204 related articles for article (PubMed ID: 32299910)
21. Functional characteristics of circulating granulocytes in severe congenital neutropenia caused by ELANE mutations.
Liu Q; Sundqvist M; Li W; Holdfeldt A; Zhang L; Björkman L; Bylund J; Dahlgren C; Wang C; Zhao X; Forsman H
BMC Pediatr; 2019 Jun; 19(1):189. PubMed ID: 31176364
[TBL] [Abstract][Full Text] [Related]
22. Dissecting ELANE neutropenia pathogenicity by human HSC gene editing.
Rao S; Yao Y; Soares de Brito J; Yao Q; Shen AH; Watkinson RE; Kennedy AL; Coyne S; Ren C; Zeng J; Serbin AV; Studer S; Ballotti K; Harris CE; Luk K; Stevens CS; Armant M; Pinello L; Wolfe SA; Chiarle R; Shimamura A; Lee B; Newburger PE; Bauer DE
Cell Stem Cell; 2021 May; 28(5):833-845.e5. PubMed ID: 33513358
[TBL] [Abstract][Full Text] [Related]
23. Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemia evolution in severe congenital neutropenia patients belonging to the original Kostmann family in northern Sweden.
Carlsson G; Aprikyan AA; Ericson KG; Stein S; Makaryan V; Dale DC; Nordenskjöld M; Fadeel B; Palmblad J; Hentera JI
Haematologica; 2006 May; 91(5):589-95. PubMed ID: 16670064
[TBL] [Abstract][Full Text] [Related]
24. Mutation, drift and selection in single-driver hematologic malignancy: Example of secondary myelodysplastic syndrome following treatment of inherited neutropenia.
Wojdyla T; Mehta H; Glaubach T; Bertolusso R; Iwanaszko M; Braun R; Corey SJ; Kimmel M
PLoS Comput Biol; 2019 Jan; 15(1):e1006664. PubMed ID: 30615612
[TBL] [Abstract][Full Text] [Related]
25. Hepatic hemangioendothelioma in an infant with severe congenital neutropenia.
Dinand V; Yadav SP; Bellanné-Chantelot C; Jain S; Bhargava M; Sachdeva A
J Pediatr Hematol Oncol; 2012 May; 34(4):298-300. PubMed ID: 22510773
[TBL] [Abstract][Full Text] [Related]
26. Reduced ELANE and SLPI expression compromises dental pulp cell activity.
Sriwattanapong K; Sa-Ard-Iam N; Boonprakong L; Subbalekha K; Trachoo V; Suratannon N; Porntaveetus T; Shotelersuk V
Cell Prolif; 2021 Nov; 54(11):e13132. PubMed ID: 34580954
[TBL] [Abstract][Full Text] [Related]
27. [Clinical and genetic analysis of two patients with congenital neutropenia caused by ELANE gene mutation].
Liu H; Liu G; Zhao P; Huang L; Zhou Y; Qiu X; Xu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1097-1101. PubMed ID: 32924109
[TBL] [Abstract][Full Text] [Related]
28. The spectrum of ELANE mutations and their implications in severe congenital and cyclic neutropenia.
Germeshausen M; Deerberg S; Peter Y; Reimer C; Kratz CP; Ballmaier M
Hum Mutat; 2013 Jun; 34(6):905-14. PubMed ID: 23463630
[TBL] [Abstract][Full Text] [Related]
29. Novel ELANE gene mutation in a Korean girl with severe congenital neutropenia.
Shim YJ; Kim HJ; Suh JS; Lee KS
J Korean Med Sci; 2011 Dec; 26(12):1646-9. PubMed ID: 22148006
[TBL] [Abstract][Full Text] [Related]
30. Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia.
Van Nieuwenhove E; Barber JS; Neumann J; Smeets E; Willemsen M; Pasciuto E; Prezzemolo T; Lagou V; Seldeslachts L; Malengier-Devlies B; Metzemaekers M; Haßdenteufel S; Kerstens A; van der Kant R; Rousseau F; Schymkowitz J; Di Marino D; Lang S; Zimmermann R; Schlenner S; Munck S; Proost P; Matthys P; Devalck C; Boeckx N; Claessens F; Wouters C; Humblet-Baron S; Meyts I; Liston A
J Allergy Clin Immunol; 2020 Nov; 146(5):1180-1193. PubMed ID: 32325141
[TBL] [Abstract][Full Text] [Related]
31. Screening for ELANE, HAX1 and GFI1 gene mutations in children with neutropenia and clinical characterization of two novel mutations in ELANE gene.
