Vanier MT - Search Results

1

Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding alpha-N-acetylglucosaminidase.

Li HH, Yu WH, Rozengurt N, Zhao HZ, Lyons KM, Anagnostaras S, Fanselow MS, Suzuki K, Vanier MT, Neufeld EF. Li HH, et al. Among authors: vanier mt. Proc Natl Acad Sci U S A. 1999 Dec 7;96(25):14505-10. doi: 10.1073/pnas.96.25.14505. Proc Natl Acad Sci U S A. 1999. PMID: 10588735 Free PMC article.

2

Induced mouse models of abnormal sphingolipid metabolism.

Suzuki K, Vanier MT. Suzuki K, et al. Among authors: vanier mt. J Biochem. 1998 Jul;124(1):8-19. doi: 10.1093/oxfordjournals.jbchem.a022101. J Biochem. 1998. PMID: 9644238 Free article. Review.

3

Recent advances in elucidating Niemann-Pick C disease.

Vanier MT, Suzuki K. Vanier MT, et al. Brain Pathol. 1998 Jan;8(1):163-74. doi: 10.1111/j.1750-3639.1998.tb00143.x. Brain Pathol. 1998. PMID: 9458174 Free PMC article. Review.

4

Biochemical and molecular aspects of late-onset GM2-gangliosidosis: B1 variant as a prototype.

Suzuki K, Vanier MT. Suzuki K, et al. Among authors: vanier mt. Dev Neurosci. 1991;13(4-5):288-94. doi: 10.1159/000112175. Dev Neurosci. 1991. PMID: 1840099 Review.

5

Drastically abnormal gluco- and galactosylceramide composition does not affect ganglioside metabolism in the brain of mice deficient in galactosylceramide synthase.

Suzuki K, Vanier MT, Coetzee T, Popko B. Suzuki K, et al. Among authors: vanier mt. Neurochem Res. 1999 Apr;24(4):471-4. doi: 10.1023/a:1022571410445. Neurochem Res. 1999. PMID: 10227678

6

Generalized CNS disease and massive GM1-ganglioside accumulation in mice defective in lysosomal acid beta-galactosidase.

Hahn CN, del Pilar Martin M, Schröder M, Vanier MT, Hara Y, Suzuki K, Suzuki K, d'Azzo A. Hahn CN, et al. Among authors: vanier mt. Hum Mol Genet. 1997 Feb;6(2):205-11. doi: 10.1093/hmg/6.2.205. Hum Mol Genet. 1997. PMID: 9063740

7

Alleviation of neuronal ganglioside storage does not improve the clinical course of the Niemann-Pick C disease mouse.

Liu Y, Wu YP, Wada R, Neufeld EB, Mullin KA, Howard AC, Pentchev PG, Vanier MT, Suzuki K, Proia RL. Liu Y, et al. Among authors: vanier mt. Hum Mol Genet. 2000 Apr 12;9(7):1087-92. doi: 10.1093/hmg/9.7.1087. Hum Mol Genet. 2000. PMID: 10767333

8

Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipids.

Fujita N, Suzuki K, Vanier MT, Popko B, Maeda N, Klein A, Henseler M, Sandhoff K, Nakayasu H, Suzuki K. Fujita N, et al. Among authors: vanier mt. Hum Mol Genet. 1996 Jun;5(6):711-25. doi: 10.1093/hmg/5.6.711. Hum Mol Genet. 1996. PMID: 8776585

9

GD3- and O-acetylated GD3-gangliosides in the GM2 synthase-deficient mouse brain and their immunohistochemical localization.

Matsuda J, Vanier MT, Popa I, Portoukalian J, Suzuki K. Matsuda J, et al. Among authors: vanier mt. Proc Jpn Acad Ser B Phys Biol Sci. 2006 Sep;82(6):189-96. doi: 10.2183/pjab.82.189. Epub 2006 Sep 21. Proc Jpn Acad Ser B Phys Biol Sci. 2006. PMID: 25792782 Free PMC article.

10

Paradoxical influence of acid beta-galactosidase gene dosage on phenotype of the twitcher mouse (genetic galactosylceramidase deficiency).

Tohyama J, Vanier MT, Suzuki K, Ezoe T, Matsuda J, Suzuki K. Tohyama J, et al. Among authors: vanier mt. Hum Mol Genet. 2000 Jul 1;9(11):1699-707. doi: 10.1093/hmg/9.11.1699. Hum Mol Genet. 2000. PMID: 10861297

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