(A, B) OncoPrint of FERMT2 co-occurring alterations in CRC cohort. The different types of genetic alterations are highlighted in different colors. (C) Correlations between FERMT2 with SYNE1, FAT4 or MUC16 at mRNA expression levels in patients with CRC. (TIF)</p
More than 1,000 mutations have been identified in the cystic fibrosis (CF) transmembrane regulator (...
<p>Associations between SEPT9 methylation rate and KRAS mutation load in tissue and plasma samples a...
MECP2 mutations are responsible for two different phenotypes in females, classical Rett syndrome and...
Frequency of co-occurring genomic alterations associated with FERMT2 in patients with CRC.</p
<p>(A) Expression of signature genes in three CRC subtypes compared to expression in normal samples....
<p>Scatter plots of gene expression (y-axis) correlating to copy number (x-axis) with differential e...
<p><i>HR</i> hazard ratio, <i>CI</i> confidence interval, <i>P</i> values in bold were statistically...
(A) The global highly correlated genes with FERMT2 identified by the Spearman test in CRC. Red and g...
<p>Among 276 CRC samples in TCGA database, we found the CRC patients with alteration in two overlap ...
<p>The relationships between germline mutation of <i>hMLH1/hMSH2</i> gene and clinicopathological fe...
<p>The relationships between somatic mutation of <i>hMLH1/hMSH2</i> gene and clinicopathological fea...
<p>The majority of genes except FUT4 were up-regulated in the CRC patients.</p>1<p>The value is the ...
More than 1,000 mutations have been identified in the cystic fibrosis (CF) transmembrane regulator (...
2013-02-19Genome-wide association studies (GWAS) have provided a powerful approach to identify CRC c...
<p>Gene breakpoint frequencies (red bars) were based on the analysis of 352 CRC samples and gene mut...
More than 1,000 mutations have been identified in the cystic fibrosis (CF) transmembrane regulator (...
<p>Associations between SEPT9 methylation rate and KRAS mutation load in tissue and plasma samples a...
MECP2 mutations are responsible for two different phenotypes in females, classical Rett syndrome and...
Frequency of co-occurring genomic alterations associated with FERMT2 in patients with CRC.</p
<p>(A) Expression of signature genes in three CRC subtypes compared to expression in normal samples....
<p>Scatter plots of gene expression (y-axis) correlating to copy number (x-axis) with differential e...
<p><i>HR</i> hazard ratio, <i>CI</i> confidence interval, <i>P</i> values in bold were statistically...
(A) The global highly correlated genes with FERMT2 identified by the Spearman test in CRC. Red and g...
<p>Among 276 CRC samples in TCGA database, we found the CRC patients with alteration in two overlap ...
<p>The relationships between germline mutation of <i>hMLH1/hMSH2</i> gene and clinicopathological fe...
<p>The relationships between somatic mutation of <i>hMLH1/hMSH2</i> gene and clinicopathological fea...
<p>The majority of genes except FUT4 were up-regulated in the CRC patients.</p>1<p>The value is the ...
More than 1,000 mutations have been identified in the cystic fibrosis (CF) transmembrane regulator (...
2013-02-19Genome-wide association studies (GWAS) have provided a powerful approach to identify CRC c...
<p>Gene breakpoint frequencies (red bars) were based on the analysis of 352 CRC samples and gene mut...
More than 1,000 mutations have been identified in the cystic fibrosis (CF) transmembrane regulator (...
<p>Associations between SEPT9 methylation rate and KRAS mutation load in tissue and plasma samples a...
MECP2 mutations are responsible for two different phenotypes in females, classical Rett syndrome and...