BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Pippucci T, Maresca A, Magini P, Cenacchi G, Donadio V, Palombo F, Papa V, Incensi A, Gasparre G, Valentino ML, Preziuso C, Pisano A, Ragno M, Liguori R, Giordano C, Tonon C, Lodi R, Parmeggiani A, Carelli V, Seri M. Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy. EMBO Mol Med 2015;7:848-58. [PMID: 25870235 DOI: 10.15252/emmm.201404399] [Cited by in Crossref: 30] [Cited by in F6Publishing: 25] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Del Gaudio F, Liu D, Lendahl U. Notch signalling in healthy and diseased vasculature. Open Biol 2022;12:220004. [PMID: 35472289 DOI: 10.1098/rsob.220004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
2 Almeida MR, Elias I, Fernandes C, Machado R, Galego O, Santo G. NOTCH3 mutations in a cohort of Portuguese patients within CADASIL spectrum phenotype. Neurogenetics 2021. [PMID: 34851492 DOI: 10.1007/s10048-021-00679-w] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
3 Schoemaker D, Arboleda-Velasquez JF. Notch3 Signaling and Aggregation as Targets for the Treatment of CADASIL and Other NOTCH3-Associated Small-Vessel Diseases. Am J Pathol 2021;191:1856-70. [PMID: 33895122 DOI: 10.1016/j.ajpath.2021.03.015] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
4 Bouck EG, de la Fuente M, Zunica ER, Li W, Mumaw MM, Nieman MT. Murine cadherin-6 mediates thrombosis in vivo in a platelet-independent manner. Res Pract Thromb Haemost 2021;5:125-31. [PMID: 33537536 DOI: 10.1002/rth2.12458] [Reference Citation Analysis]
5 Canalis E. The Skeleton of Lateral Meningocele Syndrome. Front Genet 2020;11:620334. [PMID: 33519922 DOI: 10.3389/fgene.2020.620334] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 Greisenegger EK, Llufriu S, Chamorro A, Cervera A, Jimenez-Escrig A, Rappersberger K, Marik W, Greisenegger S, Stögmann E, Kopp T, Strom TM, Henes J, Joutel A, Zimprich A. A NOTCH3 homozygous nonsense mutation in familial Sneddon syndrome with pediatric stroke. J Neurol 2021;268:810-6. [PMID: 32980981 DOI: 10.1007/s00415-020-10081-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 6] [Article Influence: 0.5] [Reference Citation Analysis]
7 Luthert PJ, Kiel C. Combining Gene-Disease Associations with Single-Cell Gene Expression Data Provides Anatomy-Specific Subnetworks in Age-Related Macular Degeneration. Netw Syst Med 2020;3:105-21. [PMID: 32789304 DOI: 10.1089/nsm.2020.0005] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
8 Andjelkovic AV, Stamatovic SM, Phillips CM, Martinez-Revollar G, Keep RF. Modeling blood-brain barrier pathology in cerebrovascular disease in vitro: current and future paradigms. Fluids Barriers CNS 2020;17:44. [PMID: 32677965 DOI: 10.1186/s12987-020-00202-7] [Cited by in Crossref: 12] [Cited by in F6Publishing: 17] [Article Influence: 6.0] [Reference Citation Analysis]
9 Palombo F, Graziano C, Al Wardy N, Nouri N, Marconi C, Magini P, Severi G, La Morgia C, Cantalupo G, Cordelli DM, Gangarossa S, Al Kindi MN, Al Khabouri M, Salehi M, Giorgio E, Brusco A, Pisani F, Romeo G, Carelli V, Pippucci T, Seri M. Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East. Hum Genet 2020;139:1429-41. [PMID: 32488467 DOI: 10.1007/s00439-020-02187-7] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
10 Mizuno T, Mizuta I, Watanabe-Hosomi A, Mukai M, Koizumi T. Clinical and Genetic Aspects of CADASIL. Front Aging Neurosci 2020;12:91. [PMID: 32457593 DOI: 10.3389/fnagi.2020.00091] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 5.0] [Reference Citation Analysis]
11 Hosseini-Alghaderi S, Baron M. Notch3 in Development, Health and Disease. Biomolecules 2020;10:E485. [PMID: 32210034 DOI: 10.3390/biom10030485] [Cited by in Crossref: 13] [Cited by in F6Publishing: 19] [Article Influence: 6.5] [Reference Citation Analysis]
12 Kinoshita K, Ishizaki Y, Yamamoto H, Sonoda M, Yonemoto K, Kira R, Sanefuji M, Ueda A, Matsui H, Ando Y, Sakai Y, Ohga S. De novo p.G696S mutation in COL4A1 causes intracranial calcification and late-onset cerebral hemorrhage: A case report and review of the literature. Eur J Med Genet 2020;63:103825. [PMID: 31857254 DOI: 10.1016/j.ejmg.2019.103825] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
