PubMed for id: 90678

Year	Number of Results
1993	2
1995	1
1998	2
2002	1
2003	3
2004	4
2005	3
2006	3
2007	2
2008	2
2009	3
2010	4
2011	6
2012	9
2013	1
2014	5
2015	2
2016	4
2017	5
2018	2
2019	4
2020	6
2021	4
2022	5
2023	2
2024	2

1

A novel mutation in the LRSAM1 gene in a family with early onset autosomal dominant Charcot-Marie-Tooth type 2P.

Milella G, Amati A, Lastella P, Zanfardino P, Petruzzella V, Zoccolella S. Milella G, et al. Clin Neurol Neurosurg. 2024 Feb;237:108158. doi: 10.1016/j.clineuro.2024.108158. Epub 2024 Feb 3. Clin Neurol Neurosurg. 2024. PMID: 38330802

2

Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2P.

Reilich P, Schlotter B, Montagnese F, Jordan B, Stock F, Schäff-Vogelsang M, Hotter B, Eger K, Diebold I, Erdmann H, Becker K, Schön U, Abicht A. Reilich P, et al. Neuromuscul Disord. 2021 Feb;31(2):123-133. doi: 10.1016/j.nmd.2020.11.011. Epub 2020 Nov 28. Neuromuscul Disord. 2021. PMID: 33414056

3

LRSAM1 E3 ubiquitin ligase promotes proteasomal clearance of E6-AP protein.

Mishra R, Joshi V, Upadhyay A, Amanullah A, Dubey AR, Singh S, Dubey VK, Poluri KM, Jana NR, Mishra A. Mishra R, et al. Cell Signal. 2021 Jan;77:109836. doi: 10.1016/j.cellsig.2020.109836. Epub 2020 Nov 15. Cell Signal. 2021. PMID: 33207262

4

Ubiquitin ligase LRSAM1 suppresses neurodegenerative diseases linked aberrant proteins induced cell death.

Mishra R, Amanullah A, Upadhyay A, Dhiman R, Dubey AR, Singh S, Prasad A, Mishra A. Mishra R, et al. Int J Biochem Cell Biol. 2020 Mar;120:105697. doi: 10.1016/j.biocel.2020.105697. Epub 2020 Jan 23. Int J Biochem Cell Biol. 2020. PMID: 31982566

5

LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2.

Peretti A, Perie M, Vincent D, Bouhour F, Dieterich K, Mallaret M, Duval F, Goizet C, Juntas-Morales R, Magy L, Solé G, Nollet S, Not A, Léonard-Louis S, Francou B, Leguern E, Lia AS, Magdelaine C, Latour P, Stojkovic T. Peretti A, et al. Eur J Hum Genet. 2019 Sep;27(9):1406-1418. doi: 10.1038/s41431-019-0403-8. Epub 2019 Apr 17. Eur J Hum Genet. 2019. PMID: 30996334 Free PMC article.

6

LRSAM1 E3 ubiquitin ligase: molecular neurobiological perspectives linked with brain diseases.

Mishra R, Upadhyay A, Prajapati VK, Dhiman R, Poluri KM, Jana NR, Mishra A. Mishra R, et al. Cell Mol Life Sci. 2019 Jun;76(11):2093-2110. doi: 10.1007/s00018-019-03055-y. Epub 2019 Mar 2. Cell Mol Life Sci. 2019. PMID: 30826859 Review.

7

A novel mutation of LRSAM1 in a Chinese family with Charcot-Marie-Tooth disease.

Zhao G, Song J, Yang M, Song X, Liu X. Zhao G, et al. J Peripher Nerv Syst. 2018 Mar;23(1):55-59. doi: 10.1111/jns.12247. Epub 2018 Feb 6. J Peripher Nerv Syst. 2018. PMID: 29341362

8

The self-association and activity regulation of LRSAM1 E3 ligase.

Bian W, Guo Y, Zhang Y, Li H. Bian W, et al. Biochem Biophys Res Commun. 2017 Mar 25;485(1):95-101. doi: 10.1016/j.bbrc.2017.02.026. Epub 2017 Feb 9. Biochem Biophys Res Commun. 2017. PMID: 28189685

9

Charcot-Marie-Tooth disease type 2G redefined by a novel mutation in LRSAM1.

Peeters K, Palaima P, Pelayo-Negro AL, García A, Gallardo E, García-Barredo R, Mateiu L, Baets J, Menten B, De Vriendt E, De Jonghe P, Timmerman V, Infante J, Berciano J, Jordanova A. Peeters K, et al. Ann Neurol. 2016 Dec;80(6):823-833. doi: 10.1002/ana.24775. Epub 2016 Sep 30. Ann Neurol. 2016. PMID: 27686364

10

A novel mutation in LRSAM1 causes axonal Charcot-Marie-Tooth disease with dominant inheritance.

Engeholm M, Sekler J, Schöndorf DC, Arora V, Schittenhelm J, Biskup S, Schell C, Gasser T. Engeholm M, et al. BMC Neurol. 2014 Jun 3;14:118. doi: 10.1186/1471-2377-14-118. BMC Neurol. 2014. PMID: 24894446 Free PMC article.

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