PubMed for id: 123606

Year	Number of Results
1993	1
1995	1
1996	1
2000	1
2002	1
2003	3
2005	3
2006	3
2007	4
2008	3
2009	1
2010	2
2011	3
2012	1
2013	2
2014	1
2015	1
2016	2
2017	1
2018	2
2019	2
2020	2
2021	3
2022	1
2023	2
2024	1

1

LncRNA NIPA1-SO confers atherosclerotic protection by suppressing the transmembrane protein NIPA1.

Jiang M, Song Y, Ren MX, He RC, Dong XH, Li XH, Lu ZF, Li S, Wu J, Bei YR, Liu F, Long Y, Wu SG, Liu XH, Wu LM, Yang HL, McVey DG, Dai XY, Ye S, Hu YW. Jiang M, et al. J Adv Res. 2023 Dec;54:29-42. doi: 10.1016/j.jare.2023.01.017. Epub 2023 Feb 2. J Adv Res. 2023. PMID: 36736696 Free PMC article.

2

Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia.

Fang SY, Chou YT, Hsu KC, Hsu SL, Yu KW, Tsai YS, Liao YC, Tsai PC, Lee YC. Fang SY, et al. Ann Clin Transl Neurol. 2023 Mar;10(3):353-362. doi: 10.1002/acn3.51724. Epub 2023 Jan 6. Ann Clin Transl Neurol. 2023. PMID: 36607129 Free PMC article. Review.

3

Analysis of the GCG repeat length in NIPA1 gene in C9orf72-mediated ALS in a large Italian ALS cohort.

Corrado L, Brunetti M, Di Pierro A, Barberis M, Croce R, Bersano E, De Marchi F, Zuccalà M, Barizzone N, Calvo A, Moglia C, Mazzini L, Chiò A, D'Alfonso S. Corrado L, et al. Neurol Sci. 2019 Dec;40(12):2537-2540. doi: 10.1007/s10072-019-04001-3. Epub 2019 Jul 9. Neurol Sci. 2019. PMID: 31286297

4

Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort.

Tazelaar GHP, Dekker AM, van Vugt JJFA, van der Spek RA, Westeneng HJ, Kool LJBG, Kenna KP, van Rheenen W, Pulit SL, McLaughlin RL, Sproviero W, Iacoangeli A, Hübers A, Brenner D, Morrison KE, Shaw PJ, Shaw CE, Panadés MP, Mora Pardina JS, Glass JD, Hardiman O, Al-Chalabi A, van Damme P, Robberecht W, Landers JE, Ludolph AC, Weishaupt JH, van den Berg LH, Veldink JH, van Es MA; Project MinE ALS Sequencing Consortium. Tazelaar GHP, et al. Neurobiol Aging. 2019 Feb;74:234.e9-234.e15. doi: 10.1016/j.neurobiolaging.2018.09.012. Epub 2018 Sep 22. Neurobiol Aging. 2019. PMID: 30342764 Free PMC article.

5

Pure hereditary spastic paraplegia due to a de novo mutation in the NIPA1 gene.

Arkadir D, Noreau A, Goldman JS, Rouleau GA, Alcvalay RN. Arkadir D, et al. Eur J Neurol. 2014;21(1):e2. doi: 10.1111/ene.12284. Epub 2013 Dec 10. Eur J Neurol. 2014. PMID: 25133278 Free PMC article. No abstract available.

6

Recurrent de novo c.316G>A mutation in NIPA1 hotspot.

Hedera P. Hedera P. J Neurol Sci. 2013 Dec 15;335(1-2):231-2. doi: 10.1016/j.jns.2013.09.015. Epub 2013 Sep 17. J Neurol Sci. 2013. PMID: 24075313

7

NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis.

Blauw HM, van Rheenen W, Koppers M, Van Damme P, Waibel S, Lemmens R, van Vught PW, Meyer T, Schulte C, Gasser T, Cuppen E, Pasterkamp RJ, Robberecht W, Ludolph AC, Veldink JH, van den Berg LH. Blauw HM, et al. Hum Mol Genet. 2012 Jun 1;21(11):2497-502. doi: 10.1093/hmg/dds064. Epub 2012 Feb 28. Hum Mol Genet. 2012. PMID: 22378146

8

NIPA1 mutation in complex hereditary spastic paraplegia with epilepsy.

Svenstrup K, Møller RS, Christensen J, Budtz-Jørgensen E, Gilling M, Nielsen JE. Svenstrup K, et al. Eur J Neurol. 2011 Sep;18(9):1197-9. doi: 10.1111/j.1468-1331.2011.03359.x. Epub 2011 Feb 22. Eur J Neurol. 2011. PMID: 21599812

9

Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1.

Du J, Hu YC, Tang BS, Chen C, Luo YY, Zhan ZX, Zhao GH, Jiang H, Xia K, Shen L. Du J, et al. Clin Neurol Neurosurg. 2011 Jul;113(6):480-2. doi: 10.1016/j.clineuro.2011.02.011. Epub 2011 Mar 17. Clin Neurol Neurosurg. 2011. PMID: 21419568

10

Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots.

Beetz C, Schüle R, Klebe S, Klimpe S, Klopstock T, Lacour A, Otto S, Sperfeld AD, van de Warrenburg B, Schöls L, Deufel T. Beetz C, et al. J Neurol Sci. 2008 May 15;268(1-2):131-5. doi: 10.1016/j.jns.2007.11.015. Epub 2008 Jan 14. J Neurol Sci. 2008. PMID: 18191948

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