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Cited by in F6Publishing
For: Duan Z, Li FQ, Wechsler J, Meade-White K, Williams K, Benson KF, Horwitz M. A novel notch protein, N2N, targeted by neutrophil elastase and implicated in hereditary neutropenia. Mol Cell Biol 2004;24:58-70. [PMID: 14673143 DOI: 10.1128/MCB.24.1.58-70.2004] [Cited by in Crossref: 44] [Cited by in F6Publishing: 20] [Article Influence: 2.4] [Reference Citation Analysis]
Number Citing Articles
1 Duan Z, Zarebski A, Montoya-Durango D, Grimes HL, Horwitz M. Gfi1 coordinates epigenetic repression of p21Cip/WAF1 by recruitment of histone lysine methyltransferase G9a and histone deacetylase 1. Mol Cell Biol 2005;25:10338-51. [PMID: 16287849 DOI: 10.1128/MCB.25.23.10338-10351.2005] [Cited by in Crossref: 128] [Cited by in F6Publishing: 93] [Article Influence: 7.5] [Reference Citation Analysis]
2 Kuchtey J, Olson LM, Rinkoski T, Mackay EO, Iverson TM, Gelatt KN, Haines JL, Kuchtey RW. Mapping of the disease locus and identification of ADAMTS10 as a candidate gene in a canine model of primary open angle glaucoma. PLoS Genet 2011;7:e1001306. [PMID: 21379321 DOI: 10.1371/journal.pgen.1001306] [Cited by in Crossref: 61] [Cited by in F6Publishing: 54] [Article Influence: 5.5] [Reference Citation Analysis]
3 Barrachina Barberá L, Pérez Martínez A, León García S, Pronzato Cuello F, Martín Arenós J, Toornador E. [Cyclic neutropenia with anti-NA2 antibodies and treatment with recombinant granulocyte colony-stimulating factor]. An Pediatr (Barc) 2005;63:180-2. [PMID: 16045884 DOI: 10.1157/13077467] [Cited by in Crossref: 3] [Article Influence: 0.2] [Reference Citation Analysis]
4 Changeux JP, Goulas A, Hilgetag CC. A Connectomic Hypothesis for the Hominization of the Brain. Cereb Cortex 2021;31:2425-49. [PMID: 33367521 DOI: 10.1093/cercor/bhaa365] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
5 Boulay JL, Miserez AR, Zweifel C, Sivasankaran B, Kana V, Ghaffari A, Luyken C, Sabel M, Zerrouqi A, Wasner M, Van Meir E, Tolnay M, Reifenberger G, Merlo A. Loss of NOTCH2 positively predicts survival in subgroups of human glial brain tumors. PLoS One 2007;2:e576. [PMID: 17593975 DOI: 10.1371/journal.pone.0000576] [Cited by in Crossref: 46] [Cited by in F6Publishing: 43] [Article Influence: 3.1] [Reference Citation Analysis]
6 Stahl M, Uemura K, Ge C, Shi S, Tashima Y, Stanley P. Roles of Pofut1 and O-fucose in mammalian Notch signaling. J Biol Chem 2008;283:13638-51. [PMID: 18347015 DOI: 10.1074/jbc.M802027200] [Cited by in Crossref: 127] [Cited by in F6Publishing: 85] [Article Influence: 9.1] [Reference Citation Analysis]
7 Fiddes IT, Lodewijk GA, Mooring M, Bosworth CM, Ewing AD, Mantalas GL, Novak AM, van den Bout A, Bishara A, Rosenkrantz JL, Lorig-Roach R, Field AR, Haeussler M, Russo L, Bhaduri A, Nowakowski TJ, Pollen AA, Dougherty ML, Nuttle X, Addor MC, Zwolinski S, Katzman S, Kriegstein A, Eichler EE, Salama SR, Jacobs FMJ, Haussler D. Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis. Cell 2018;173:1356-1369.e22. [PMID: 29856954 DOI: 10.1016/j.cell.2018.03.051] [Cited by in Crossref: 170] [Cited by in F6Publishing: 161] [Article Influence: 42.5] [Reference Citation Analysis]
8 Sheshachalam A, Srivastava N, Mitchell T, Lacy P, Eitzen G. Granule protein processing and regulated secretion in neutrophils. Front Immunol 2014;5:448. [PMID: 25285096 DOI: 10.3389/fimmu.2014.00448] [Cited by in Crossref: 78] [Cited by in F6Publishing: 78] [Article Influence: 9.8] [Reference Citation Analysis]
9 Horwitz MS, Duan Z, Korkmaz B, Lee HH, Mealiffe ME, Salipante SJ. Neutrophil elastase in cyclic and severe congenital neutropenia. Blood 2007;109:1817-24. [PMID: 17053055 DOI: 10.1182/blood-2006-08-019166] [Cited by in Crossref: 179] [Cited by in F6Publishing: 143] [Article Influence: 11.2] [Reference Citation Analysis]
10 Suzuki IK, Gacquer D, Van Heurck R, Kumar D, Wojno M, Bilheu A, Herpoel A, Lambert N, Cheron J, Polleux F, Detours V, Vanderhaeghen P. Human-Specific NOTCH2NL Genes Expand Cortical Neurogenesis through Delta/Notch Regulation. Cell 2018;173:1370-1384.e16. [PMID: 29856955 DOI: 10.1016/j.cell.2018.03.067] [Cited by in Crossref: 135] [Cited by in F6Publishing: 122] [Article Influence: 33.8] [Reference Citation Analysis]
