D'Hooge R - Search Results

1

Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1.

Kollmann K, Damme M, Deuschl F, Kahle J, D'Hooge R, Lüllmann-Rauch R, Lübke T. Kollmann K, et al. FEBS J. 2009 Mar;276(5):1356-69. doi: 10.1111/j.1742-4658.2009.06877.x. FEBS J. 2009. PMID: 19187242 Free article.

2

Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in α-mannosidosis.

Damme M, Stroobants S, Walkley SU, Lüllmann-Rauch R, D'Hooge R, Fogh J, Saftig P, Lübke T, Blanz J. Damme M, et al. J Neuropathol Exp Neurol. 2011 Jan;70(1):83-94. doi: 10.1097/NEN.0b013e31820428fa. J Neuropathol Exp Neurol. 2011. PMID: 21157375 Free PMC article.

3

A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease.

Wolf H, Damme M, Stroobants S, D'Hooge R, Beck HC, Hermans-Borgmeyer I, Lüllmann-Rauch R, Dierks T, Lübke T. Wolf H, et al. Dis Model Mech. 2016 Sep 1;9(9):1015-28. doi: 10.1242/dmm.025122. Epub 2016 Aug 4. Dis Model Mech. 2016. PMID: 27491075 Free PMC article.

4

Arylsulfatase G inactivation causes loss of heparan sulfate 3-O-sulfatase activity and mucopolysaccharidosis in mice.

Kowalewski B, Lamanna WC, Lawrence R, Damme M, Stroobants S, Padva M, Kalus I, Frese MA, Lübke T, Lüllmann-Rauch R, D'Hooge R, Esko JD, Dierks T. Kowalewski B, et al. Proc Natl Acad Sci U S A. 2012 Jun 26;109(26):10310-5. doi: 10.1073/pnas.1202071109. Epub 2012 Jun 11. Proc Natl Acad Sci U S A. 2012. PMID: 22689975 Free PMC article.

5

Aged Tmem106b knockout mice display gait deficits in coincidence with Purkinje cell loss and only limited signs of non-motor dysfunction.

Stroobants S, D'Hooge R, Damme M. Stroobants S, et al. Brain Pathol. 2021 Mar;31(2):223-238. doi: 10.1111/bpa.12903. Epub 2020 Nov 1. Brain Pathol. 2021. PMID: 33016371 Free PMC article.

6

LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice.

Gamp AC, Tanaka Y, Lüllmann-Rauch R, Wittke D, D'Hooge R, De Deyn PP, Moser T, Maier H, Hartmann D, Reiss K, Illert AL, von Figura K, Saftig P. Gamp AC, et al. Hum Mol Genet. 2003 Mar 15;12(6):631-46. Hum Mol Genet. 2003. PMID: 12620969

7

Induction of tolerance to human arylsulfatase A in a mouse model of metachromatic leukodystrophy.

Matzner U, Matthes F, Herbst E, Lüllmann-Rauch R, Callaerts-Vegh Z, D'Hooge R, Weigelt C, Eistrup C, Fogh J, Gieselmann V. Matzner U, et al. Mol Med. 2007 Sep-Oct;13(9-10):471-9. doi: 10.2119/2007-00063.Matzner. Mol Med. 2007. PMID: 17660863 Free PMC article.

8

The FTLD Risk Factor TMEM106B Regulates the Transport of Lysosomes at the Axon Initial Segment of Motoneurons.

Lüningschrör P, Werner G, Stroobants S, Kakuta S, Dombert B, Sinske D, Wanner R, Lüllmann-Rauch R, Wefers B, Wurst W, D'Hooge R, Uchiyama Y, Sendtner M, Haass C, Saftig P, Knöll B, Capell A, Damme M. Lüningschrör P, et al. Cell Rep. 2020 Mar 10;30(10):3506-3519.e6. doi: 10.1016/j.celrep.2020.02.060. Cell Rep. 2020. PMID: 32160553 Free article.

9

Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy.

Hess B, Saftig P, Hartmann D, Coenen R, Lüllmann-Rauch R, Goebel HH, Evers M, von Figura K, D'Hooge R, Nagels G, De Deyn P, Peters C, Gieselmann V. Hess B, et al. Proc Natl Acad Sci U S A. 1996 Dec 10;93(25):14821-6. doi: 10.1073/pnas.93.25.14821. Proc Natl Acad Sci U S A. 1996. PMID: 8962139 Free PMC article.

10

Reversal of peripheral and central neural storage and ataxia after recombinant enzyme replacement therapy in alpha-mannosidosis mice.

Blanz J, Stroobants S, Lüllmann-Rauch R, Morelle W, Lüdemann M, D'Hooge R, Reuterwall H, Michalski JC, Fogh J, Andersson C, Saftig P. Blanz J, et al. Hum Mol Genet. 2008 Nov 15;17(22):3437-45. doi: 10.1093/hmg/ddn237. Epub 2008 Aug 19. Hum Mol Genet. 2008. PMID: 18713755

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