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Items: 1 to 20 of 38

1.

Duration of antigen expression in vivo following DNA immunization modifies the magnitude, contraction, and secondary responses of CD8+ T lymphocytes.

Hovav AH, Panas MW, Rahman S, Sircar P, Gillard G, Cayabyab MJ, Letvin NL.

J Immunol. 2007 Nov 15;179(10):6725-33.

2.

The impact of a boosting immunogen on the differentiation of secondary memory CD8+ T cells.

Hovav AH, Panas MW, Osuna CE, Cayabyab MJ, Autissier P, Letvin NL.

J Virol. 2007 Dec;81(23):12793-802. Epub 2007 Sep 19.

3.

Complete correction of murine Artemis immunodeficiency by lentiviral vector-mediated gene transfer.

Mostoslavsky G, Fabian AJ, Rooney S, Alt FW, Mulligan RC.

Proc Natl Acad Sci U S A. 2006 Oct 31;103(44):16406-11. Epub 2006 Oct 24.

4.

Gene therapy: therapeutic gene causing lymphoma.

Woods NB, Bottero V, Schmidt M, von Kalle C, Verma IM.

Nature. 2006 Apr 27;440(7088):1123.

PMID:
16641981
5.

Endothelial protein C receptor (CD201) explicitly identifies hematopoietic stem cells in murine bone marrow.

Balazs AB, Fabian AJ, Esmon CT, Mulligan RC.

Blood. 2006 Mar 15;107(6):2317-21. Epub 2005 Nov 22.

6.

Failure of bone marrow to reconstitute lung epithelium.

Kotton DN, Fabian AJ, Mulligan RC.

Am J Respir Cell Mol Biol. 2005 Oct;33(4):328-34. Epub 2005 Jun 16.

7.
8.

A novel stem-cell population in adult liver with potent hematopoietic-reconstitution activity.

Kotton DN, Fabian AJ, Mulligan RC.

Blood. 2005 Sep 1;106(5):1574-80. Epub 2005 May 3.

9.

Serine protease inhibitors serpina1 and serpina3 are down-regulated in bone marrow during hematopoietic progenitor mobilization.

Winkler IG, Hendy J, Coughlin P, Horvath A, Lévesque JP.

J Exp Med. 2005 Apr 4;201(7):1077-88. Epub 2005 Mar 28.

10.

Coordinate dual-gene transgenesis by lentiviral vectors carrying synthetic bidirectional promoters.

Amendola M, Venneri MA, Biffi A, Vigna E, Naldini L.

Nat Biotechnol. 2005 Jan;23(1):108-16. Epub 2004 Dec 26.

PMID:
15619618
11.

Gene therapy for human alpha1-antitrypsin deficiency in an animal model using SV40-derived vectors.

Duan YY, Wu J, Zhu JL, Liu SL, Ozaki I, Strayer DS, Zern MA.

Gastroenterology. 2004 Oct;127(4):1222-32. Erratum in: Gastroenterology. 2005 Mar;128(3):808.

PMID:
15480999
12.

Translational physiology: origin and phenotype of lung side population cells.

Summer R, Kotton DN, Sun X, Fitzsimmons K, Fine A.

Am J Physiol Lung Cell Mol Physiol. 2004 Sep;287(3):L477-83. Epub 2004 Mar 26.

13.

Gene therapy progress and prospects: alpha-1 antitrypsin.

Stecenko AA, Brigham KL.

Gene Ther. 2003 Jan;10(2):95-9. Review.

PMID:
12571637
15.

Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy.

Hacein-Bey-Abina S, Le Deist F, Carlier F, Bouneaud C, Hue C, De Villartay JP, Thrasher AJ, Wulffraat N, Sorensen R, Dupuis-Girod S, Fischer A, Davies EG, Kuis W, Leiva L, Cavazzana-Calvo M.

N Engl J Med. 2002 Apr 18;346(16):1185-93.

16.
17.

Costimulation blockade, busulfan, and bone marrow promote titratable macrochimerism, induce transplantation tolerance, and correct genetic hemoglobinopathies with minimal myelosuppression.

Adams AB, Durham MM, Kean L, Shirasugi N, Ha J, Williams MA, Rees PA, Cheung MC, Mittelstaedt S, Bingaman AW, Archer DR, Pearson TC, Waller EK, Larsen CP.

J Immunol. 2001 Jul 15;167(2):1103-11.

18.

Sustained secretion of human alpha-1-antitrypsin from murine muscle transduced with adeno-associated virus vectors.

Song S, Morgan M, Ellis T, Poirier A, Chesnut K, Wang J, Brantly M, Muzyczka N, Byrne BJ, Atkinson M, Flotte TR.

Proc Natl Acad Sci U S A. 1998 Nov 24;95(24):14384-8.

19.

Transfer of the human Alpha1-antitrypsin gene into pulmonary macrophages in vivo.

Ferkol T, Mularo F, Hilliard J, Lodish S, Perales JC, Ziady A, Konstan M.

Am J Respir Cell Mol Biol. 1998 May;18(5):591-601.

PMID:
9569229
20.

Comparison of picornaviral IRES-driven internal initiation of translation in cultured cells of different origins.

Borman AM, Le Mercier P, Girard M, Kean KM.

Nucleic Acids Res. 1997 Mar 1;25(5):925-32.

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