Olsson K - Search Results

1

Real-time t(11;14) and t(14;18) PCR assays provide sensitive and quantitative assessments of minimal residual disease (MRD).

Olsson K, Gerard CJ, Zehnder J, Jones C, Ramanathan R, Reading C, Hanania EG. Olsson K, et al. Leukemia. 1999 Nov;13(11):1833-42. doi: 10.1038/sj.leu.2401575. Leukemia. 1999. PMID: 10557059

2

Improved quantitation of minimal residual disease in multiple myeloma using real-time polymerase chain reaction and plasmid-DNA complementarity determining region III standards.

Gerard CJ, Olsson K, Ramanathan R, Reading C, Hanania EG. Gerard CJ, et al. Among authors: olsson k. Cancer Res. 1998 Sep 1;58(17):3957-64. Cancer Res. 1998. PMID: 9731509

3

Addition of the human interferon beta scaffold attachment region to retroviral vector backbones increases the level of in vivo transgene expression among progeny of engrafted human hematopoietic stem cells.

Murray L, Travis M, Luens-Abitorabi K, Olsson K, Plavec I, Forestell S, Hanania EG, Hill B. Murray L, et al. Among authors: olsson k. Hum Gene Ther. 2000 Sep 20;11(14):2039-50. doi: 10.1089/10430340050143453. Hum Gene Ther. 2000. PMID: 11020802

4

Efficient oncoretroviral transduction of extended long-term culture-initiating cells and NOD/SCID repopulating cells: enhanced reconstitution with gene-marked cells through an ex vivo expansion approach.

Björgvinsdóttir H, Bryder D, Sitnicka E, Ramsfjell V, De Jong I, Olsson K, Rusterholz C, Karlsson S, Jacobsen SE. Björgvinsdóttir H, et al. Among authors: olsson k. Hum Gene Ther. 2002 Jun 10;13(9):1061-73. doi: 10.1089/104303402753812467. Hum Gene Ther. 2002. PMID: 12067439

5

Overexpression of gibbon ape leukemia virus (GALV) receptor (GLVR1) on human CD34(+) cells increases gene transfer mediated by GALV pseudotyped vectors.

Relander T, Brun AC, Olsson K, Pedersen L, Richter J. Relander T, et al. Among authors: olsson k. Mol Ther. 2002 Sep;6(3):400-6. doi: 10.1006/mthe.2002.0678. Mol Ther. 2002. PMID: 12231177 Free article.

6

Gene transfer to repopulating human CD34+ cells using amphotropic-, GALV-, or RD114-pseudotyped HIV-1-based vectors from stable producer cells.

Relander T, Johansson M, Olsson K, Ikeda Y, Takeuchi Y, Collins M, Richter J. Relander T, et al. Among authors: olsson k. Mol Ther. 2005 Mar;11(3):452-9. doi: 10.1016/j.ymthe.2004.10.014. Mol Ther. 2005. PMID: 15727942 Free article.

7

Lentiviral-mediated gene transfer into haematopoietic stem cells.

Woods NB, Mikkola H, Nilsson E, Olsson K, Trono D, Karlsson S. Woods NB, et al. Among authors: olsson k. J Intern Med. 2001 Apr;249(4):339-43. doi: 10.1046/j.1365-2796.2001.00806.x. J Intern Med. 2001. PMID: 11298854 Free article.

8

Lentiviral gene transfer into primary and secondary NOD/SCID repopulating cells.

Woods NB, Fahlman C, Mikkola H, Hamaguchi I, Olsson K, Zufferey R, Jacobsen SE, Trono D, Karlsson S. Woods NB, et al. Among authors: olsson k. Blood. 2000 Dec 1;96(12):3725-33. Blood. 2000. PMID: 11090053 Free article.

9

Lentiviral vector transduction of NOD/SCID repopulating cells results in multiple vector integrations per transduced cell: risk of insertional mutagenesis.

Woods NB, Muessig A, Schmidt M, Flygare J, Olsson K, Salmon P, Trono D, von Kalle C, Karlsson S. Woods NB, et al. Among authors: olsson k. Blood. 2003 Feb 15;101(4):1284-9. doi: 10.1182/blood-2002-07-2238. Epub 2002 Oct 17. Blood. 2003. PMID: 12393514 Free article.

10

Lentiviral gene therapy using cellular promoters cures type 1 Gaucher disease in mice.

Dahl M, Doyle A, Olsson K, Månsson JE, Marques ARA, Mirzaian M, Aerts JM, Ehinger M, Rothe M, Modlich U, Schambach A, Karlsson S. Dahl M, et al. Among authors: olsson k. Mol Ther. 2015 May;23(5):835-844. doi: 10.1038/mt.2015.16. Epub 2015 Feb 6. Mol Ther. 2015. PMID: 25655314 Free PMC article.

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