Documents (40) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
@dpavot	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	1	3	-
@dpavot	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	1	3	-
@dpavot	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	1	3	-
@dpavot	24386311	Clinically, low expression of CLCA4 signaled lower relapse-free survival in basal and luminal B breast cancers.	111 Bytes	2020-02-26	1	3	-
@dpavot	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	1	3	-
@dpavot	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	1	3	-
@dpavot	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	1	3	-
@dpavot	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	1	3	-
@dpavot	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	1	3	-
@dpavot	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	1	3	-