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

[Application of Next Generation Sequencing for AML/MDS Diagnosis and Treatment].

Zhongguo shi yan xue ye xue za zhi - 1 Dec 2017

Cheng Huan-Chen, Liu Sheng-Wei, Liu Yu, Zhao Xue-Fei, Li Wei, Qiu Lin, Ma Jun

Abstract excerpt

OBJECTIVE: To detect the mutations of AML/MDS- related genes by using next generation sequencing (NGS), to analyze the mutation levels of each genes in the AML/MDS and the sensitivity of NGS, and to evaluate the feasibility of gene mutations for monitoring the MRD and predicating the progression of diseases. METHODS: The specimens were collected from primary AML (68 cases) and MDS (57 cases) patients from August...

Read the complete abstract on PubMed

Topics

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

Share to SRSF2 gene
Share to Genes, Neoplasm
Share to High-Throughput Nucleotide Sequencing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukemia, Myeloid, Acute

Share to Mutation

Share to Myelodysplastic Syndromes

Share to Neoplasms, Second Primary

Share to Prognosis

Source

Identifiers

PMID: 29262888
DOI: 10.7534/j.issn.1009-2137.2017.06.009

Genes

FLT3
KIT
TET2
SRSF2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Application of Next Generation Sequencing for AML/MDS Diagnosis and Treatment].PMID 29262888Read ↗

[Using next generation sequencing technology to analyze gene mutations in patients with acute myeloid leukemia and the impact on prognosis].Semantic proximity Read ↗

[Comparision of Mutational Spectrum between Elderly and Young Adults with Acute Myeloid Leukemia Based on Next Generation Sequencing].Semantic proximity Read ↗

Next generation sequencing reveals the mutation landscape of Chinese MDS patients and the association between mutations and AML transformations.Semantic proximity Read ↗

[Mutational Spectrum and Prognosis Analysis of AML Patients Based on High-Throughput Sequencing].Semantic proximity Read ↗

Gene mutation analysis using next-generation sequencing and its clinical significance in patients with myeloid neoplasm: A multi-center study from China.Semantic proximity Read ↗

Gene mutational analysis by NGS and its clinical significance in patients with myelodysplastic syndrome and acute myeloid leukemiaSemantic proximity Read ↗

Gene mutation patterns of Chinese acute myeloid leukemia patients by targeted next-generation sequencing and bioinformatic analysis.Semantic proximity Read ↗

Genomic Mutation Profiles of Patients with Acute Myeloid Leukemia in Korea: a Single-Center Experience.Semantic proximity Read ↗

Acute Myeloid Leukemia and Next-Generation Sequencing Panels for Diagnosis: A Comprehensive Review.Semantic proximity Read ↗

Analysis of gene mutation characteristics and its correlation with prognosis in patients with myelodysplastic syndromes.Semantic proximity Read ↗

Difference in gene mutation profile in patients with refractory/relapsed versus newly diagnosed acute myeloid leukemia based on targeted next-generation sequencing.Semantic proximity Read ↗

[Analysis of Genomic Landscape in Patients with Acute Myeloid Leukemia].Semantic proximity Read ↗

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