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Items: 11

1.

In vivo gene transfer into adult stem cells in unconditioned mice by in situ delivery of a lentiviral vector.

Worsham DN, Schuesler T, von Kalle C, Pan D.

Mol Ther. 2006 Oct;14(4):514-24. Epub 2006 Aug 7.

2.

Potential use of T cell receptor genes to modify hematopoietic stem cells for the gene therapy of cancer.

Clay TM, Custer MC, Spiess PJ, Nishimura MI.

Pathol Oncol Res. 1999;5(1):3-15. Review.

3.

Animal xenograft models for evaluation of gene transfer into human hematopoietic stem cells.

Dao MA, Tsark E, Nolta JA.

Curr Opin Mol Ther. 1999 Oct;1(5):553-7. Review.

PMID:
11249661
4.

Role of the mammalian target of rapamycin pathway in lentiviral vector transduction of hematopoietic stem cells.

Wang CX, Torbett BE.

Curr Opin Hematol. 2015 Jul;22(4):302-8. doi: 10.1097/MOH.0000000000000150. Review.

6.

Gene transfer into hematopoietic stem cells of nonhuman primates.

Van Beusechem VW, Valerio D.

Hum Gene Ther. 1996 Sep 10;7(14):1649-68. Review.

PMID:
8886837
7.

Gene therapy for adenosine deaminase deficiency.

Parkman R, Weinberg K, Crooks G, Nolta J, Kapoor N, Kohn D.

Annu Rev Med. 2000;51:33-47. Review.

PMID:
10774451
8.

Myeloprotection with drug-resistance genes.

Banerjee D, Bertino JR.

Lancet Oncol. 2002 Mar;3(3):154-8. Review.

PMID:
11902501
9.

Lentiviral hematopoietic stem cell gene therapy in inherited metabolic disorders.

Wagemaker G.

Hum Gene Ther. 2014 Oct;25(10):862-5. doi: 10.1089/hum.2014.102. Epub 2014 Sep 17. Review.

10.

Gene marking.

Brenner M.

Hum Gene Ther. 1996 Oct 20;7(16):1927-36. Review.

PMID:
8930652
11.

Hematopoietic stem cell gene therapy:assessing the relevance of preclinical models.

Larochelle A, Dunbar CE.

Semin Hematol. 2013 Apr;50(2):101-30. Review. No abstract available.

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