Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiency

Haematopoietic stem cells in umbilical cord blood are an attractive target for gene therapy of inborn errors of metabolism. Three neonates with severe combined immunodeficiency were treated by retroviral-mediated transduction of the CD34+ cells from their umbilical cord blood with a normal human ade...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Kohn, Donald B., Weinberg, Kenneth I., Nolta, Jan A., Heiss, Linda N., Lenarsky, Carl, Crooks, Gay M., Hanley, Mary E., Annett, Geralyn, Brooks, Judith S., El-Khoureiy, Anthony, Lawrence, Kim, Wells, Susie, Moen, Robert C., Bastian, John, Williams-Herman, Debora E., Elder, Melissa, Wara, Diane, Bowen, Thomas, Hershfield, Michael S., Mullen, Craig A., Blaese, R. Michael, Parkman, Robertson
Médium: Artigo
Jazyk:Inglês
Vydáno: 1995
Témata:
Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3013367/
https://ncbi.nlm.nih.gov/pubmed/7489356
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky