Mann LW - Search Results

1

Lack of PPCA expression only partially coincides with lysosomal storage in galactosialidosis mice: indirect evidence for spatial requirement of the catalytic rather than the protective function of PPCA.

Rottier RJ, Hahn CN, Mann LW, del Pilar Martin M, Smeyne RJ, Suzuki K, d'Azzo A. Rottier RJ, et al. Among authors: mann lw. Hum Mol Genet. 1998 Oct;7(11):1787-94. doi: 10.1093/hmg/7.11.1787. Hum Mol Genet. 1998. PMID: 9736781

2

Systemic and neurologic abnormalities distinguish the lysosomal disorders sialidosis and galactosialidosis in mice.

de Geest N, Bonten E, Mann L, de Sousa-Hitzler J, Hahn C, d'Azzo A. de Geest N, et al. Hum Mol Genet. 2002 Jun 1;11(12):1455-64. doi: 10.1093/hmg/11.12.1455. Hum Mol Genet. 2002. PMID: 12023988

3

Correction of murine galactosialidosis by bone marrow-derived macrophages overexpressing human protective protein/cathepsin A under control of the colony-stimulating factor-1 receptor promoter.

Hahn CN, del Pilar Martin M, Zhou XY, Mann LW, d'Azzo A. Hahn CN, et al. Among authors: mann lw. Proc Natl Acad Sci U S A. 1998 Dec 8;95(25):14880-5. doi: 10.1073/pnas.95.25.14880. Proc Natl Acad Sci U S A. 1998. PMID: 9843984 Free PMC article.

4

Functional amelioration of murine galactosialidosis by genetically modified bone marrow hematopoietic progenitor cells.

Leimig T, Mann L, Martin Mdel P, Bonten E, Persons D, Knowles J, Allay JA, Cunningham J, Nienhuis AW, Smeyne R, d'Azzo A. Leimig T, et al. Blood. 2002 May 1;99(9):3169-78. doi: 10.1182/blood.v99.9.3169. Blood. 2002. PMID: 11964280 Free article.

5

Targeting macrophages with baculovirus-produced lysosomal enzymes: implications for enzyme replacement therapy of the glycoprotein storage disorder galactosialidosis.

Bonten EJ, Wang D, Toy JN, Mann L, Mignardot A, Yogalingam G, D'Azzo A. Bonten EJ, et al. FASEB J. 2004 Jun;18(9):971-3. doi: 10.1096/fj.03-0941fje. Epub 2004 Apr 14. FASEB J. 2004. PMID: 15084520

6

Short-term, high dose enzyme replacement therapy in sialidosis mice.

Wang D, Bonten EJ, Yogalingam G, Mann L, d'Azzo A. Wang D, et al. Mol Genet Metab. 2005 Jul;85(3):181-9. doi: 10.1016/j.ymgme.2005.03.007. Epub 2005 Apr 25. Mol Genet Metab. 2005. PMID: 15979029

7

Ozz-E3, a muscle-specific ubiquitin ligase, regulates beta-catenin degradation during myogenesis.

Nastasi T, Bongiovanni A, Campos Y, Mann L, Toy JN, Bostrom J, Rottier R, Hahn C, Conaway JW, Harris AJ, D'Azzo A. Nastasi T, et al. Dev Cell. 2004 Feb;6(2):269-82. doi: 10.1016/s1534-5807(04)00020-6. Dev Cell. 2004. PMID: 14960280 Free article.

8

Correction of Hunter syndrome in the MPSII mouse model by AAV2/8-mediated gene delivery.

Cardone M, Polito VA, Pepe S, Mann L, D'Azzo A, Auricchio A, Ballabio A, Cosma MP. Cardone M, et al. Hum Mol Genet. 2006 Apr 1;15(7):1225-36. doi: 10.1093/hmg/ddl038. Epub 2006 Feb 27. Hum Mol Genet. 2006. PMID: 16505002

9

GM1-ganglioside-mediated activation of the unfolded protein response causes neuronal death in a neurodegenerative gangliosidosis.

Tessitore A, del P Martin M, Sano R, Ma Y, Mann L, Ingrassia A, Laywell ED, Steindler DA, Hendershot LM, d'Azzo A. Tessitore A, et al. Mol Cell. 2004 Sep 10;15(5):753-66. doi: 10.1016/j.molcel.2004.08.029. Mol Cell. 2004. PMID: 15350219 Free article.

10

Muscle degeneration in neuraminidase 1-deficient mice results from infiltration of the muscle fibers by expanded connective tissue.

Zanoteli E, van de Vlekkert D, Bonten EJ, Hu H, Mann L, Gomero EM, Harris AJ, Ghersi G, d'Azzo A. Zanoteli E, et al. Biochim Biophys Acta. 2010 Jul-Aug;1802(7-8):659-72. doi: 10.1016/j.bbadis.2010.04.002. Epub 2010 Apr 11. Biochim Biophys Acta. 2010. PMID: 20388541 Free PMC article.

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