Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Identification of novel mutations in endometrial cancer patients by whole-exome sequencing.

International journal of oncology - 1 May 2017

Chang Ya-Sian, Huang Hsien-Da, Yeh Kun-Tu, Chang Jan-Gowth

Abstract excerpt

The aim of the present study was to identify genomic alterations in Taiwanese endometrial cancer patients. This information is vitally important in Taiwan, where endometrial cancer is the second most common gynecological cancer. We performed whole-exome sequencing on DNA from 14 tumor tissue samples from Taiwanese endometrial cancer patients. We used the Genome Analysis Tool kit software package for data...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Endometrial Neoplasms
Share to Exome
Share to Genome, Human

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genomics

Share to High-Throughput Nucleotide Sequencing

Share to Neoplasm Proteins

Share to Polymorphism, Single Nucleotide

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 28339086
DOI: 10.3892/ijo.2017.3919

Genes

CASP8
CIITA
CMYA5
CYFIP2
DCT
DNAH14
DST
IGSF10
IMP4
JAKMIP1
KRAS
MACF1
MAPT
MCM6
MOCOS
NOTCH2
NUDT5
PCDH17
PCDHGB4
PCMTD1
PTEN
SNX6
TLN1
TSC1
ZSCAN29

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of novel mutations in endometrial cancer patients by whole-exome sequencing.PMID 28339086Read ↗

Genetic alterations in endometrial cancer by targeted next-generation sequencing.Semantic proximity Read ↗

Whole-exome sequencing combined with functional genomics reveals novel candidate driver cancer genes in endometrial cancer.Semantic proximity Read ↗

Next-Generation Sequencing.Semantic proximity Read ↗

Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genes.Semantic proximity Read ↗

Genomic Comparison of Endometrioid Endometrial Carcinoma and Its Precancerous Lesions in Chinese Patients by High-Depth Next Generation SequencingSemantic proximity Read ↗

Clinical relevance of oncogenic driver mutations identified in endometrial carcinomaSemantic proximity Read ↗

Somatic and germline mutations in endometrial cancer.Semantic proximity Read ↗

The mutational landscape of endometrial cancer.Semantic proximity Read ↗

Whole-Exome Sequencing Reveals Clinical Potential of Circulating Tumor DNA from Peritoneal Fluid and Plasma in Endometrial CancerSemantic proximity Read ↗

Clinical Relevance of Oncogenic Driver Mutations Identified in Endometrial CarcinomaSemantic proximity Read ↗

Molecular characterization of colorectal cancer using whole‐exome sequencing in a Taiwanese populationSemantic proximity Read ↗

Met Mutation is a Potential Therapeutic Target for Advanced Endometrial Cancer Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.