1
|
A unified nomenclature for the superfamily of TRP cation channels.
|
Mol Cell
|
2002
|
2.99
|
2
|
TRPM5 regulates glucose-stimulated insulin secretion.
|
Pflugers Arch
|
2010
|
1.74
|
3
|
Premature senescence is a primary fail-safe mechanism of ERBB2-driven tumorigenesis in breast carcinoma cells.
|
Cancer Res
|
2005
|
1.23
|
4
|
The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites.
|
Hum Mol Genet
|
2012
|
1.16
|
5
|
Beckwith-Wiedemann syndrome: multiple molecular mechanisms.
|
Expert Rev Mol Med
|
2006
|
1.16
|
6
|
ERBB2-mediated transcriptional up-regulation of the alpha5beta1 integrin fibronectin receptor promotes tumor cell survival under adverse conditions.
|
Cancer Res
|
2006
|
1.06
|
7
|
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor.
|
Nat Genet
|
2005
|
1.05
|
8
|
Linking C5 deficiency to an exonic splicing enhancer mutation.
|
J Immunol
|
2005
|
1.03
|
9
|
Allelic loss but absence of mutations in the polyspecific transporter gene BWR1A on 11p15.5 in hepatoblastoma.
|
Int J Cancer
|
2004
|
0.99
|
10
|
High calcium concentration in bones promotes bone metastasis in renal cell carcinomas expressing calcium-sensing receptor.
|
Mol Cancer
|
2014
|
0.94
|
11
|
Switching off HER-2/neu in a tetracycline-controlled mouse tumor model leads to apoptosis and tumor-size-dependent remission.
|
Cancer Res
|
2003
|
0.93
|
12
|
Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesis.
|
Cancer Res
|
2007
|
0.92
|
13
|
Transcriptional regulation of Nox4 by histone deacetylases in human endothelial cells.
|
Basic Res Cardiol
|
2012
|
0.88
|
14
|
Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene.
|
J Clin Endocrinol Metab
|
2002
|
0.85
|
15
|
Migration of renal tumor cells depends on dephosphorylation of Shc by PTEN.
|
Int J Oncol
|
2010
|
0.82
|
16
|
Frequency and characterization of DNA methylation defects in children born SGA.
|
Eur J Hum Genet
|
2012
|
0.79
|
17
|
Dephosphorylation of p-ERK1/2 in relation to tumor remission after HER-2 and Raf1 blocking therapy in a conditional mouse tumor model.
|
Mol Carcinog
|
2006
|
0.77
|
18
|
Adding efficiency: the role of the CAN ion channels TRPM4 and TRPM5 in pancreatic islets.
|
Islets
|
2010
|
0.76
|
19
|
In vitro cultured islet-derived progenitor cells of human origin express human albumin in severe combined immunodeficiency mouse liver in vivo.
|
Stem Cells
|
2004
|
0.75
|
20
|
Two novel mutations in the human thyroid peroxidase (TPO) gene: genetics and clinical findings in four children.
|
Acta Paediatr
|
2009
|
0.75
|