Common genetic variants in NEFL influence gene expression and neuroblastoma risk. - Wikidata - wikimedia - TriplyDB

Common genetic variants in NEFL influence gene expression and neuroblastoma risk.

Common genetic variants in NEFL influence gene expression and neuroblastoma risk.

http://www.wikidata.org/entity/Q38948164

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Neuroblastoma, a Paradigm for Big Data Science in Pediatric Oncology.HSD17B12 gene rs11037575 C>T polymorphism confers neuroblastoma susceptibility in a Southern Chinese population The TP53 gene rs1042522 C>G polymorphism and neuroblastoma risk in Chinese children.An 18 gene expression-based score classifier predicts the clinical outcome in stage 4 neuroblastoma.Potentially functional polymorphisms in the LIN28B gene contribute to neuroblastoma susceptibility in Chinese children.Exome and deep sequencing of clinically aggressive neuroblastoma reveal somatic mutations that affect key pathways involved in cancer progression LMO1 gene polymorphisms contribute to decreased neuroblastoma susceptibility in a Southern Chinese population.Lack of Associations between XPC Gene Polymorphisms and Neuroblastoma Susceptibility in a Chinese Population.Common variations within HACE1 gene and neuroblastoma susceptibility in a Southern Chinese population.Advances in the translational genomics of neuroblastoma: From improving risk stratification and revealing novel biology to identifying actionable genomic alterations.The functional variant rs34330 of CDKN1B is associated with risk of neuroblastoma.Genetic susceptibility to neuroblastoma.A comprehensive characterization of rare mitochondrial DNA variants in neuroblastoma.Single nucleotide polymorphism rs11669203 in TGFBR3L is associated with the risk of neuroblastoma in a Chinese population.LMO1 polymorphisms reduce neuroblastoma risk in Chinese children: a two-center case-control study.Genetic Variations of GWAS-Identified Genes and Neuroblastoma Susceptibility: a Replication Study in Southern Chinese Children.CASC15 gene polymorphisms reduce neuroblastoma risk in Chinese children.Dualistic Role of BARD1 in Cancer.CDC20siRNA and paclitaxel co-loaded nanometric liposomes of a nipecotic acid-derived cationic amphiphile inhibit xenografted neuroblastoma.CANT1 lncRNA Triggers Efficient Therapeutic Efficacy by Correcting Aberrant lncing Cascade in Malignant Uveal Melanoma.Associations between lncRNA MEG3 polymorphisms and neuroblastoma risk in Chinese children.Functional Polymorphisms at ERCC1/XPF Genes Confer Neuroblastoma Risk in Chinese Children.Association between NEFL Gene Polymorphisms and Neuroblastoma Risk in Chinese Children: A Two-Center Case-Control Study.Serum Interleukin-6 Level and the rs1800795 Polymorphism in its Gene Associated with Neuroblastoma Risk in Chinese Children.RAN/RANBP2 polymorphisms and neuroblastoma risk in Chinese children: a three-center case-control study.Relevance of polymorphisms to neuroblastoma risk in Chinese children: a four-center case-control study

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P2860

Common genetic variants in NEFL influence gene expression and neuroblastoma risk.

http://www.wikidata.org/entity/Q38948164

description

2014 nî lūn-bûn

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

@wuu

2014年论文

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2014年论文

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name

Common genetic variants in NEFL influence gene expression and neuroblastoma risk.

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type

label

Common genetic variants in NEFL influence gene expression and neuroblastoma risk.

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prefLabel

Common genetic variants in NEFL influence gene expression and neuroblastoma risk.

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0008-5472.CAN-14-0431

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Cancer Research

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Common genetic variants in NEFL influence gene expression and neuroblastoma risk.

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Achille Iolascon

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Francesca Totaro

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Giovanni Acierno

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Giuseppe Petrosino

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Hakon Hakonarson

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John M Maris

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Lee McDaniel

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Lucia Pezone

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Maura Diamond

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Sharon Diskin

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P2860

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

Identification of ALK as a major familial neuroblastoma predisposition gene

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

PLINK: a tool set for whole-genome association and population-based linkage analyses

Distinct neuroblastoma-associated alterations of PHOX2B impair sympathetic neuronal differentiation in zebrafish models

Haploview: analysis and visualization of LD and haplotype maps

Deficiency in ubiquitin ligase TRIM2 causes accumulation of neurofilament light chain and neurodegeneration

Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma

A new multipoint method for genome-wide association studies by imputation of genotypes

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6913-6924

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scholarly article

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10.1158/0008-5472.CAN-14-0431

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23

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74

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Marcella Devoto

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2014-10-13T00:00:00Z

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25312269

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4253722

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