Cargando…

Integrated whole genome microarray analysis and immunohistochemical assay identifies COL11A1, GJB2 and CTRL as predictive biomarkers for pancreatic cancer

BACKGROUND: Pancreatic cancer is characterized by its unsatisfying early detection rate, rapid disease progression and poor prognosis. Further studies on molecular mechanism and novel predictive biomarkers for pancreatic cancer based on a large sample volume are required. METHODS: Multiple bioinform...

Descripción completa

Detalles Bibliográficos
Autores principales:	Sun, Defeng, Jin, Haoyi, Zhang, Jun, Tan, Xiaodong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2018
Materias:	Primary Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219000/ https://www.ncbi.nlm.nih.gov/pubmed/30410422 http://dx.doi.org/10.1186/s12935-018-0669-x

Ejemplares similares

Ctrl alt share
Publicado: (2015)

Differential secretome of pancreatic cancer cells in serum-containing conditioned medium reveals CCT8 as a new biomarker of pancreatic cancer invasion and metastasis
por: Liu, Peng, et al.
Publicado: (2019)

Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta
por: Maasalu, Katre, et al.
Publicado: (2015)

Loss of chymotrypsin-like protease (CTRL) alters intrapancreatic protease activation but not pancreatitis severity in mice
por: Mosztbacher, Dóra, et al.
Publicado: (2020)

Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta
por: Ho Duy, Binh, et al.
Publicado: (2016)

CTRL: Closed-Loop Transcription to an LDR via Minimaxing Rate Reduction
por: Dai, Xili, et al.
Publicado: (2022)

Mutational analysis of COL1A1 and COL1A2 genes among Estonian osteogenesis imperfecta patients
por: Zhytnik, Lidiia, et al.
Publicado: (2017)

Heterogeneous programmed death-ligand 1 expression in gastric cancer: comparison of tissue microarrays and whole sections
por: Ye, Min, et al.
Publicado: (2020)

Over-expression of CDX2 alleviates breast cancer by up-regulating microRNA let-7b and inhibiting COL11A1 expression
por: Wang, Hongbin, et al.
Publicado: (2020)

Ctrl+Alt+Delete in the name of COVID-19: When a reset leads to misrecognition()
por: Laursen, Klaus Brønd, et al.
Publicado: (2023)

Regulatory effects of COL1A1 on apoptosis induced by radiation in cervical cancer cells
por: Liu, Shurong, et al.
Publicado: (2017)

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy
por: Zhang, Linlin, et al.
Publicado: (2020)

Associations of high-altitude polycythemia with polymorphisms in PIK3CD and COL4A3 in Tibetan populations
por: Fan, Xiaowei, et al.
Publicado: (2018)

Clinical value and potential mechanisms of COL8A1 upregulation in breast cancer: a comprehensive analysis
por: Peng, Wei, et al.
Publicado: (2020)

Open Up – the Mission Statement of the Control of Impulsive Action (Ctrl-ImpAct) Lab on Open Science
por: Reimer, Christina B., et al.
Publicado: (2019)

Allele-Specific Impairment of GJB2 Expression by GJB6 Deletion del(GJB6-D13S1854)
por: Rodriguez-Paris, Juan, et al.
Publicado: (2011)

Whole genome DNA copy number changes identified by high density oligonucleotide arrays
por: Huang, Jing, et al.
Publicado: (2004)

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera
por: Hirvonen, Elina A. M., et al.
Publicado: (2017)

Relationship between TRAF6 and deterioration of HCC: an immunohistochemical and in vitro study
por: Li, Jian-jun, et al.
Publicado: (2016)

Cloning a Chymotrypsin-Like 1 (CTRL-1) Protease cDNA from the Jellyfish Nemopilema nomurai
por: Heo, Yunwi, et al.
Publicado: (2016)

‘CTRL’: an online, Dynamic Consent and participant engagement platform working towards solving the complexities of consent in genomic research
por: Haas, Matilda A., et al.
Publicado: (2021)

Ctrl-C: a cross-sectional study of the electronic health record usage patterns of US oncology clinicians
por: Sinha, Sumi, et al.
Publicado: (2023)

Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility
por: Bruse, Shannon, et al.
Publicado: (2016)

Genome-scale analysis identifies GJB2 and ERO1LB as prognosis markers in patients with pancreatic cancer
por: Zhu, Tao, et al.
Publicado: (2017)

Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation
por: Parzefall, Thomas, et al.
Publicado: (2017)

GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana
por: Adadey, Samuel M., et al.
Publicado: (2019)

IMUP and GPRC5A: two newly identified risk score indicators in pancreatic ductal adenocarcinoma
por: Wei, Rong, et al.
Publicado: (2021)

KinSNP software for homozygosity mapping of disease genes using SNP microarrays
por: Amir, El-Ad David, et al.
Publicado: (2010)

Exosomal LINC00460/miR-503-5p/ANLN positive feedback loop aggravates pancreatic cancer progression through regulating T cell–mediated cytotoxicity and PD-1 checkpoint
por: Yao, Jun, et al.
Publicado: (2022)

Erratum: GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana
Publicado: (2019)

GJB2 and GJB6 Mutations in Hereditary Recessive Non-Syndromic Hearing Impairment in Cameroon
por: Tingang Wonkam, Edmond, et al.
Publicado: (2019)

LncRNA LIFR-AS1 promotes proliferation and invasion of gastric cancer cell via miR-29a-3p/COL1A2 axis
por: Pan, Haiyan, et al.
Publicado: (2021)

Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patients
por: Fichna, Jakub Piotr, et al.
Publicado: (2018)

Deletion of the CTRL2 Insulator in HSV-1 Results in the Decreased Expression of Genes Involved in Axonal Transport and Attenuates Reactivation In Vivo
por: Singh, Pankaj, et al.
Publicado: (2022)

Exon-Trapping Assay Improves Clinical Interpretation of COL11A1 and COL11A2 Intronic Variants in Stickler Syndrome Type 2 and Otospondylomegaepiphyseal Dysplasia
por: Micale, Lucia, et al.
Publicado: (2020)

Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis
por: Pang, Herbert, et al.
Publicado: (2010)

Hospital care for opioid use disorder in pregnancy: Challenges and opportunities identified from a Minnesota survey
por: Dopp, Alana, et al.
Publicado: (2020)

GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort
por: Buonfiglio, Paula, et al.
Publicado: (2020)

Evaluation of the GJB2 and GJB6 Polymorphisms with Autosomal Recessive Nonsyndromic Hearing Loss in Iranian Population
por: Ebrahimkhani, Somayeh, et al.
Publicado: (2021)

Identifying SLC27A5 as a potential prognostic marker of hepatocellular carcinoma by weighted gene co-expression network analysis and in vitro assays
por: Zhang, Fan, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_v89jji13oomvrftmmosc58o35b