Cargando…

Whole-Exome Sequencing on Circulating Tumor Cells Explores Platinum-Drug Resistance Mutations in Advanced Non-small Cell Lung Cancer

Circulating tumor cells (CTCs) have important applications in clinical practice on early tumor diagnosis, prognostic prediction, and treatment evaluation. Platinum-based chemotherapy is a fundamental treatment for non-small cell lung cancer (NSCLC) patients who are not suitable for targeted drug the...

Descripción completa

Detalles Bibliográficos
Autores principales:	Chang, Yuanyuan, Wang, Yin, Li, Boyi, Lu, Xingzhong, Wang, Ruiru, Li, Hui, Yan, Bo, Gu, Aiqin, Wang, Weimin, Huang, Aimi, Wu, Shuangxiu, Li, Rong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8488217/ https://www.ncbi.nlm.nih.gov/pubmed/34616428 http://dx.doi.org/10.3389/fgene.2021.722078

Ejemplares similares

Whole Exome Sequencing Identifies Genes Associated With Non-Obstructive Azoospermia
por: Zhang, Hongguo, et al.
Publicado: (2022)

Whole Exome Sequencing Aids the Diagnosis of Fetal Skeletal Dysplasia
por: Tang, Hui, et al.
Publicado: (2021)

Prognosis and personalized medicine prediction by integrated whole exome and transcriptome sequencing of hepatocellular carcinoma
por: Li, Debao, et al.
Publicado: (2023)

Clinical Application of Whole Exome Sequencing for Monogenic Disorders in PICU of China
por: Liu, Yingchao, et al.
Publicado: (2021)

Whole exome sequencing reveals novel variants associated with diminished ovarian reserve in young women
por: Li, Na, et al.
Publicado: (2023)

SECNVs: A Simulator of Copy Number Variants and Whole-Exome Sequences From Reference Genomes
por: Xing, Yue, et al.
Publicado: (2020)

Identification of the Germline Mutation Profile in Esophageal Squamous Cell Carcinoma by Whole Exome Sequencing
por: Deng, Jiaying, et al.
Publicado: (2019)

Familial Whole Exome Sequencing Study of 30 Families With Early-Onset High Myopia
por: Yang, Entuan, et al.
Publicado: (2023)

Whole Exome Sequencing Identifies a Novel Predisposing Gene, MAPKAP1, for Familial Mixed Mood Disorder
por: Yang, Chunxia, et al.
Publicado: (2019)

Use of whole-exome sequencing to identify novel monogenic gene mutations and genotype–phenotype correlations in Chinese Han children with urolithiasis
por: Wang, Zhi, et al.
Publicado: (2023)

Whole Exome Sequencing Identified a Novel Biallelic SMARCAL1 Mutation in the Extremely Rare Disease SIOD
por: Jin, Jing, et al.
Publicado: (2019)

Genetic Diagnostic Evaluation of Trio-Based Whole Exome Sequencing Among Children With Diagnosed or Suspected Autism Spectrum Disorder
por: Du, Xiujuan, et al.
Publicado: (2018)

Protein Network Analysis of Whole Exome Sequencing of Severe Preeclampsia
por: Schuster, Jessica, et al.
Publicado: (2022)

Multilayer-omics analysis of renal cell carcinoma, including the whole exome, methylome and transcriptome
por: Arai, Eri, et al.
Publicado: (2014)

Whole Exome Sequencing Identifies a Novel Pathogenic RET Variant in Hirschsprung Disease
por: Wu, Wei, et al.
Publicado: (2019)

Whole-Exome Sequencing Identifies Somatic Mutations Associated With Mortality in Metastatic Clear Cell Kidney Carcinoma
por: Mendoza-Alvarez, Alejandro, et al.
Publicado: (2019)

Whole-Genome/Exome Sequencing Uncovers Mutations and Copy Number Variations in Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System
por: Zhu, Qiong, et al.
Publicado: (2022)