Komvilaisak P; Yudhasompop N; Kanchanakamhaeng K; Hongeng S; Pakakasama S; Anurathapan U; Pongphitcha P; Songdej D; Sasanakul W; Sirachainan N
BMC Pediatr; 2023 Nov; 23(1):592. PubMed ID: 37993852
[TBL] [Abstract][Full Text] [Related]
32. CRISPR/Cas9-mediated
Nasri M; Ritter M; Mir P; Dannenmann B; Aghaallaei N; Amend D; Makaryan V; Xu Y; Fletcher B; Bernhard R; Steiert I; Hahnel K; Berger J; Koch I; Sailer B; Hipp K; Zeidler C; Klimiankou M; Bajoghli B; Dale DC; Welte K; Skokowa J
Haematologica; 2020 Mar; 105(3):598-609. PubMed ID: 31248972
[TBL] [Abstract][Full Text] [Related]
33. Neutropenia-associated ELANE mutations disrupting translation initiation produce novel neutrophil elastase isoforms.
Tidwell T; Wechsler J; Nayak RC; Trump L; Salipante SJ; Cheng JC; Donadieu J; Glaubach T; Corey SJ; Grimes HL; Lutzko C; Cancelas JA; Horwitz MS
Blood; 2014 Jan; 123(4):562-9. PubMed ID: 24184683
[TBL] [Abstract][Full Text] [Related]
34. Case Report: Characterization of known (c.607G>C) and novel (c.416C>G)
Núñez-Núñez ME; Lona-Reyes JC; López-Barragán B; Cruz-Osorio RM; Gutiérrez-Zepeda BM; Quintero-Ramos A; Becerra-Loaiza DS
Front Immunol; 2023; 14():1194262. PubMed ID: 37795094
[TBL] [Abstract][Full Text] [Related]
35. Mutations in the ELANE gene are associated with development of periodontitis in patients with severe congenital neutropenia.
Ye Y; Carlsson G; Wondimu B; Fahlén A; Karlsson-Sjöberg J; Andersson M; Engstrand L; Yucel-Lindberg T; Modéer T; Pütsep K
J Clin Immunol; 2011 Dec; 31(6):936-45. PubMed ID: 21796505
[TBL] [Abstract][Full Text] [Related]
36. Severe congenital neutropenias.
Skokowa J; Dale DC; Touw IP; Zeidler C; Welte K
Nat Rev Dis Primers; 2017 Jun; 3():17032. PubMed ID: 28593997
[TBL] [Abstract][Full Text] [Related]
37. Elastase inhibitors as potential therapies for
Makaryan V; Kelley ML; Fletcher B; Bolyard AA; Aprikyan AA; Dale DC
J Leukoc Biol; 2017 Oct; 102(4):1143-1151. PubMed ID: 28754797
[TBL] [Abstract][Full Text] [Related]
38. Aberrant subcellular targeting of the G185R neutrophil elastase mutant associated with severe congenital neutropenia induces premature apoptosis of differentiating promyelocytes.
Massullo P; Druhan LJ; Bunnell BA; Hunter MG; Robinson JM; Marsh CB; Avalos BR
Blood; 2005 May; 105(9):3397-404. PubMed ID: 15657182
[TBL] [Abstract][Full Text] [Related]
39. A patient with severe congenital neutropenia harbors a missense ELANE mutation due to paternal germline mosaicism.
Ying Y; Ye J; Chen Y; Chen Q; Chen Y; Lu X; Xi H; Gu F; Pan D; Zhao J
Clin Chim Acta; 2022 Feb; 526():14-20. PubMed ID: 34968504
[TBL] [Abstract][Full Text] [Related]
40. Wnt3a stimulates maturation of impaired neutrophils developed from severe congenital neutropenia patient-derived pluripotent stem cells.
Hiramoto T; Ebihara Y; Mizoguchi Y; Nakamura K; Yamaguchi K; Ueno K; Nariai N; Mochizuki S; Yamamoto S; Nagasaki M; Furukawa Y; Tani K; Nakauchi H; Kobayashi M; Tsuji K
Proc Natl Acad Sci U S A; 2013 Feb; 110(8):3023-8. PubMed ID: 23382209
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]