |
26077881 |
The findings in this study expand our understanding of SRPS locus heterogeneity and demonstrate the |
210 Bytes |
2020-02-26 |
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1 |
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3 |
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@dpavot |
26211651 |
In addition, polymorphisms in apoptosis-related genes such as RNF7, TULP1, and MERTK are associated |
213 Bytes |
2020-02-26 |
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1 |
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3 |
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