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DNAJC11  -  DnaJ (Hsp40) homolog, subfamily C, member 11

Homo sapiens

Synonyms: DnaJ homolog subfamily C member 11, FLJ10737
 
 
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Disease relevance of DNAJC11

 

High impact information on DNAJC11

 

Biological context of DNAJC11

  • The present study surveys CAMTA1 and FLJ10737 for genetic alterations by fluorescence-based single strand conformation polymorphism (SSCP) using a panel of DNAs from 88 neuroblastomas, their matching blood samples and 97 unaffected individuals [1].
 

Other interactions of DNAJC11

References

  1. Allelic variants of CAMTA1 and FLJ10737 within a commonly deleted region at 1p36 in neuroblastoma. Henrich, K.O., Claas, A., Praml, C., Benner, A., Mollenhauer, J., Poustka, A., Schwab, M., Westermann, F. Eur. J. Cancer (2007) [Pubmed]
  2. Reduced expression of CAMTA1 correlates with adverse outcome in neuroblastoma patients. Henrich, K.O., Fischer, M., Mertens, D., Benner, A., Wiedemeyer, R., Brors, B., Oberthuer, A., Berthold, F., Wei, J.S., Khan, J., Schwab, M., Westermann, F. Clin. Cancer Res. (2006) [Pubmed]
  3. Identification and characterization of FLJ10737 and CAMTA1 genes on the commonly deleted region of neuroblastoma at human chromosome 1p36.31-p36.23. Katoh, M., Katoh, M. Int. J. Oncol. (2003) [Pubmed]
 
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