Kuhlbrodt K - Search Results

1

The Machado-Joseph disease deubiquitylase ATX-3 couples longevity and proteostasis.

Kuhlbrodt K, Janiesch PC, Kevei É, Segref A, Barikbin R, Hoppe T. Kuhlbrodt K, et al. Nat Cell Biol. 2011 Mar;13(3):273-81. doi: 10.1038/ncb2200. Epub 2011 Feb 13. Nat Cell Biol. 2011. PMID: 21317884

2

Orchestra for assembly and fate of polyubiquitin chains.

Kuhlbrodt K, Mouysset J, Hoppe T. Kuhlbrodt K, et al. Essays Biochem. 2005;41:1-14. doi: 10.1042/EB0410001. Essays Biochem. 2005. PMID: 16250894 Review.

3

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.

4

Polyglutamine-Expanded Ataxin-3: A Target Engagement Marker for Spinocerebellar Ataxia Type 3 in Peripheral Blood.

Hübener-Schmid J, Kuhlbrodt K, Peladan J, Faber J, Santana MM, Hengel H, Jacobi H, Reetz K, Garcia-Moreno H, Raposo M, van Gaalen J, Infante J, Steiner KM, de Vries J, Verbeek MM, Giunti P, Pereira de Almeida L, Lima M, van de Warrenburg B, Schöls L, Klockgether T, Synofzik M; 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. 2021 Nov;36(11):2675-2681. doi: 10.1002/mds.28749. Epub 2021 Aug 16. Mov Disord. 2021. PMID: 34397117

5

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.

6

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.

7

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.

8

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.

9

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

10

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

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