LitCoin-SeqVar

Documents (400) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	17006606	A polymorphism of C-to-T substitution at -31 IL1B is associated with the risk of advanced gastric adenocarcinoma in a Japanese population. Proinflammatory cytokine gene polymorphisms have been demonst	1.74 KB	2015-11-23	25	8	2021-12-16
PubMed	16277682	Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian family. Mutations of the p62/Sequestosome 1 gene (p62/SQSTM1) account	1.92 KB	2015-08-06	44	6	2021-12-16
PubMed	27959382	Bach1 siRNA attenuates bleomycin-induced pulmonary fibrosis by modulating oxidative stress in mice. Oxidative stress plays an essential role in inflammation and fibrosis. Bach1 is an important transcr	1.96 KB	2017-08-30	27	0	2021-12-16
PubMed	16364460	Microinjection of ritanserin into the CA1 region of hippocampus improves scopolamine-induced amnesia in adult male rats. The effect of ritanserin (5-HT2 antagonist) on scopolamine (muscarinic choliner	1.6 KB	2021-11-28	24	0	2021-12-16
PubMed	22859398	Variation in IL10 and other genes involved in the immune response and in oxidation and prostate cancer recurrence. BACKGROUND: To evaluate the association of variation in genes involved in immune resp	1.78 KB	2015-11-26	27	2	2021-12-16
PubMed	24709919	Effects of ginsenosides on opioid-induced hyperalgesia in mice. Opioid-induced hyperalgesia (OIH) is characterized by nociceptive sensitization caused by the cessation of chronic opioid use. OIH can l	1.12 KB	2017-02-10	24	0	2021-12-16
PubMed	27103577	On the pivotal role of PPARα in adaptation of the heart to hypoxia and why fat in the diet increases hypoxic injury. The role of peroxisome proliferator-activated receptor α (PPARα)-mediated metabolic	1.92 KB	2017-09-04	41	0	2021-12-16
PubMed	19759529	The glycine transporter-1 inhibitor SSR103800 displays a selective and specific antipsychotic-like profile in normal and transgenic mice. Schizophrenia has been initially associated with dysfunction i	2.03 KB	2016-07-04	40	0	2021-12-16
PubMed	17304550	Disruption of a synaptotagmin (SYT14) associated with neurodevelopmental abnormalities. We report cytogenetic and molecular studies of a de novo, apparently balanced t(1;3)(q32.1;q25.1) identified in	1.02 KB	2015-11-23	28	0	2021-12-16
PubMed	21405999	Mutation screening of the GUCA1B gene in patients with autosomal dominant cone and cone rod dystrophy. BACKGROUND: Heterozygous mutations in GUCA1A (MIM # 600364) have been identified to cause autosom	1.5 KB	2015-11-26	29	5	2021-12-16