Similar articles for PMID: 15122254

Year	Number of Results
1990	1
1991	3
1992	1
1993	3
1994	1
1995	2
1996	3
1997	4
1998	4
1999	9
2000	8
2001	12
2002	11
2003	14
2004	15
2005	14
2006	16
2007	12
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2009	8
2010	18
2011	25
2012	17
2013	16
2014	13
2015	22
2016	28
2017	28
2018	15
2019	13
2020	19
2021	15
2022	18
2023	6
2024	1

1

Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.

Evgrafov OV, Mersiyanova I, Irobi J, Van Den Bosch L, Dierick I, Leung CL, Schagina O, Verpoorten N, Van Impe K, Fedotov V, Dadali E, Auer-Grumbach M, Windpassinger C, Wagner K, Mitrovic Z, Hilton-Jones D, Talbot K, Martin JJ, Vasserman N, Tverskaya S, Polyakov A, Liem RK, Gettemans J, Robberecht W, De Jonghe P, Timmerman V. Evgrafov OV, et al. Nat Genet. 2004 Jun;36(6):602-6. doi: 10.1038/ng1354. Epub 2004 May 2. Nat Genet. 2004. PMID: 15122254

2

Disruption of neurofilament network with aggregation of light neurofilament protein: a common pathway leading to motor neuron degeneration due to Charcot-Marie-Tooth disease-linked mutations in NFL and HSPB1.

Zhai J, Lin H, Julien JP, Schlaepfer WW. Zhai J, et al. Hum Mol Genet. 2007 Dec 15;16(24):3103-16. doi: 10.1093/hmg/ddm272. Epub 2007 Sep 19. Hum Mol Genet. 2007. PMID: 17881652

3

Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth disease.

Tang B, Liu X, Zhao G, Luo W, Xia K, Pan Q, Cai F, Hu Z, Zhang C, Chen B, Zhang F, Shen L, Zhang R, Jiang H. Tang B, et al. Arch Neurol. 2005 Aug;62(8):1201-7. doi: 10.1001/archneur.62.8.1201. Arch Neurol. 2005. PMID: 16087758

4

[Molecular genetics of inherited neuropathies].

Takashima H. Takashima H. Rinsho Shinkeigaku. 2006 Jan;46(1):1-18. Rinsho Shinkeigaku. 2006. PMID: 16541790 Review. Japanese.

5

[Distal hereditary motor neuropathy type II with mutation in heat shock protein 27 gene. A case report].

Nishibayashi M, Kokubun N, Nakamura A, Hirata K, Yamamoto M, Sobue G. Nishibayashi M, et al. Rinsho Shinkeigaku. 2007 Jan;47(1):50-2. Rinsho Shinkeigaku. 2007. PMID: 17491338 Japanese.

6

Mitochondrial and axonal abnormalities precede disruption of the neurofilament network in a model of charcot-marie-tooth disease type 2E and are prevented by heat shock proteins in a mutant-specific fashion.

Tradewell ML, Durham HD, Mushynski WE, Gentil BJ. Tradewell ML, et al. J Neuropathol Exp Neurol. 2009 Jun;68(6):642-52. doi: 10.1097/NEN.0b013e3181a5deeb. J Neuropathol Exp Neurol. 2009. PMID: 19458545

7

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21.

Ismailov SM, Fedotov VP, Dadali EL, Polyakov AV, Van Broeckhoven C, Ivanov VI, De Jonghe P, Timmerman V, Evgrafov OV. Ismailov SM, et al. Eur J Hum Genet. 2001 Aug;9(8):646-50. doi: 10.1038/sj.ejhg.5200686. Eur J Hum Genet. 2001. PMID: 11528513

8

The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy.

Bomont P, Cavalier L, Blondeau F, Ben Hamida C, Belal S, Tazir M, Demir E, Topaloglu H, Korinthenberg R, Tüysüz B, Landrieu P, Hentati F, Koenig M. Bomont P, et al. Nat Genet. 2000 Nov;26(3):370-4. doi: 10.1038/81701. Nat Genet. 2000. PMID: 11062483

9

Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response.

Dierick I, Irobi J, Janssens S, Theuns J, Lemmens R, Jacobs A, Corsmit E, Hersmus N, Van Den Bosch L, Robberecht W, De Jonghe P, Van Broeckhoven C, Timmerman V. Dierick I, et al. Hum Mutat. 2007 Aug;28(8):830. doi: 10.1002/humu.9503. Hum Mutat. 2007. PMID: 17623484

10

Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy.

Jordanova A, Irobi J, Thomas FP, Van Dijck P, Meerschaert K, Dewil M, Dierick I, Jacobs A, De Vriendt E, Guergueltcheva V, Rao CV, Tournev I, Gondim FA, D'Hooghe M, Van Gerwen V, Callaerts P, Van Den Bosch L, Timmermans JP, Robberecht W, Gettemans J, Thevelein JM, De Jonghe P, Kremensky I, Timmerman V. Jordanova A, et al. Nat Genet. 2006 Feb;38(2):197-202. doi: 10.1038/ng1727. Epub 2006 Jan 22. Nat Genet. 2006. PMID: 16429158 Free article.

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