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Zinc finger protein 350
Identifiers
Symbols ZNF350; ZBRK1; ZFQR
External IDs OMIM: 605422
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 59348 n/a
Ensembl ENSG00000171032 n/a
Uniprot Q9GZX5 n/a
Refseq NM_021632 (mRNA)
NP_067645 (protein)
n/a (mRNA)
n/a (protein)
Location Chr 19: 57.16 - 57.18 Mb n/a
Pubmed search [1] n/a

Zinc finger protein 350, also known as ZNF350, is a human gene.[1]


Contents

See also

References

Further reading

  • Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery.". Genome Res. 6 (9): 791–806. PMID 8889548. 
  • Zheng L, Pan H, Li S, et al. (2000). "Sequence-specific transcriptional corepressor function for BRCA1 through a novel zinc finger protein, ZBRK1.". Mol. Cell 6 (4): 757–68. PMID 11090615. 
  • Ran Q, Wadhwa R, Bischof O, et al. (2001). "Characterization of a novel zinc finger gene with increased expression in nondividing normal human cells.". Exp. Cell Res. 263 (1): 156–62. doi:10.1006/excr.2000.5068. PMID 11161714. 
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932. 
  • Rutter JL, Smith AM, Dávila MR, et al. (2004). "Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals.". Hum. Mutat. 22 (2): 121–8. doi:10.1002/humu.10238. PMID 12872252. 
  • Yun J, Lee WH (2003). "Degradation of transcription repressor ZBRK1 through the ubiquitin-proteasome pathway relieves repression of Gadd45a upon DNA damage.". Mol. Cell. Biol. 23 (20): 7305–14. PMID 14517299. 
  • Tan W, Zheng L, Lee WH, Boyer TG (2004). "Functional dissection of transcription factor ZBRK1 reveals zinc fingers with dual roles in DNA-binding and BRCA1-dependent transcriptional repression.". J. Biol. Chem. 279 (8): 6576–87. doi:10.1074/jbc.M312270200. PMID 14660588. 
  • Surpili MJ, Delben TM, Kobarg J (2004). "Identification of proteins that interact with the central coiled-coil region of the human protein kinase NEK1.". Biochemistry 42 (51): 15369–76. doi:10.1021/bi034575v. PMID 14690447. 
  • Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039. 
  • Li H, Seth A (2004). "An RNF11: Smurf2 complex mediates ubiquitination of the AMSH protein.". Oncogene 23 (10): 1801–8. doi:10.1038/sj.onc.1207319. PMID 14755250. 
  • Tan W, Kim S, Boyer TG (2005). "Tetrameric oligomerization mediates transcriptional repression by the BRCA1-dependent Kruppel-associated box-zinc finger protein ZBRK1.". J. Biol. Chem. 279 (53): 55153–60. doi:10.1074/jbc.M410926200. PMID 15496401. 
  • Liao G, Huang J, Fixman ED, Hayward SD (2005). "The Epstein-Barr virus replication protein BBLF2/3 provides an origin-tethering function through interaction with the zinc finger DNA binding protein ZBRK1 and the KAP-1 corepressor.". J. Virol. 79 (1): 245–56. doi:10.1128/JVI.79.1.245-256.2005. PMID 15596820. 
  • Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMID 16344560. 
  • Bulliard Y, Wiznerowicz M, Barde I, Trono D (2007). "KRAB can repress lentivirus proviral transcription independently of integration site.". J. Biol. Chem. 281 (47): 35742–6. doi:10.1074/jbc.M602843200. PMID 16997916. 
  • Desjardins S, Belleau P, Labrie Y, et al. (2007). "Genetic variants and haplotype analyses of the ZBRK1/ZNF350 gene in high-risk non BRCA1/2 French Canadian breast and ovarian cancer families.". Int. J. Cancer 122 (1): 108–16. doi:10.1002/ijc.23058. PMID 17764113. 

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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