BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

216 related articles for article (PubMed ID: 20008220)

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

  • 2. [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]  

  • 3. 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]  

  • 4. Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia.
    Xia J; Bolyard AA; Rodger E; Stein S; Aprikyan AA; Dale DC; Link DC
    Br J Haematol; 2009 Nov; 147(4):535-42. PubMed ID: 19775295
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic analysis and clinical picture of severe congenital neutropenia in Israel.
    Lebel A; Yacobovich J; Krasnov T; Koren A; Levin C; Kaplinsky C; Ravel-Vilk S; Laor R; Attias D; Ben Barak A; Shtager D; Stein J; Kuperman A; Miskin H; Dgany O; Giri N; Alter BP; Tamary H
    Pediatr Blood Cancer; 2015 Jan; 62(1):103-8. PubMed ID: 25284454
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic insights into congenital neutropenia.
    Klein C; Welte K
    Clin Rev Allergy Immunol; 2010 Feb; 38(1):68-74. PubMed ID: 19440858
    [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. 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]  

  • 9. Genetics and pathophysiology of severe congenital neutropenia syndromes unrelated to neutrophil elastase.
    Boztug K; Klein C
    Hematol Oncol Clin North Am; 2013 Feb; 27(1):43-60, vii. PubMed ID: 23351987
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pathogenic mechanisms and clinical implications of congenital neutropenia syndromes.
    Hauck F; Klein C
    Curr Opin Allergy Clin Immunol; 2013 Dec; 13(6):596-606. PubMed ID: 24145314
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Different pattern of gene mutations in Iranian patients with severe congenital neutropenia (including 2 new mutations).
    Alizadeh Z; Fazlollahi MR; Houshmand M; Maddah M; Chavoshzadeh Z; Hamidieh AA; Shamsian BS; Eshghi P; Bolandghamat Pour S; Sadaaie Jahromi H; Mansouri M; Movahedi M; Nayebpour M; Pourpak Z; Moin M
    Iran J Allergy Asthma Immunol; 2013 Mar; 12(1):86-92. PubMed ID: 23454784
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Game of clones: the genomic evolution of severe congenital neutropenia.
    Touw IP
    Hematology Am Soc Hematol Educ Program; 2015; 2015():1-7. PubMed ID: 26637693
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neurological findings and genetic alterations in patients with Kostmann syndrome and HAX1 mutations.
    Roques G; Munzer M; Barthez MA; Beaufils S; Beaupain B; Flood T; Keren B; Bellanné-Chantelot C; Donadieu J
    Pediatr Blood Cancer; 2014 Jun; 61(6):1041-8. PubMed ID: 24482108
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.