(Q85107061)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20878554%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

title

Investigation of copy-number variations of C8orf4 in hematological malignancies (English)

1 reference

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14 February 2020

6

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14 February 2020

author name string

Jiahao Zhang

1

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14 February 2020

Yan Gao

2

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14 February 2020

Xiaosu Zhao

3

1 reference

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14 February 2020

Ming Guan

4

1 reference

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14 February 2020

Wei Zhang

5

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14 February 2020

Bo Yu

7

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14 February 2020

publication date

29 September 2010

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14 February 2020

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14 February 2020

volume

28 Suppl 1

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14 February 2020

page(s)

S647-52

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Segmental copy number variation shapes tissue transcriptomes

14 February 2020

cites work

1 reference

12 December 2020

TC1(C8orf4) is a novel endothelial inflammatory regulator enhancing NF-kappaB activity

1 reference

12 December 2020

Genetic variation in human gene expression

1 reference

12 December 2020

Transforming properties of TC-1 in human breast cancer: interaction with FGFR2 and beta-catenin signaling pathways

1 reference

12 December 2020

The intrinsically disordered TC-1 interacts with Chibby via regions with high helical propensity

1 reference

12 December 2020

Side effects of genome structural changes

1 reference

12 December 2020

Copy-number variation: the end of the human genome?

1 reference

12 December 2020

The role of transcription factories in large-scale structure and dynamics of interphase chromatin.

1 reference

12 December 2020

Integrated analysis of copy number alterations and gene expression: a bivariate assessment of equally directed abnormalities

1 reference

12 December 2020

A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups.

1 reference

12 December 2020

Cloning of TC-1 (C8orf4), a novel gene found to be overexpressed in thyroid cancer

1 reference

12 December 2020

TC1(C8orf4) is upregulated by IL-1beta/TNF-alpha and enhances proliferation of human follicular dendritic cells

1 reference

12 December 2020

Mapping and sequencing of structural variation from eight human genomes

1 reference

12 December 2020

Acquired copy number alterations in adult acute myeloid leukemia genomes

1 reference

12 December 2020

Multi-platform whole-genome microarray analyses refine the epigenetic signature of breast cancer metastasis with gene expression and copy number

1 reference

12 December 2020

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

1 reference

12 December 2020

Fine-scale structural variation of the human genome

1 reference

12 December 2020

TC1 (C8orf4) is involved in ERK1/2 pathway-regulated G(1)- to S-phase transition

1 reference

12 December 2020

A high-resolution survey of deletion polymorphism in the human genome

1 reference

12 December 2020

Copy number variation at 1q21.1 associated with neuroblastoma

1 reference

12 December 2020

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

1 reference

12 December 2020

Large-scale copy number polymorphism in the human genome

1 reference

12 December 2020

alpha-Synuclein locus triplication causes Parkinson's disease

1 reference

12 December 2020

Distribution and functional impact of DNA copy number variation in the rat.

1 reference

12 December 2020

Global variation in copy number in the human genome

1 reference

12 December 2020

Detection of large-scale variation in the human genome

1 reference

12 December 2020

TC1(C8orf4) correlates with Wnt/beta-catenin target genes and aggressive biological behavior in gastric cancer

1 reference

12 December 2020

Paired-end mapping reveals extensive structural variation in the human genome

1 reference

12 December 2020

Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia--a comparative study of four differently designed, high resolution microarray platforms

1 reference

12 December 2020

Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome

1 reference

12 December 2020

Common deletion polymorphisms in the human genome.

1 reference

12 December 2020

Common deletions and SNPs are in linkage disequilibrium in the human genome

1 reference

12 December 2020

Novel genomic alterations and clonal evolution in chronic lymphocytic leukemia revealed by representational oligonucleotide microarray analysis (ROMA)

1 reference

12 December 2020

C8orf4 is a transforming growth factor B induced transcript downregulated in metastatic colon cancer

1 reference

12 December 2020

Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome

1 reference

12 December 2020

Evidence for an influence of chemokine ligand 3-like 1 (CCL3L1) gene copy number on susceptibility to rheumatoid arthritis

1 reference

12 December 2020

TC-1 is a novel tumorigenic and natively disordered protein associated with thyroid cancer

1 reference

12 December 2020

Association of a germ-line copy number variation at 2p24.3 and risk for aggressive prostate cancer

1 reference

12 December 2020

TC1 (C8orf4) enhances the Wnt/beta-catenin pathway by relieving antagonistic activity of Chibby

1 reference

12 December 2020

Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21.

1 reference

12 December 2020