Kurz T - Search Results

1

ROMK expression remains unaltered in a mouse model of familial hyperkalemic hypertension caused by the CUL3Δ403-459 mutation.

Murthy M, Kurz T, O'Shaughnessy KM. Murthy M, et al. Among authors: kurz t. Physiol Rep. 2016 Jul;4(13):e12850. doi: 10.14814/phy2.12850. Physiol Rep. 2016. PMID: 27378813 Free PMC article.

2

The CUL3-KLHL3 E3 ligase complex mutated in Gordon's hypertension syndrome interacts with and ubiquitylates WNK isoforms: disease-causing mutations in KLHL3 and WNK4 disrupt interaction.

Ohta A, Schumacher FR, Mehellou Y, Johnson C, Knebel A, Macartney TJ, Wood NT, Alessi DR, Kurz T. Ohta A, et al. Among authors: kurz t. Biochem J. 2013 Apr 1;451(1):111-22. doi: 10.1042/BJ20121903. Biochem J. 2013. PMID: 23387299 Free PMC article.

3

Structural and biochemical characterization of the KLHL3-WNK kinase interaction important in blood pressure regulation.

Schumacher FR, Sorrell FJ, Alessi DR, Bullock AN, Kurz T. Schumacher FR, et al. Among authors: kurz t. Biochem J. 2014 Jun 1;460(2):237-46. doi: 10.1042/BJ20140153. Biochem J. 2014. PMID: 24641320 Free PMC article.

4

Characterisation of the Cullin-3 mutation that causes a severe form of familial hypertension and hyperkalaemia.

Schumacher FR, Siew K, Zhang J, Johnson C, Wood N, Cleary SE, Al Maskari RS, Ferryman JT, Hardege I, Yasmin, Figg NL, Enchev R, Knebel A, O'Shaughnessy KM, Kurz T. Schumacher FR, et al. Among authors: kurz t. EMBO Mol Med. 2015 Oct;7(10):1285-306. doi: 10.15252/emmm.201505444. EMBO Mol Med. 2015. PMID: 26286618 Free PMC article.

5

WNK signalling pathways in blood pressure regulation.

Murthy M, Kurz T, O'Shaughnessy KM. Murthy M, et al. Among authors: kurz t. Cell Mol Life Sci. 2017 Apr;74(7):1261-1280. doi: 10.1007/s00018-016-2402-z. Epub 2016 Nov 4. Cell Mol Life Sci. 2017. PMID: 27815594 Free PMC article. Review.

6

Changes in the ratio of free NEDD8 to ubiquitin triggers NEDDylation by ubiquitin enzymes.

Hjerpe R, Thomas Y, Chen J, Zemla A, Curran S, Shpiro N, Dick LR, Kurz T. Hjerpe R, et al. Among authors: kurz t. Biochem J. 2012 Feb 1;441(3):927-36. doi: 10.1042/BJ20111671. Biochem J. 2012. PMID: 22004789 Free PMC article.

7

CSN- and CAND1-dependent remodelling of the budding yeast SCF complex.

Zemla A, Thomas Y, Kedziora S, Knebel A, Wood NT, Rabut G, Kurz T. Zemla A, et al. Among authors: kurz t. Nat Commun. 2013;4:1641. doi: 10.1038/ncomms2628. Nat Commun. 2013. PMID: 23535662 Free article.

8

The COP9 signalosome is vital for timely repair of DNA double-strand breaks.

Meir M, Galanty Y, Kashani L, Blank M, Khosravi R, Fernández-Ávila MJ, Cruz-García A, Star A, Shochot L, Thomas Y, Garrett LJ, Chamovitz DA, Bodine DM, Kurz T, Huertas P, Ziv Y, Shiloh Y. Meir M, et al. Among authors: kurz t. Nucleic Acids Res. 2015 May 19;43(9):4517-30. doi: 10.1093/nar/gkv270. Epub 2015 Apr 8. Nucleic Acids Res. 2015. PMID: 25855810 Free PMC article.

9

Characterization of the mammalian family of DCN-type NEDD8 E3 ligases.

Keuss MJ, Thomas Y, Mcarthur R, Wood NT, Knebel A, Kurz T. Keuss MJ, et al. Among authors: kurz t. J Cell Sci. 2016 Apr 1;129(7):1441-54. doi: 10.1242/jcs.181784. Epub 2016 Feb 18. J Cell Sci. 2016. PMID: 26906416 Free PMC article.

10

UBQLN2 Mediates Autophagy-Independent Protein Aggregate Clearance by the Proteasome.

Hjerpe R, Bett JS, Keuss MJ, Solovyova A, McWilliams TG, Johnson C, Sahu I, Varghese J, Wood N, Wightman M, Osborne G, Bates GP, Glickman MH, Trost M, Knebel A, Marchesi F, Kurz T. Hjerpe R, et al. Among authors: kurz t. Cell. 2016 Aug 11;166(4):935-949. doi: 10.1016/j.cell.2016.07.001. Epub 2016 Jul 28. Cell. 2016. PMID: 27477512 Free PMC article.

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