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Displaying 14 of 14 results for "ZNF382"
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  1. Mycoplasma putrefaciens KS1 : Mycoplasma putrefaciens KS1 Genome sequencing BioProject

    ID: PRJNA46453

    Keywords: Genome sequencing

    Access Type: download

  2. Paenibacillus sp. KS1 : Paenibacillus sp. KS1 Genome sequencing and assembly BioProject

    ID: PRJNA321323

    Keywords: Genome sequencing and assembly

    Access Type: download

  3. KS1-alignment Dryad

    DateIssued: 09-03-2015

    Description: Aligned sequences of KS1 gene fragment from 307 individuals of Oryza nivara and O. rufipogon and two individuals of O.barthii used as outgroup....

  4. Streptomcyes albus JA3453 oxazolomycin ketosynthase domain OzmQ KS1 PDB

    ID: PDB:4OQJ

    Description: PKS

  5. Thiocapsa sp. KS1 draft genome sequence : Genomic Characterization of a Phototrophic Nitrite Oxidizer: Insights into the Evolution of Oxygenic Ph... BioProject

    ID: PRJEB9229

    Keywords: Genome sequencing and assembly

    Access Type: download

  6. Large-scale characterization of DNA methylation changes in human gastric carcinomas with and without metastasis ArrayExpress

    ID: E-GEOD-47724

    Description: NH1, PSMD10, PTPRT, SIGIRR, SRF, TBX5, TFPI2, and ZNF382. Hypomethylation of CGIs correlated with up-regulation of GFRA1 expression in GCs, while hypermethylation of other genes inactivated their transcription. Most importantly, prevalence of GFRA1, SRF, and ZNF382 methylation alterations were inversely and coordinately associated with GC metastasis and the patients’ overall survival throughout discovery and testing cohorts in China as well as independent validation cohorts in Japan and Korea. In conclusion, methylation changes in the CGIs of 15 genes correlated strongly with GC development. GFRA1 hypomethylation and SRF and ZNF382 hypermethylation are potential synergistic biomarkers for the prediction of GC metastasis. To identify differential methylation of CGIs related to GC development and metastasis, genome-wide DNA methylation changes in 8 pairs of GC and SM samples were analysed using the MCAM assay with a 99K custom-designed Agilent oligonucleotide microarray composed of 99,027 probes targeting 6,177 unique protein-coding genes containing at least two methylation-sensitive/insensitive SmaI/ XmaI restriction sites (CCC|GGG/ C|CmCGGG) as described in Shen et al, PLoS Genet 3, 2023-2036 (2...

  7. Large-scale characterization of DNA methylation changes in human gastric carcinomas with and without metastasis OmicsDI

    ID: E-GEOD-47724

    Date Released: 06-07-2014

    Description: NH1, PSMD10, PTPRT, SIGIRR, SRF, TBX5, TFPI2, and ZNF382. Hypomethylation of CGIs correlated with up-regulation of GFRA1 expression in GCs, while hypermethylation of other genes inactivated their transcription. Most importantly, prevalence of GFRA1, SRF, and ZNF382 methylation alterations were inversely and coordinately associated with GC metastasis and the patients’ overall survival throughout discovery and testing cohorts in China as well as independent validation cohorts in Japan and Korea. In conclusion, methylation changes in the CGIs of 15 genes correlated strongly with GC development. GFRA1 hypomethylation and SRF and ZNF382 hypermethylation are potential synergistic biomarkers for the prediction of GC metastasis. To identify differential methylation of CGIs related to GC development and metastasis, genome-wide DNA methylation changes in 8 pairs of GC and SM samples were analysed using the MCAM assay with a 99K custom-designed Agilent oligonucleotide microarray composed of 99,027 probes targeting 6,177 unique protein-coding genes containing at least two methylation-sensitive/insensitive SmaI/ XmaI restriction sites (CCC|GGG/ C|CmCGGG) as described in Shen et al, PLoS Genet 3, 2023-2036 (2...

  8. Large-scale characterization of DNA methylation changes in human gastric carcinomas with and without metastasis BioProject

    ID: PRJNA209300

    Keywords: Epigenomics

    Access Type: download

    dataset.description: NH1, PSMD10, PTPRT, SIGIRR, SRF, TBX5, TFPI2, and ZNF382. Hypomethylation of CGIs correlated with up-regulation of GFRA1 expression in GCs, while hypermethylation of other genes inactivated their transcription. Most importantly, prevalence of GFRA1, SRF, and ZNF382 methylation alterations were inversely and coordinately associated with GC metastasis and the patients’ overall survival throughout discovery and testing cohorts in China as well as independent validation cohorts in Japan and Korea. In conclusion, methylation changes in the CGIs of 15 genes correlated strongly with GC development. GFRA1 hypomethylation and SRF and ZNF382 hypermethylation are potential synergistic biomarkers for the prediction of GC metastasis. Overall design: To identify differential methylation of CGIs related to GC development and metastasis, genome-wide DNA methylation changes in 8 pairs of GC and SM samples were analysed using the MCAM assay with a 99K custom-designed Agilent oligonucleotide microarray composed of 99,027 probes targeting 6,177 unique protein-coding genes containing at least two methylation-sensitive/insensitive SmaI/ XmaI restriction sites (CCC|GGG/ C|CmCGGG) as described in Shen et al, PLoS Genet...
  9. KS1_HYDVU UniProt:Swiss-Prot

    ID: P38978

    Description: KS1 protein 1 2 2 X 50 AA approximate repeats Arg/Lys-rich (basic) Asp/Glu-rich (acidic) Arg/Lys-rich (basic) As...

  10. Millennium Cohort Study: Linked Education Administrative Dataset (KS1), Scotland: Secure Access UKDA

    ID: doi:10.5255/UKDA-SN-7414-1

    Release Date: 05-01-2015

  11. Millennium Cohort Study: Linked Education Administrative Dataset (KS1), England: Secure Access UKDA

    ID: doi:10.5255/UKDA-SN-6862-3

    Release Date: 06-03-2015

  12. Millennium Cohort Study: Linked Education Administrative Dataset (KS1), Wales: Secure Access UKDA

    ID: doi:10.5255/UKDA-SN-7415-1

    Release Date: 05-01-2015

  13. Millennium Cohort Study: Linked Education Administrative Dataset (KS1), England: Secure Access UKDA

    ID: doi:10.5255/UKDA-SN-6862-2

    Release Date: 05-01-2015

  14. Crystal structure of the 3-MBT domain from human L3MBTL1 in complex with p53K382me1 PDB

    ID: PDB:3OQ5

    Description: Lethal(3)malignant brain tumor-like protein, Cellular tumor antigen p53


Displaying 14 of 14 results for "ZNF382"