BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 18334177)

  • 1. [Granulopoeisis and leukemogenesis: lessons from congenital neutropenia].
    Donadieu J; Beaupain B; Bellanné-Chantelot C
    Med Sci (Paris); 2008 Mar; 24(3):284-9. PubMed ID: 18334177
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Congenital neutropenia.
    Klein C
    Hematology Am Soc Hematol Educ Program; 2009; ():344-50. PubMed ID: 20008220
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Severe congenital neutropenia and the unfolded protein response.
    Xia J; Link DC
    Curr Opin Hematol; 2008 Jan; 15(1):1-7. PubMed ID: 18043239
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel genetic etiologies of severe congenital neutropenia.
    Boztug K; Klein C
    Curr Opin Immunol; 2009 Oct; 21(5):472-80. PubMed ID: 19782549
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chronic idiopathic neutropenias and severe congenital neutropenia.
    Palmblad J; Papadaki HA
    Curr Opin Hematol; 2008 Jan; 15(1):8-14. PubMed ID: 18043240
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds.
    Smith BN; Ancliff PJ; Pizzey A; Khwaja A; Linch DC; Gale RE
    Br J Haematol; 2009 Mar; 144(5):762-70. PubMed ID: 19036076
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations associated with neutropenia in dogs and humans disrupt intracellular transport of neutrophil elastase.
    Benson KF; Li FQ; Person RE; Albani D; Duan Z; Wechsler J; Meade-White K; Williams K; Acland GM; Niemeyer G; Lothrop CD; Horwitz M
    Nat Genet; 2003 Sep; 35(1):90-6. PubMed ID: 12897784
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Molecular screening of the neutrophil elastase gene in congenital neutropenia.
    Thomas M; Jayandharan G; Chandy M
    Indian Pediatr; 2006 Dec; 43(12):1081-4. PubMed ID: 17202606
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Neutrophil elastase mutations in congenital neutropenia.
    Ancliff PJ; Gale RE; Linch DC
    Hematology; 2003 Jun; 8(3):165-71. PubMed ID: 12745650
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Double de novo mutations of ELANE (ELA2) in a patient with severe congenital neutropenia requiring high-dose G-CSF therapy.
    Lundén L; Boxhammer S; Carlsson G; Ellström KG; Nordenskjöld M; Lagerstedt-Robinson K; Fadeel B
    Br J Haematol; 2009 Nov; 147(4):587-90. PubMed ID: 19694719
    [No Abstract]   [Full Text] [Related]  

  • 16. Double de novo mutations of ELA2 in cyclic and severe congenital neutropenia.
    Salipante SJ; Benson KF; Luty J; Hadavi V; Kariminejad R; Kariminejad MH; Rezaei N; Horwitz MS
    Hum Mutat; 2007 Sep; 28(9):874-81. PubMed ID: 17436313
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital dysgranulopoietic neutropenia.
    Olcay L; Yetgin S; Erdemli E; Germeshausen M; Aktaş D; Büyükaşik Y; Okur H
    Pediatr Blood Cancer; 2008 Jan; 50(1):115-9. PubMed ID: 16652351
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Severe congenital neutropenia: new genes explain an old disease.
    Bohn G; Welte K; Klein C
    Curr Opin Rheumatol; 2007 Nov; 19(6):644-50. PubMed ID: 17917547
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Cyclic neutropenia. Detection of a mutation in the gene for neutrophil elastase (ELA2)].
    Schiller M; Böhm M; Zeidler C; Germeshausen M; Welte K; Luger TA; Bonsmann G
    Hautarzt; 2001 Sep; 52(9):790-6. PubMed ID: 11572070
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.