Whole Exome Sequencing Identified Novel ARMC9 Variations in Two Cases With Joubert Syndrome
por: Wang, Hao, et al.
Publicado: (2022)

Genetic Analysis of Children With Unexplained Developmental Delay and/or Intellectual Disability by Whole-Exome Sequencing
por: Xiang, Jingjing, et al.
Publicado: (2021)

The Added Value of Whole-Exome Sequencing for Anomalous Fetuses With Detailed Prenatal Ultrasound and Postnatal Phenotype
por: He, Miao, et al.
Publicado: (2021)

Occurrence of Chordoid Glioma With Sodium Ion Metabolism Disorder 5 Years After Meningioma Surgery and Whole-Exome Sequencing: A Case Report and Literature Review
por: Zhang, Mei, et al.
Publicado: (2021)

Whole-Exome Sequencing Enables the Diagnosis of Variant-Type Xeroderma Pigmentosum
por: Fang, Xiaokai, et al.
Publicado: (2019)

De novo Mutations From Whole Exome Sequencing in Neurodevelopmental and Psychiatric Disorders: From Discovery to Application
por: Wang, Weidi, et al.
Publicado: (2019)

Whole-Exome Sequencing of Discordant Monozygotic Twin Families for Identification of Candidate Genes for Microtia-Atresia
por: Fan, Xinmiao, et al.
Publicado: (2020)

Whole Exome Sequencing Analysis in Fetal Skeletal Dysplasia Detected by Ultrasonography: An Analysis of 38 Cases
por: Peng, Ying, et al.
Publicado: (2021)

Novel Partial Exon 51 Deletion in the Duchenne Muscular Dystrophy Gene Identified via Whole Exome Sequencing and Long-Read Whole-Genome Sequencing
por: Li, Qianqian, et al.
Publicado: (2021)

A Protocol for Preconceptional Screening of Consanguineous Couples Using Whole Exome Sequencing
por: dos Santos, Carolina Maria de Araújo, et al.
Publicado: (2021)

Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation
por: Vad, Oliver Bundgaard, et al.
Publicado: (2022)

Fusion Gene Detection Using Whole-Exome Sequencing Data in Cancer Patients
por: Deng, Wenjiang, et al.
Publicado: (2022)

Whole-Exome Sequencing Analysis of Human Semen Quality in Russian Multiethnic Population
por: Kolmykov, Semyon, et al.
Publicado: (2021)

Whole-Exome Sequencing Identified CFTR Variants in Two Consanguineous Families in China
por: Yang, Binyi, et al.
Publicado: (2021)

Whole-Exome Sequencing Reveals Rare Germline Mutations in Patients With Hemifacial Microsomia
por: Chen, Xiaojun, et al.
Publicado: (2021)

Whole-exome identifies germline variants in families with obstructive sleep apnea syndrome
por: de Azevedo, Pedro Guimarães, et al.
Publicado: (2023)

Whole-Exome Sequencing Identified Genes Responsible for Thoracic Aortic Aneurysms and Dissections in three Chinese Families
por: Guo, Renle, et al.
Publicado: (2022)

Family-based whole-exome sequencing identifies novel loss-of-function mutations of FBN1 for Marfan syndrome
por: Pu, Zhening, et al.
Publicado: (2018)

Clinical Utility of Exome Sequencing and Reinterpreting Genetic Test Results in Children and Adults With Epilepsy
por: Jiang, Yong-li, et al.
Publicado: (2020)

Identification of a Rare Case With Nagashima-Type Palmoplantar Keratoderma and 18q Deletion Syndrome via Exome Sequencing and Low-Coverage Whole-Genome Sequencing
por: Li, Qianqian, et al.
Publicado: (2021)

Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing
por: Roberts, Lisa, et al.
Publicado: (2016)

Advancing Personalized Medicine Through the Application of Whole Exome Sequencing and Big Data Analytics
por: Suwinski, Pawel, et al.
Publicado: (2019)

Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencing
por: Varzari, Alexander, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_v0ahfhdqmjm2bt3bn27lhqdh65