Büssow H - Search Results

1

Oligodendrocyte-specific ceramide galactosyltransferase (CGT) expression phenotypically rescues CGT-deficient mice and demonstrates that CGT activity does not limit brain galactosylceramide level.

Zöller I, Büssow H, Gieselmann V, Eckhardt M. Zöller I, et al. Among authors: bussow h. Glia. 2005 Nov 15;52(3):190-8. doi: 10.1002/glia.20230. Glia. 2005. PMID: 15968630

2

Reversal of non-hydroxy:alpha-hydroxy galactosylceramide ratio and unstable myelin in transgenic mice overexpressing UDP-galactose:ceramide galactosyltransferase.

Fewou SN, Büssow H, Schaeren-Wiemers N, Vanier MT, Macklin WB, Gieselmann V, Eckhardt M. Fewou SN, et al. Among authors: bussow h. J Neurochem. 2005 Jul;94(2):469-81. doi: 10.1111/j.1471-4159.2005.03221.x. J Neurochem. 2005. PMID: 15998297 Free article.

3

Absence of 2-hydroxylated sphingolipids is compatible with normal neural development but causes late-onset axon and myelin sheath degeneration.

Zöller I, Meixner M, Hartmann D, Büssow H, Meyer R, Gieselmann V, Eckhardt M. Zöller I, et al. Among authors: bussow h. J Neurosci. 2008 Sep 24;28(39):9741-54. doi: 10.1523/JNEUROSCI.0458-08.2008. J Neurosci. 2008. PMID: 18815260 Free PMC article.

4

A spontaneously immortalized Schwann cell line to study the molecular aspects of metachromatic leukodystrophy.

Saravanan K, Büssow H, Weiler N, Gieselmann V, Franken S. Saravanan K, et al. Among authors: bussow h. J Neurosci Methods. 2007 Apr 15;161(2):223-33. doi: 10.1016/j.jneumeth.2006.11.009. Epub 2007 Jan 3. J Neurosci Methods. 2007. PMID: 17204333

5

Down-regulation of polysialic acid is required for efficient myelin formation.

Fewou SN, Ramakrishnan H, Büssow H, Gieselmann V, Eckhardt M. Fewou SN, et al. Among authors: bussow h. J Biol Chem. 2007 Jun 1;282(22):16700-11. doi: 10.1074/jbc.M610797200. Epub 2007 Apr 9. J Biol Chem. 2007. PMID: 17420257 Free article.

6

Exocytosis of storage material in a lysosomal disorder.

Klein D, Büssow H, Fewou SN, Gieselmann V. Klein D, et al. Among authors: bussow h. Biochem Biophys Res Commun. 2005 Feb 18;327(3):663-7. doi: 10.1016/j.bbrc.2004.12.054. Biochem Biophys Res Commun. 2005. PMID: 15649398

7

Missense mutations as a cause of metachromatic leukodystrophy. Degradation of arylsulfatase A in the endoplasmic reticulum.

Poeppel P, Habetha M, Marcão A, Büssow H, Berna L, Gieselmann V. Poeppel P, et al. Among authors: bussow h. FEBS J. 2005 Mar;272(5):1179-88. doi: 10.1111/j.1742-4658.2005.04553.x. FEBS J. 2005. PMID: 15720392 Free article.

8

Expression pattern and functional characterization of connexin29 in transgenic mice.

Eiberger J, Kibschull M, Strenzke N, Schober A, Büssow H, Wessig C, Djahed S, Reucher H, Koch DA, Lautermann J, Moser T, Winterhager E, Willecke K. Eiberger J, et al. Among authors: bussow h. Glia. 2006 Apr 15;53(6):601-11. doi: 10.1002/glia.20315. Glia. 2006. PMID: 16435366

9

Oligodendrocytes expressing exclusively the DM20 isoform of the proteolipid protein gene: myelination and development.

Spörkel O, Uschkureit T, Büssow H, Stoffel W. Spörkel O, et al. Among authors: bussow h. Glia. 2002 Jan;37(1):19-30. doi: 10.1002/glia.10014. Glia. 2002. PMID: 11746780

10

Rumpshaker-like proteolipid protein (PLP) ratio in a mouse model with unperturbed structural and functional integrity of the myelin sheath and axons in the central nervous system.

Uschkureit T, Spörkel O, Büssow H, Stoffel W. Uschkureit T, et al. Among authors: bussow h. Glia. 2001 Jul;35(1):63-71. doi: 10.1002/glia.1071. Glia. 2001. PMID: 11424193

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