Kuhlbrodt K - Search Results

1

High-affinity glutamate transporters in the rat retina: a major role of the glial glutamate transporter GLAST-1 in transmitter clearance.

Rauen T, Taylor WR, Kuhlbrodt K, Wiessner M. Rauen T, et al. Among authors: kuhlbrodt k. Cell Tissue Res. 1998 Jan;291(1):19-31. doi: 10.1007/s004410050976. Cell Tissue Res. 1998. PMID: 9394040

2

Sox10, a novel transcriptional modulator in glial cells.

Kuhlbrodt K, Herbarth B, Sock E, Hermans-Borgmeyer I, Wegner M. Kuhlbrodt K, et al. J Neurosci. 1998 Jan 1;18(1):237-50. doi: 10.1523/JNEUROSCI.18-01-00237.1998. J Neurosci. 1998. PMID: 9412504 Free PMC article.

3

Expression of Krox proteins during differentiation of the O-2A progenitor cell line CG-4.

Sock E, Leger H, Kuhlbrodt K, Schreiber J, Enderich J, Richter-Landsberg C, Wegner M. Sock E, et al. Among authors: kuhlbrodt k. J Neurochem. 1997 May;68(5):1911-9. doi: 10.1046/j.1471-4159.1997.68051911.x. J Neurochem. 1997. PMID: 9109517 Free article.

4

Cooperative function of POU proteins and SOX proteins in glial cells.

Kuhlbrodt K, Herbarth B, Sock E, Enderich J, Hermans-Borgmeyer I, Wegner M. Kuhlbrodt K, et al. J Biol Chem. 1998 Jun 26;273(26):16050-7. doi: 10.1074/jbc.273.26.16050. J Biol Chem. 1998. PMID: 9632656 Free article.

5

Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients.

Kuhlbrodt K, Schmidt C, Sock E, Pingault V, Bondurand N, Goossens M, Wegner M. Kuhlbrodt K, et al. J Biol Chem. 1998 Sep 4;273(36):23033-8. doi: 10.1074/jbc.273.36.23033. J Biol Chem. 1998. PMID: 9722528 Free article.

6

Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease.

Herbarth B, Pingault V, Bondurand N, Kuhlbrodt K, Hermans-Borgmeyer I, Puliti A, Lemort N, Goossens M, Wegner M. Herbarth B, et al. Among authors: kuhlbrodt k. Proc Natl Acad Sci U S A. 1998 Apr 28;95(9):5161-5. doi: 10.1073/pnas.95.9.5161. Proc Natl Acad Sci U S A. 1998. PMID: 9560246 Free PMC article.

7

A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies.

Bondurand N, Kuhlbrodt K, Pingault V, Enderich J, Sajus M, Tommerup N, Warburg M, Hennekam RC, Read AP, Wegner M, Goossens M. Bondurand N, et al. Among authors: kuhlbrodt k. Hum Mol Genet. 1999 Sep;8(9):1785-9. doi: 10.1093/hmg/8.9.1785. Hum Mol Genet. 1999. PMID: 10441344

8

SOX10 mutations in patients with Waardenburg-Hirschsprung disease.

Pingault V, Bondurand N, Kuhlbrodt K, Goerich DE, Préhu MO, Puliti A, Herbarth B, Hermans-Borgmeyer I, Legius E, Matthijs G, Amiel J, Lyonnet S, Ceccherini I, Romeo G, Smith JC, Read AP, Wegner M, Goossens M. Pingault V, et al. Among authors: kuhlbrodt k. Nat Genet. 1998 Feb;18(2):171-3. doi: 10.1038/ng0298-171. Nat Genet. 1998. PMID: 9462749

9

Benefits of global mutant huntingtin lowering diminish over time in a Huntington's disease mouse model.

Marchionini DM, Liu JP, Ambesi-Impiombato A, Kerker K, Cirillo K, Bansal M, Mushlin R, Brunner D, Ramboz S, Kwan M, Kuhlbrodt K, Tillack K, Peters F, Rauhala L, Obenauer J, Greene JR, Hartl C, Khetarpal V, Lager B, Rosinski J, Aaronson J, Alam M, Signer E, Muñoz-Sanjuán I, Howland D, Zeitlin SO. Marchionini DM, et al. Among authors: kuhlbrodt k. JCI Insight. 2022 Oct 24;7(20):e161769. doi: 10.1172/jci.insight.161769. JCI Insight. 2022. PMID: 36278490 Free PMC article.

10

Reply to: "Comment on: Polyglutamine-Expanded Ataxin-3: A Target Engagement Marker for Spinocerebellar Ataxia Type 3 in Peripheral Blood".

Hübener-Schmid J, Kuhlbrodt K, Peladan J; European Spinocerebellar Ataxia Type 3/Machado-Joseph Disease Initiative (ESMI) Study Group; Rieß O. Hübener-Schmid J, et al. Among authors: kuhlbrodt k. Mov Disord. 2022 May;37(5):1121-1122. doi: 10.1002/mds.29003. Mov Disord. 2022. PMID: 35587632 No abstract available.

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