11 Kubanov AA, Karamova AE, Chikin VV, Verbenko DA, Znamenskaya LF, Artamonova OG. Genetic markers for psoriatic arthritis in patients with psoriasis. Part I: non-HLA genes. Vestnik dermatologii i venerologii 2021;97:33-47. [DOI: 10.25208/vdv1260] [Reference Citation Analysis]
12 Massullo P, Druhan LJ, Bunnell BA, Hunter MG, Robinson JM, Marsh CB, Avalos BR. Aberrant subcellular targeting of the G185R neutrophil elastase mutant associated with severe congenital neutropenia induces premature apoptosis of differentiating promyelocytes. Blood 2005;105:3397-404. [PMID: 15657182 DOI: 10.1182/blood-2004-07-2618] [Cited by in Crossref: 50] [Cited by in F6Publishing: 47] [Article Influence: 2.9] [Reference Citation Analysis]
13 Köster L, Harper C, Goddard A. Cyclic neutropenia in a basset hound. Vet rec case rep 2015;3. [DOI: 10.1136/vetreccr-2014-000135] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
14 Peters HL, Tripathi SC, Kerros C, Katayama H, Garber HR, St John LS, Federico L, Meraz IM, Roth JA, Sepesi B, Majidi M, Ruisaard K, Clise-Dwyer K, Roszik J, Gibbons DL, Heymach JV, Swisher SG, Bernatchez C, Alatrash G, Hanash S, Molldrem JJ. Serine Proteases Enhance Immunogenic Antigen Presentation on Lung Cancer Cells. Cancer Immunol Res 2017;5:319-29. [PMID: 28254787 DOI: 10.1158/2326-6066.CIR-16-0141] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 1.6] [Reference Citation Analysis]
15 Schäffer AA, Klein C. Genetic heterogeneity in severe congenital neutropenia: how many aberrant pathways can kill a neutrophil? Curr Opin Allergy Clin Immunol 2007;7:481-94. [PMID: 17989524 DOI: 10.1097/ACI.0b013e3282f1d690] [Cited by in Crossref: 33] [Cited by in F6Publishing: 8] [Article Influence: 2.4] [Reference Citation Analysis]
16 Grenda DS, Murakami M, Ghatak J, Xia J, Boxer LA, Dale D, Dinauer MC, Link DC. Mutations of the ELA2 gene found in patients with severe congenital neutropenia induce the unfolded protein response and cellular apoptosis. Blood 2007;110:4179-87. [PMID: 17761833 DOI: 10.1182/blood-2006-11-057299] [Cited by in Crossref: 137] [Cited by in F6Publishing: 128] [Article Influence: 9.1] [Reference Citation Analysis]
17 Rydzynska Z, Pawlik B, Krzyzanowski D, Mlynarski W, Madzio J. Neutrophil Elastase Defects in Congenital Neutropenia. Front Immunol 2021;12:653932. [PMID: 33968054 DOI: 10.3389/fimmu.2021.653932] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
18 Wu CL, Zhao SP, Yu BL. Microarray analysis provides new insights into the function of apolipoprotein O in HepG2 cell line. Lipids Health Dis. 2013;12:186. [PMID: 24341743 DOI: 10.1186/1476-511X-12-186] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 0.9] [Reference Citation Analysis]
19 Zhou L, Gao R, Hong H, Li X, Yang J, Shen W, Wang Z, Yang J. Emodin inhibiting neutrophil elastase-induced epithelial-mesenchymal transition through Notch1 signalling in alveolar epithelial cells. J Cell Mol Med 2020;24:11998-2007. [PMID: 32935466 DOI: 10.1111/jcmm.15827] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
20 Richard I. The genetic and molecular bases of monogenic disorders affecting proteolytic systems. J Med Genet 2005;42:529-39. [PMID: 15994873 DOI: 10.1136/jmg.2004.028118] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 1.0] [Reference Citation Analysis]
21 Huang H, Wang X, Guo AN, Li W, Duan RH, Fang JH, Yin B, Li DD. De novo brain arteriovenous malformation formation and development: A case report. World J Clin Cases 2022; 10(18): 6277-6282 [DOI: 10.12998/wjcc.v10.i18.6277] [Reference Citation Analysis]
22 McDaniell R, Warthen DM, Sanchez-Lara PA, Pai A, Krantz ID, Piccoli DA, Spinner NB. NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway. Am J Hum Genet 2006;79:169-73. [PMID: 16773578 DOI: 10.1086/505332] [Cited by in Crossref: 526] [Cited by in F6Publishing: 422] [Article Influence: 32.9] [Reference Citation Analysis]
23 Lodewijk GA, Fernandes DP, Vretzakis I, Savage JE, Jacobs FMJ. Evolution of Human Brain Size-Associated NOTCH2NL Genes Proceeds toward Reduced Protein Levels. Mol Biol Evol 2020;37:2531-48. [PMID: 32330268 DOI: 10.1093/molbev/msaa104] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
24 Huang XR, Tang BS, Jin P, Guo JF. The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review. Mol Neurobiol 2021. [PMID: 34718964 DOI: 10.1007/s12035-021-02616-2] [Reference Citation Analysis]