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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Sheng Zhou

Division of Experimental Hematology

Department of Hematology

St Jude Children's Research Hospital

262 Danny Thomas Pl.

USA

[email]@stjude.org

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Division of Experimental Hematology, Department of Hematology, St Jude Children's Research Hospital, 262 Danny Thomas Pl., USA. 2002 - 2010

References

  1. A self-inactivating lentiviral vector for SCID-X1 gene therapy that does not activate LMO2 expression in human T cells. Zhou, S., Mody, D., DeRavin, S.S., Hauer, J., Lu, T., Ma, Z., Hacein-Bey Abina, S., Gray, J.T., Greene, M.R., Cavazzana-Calvo, M., Malech, H.L., Sorrentino, B.P. Blood (2010) [Pubmed]
  2. Increased expression of the Abcg2 transporter during erythroid maturation plays a role in decreasing cellular protoporphyrin IX levels. Zhou, S., Zong, Y., Ney, P.A., Nair, G., Stewart, C.F., Sorrentino, B.P. Blood (2005) [Pubmed]
  3. Hematopoietic cells from mice that are deficient in both Bcrp1/Abcg2 and Mdr1a/1b develop normally but are sensitized to mitoxantrone. Zhou, S., Zong, Y., Lu, T., Sorrentino, B.P. BioTechniques (2003) [Pubmed]
  4. Bcrp1 gene expression is required for normal numbers of side population stem cells in mice, and confers relative protection to mitoxantrone in hematopoietic cells in vivo. Zhou, S., Morris, J.J., Barnes, Y., Lan, L., Schuetz, J.D., Sorrentino, B.P. Proc. Natl. Acad. Sci. U.S.A. (2002) [Pubmed]
 
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