Hossle JP - Search Results

1

Correction of respiratory burst activity in X-linked chronic granulomatous cells to therapeutically relevant levels after gene transfer into bone marrow CD34+ cells.

Becker S, Wasser S, Hauses M, Hossle JP, Ott MG, Dinauer MC, Ganser A, Hoelzer D, Seger R, Grez M. Becker S, et al. Among authors: hossle jp. Hum Gene Ther. 1998 Jul 20;9(11):1561-70. doi: 10.1089/hum.1998.9.11-1561. Hum Gene Ther. 1998. PMID: 9694155

2

Mobilization and transduction of CD34(+) peripheral blood stem cells in patients with X-linked chronic granulomatous disease.

Ott MG, Merget-Millitzer H, Ottmann OG, Martin H, Brüggenolte N, Bialek H, Seger R, Hossle JP, Hoelzer D, Grez M. Ott MG, et al. Among authors: hossle jp. J Hematother Stem Cell Res. 2002 Aug;11(4):683-94. doi: 10.1089/15258160260194839. J Hematother Stem Cell Res. 2002. PMID: 12201957

3

Long-term high-level reconstitution of NADPH oxidase activity in murine X-linked chronic granulomatous disease using a bicistronic vector expressing gp91phox and a Delta LNGFR cell surface marker.

Sadat MA, Pech N, Saulnier S, Leroy BA, Hossle JP, Grez M, Dinauer MC. Sadat MA, et al. Among authors: hossle jp. Hum Gene Ther. 2003 May 1;14(7):651-66. doi: 10.1089/104303403321618164. Hum Gene Ther. 2003. PMID: 12804147

4

Adenovirus-mediated gene transfer into monocyte-derived macrophages of patients with X-linked chronic granulomatous disease: ex vivo correction of deficient respiratory burst.

Schneider SD, Rusconi S, Seger RA, Hossle JP. Schneider SD, et al. Among authors: hossle jp. Gene Ther. 1997 Jun;4(6):524-32. doi: 10.1038/sj.gt.3300432. Gene Ther. 1997. PMID: 9231068

5

Gene therapy of chronic granulomatous disease.

Grez M, Becker S, Saulnier S, Knöss H, Ott MG, Maurer A, Dinauer MC, Hoelzer D, Seger R, Hossle JP. Grez M, et al. Among authors: hossle jp. Bone Marrow Transplant. 2000 May;25 Suppl 2:S99-104. doi: 10.1038/sj.bmt.1702365. Bone Marrow Transplant. 2000. PMID: 10933200

6

Lentivirus-mediated gene transfer of gp91phox corrects chronic granulomatous disease (CGD) phenotype in human X-CGD cells.

Saulnier SO, Steinhoff D, Dinauer MC, Zufferey R, Trono D, Seger RA, Hossle JP. Saulnier SO, et al. Among authors: hossle jp. J Gene Med. 2000 Sep-Oct;2(5):317-25. doi: 10.1002/1521-2254(200009/10)2:5<317::AID-JGM127>3.0.CO;2-P. J Gene Med. 2000. PMID: 11045425

7

Identification of allele-specific p22-phox mutations in a compound heterozygous patient with chronic granulomatous disease by mismatch PCR and restriction enzyme analysis.

Hossle JP, de Boer M, Seger RA, Roos D. Hossle JP, et al. Hum Genet. 1994 Apr;93(4):437-42. doi: 10.1007/BF00201671. Hum Genet. 1994. PMID: 8168815

8

Characterization of 17 new cases of X-linked chronic granulomatous disease with seven novel mutations in the CYBB gene.

von Goessel H, Hossle JP, Seger R, Gungor T. von Goessel H, et al. Among authors: hossle jp. Exp Hematol. 2006 Apr;34(4):528-35. doi: 10.1016/j.exphem.2006.01.005. Exp Hematol. 2006. PMID: 16569599 Free article.

9

Gene therapy of hematopoietic stem cells: strategies for improvement.

Hossle JP, Seger RA, Steinhoff D. Hossle JP, et al. News Physiol Sci. 2002 Jun;17:87-92. doi: 10.1152/nips.01343.2001. News Physiol Sci. 2002. PMID: 12021377 Review.

10

Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).

de Boer M, de Klein A, Hossle JP, Seger R, Corbeel L, Weening RS, Roos D. de Boer M, et al. Among authors: hossle jp. Am J Hum Genet. 1992 Nov;51(5):1127-35. Am J Hum Genet. 1992. PMID: 1415254 Free PMC article.

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