English
日本語
signup
login
Repository
Search
Annotators
Editors
Evaluators
NEWS
Documentation
>
top
>
projects
>
DisGeNet-2017-sample
> docs
DisGeNet-2017-sample
Documents
(986)
JSON
TSV
source DB
source ID
text
size
updated at
# proj.
# Ann.
updated_at
PubMed
16333527
Elevated Src activity promotes cellular invasion and motility in tamoxifen resistant breast cancer cells. Src kinase plays a central role in growth factor signalling, regulating a diverse array of cel
1.81 KB
2015-11-19
8
3
-
PubMed
16387423
STAT6 specific shRNA inhibits proliferation and induces apoptosis in colon cancer HT-29 cells. RNA interference (RNAi) has been employed as an effective tool for studying gene functions. Here, we have
638 Bytes
2015-11-19
8
4
-
PubMed
16402914
The TLX2 homeobox gene is a transcriptional target of PHOX2B in neural-crest-derived cells. The TLX2 (HOX11L1, Ncx, Enx) and PHOX2B genes encode transcription factors crucial in the development of neu
1.67 KB
2015-11-20
7
4
-
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
16513230
DNA hypomethylation therapy for hemoglobin disorders: molecular mechanisms and clinical applications. Reactivation of fetal hemoglobin (HbF) expression is an important therapeutic option in patients w
1.09 KB
2015-11-19
7
4
-
PubMed
16525693
Comparative study of intelligent models for the prediction of bladder cancer progression. New techniques for the prediction of tumour behaviour are needed since statistical analysis has low accuracy a
967 Bytes
2015-11-19
8
3
-
PubMed
16538531
Identification of BAF57 mutations in human breast cancer cell lines. Accumulating genetic and biochemical evidences support a role for the SWI/SNF chromatin-remodeling complex in cancer development an
1.8 KB
2015-11-19
8
4
-
PubMed
16546171
Two novel presenilin 1 gene mutations connected with frontotemporal dementia-like clinical phenotype: genetic and bioinformatic assessment. Mutations in the amyloid precursor protein (APP), presenilin
1.32 KB
2015-11-19
9
4
-
PubMed
16606914
Altered brain white matter integrity in healthy carriers of the APOE epsilon4 allele: a risk for AD? BACKGROUND: Previous research has shown that polymorphisms of apolipoprotein E (APOE) represent gen
1.45 KB
2015-11-19
8
4
-
PubMed
16637064
Inactivation of IkappaB contributes to transcriptional activation of spermidine/spermine N(1)-acetyltransferase. Spermidine/spermine N(1)-acetyltransferase (SSAT) is a key enzyme in polyamine cataboli
1.72 KB
2015-11-20
8
4
-
Page 8