Documents (986) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	16061662	Activation of ErbB2 by overexpression or by transmembrane neuregulin results in differential signaling and sensitivity to herceptin. The ligands of the epidermal growth factor family and their recepto	1.74 KB	2015-11-19	8	4	-
PubMed	24916015	Corneal dystrophy-causing SLC4A11 mutants: suitability for folding-correction therapy. SLC4A11 mutations cause some cases of the corneal endothelial dystrophies, congenital hereditary endothelial corn	1.48 KB	2016-01-15	8	4	-
PubMed	20212155	Monomeric red fluorescent proteins with a large Stokes shift. Two-photon microscopy has advanced fluorescence imaging of cellular processes in living animals. Fluorescent proteins in the blue-green wa	1.28 KB	2015-11-25	8	4	-
PubMed	16949912	Infrequent COX-2 expression due to promoter hypermethylation in gastric cancers in Dalian, China. Cyclooxygenase-2 (COX-2) has been shown to play oncogenic roles during stepwise gastrocarcinogenesis,	1.96 KB	2015-11-20	8	4	-
PubMed	15770521	Phenotypic characterization of BRCA1 and BRCA2 tumors based in a tissue microarray study with 37 immunohistochemical markers. Familial breast cancers that are associated with BRCA1 or BRCA2 germline m	1.83 KB	2015-11-19	7	13	-
PubMed	18449914	The significance of ANXA7 expression and its correlation with poor cellular differentiation and enhanced metastatic potential of gastric cancer. BACKGROUND: Annexin-A7 (ANXA7) exhibits biological and	1.53 KB	2015-11-24	7	3	-
PubMed	24469904	Exploring the Wnt pathway-associated LncRNAs and genes involved in pancreatic carcinogenesis driven by Tp53 mutation. PURPOSE: Study the contribution of long non-coding RNAs (lncRNAs) to progression o	1.46 KB	2016-01-16	11	17	-
PubMed	16513216	Selective decrease of SN1(SNAT3) mRNA expression in human and rat glioma cells adapted to grow in acidic medium. The system N glutamine (Gln) transporter SN1(SNAT3) is overexpressed in human malignant	1.92 KB	2015-11-19	7	3	-
PubMed	24454829	Altered dynamics in the circadian oscillation of clock genes in dermal fibroblasts of patients suffering from idiopathic hypersomnia. From single cell organisms to the most complex life forms, the 24-	1.98 KB	2015-11-26	10	4	-
PubMed	18669490	Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A. Lissencephalies are congenital malformations responsible for epilepsy and mental retardation in chi	2.09 KB	2015-11-24	13	4	-