185 related articles for article (PubMed ID: 37795094)
1. 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]
2. [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]
3. Severe congenital neutropenia with elastase, neutrophil expressed (ELANE) gene mutation in a Tanzanian child.
Shoo A; Swai P; Kindole C; Ngailo E; Godfrey E; Massawe E; Warren AJ; Luzzatto L
Br J Haematol; 2022 Mar; 196(5):1271-1274. PubMed ID: 34725814
[No Abstract] [Full Text] [Related]
4. 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]
5. CRISPR-Cas9-Mediated ELANE Mutation Correction in Hematopoietic Stem and Progenitor Cells to Treat Severe Congenital Neutropenia.
Tran NT; Graf R; Wulf-Goldenberg A; Stecklum M; Strauß G; Kühn R; Kocks C; Rajewsky K; Chu VT
Mol Ther; 2020 Dec; 28(12):2621-2634. PubMed ID: 32822592
[TBL] [Abstract][Full Text] [Related]
6. Inducible expression of a disease-associated
Garg B; Mehta HM; Wang B; Kamel R; Horwitz MS; Corey SJ
J Biol Chem; 2020 May; 295(21):7492-7500. PubMed ID: 32299910
[TBL] [Abstract][Full Text] [Related]
7. CRISPR-Cas9n-mediated ELANE promoter editing for gene therapy of severe congenital neutropenia.
Nasri M; Ritter MU; Mir P; Dannenmann B; Kaufmann MM; Arreba-Tutusaus P; Xu Y; Borbaran-Bravo N; Klimiankou M; Lengerke C; Zeidler C; Cathomen T; Welte K; Skokowa J
Mol Ther; 2024 Jun; 32(6):1628-1642. PubMed ID: 38556793
[TBL] [Abstract][Full Text] [Related]
8. Clinical characteristics of severe congenital neutropenia caused by novel ELANE gene mutations.
Shu Z; Li XH; Bai XM; Zhang ZY; Jiang LP; Tang XM; Zhao XD
Pediatr Infect Dis J; 2015 Feb; 34(2):203-7. PubMed ID: 25162927
[TBL] [Abstract][Full Text] [Related]
9. Four novel ELANE mutations in patients with congenital neutropenia.
Kurnikova M; Maschan M; Dinova E; Shagina I; Finogenova N; Mamedova E; Polovtseva T; Shagin D; Shcherbina A
Pediatr Blood Cancer; 2011 Aug; 57(2):332-5. PubMed ID: 21425445
[TBL] [Abstract][Full Text] [Related]
10. Screening of genetic variants in
Arunachalam AK; Suresh H; Edison ES; Korula A; Aboobacker FN; George B; Shaji RV; Mathews V; Balasubramanian P
J Clin Pathol; 2020 Jun; 73(6):322-327. PubMed ID: 31732620
[TBL] [Abstract][Full Text] [Related]
11. Differential transcriptional control of hematopoiesis in congenital and cyclic neutropenia patients harboring
Zeidler A; Borbaran-Bravo N; Dannenmann B; Ritter M; Nasri M; Klimiankou M; Kandabarau S; Zahabi A; König J; Zeidler C; Skokowa J; Welte K
Haematologica; 2024 May; 109(5):1393-1402. PubMed ID: 37855057
[TBL] [Abstract][Full Text] [Related]
12. Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation.
van de Vosse E; Verhard EM; Tool AJ; de Visser AW; Kuijpers TW; Hiemstra PS; van Dissel JT
Ann Hematol; 2011 Feb; 90(2):151-8. PubMed ID: 20803142
[TBL] [Abstract][Full Text] [Related]
13. The Clinical and Molecular Assessment of Iranian Families with Severe Congenital Neutropenia, Identification of HYOU1 and SHOC2 as Potential Novel Gene Defects.
Arab F; Rezaei N; Taheri F; Kouhpeikar H; Rayzan E; Mirbeyk M; Zare-Abdollahi D; Ghadami M
Iran J Allergy Asthma Immunol; 2022 Jun; 21(3):344-354. PubMed ID: 35822684
[TBL] [Abstract][Full Text] [Related]
14. Neutrophil Elastase Defects in Congenital Neutropenia.
Rydzynska Z; Pawlik B; Krzyzanowski D; Mlynarski W; Madzio J
Front Immunol; 2021; 12():653932. PubMed ID: 33968054
[TBL] [Abstract][Full Text] [Related]
15. Congenital neutropenia: From lab bench to clinic bedside and back.
Dobrewa W; Bielska M; Bąbol-Pokora K; Janczar S; Młynarski W
Mutat Res Rev Mutat Res; 2024; 793():108476. PubMed ID: 37989463
[TBL] [Abstract][Full Text] [Related]
16. [Clinical and genetic analysis of four patients with congenital neutropenia].
Zhu H; Liao Q; Gong Y; Xu B; Zhang C; Zhao H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Nov; 37(11):1222-1225. PubMed ID: 33179225
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. ELANE mutations in cyclic and severe congenital neutropenia: genetics and pathophysiology.
Horwitz MS; Corey SJ; Grimes HL; Tidwell T
Hematol Oncol Clin North Am; 2013 Feb; 27(1):19-41, vii. PubMed ID: 23351986
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]