Cargando…

Association between plasma somatic copy number variations and response to immunotherapy in patients with programmed death-ligand 1-negative non-small cell lung cancer

OBJECTIVE: To determine how patients with non-small cell lung cancer (NSCLC) with programmed death-ligand 1 (PD-L1)-negative and/or a low tumor mutation burden status benefit from immune checkpoint inhibitors (ICI). METHODS: We determined the plasma cell-free DNA profiles of 25 patients with PD-L1-n...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhang, Xiaochen, Wang, Yina, Xiang, Jingjing, Zhao, Pan, Xun, Yanping, Zhang, Shirong, Xu, Nong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2022
Materias:	Pre-Clinical Research Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047987/ https://www.ncbi.nlm.nih.gov/pubmed/35466753 http://dx.doi.org/10.1177/03000605221093222

Ejemplares similares

SCNVSim: somatic copy number variation and structure variation simulator
por: Qin, Maochun, et al.
Publicado: (2015)

Controlled Somatic and Germline Copy Number Variation in the Mouse Model
por: Hérault, Yann, et al.
Publicado: (2010)

Identification of somatic copy number variations in plasma cell free DNA correlating with intrinsic resistances to EGFR targeted therapy in T790M negative non-small cell lung cancer
por: Zhu, Lucheng, et al.
Publicado: (2020)

The Human Genome Puzzle – the Role of Copy Number Variation in Somatic Mosaicism
por: Mkrtchyan, Hasmik, et al.
Publicado: (2010)

Short somatic alterations at the site of copy number variation in breast cancer
por: Murakami, Fumi, et al.
Publicado: (2020)

Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome
por: Žilina, Olga, et al.
Publicado: (2015)

Comprehensive identification and characterization of somatic copy number alterations in triple-negative breast cancer
por: Li, Zaibing, et al.
Publicado: (2019)

cnvCurator: an interactive visualization and editing tool for somatic copy number variations
por: Ma, Lingnan, et al.
Publicado: (2015)

CNValidator: validating somatic copy-number inference
por: Smith, Lucian P, et al.
Publicado: (2019)

Assessment of megabase-scale somatic copy number variation using single-cell sequencing
por: Knouse, Kristin A., et al.
Publicado: (2016)

Somatic mutations and copy number variations in breast cancers with heterogeneous HER2 amplification
por: Van Bockstal, Mieke R., et al.
Publicado: (2020)

Pan-cancer patterns of somatic copy-number alteration
por: Zack, Travis I., et al.
Publicado: (2013)

In vivo optical signatures of neuronal death in a mouse model of Alzheimer's disease
por: Lin, Alexander J, et al.
Publicado: (2014)

Identification of mutated core cancer modules by integrating somatic mutation, copy number variation, and gene expression data
por: Zhang, Junhua, et al.
Publicado: (2013)

Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencing
por: Bai, Wei, et al.
Publicado: (2023)

Robustness of the Autophagy Pathway to Somatic Copy Number Losses
por: Polo, Pierfrancesco, et al.
Publicado: (2022)

Copy number variations among silkworms
por: Zhao, Qian, et al.
Publicado: (2014)

Anaconda: AN automated pipeline for somatic COpy Number variation Detection and Annotation from tumor exome sequencing data
por: Gao, Jianing, et al.
Publicado: (2017)

Copy number variations and cancer
por: Shlien, Adam, et al.
Publicado: (2009)

Copy number variations and stroke
por: Colaianni, Valeria, et al.
Publicado: (2016)

Copy Number Variations and Schizophrenia
por: Szecówka, Kamila, et al.
Publicado: (2022)

Copy Number Variation and Osteoporosis
por: Lovšin, Nika
Publicado: (2023)

Somatic copy number changes in DPYD are associated with lower risk of recurrence in triple-negative breast cancers
por: Gross, E, et al.
Publicado: (2013)

Genomic Copy Number Variation Affecting Genes Involved in the Cell Cycle Pathway: Implications for Somatic Mosaicism
por: Iourov, Ivan Y., et al.
Publicado: (2015)

Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain
por: Cai, Xuyu, et al.
Publicado: (2014)

Copy-number-variation and copy-number-alteration region detection by cumulative plots
por: Li, Wentian, et al.
Publicado: (2009)

The landscape of somatic copy-number alteration across human cancers
por: Beroukhim, Rameen, et al.
Publicado: (2010)

Copy number variations of cytochrome P450 genes in Kinh Vietnamese
por: Vu, Nhung Phuong, et al.
Publicado: (2023)

Prognostic value of integrated cytogenetic, somatic variation, and copy number variation analyses in Korean patients with newly diagnosed multiple myeloma
por: Lee, Nuri, et al.
Publicado: (2021)

Association Analysis of Somatic Copy Number Alteration Burden With Breast Cancer Survival
por: Zhang, Linfan, et al.
Publicado: (2018)

AB201. Whole-exome sequencing characterizes the landscape of somatic mutations and copy number variations in testicular germ cell tumor
por: Wu, Song, et al.
Publicado: (2015)

New Copy Number Variations in Schizophrenia
por: Magri, Chiara, et al.
Publicado: (2010)

Copy number variation in African Americans
por: McElroy, Joseph P, et al.
Publicado: (2009)

Copy number variation goes clinical
por: Le Caignec, Cédric, et al.
Publicado: (2009)

Copy number variation in Parkinson's disease
por: Toft, Mathias, et al.
Publicado: (2010)

Copy number variation in the bovine genome
por: Fadista, João, et al.
Publicado: (2010)

Copy Number Variation in Thai Population
por: Suktitipat, Bhoom, et al.
Publicado: (2014)

Copy Number Variation in the Horse Genome
por: Ghosh, Sharmila, et al.
Publicado: (2014)

Copy number variation in bipolar disorder
por: Green, E K, et al.
Publicado: (2016)

Copy number variation and neuropsychiatric illness
por: Rees, Elliott, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_e413etb14rslqtl269bsrt6hl3