BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 18354489)

  • 1. Transformation of severe congenital neutropenia to early acute lymphoblastic leukemia in a patient with HAX1 mutation and without G-CSF administration or receptor mutation.
    Yetgin S; Olcay L; Koç A; Germeshausen M
    Leukemia; 2008 Sep; 22(9):1797. PubMed ID: 18354489
    [No Abstract]   [Full Text] [Related]  

  • 2. Screening for G-CSF receptor mutations in patients with secondary myeloid or lymphoid transformation of severe congenital neutropenia. A report from the French neutropenia register.
    Cassinat B; Bellanné-Chantelot C; Notz-Carrère A; Menot ML; Vaury C; Micheau M; Bader-Meunier B; Perel Y; Leblanc T; Donadieu J; Chomienne C
    Leukemia; 2004 Sep; 18(9):1553-5. PubMed ID: 15284863
    [No Abstract]   [Full Text] [Related]  

  • 3. Acute lymphoblastic leukemia in a patient with congenital neutropenia without G-CSF-R and ELA2 mutations.
    Yetgin S; Germeshausen M; Touw I; Koç A; Olcay L
    Leukemia; 2005 Sep; 19(9):1710-1. PubMed ID: 15973448
    [No 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. 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]  

  • 6. 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]  

  • 7. Granulocyte colony-stimulating factor receptor signaling: implications for G-CSF responses and leukemic progression in severe congenital neutropenia.
    Touw IP; Palande K; Beekman R
    Hematol Oncol Clin North Am; 2013 Feb; 27(1):61-73, viii. PubMed ID: 23351988
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Survivin expression in the bone marrow of patients with severe congenital neutropenia.
    Carlsson G; Boxhammer S; Garwicz D; Henter JI; Palmblad J; Nordenskjöld M; Porwit A; Fadeel B
    Leukemia; 2009 Mar; 23(3):622-5. PubMed ID: 18818705
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. HAX1 mutation in an infant with severe congenital neutropenia.
    Eghbali A; Eshghi P; Malek F; Abdollahpour H; Rezaei N
    Turk J Pediatr; 2010; 52(1):81-4. PubMed ID: 20402072
    [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. 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]  

  • 15. 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]  

  • 16. Acute myeloid/NK precursor cell leukemia with trisomy 4 and a novel point mutation in the extracellular domain of the G-CSF receptor in a patient with chronic idiopathic neutropenia.
    Papadaki HA; Kosteas T; Gemetzi C; Damianaki A; Anagnou NP; Eliopoulos GD
    Ann Hematol; 2004 Jun; 83(6):345-8. PubMed ID: 15014900
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Molecular analysis of two cases of severe congenital neutropenia].
    Park J; Kim M; Lim J; Kim Y; Cho B; Park YJ; Han K
    Korean J Lab Med; 2010 Apr; 30(2):111-6. PubMed ID: 20445326
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel mutation in the juxtamembrane intracellular sequence of the granulocyte colony-stimulating factor (G-CSF) receptor gene in a patient with severe congenital neutropenia augments GCSF proliferation activity but not through the MAP kinase cascade.
    Yokoyama T; Okamura S; Asano Y; Kamezaki K; Numata A; Kakumitsu H; Shide K; Nakashima H; Taisuke K; Sekine Y; Mizuno Y; Okamura J; Matsuda T; Harada M; Yoshiyuki N; Shimoda K
    Int J Hematol; 2005 Jul; 82(1):28-34. PubMed ID: 16229088
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An acquired G-CSF receptor mutation results in increased proliferation of CMML cells from a patient with severe congenital neutropenia.
    Germeshausen M; Schulze H; Kratz C; Wilkens L; Repp R; Shannon K; Welte K; Ballmaier M
    Leukemia; 2005 Apr; 19(4):611-7. PubMed ID: 15729385
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Heterozygous M1V variant of ELA-2 gene mutation associated with G-CSF refractory severe congenital neutropenia.
    Setty BA; Yeager ND; Bajwa RP
    Pediatr Blood Cancer; 2011 Sep; 57(3):514-5. PubMed ID: 21618407
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.