BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

666 related articles for article (PubMed ID: 16670064)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Frequency of point mutations in the gene for the G-CSF receptor in patients with chronic neutropenia undergoing G-CSF therapy.
    Tidow N; Pilz C; Kasper B; Welte K
    Stem Cells; 1997; 15 Suppl 1():113-9; discussion 120. PubMed ID: 9368331
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutations.
    Carlsson G; van't Hooft I; Melin M; Entesarian M; Laurencikas E; Nennesmo I; Trebińska A; Grzybowska E; Palmblad J; Dahl N; Nordenskjöld M; Fadeel B; Henter JI
    J Intern Med; 2008 Oct; 264(4):388-400. PubMed ID: 18513342
    [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. A comparison of the defective granulopoiesis in childhood cyclic neutropenia and in severe congenital neutropenia.
    Sera Y; Kawaguchi H; Nakamura K; Sato T; Habara M; Okada S; Ishikawa N; Kojima S; Katoh O; Kobayashi M
    Haematologica; 2005 Aug; 90(8):1032-41. PubMed ID: 16079102
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene.
    Ishikawa N; Okada S; Miki M; Shirao K; Kihara H; Tsumura M; Nakamura K; Kawaguchi H; Ohtsubo M; Yasunaga S; Matsubara K; Sako M; Hara J; Shiohara M; Kojima S; Sato T; Takihara Y; Kobayashi M
    J Med Genet; 2008 Dec; 45(12):802-7. PubMed ID: 18611981
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities.
    Carlsson G; Elinder G; Malmgren H; Trebinska A; Grzybowska E; Dahl N; Nordenskjöld M; Fadeel B
    Pediatr Blood Cancer; 2009 Dec; 53(6):1143-6. PubMed ID: 19499579
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Defects of granulopoiesis in patients with severe congenital neutropenia.
    Nakamura K; Kobayashi M; Konishi N; Kawaguchi H; Miyagawa S; Sato T; Katoh O; Ueda K
    Hiroshima J Med Sci; 2002 Sep; 51(3):63-74. PubMed ID: 12422946
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acute lymphoblastic leukemia following severe congenital neutropenia or de novo ALL?
    Valera ET; Brassesco MS; Germeshausen M; Silveira Vda S; Queiroz RG; Roxo P; Scrideli CA; de Menezes UP; Ferriani V; Tone LG
    Leuk Res; 2009 Sep; 33(9):e139-42. PubMed ID: 19398129
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Congenital neutropenias.
    Zeidler C; Schwinzer B; Welte K
    Rev Clin Exp Hematol; 2003 Mar; 7(1):72-83. PubMed ID: 14692235
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Novel variant isoform of G-CSF receptor involved in induction of proliferation of FDCP-2 cells: relevance to the pathogenesis of myelodysplastic syndrome.
    Awaya N; Uchida H; Miyakawa Y; Kinjo K; Matsushita H; Nakajima H; Ikeda Y; Kizaki M
    J Cell Physiol; 2002 Jun; 191(3):327-35. PubMed ID: 12012328
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 34.