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17982252 |
The glutamatergic hypothesis of schizophrenia lead recently to a first successful mGlu2/3 receptor agonistic drug and is underpinned by significant findings in genes regulating the glutamatergic syste |
281 Bytes |
2020-02-26 |
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23781959 |
Recent clinical, morphological and molecular investigations of CMT families with autosomal recessive inheritance allowed the identification of many genes such as GDAP1, MTMR2, SBF2, NDRG1, EGR2, SH3TC |
361 Bytes |
2020-02-26 |
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24269018 |
We analyzed the nucleotide repeat lengths of 6 genes (ATXN8, ATXN10, PPP2R2B, NOP56, DMPK, and JPH3) that have previously been associated with neurologic or neuromuscular disorders, in several hundred |
257 Bytes |
2020-02-26 |
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24386311 |
Clinically, low expression of CLCA4 signaled lower relapse-free survival in basal and luminal B breast cancers. |
111 Bytes |
2020-02-26 |
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24662834 |
Rather, we observed that, in ADAM23-heterotypic environments, ADAM23-negative cells promote tumor growth and metastasis by enhancing the proliferation and invasion of adjacent A23-positive cells throu |
284 Bytes |
2020-02-26 |
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25157627 |
Though KRT5 has been identified to be the causal gene of DDD, the heterogeneity of this disease was displayed: for example, POFUT1 and POGLUT1 were recently identified and confirmed to be additional p |
223 Bytes |
2020-02-26 |
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25357075 |
In Mfrprd6 eyes, a significant 1.5- to 2.0-fold decrease was observed among transcripts of genes linked to retinal degeneration, including those involved in visual cycle (Rpe65, Lrat, Rgr), phototrans |
288 Bytes |
2020-02-26 |
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26023803 |
In vitro test on colon cancer resistant/susceptible to chemoradioterapy cells, finally prove that XRCC3 deregulation is extensively involved in the chemoresistance mechanisms. |
175 Bytes |
2020-02-26 |
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26035073 |
Next, using DLD-1 colon cancer cells inducibly expressing SASS6, SASS6 overexpression was shown to induce centrosome amplification, mitotic abnormalities such as chromosomal misalignment and lagging c |
245 Bytes |
2020-02-26 |
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26680691 |
CGD is a genetically heterogeneous disease with an X-linked recessive (XR-CGD) form caused by mutations in the CYBB gene encoding the gp91(phox) protein, and an autosomal recessive (AR-CGD) form cause |
328 Bytes |
2020-02-26 |
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