198 related articles for article (PubMed ID: 17133096)
1. Severe congenital neutropenia: inheritance and pathophysiology.
Skokowa J; Germeshausen M; Zeidler C; Welte K
Curr Opin Hematol; 2007 Jan; 14(1):22-8. PubMed ID: 17133096
[TBL] [Abstract][Full Text] [Related]
2. G-CSF receptor mutations in patients with congenital neutropenia.
Germeshausen M; Skokowa J; Ballmaier M; Zeidler C; Welte K
Curr Opin Hematol; 2008 Jul; 15(4):332-7. PubMed ID: 18536571
[TBL] [Abstract][Full Text] [Related]
3. Clinical implications of ELA2-, HAX1-, and G-CSF-receptor (CSF3R) mutations in severe congenital neutropenia.
Zeidler C; Germeshausen M; Klein C; Welte K
Br J Haematol; 2009 Feb; 144(4):459-67. PubMed ID: 19120359
[TBL] [Abstract][Full Text] [Related]
4. Severe congenital neutropenia.
Welte K; Zeidler C
Hematol Oncol Clin North Am; 2009 Apr; 23(2):307-20. PubMed ID: 19327585
[TBL] [Abstract][Full Text] [Related]
5. Severe congenital neutropenia.
Welte K; Zeidler C; Dale DC
Semin Hematol; 2006 Jul; 43(3):189-95. PubMed ID: 16822461
[TBL] [Abstract][Full Text] [Related]
6. Dysregulation of myeloid-specific transcription factors in congenital neutropenia.
Skokowa J; Welte K
Ann N Y Acad Sci; 2009 Sep; 1176():94-100. PubMed ID: 19796237
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Mice expressing a neutrophil elastase mutation derived from patients with severe congenital neutropenia have normal granulopoiesis.
Grenda DS; Johnson SE; Mayer JR; McLemore ML; Benson KF; Horwitz M; Link DC
Blood; 2002 Nov; 100(9):3221-8. PubMed ID: 12384420
[TBL] [Abstract][Full Text] [Related]
9. Neutrophil elastase is severely down-regulated in severe congenital neutropenia independent of ELA2 or HAX1 mutations but dependent on LEF-1.
Skokowa J; Fobiwe JP; Dan L; Thakur BK; Welte K
Blood; 2009 Oct; 114(14):3044-51. PubMed ID: 19620402
[TBL] [Abstract][Full Text] [Related]
10. Mutations in the gene for the granulocyte colony-stimulating-factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia.
Dong F; Brynes RK; Tidow N; Welte K; Löwenberg B; Touw IP
N Engl J Med; 1995 Aug; 333(8):487-93. PubMed ID: 7542747
[TBL] [Abstract][Full Text] [Related]
11. Kostmann syndrome or infantile genetic agranulocytosis, part two: Understanding the underlying genetic defects in severe congenital neutropenia.
Carlsson G; Melin M; Dahl N; Ramme KG; Nordenskjöld M; Palmblad J; Henter JI; Fadeel B
Acta Paediatr; 2007 Jun; 96(6):813-9. PubMed ID: 17537008
[TBL] [Abstract][Full Text] [Related]
12. Defective G-CSFR signaling pathways in congenital neutropenia.
Skokowa J; Welte K
Hematol Oncol Clin North Am; 2013 Feb; 27(1):75-88, viii. PubMed ID: 23351989
[TBL] [Abstract][Full Text] [Related]
13. Granulocyte colony-stimulating factor, congenital neutropenia, and acute myeloid leukemia.
Naparstek E
N Engl J Med; 1995 Aug; 333(8):516-8. PubMed ID: 7542748
[No Abstract] [Full Text] [Related]
14. Severe congenital neutropenia terminating in acute myeloid leukemia: disease progression associated with mutations in the granulocyte-colony stimulating factor receptor gene.
Touw IP; Dong F
Leuk Res; 1996 Aug; 20(8):629-31. PubMed ID: 8913314
[TBL] [Abstract][Full Text] [Related]
15. Kostmann syndrome and severe congenital neutropenia.
Zeidler C; Welte K
Semin Hematol; 2002 Apr; 39(2):82-8. PubMed ID: 11957189
[TBL] [Abstract][Full Text] [Related]
16. Increased granulocyte colony-stimulating factor responsiveness but normal resting granulopoiesis in mice carrying a targeted granulocyte colony-stimulating factor receptor mutation derived from a patient with severe congenital neutropenia.
McLemore ML; Poursine-Laurent J; Link DC
J Clin Invest; 1998 Aug; 102(3):483-92. PubMed ID: 9691084
[TBL] [Abstract][Full Text] [Related]
17. [Hematological malignancies in congenital neutropenia].
Okada S; Nakamura K; Kobayashi M
Rinsho Ketsueki; 2010 Jul; 51(7):553-8. PubMed ID: 20693776
[No Abstract] [Full Text] [Related]
18. Functional interaction between mutations in the granulocyte colony-stimulating factor receptor in severe congenital neutropenia.
Ward AC; Gits J; Majeed F; Aprikyan AA; Lewis RS; O'Sullivan LA; Freedman M; Shigdar S; Touw IP; Dale DC; Dror Y
Br J Haematol; 2008 Aug; 142(4):653-6. PubMed ID: 18513286
[TBL] [Abstract][Full Text] [Related]
19. Clinical relevance of point mutations in the cytoplasmic domain of the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropenia.
Tidow N; Pilz C; Teichmann B; Müller-Brechlin A; Germeshausen M; Kasper B; Rauprich P; Sykora KW; Welte K
Blood; 1997 Apr; 89(7):2369-75. PubMed ID: 9116280
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
