Similar articles for PMID: 21702048

Year	Number of Results
2001	2
2002	1
2003	1
2004	4
2005	4
2006	6
2007	5
2008	8
2009	7
2010	5
2011	6
2012	8
2013	6
2014	9
2015	7
2016	1
2017	1
2018	1
2020	2
2021	2
2022	1
2023	1
2024	0

1

Human peripheral blood lymphocytes and fibroblasts as Notch3 expression models.

Di Maio G, Formichi P, Radi E, Bianchi S, Onnis A, Tarquini E, Leoncini L, Federico A. Di Maio G, et al. J Cell Physiol. 2012 Apr;227(4):1771-5. doi: 10.1002/jcp.22901. J Cell Physiol. 2012. PMID: 21702048

2

[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].

Ueda M, Nakaguma R, Ando Y. Ueda M, et al. Rinsho Byori. 2009 Mar;57(3):242-51. Rinsho Byori. 2009. PMID: 19363995 Review. Japanese.

3

A new de novo Notch3 mutation causing CADASIL.

Coto E, Menéndez M, Navarro R, García-Castro M, Alvarez V. Coto E, et al. Eur J Neurol. 2006 Jun;13(6):628-31. doi: 10.1111/j.1468-1331.2006.01337.x. Eur J Neurol. 2006. PMID: 16796587

4

Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Ruchoux MM, Domenga V, Brulin P, Maciazek J, Limol S, Tournier-Lasserve E, Joutel A. Ruchoux MM, et al. Am J Pathol. 2003 Jan;162(1):329-42. doi: 10.1016/S0002-9440(10)63824-2. Am J Pathol. 2003. PMID: 12507916 Free PMC article.

5

Archetypal Arg169Cys mutation in NOTCH3 does not drive the pathogenesis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy via a loss-of-function mechanism.

Cognat E, Baron-Menguy C, Domenga-Denier V, Cleophax S, Fouillade C, Monet-Leprêtre M, Dewerchin M, Joutel A. Cognat E, et al. Stroke. 2014 Mar;45(3):842-9. doi: 10.1161/STROKEAHA.113.003339. Epub 2014 Jan 14. Stroke. 2014. PMID: 24425116

6

New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

Abramycheva N, Stepanova M, Kalashnikova L, Zakharova M, Maximova M, Tanashyan M, Lagoda O, Fedotova E, Klyushnikov S, Konovalov R, Sakharova A, Illarioshkin S. Abramycheva N, et al. J Neurol Sci. 2015 Feb 15;349(1-2):196-201. doi: 10.1016/j.jns.2015.01.018. Epub 2015 Jan 17. J Neurol Sci. 2015. PMID: 25623805

7

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) associated with a novel C82R mutation in the NOTCH3 gene.

Zea-Sevilla MA, Bermejo-Velasco P, Serrano-Heranz R, Calero M. Zea-Sevilla MA, et al. J Alzheimers Dis. 2015;43(2):363-7. doi: 10.3233/JAD-141218. J Alzheimers Dis. 2015. PMID: 25096610

8

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese.

Lee YC, Yang AH, Liu HC, Wong WJ, Lu YC, Chang MH, Soong BW. Lee YC, et al. J Neurol Sci. 2006 Jul 15;246(1-2):111-5. doi: 10.1016/j.jns.2006.02.011. Epub 2006 Mar 31. J Neurol Sci. 2006. PMID: 16580020

9

Nephroangiosclerosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: is NOTCH3 mutation the common culprit?

Guerrot D, François A, Boffa JJ, Boulos N, Hanoy M, Legallicier B, Triquenot-Bagan A, Guyant-Marechal L, Laquerriere A, Freguin-Bouilland C, Ronco P, Godin M. Guerrot D, et al. Am J Kidney Dis. 2008 Aug;52(2):340-5. doi: 10.1053/j.ajkd.2008.04.017. Epub 2008 Jun 24. Am J Kidney Dis. 2008. PMID: 18572291

10

[Identification of a novel NOTCH3 mutation in a family featuring cerebral autosomal dominant arteriopathy with subcortical infarct and leucoencephalopathy].

Zhu Y, Wang J, Wu Y, Wang G, Hu B, Xu A. Zhu Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Oct;31(5):578-81. doi: 10.3760/cma.j.issn.1003-9406.2014.01.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25297585 Chinese.

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