13 Yu J, Siebel CW, Schilling L, Canalis E. An antibody to Notch3 reverses the skeletal phenotype of lateral meningocele syndrome in male mice. J Cell Physiol 2020;235:210-20. [PMID: 31188489 DOI: 10.1002/jcp.28960] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
14 Zhang J, Liu M, Zhang Z, Zhou L, Kong W, Jiang Y, Wang J, Xiao J, Wu Y. Genotypic Spectrum and Natural History of Cavitating Leukoencephalopathies in Childhood. Pediatr Neurol 2019;94:38-47. [PMID: 30770271 DOI: 10.1016/j.pediatrneurol.2019.01.002] [Cited by in Crossref: 9] [Cited by in F6Publishing: 14] [Article Influence: 3.0] [Reference Citation Analysis]
15 Hung LY, Ling TK, Lau NKC, Cheung WL, Chong YK, Sheng B, Kwok KM, Mak CM. Genetic diagnosis of CADASIL in three Hong Kong Chinese patients: A novel mutation within the intracellular domain of NOTCH3. J Clin Neurosci 2018;56:95-100. [PMID: 29980472 DOI: 10.1016/j.jocn.2018.06.050] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
16 Zellner A, Scharrer E, Arzberger T, Oka C, Domenga-Denier V, Joutel A, Lichtenthaler SF, Müller SA, Dichgans M, Haffner C. CADASIL brain vessels show a HTRA1 loss-of-function profile. Acta Neuropathol 2018;136:111-25. [PMID: 29725820 DOI: 10.1007/s00401-018-1853-8] [Cited by in Crossref: 33] [Cited by in F6Publishing: 29] [Article Influence: 8.3] [Reference Citation Analysis]
17 Meester J, Verstraeten A, Alaerts M, Schepers D, Van Laer L, Loeys B. Overlapping but distinct roles for NOTCH receptors in human cardiovascular disease. Clin Genet 2018;95:85-94. [DOI: 10.1111/cge.13382] [Cited by in Crossref: 22] [Cited by in F6Publishing: 27] [Article Influence: 5.5] [Reference Citation Analysis]
18 Siebel C, Lendahl U. Notch Signaling in Development, Tissue Homeostasis, and Disease. Physiol Rev. 2017;97:1235-1294. [PMID: 28794168 DOI: 10.1152/physrev.00005.2017] [Cited by in Crossref: 291] [Cited by in F6Publishing: 361] [Article Influence: 58.2] [Reference Citation Analysis]
19 Mašek J, Andersson ER. The developmental biology of genetic Notch disorders. Development 2017;144:1743-63. [PMID: 28512196 DOI: 10.1242/dev.148007] [Cited by in Crossref: 93] [Cited by in F6Publishing: 82] [Article Influence: 18.6] [Reference Citation Analysis]
20 Guo T, Tan ZP, Chen HM, Zheng DY, Liu L, Huang XG, Chen P, Luo H, Yang YF. An effective combination of whole-exome sequencing and runs of homozygosity for the diagnosis of primary ciliary dyskinesia in consanguineous families. Sci Rep 2017;7:7905. [PMID: 28801648 DOI: 10.1038/s41598-017-08510-z] [Cited by in Crossref: 16] [Cited by in F6Publishing: 21] [Article Influence: 3.2] [Reference Citation Analysis]
21 Machuca-Parra AI, Bigger-Allen AA, Sanchez AV, Boutabla A, Cardona-Vélez J, Amarnani D, Saint-Geniez M, Siebel CW, Kim LA, D'Amore PA, Arboleda-Velasquez JF. Therapeutic antibody targeting of Notch3 signaling prevents mural cell loss in CADASIL. J Exp Med 2017;214:2271-82. [PMID: 28698285 DOI: 10.1084/jem.20161715] [Cited by in Crossref: 29] [Cited by in F6Publishing: 30] [Article Influence: 5.8] [Reference Citation Analysis]
22 Di Donato I, Bianchi S, De Stefano N, Dichgans M, Dotti MT, Duering M, Jouvent E, Korczyn AD, Lesnik-Oberstein SA, Malandrini A, Markus HS, Pantoni L, Penco S, Rufa A, Sinanović O, Stojanov D, Federico A. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects. BMC Med 2017;15:41. [PMID: 28231783 DOI: 10.1186/s12916-017-0778-8] [Cited by in Crossref: 90] [Cited by in F6Publishing: 81] [Article Influence: 18.0] [Reference Citation Analysis]
23 Baeten JT, Lilly B. Notch Signaling in Vascular Smooth Muscle Cells. Adv Pharmacol 2017;78:351-82. [PMID: 28212801 DOI: 10.1016/bs.apha.2016.07.002] [Cited by in Crossref: 36] [Cited by in F6Publishing: 44] [Article Influence: 6.0] [Reference Citation Analysis]
24 Lu J, Xia Y, Chen K, Zheng Y, Wang J, Lu W, Yin Q, Wang F, Zhou Y, Guo C. Oncogenic role of the Notch pathway in primary liver cancer. Oncol Lett. 2016;12:3-10. [PMID: 27347091 DOI: 10.3892/ol.2016.4609] [Cited by in Crossref: 28] [Cited by in F6Publishing: 24] [Article Influence: 4.7] [Reference Citation Analysis]
25 Li Y, Liu N, Chen H, Huang Y, Zhang W. Association of Notch3 single-nucleotide polymorphisms and lacunar infarctions in patients. Exp Ther Med 2016;11:28-32. [PMID: 26889213 DOI: 10.3892/etm.2015.2898] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]