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Journal Abstract Search

164 related items for PubMed ID: 26324699

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  • 5. Effect of granulocyte colony-stimulating factor on granulopoiesis of congenital neutropenic children.
    Benkö I, Maródi L, Megyeri A, Káposzta R, Kovács P.
    Acta Physiol Hung; 1996; 84(3):261-2. PubMed ID: 9219597
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  • 6. A GCSFR/CSF3R zebrafish mutant models the persistent basal neutrophil deficiency of severe congenital neutropenia.
    Pazhakh V, Clark S, Keightley MC, Lieschke GJ.
    Sci Rep; 2017 Mar 10; 7():44455. PubMed ID: 28281657
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  • 8. Congenital Neutropenia Patient With Hypomorphic Biallelic CSF3R Mutation Responding to GCSF.
    Yilmaz Karapinar D, Akinci B, Şahin Yaşar A, Hekimci Özdemir H, Önder Siviş Z, Onay H, Özkinay F.
    J Pediatr Hematol Oncol; 2019 Apr 10; 41(3):e190-e192. PubMed ID: 30028820
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  • 10. Severe congenital neutropenia and chronic neutrophilic leukemia: an intriguing molecular connection unveiled by oncogenic mutations in CSF3R.
    Touw IP, Beekman R.
    Haematologica; 2013 Oct 10; 98(10):1490-2. PubMed ID: 24091926
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  • 11. In vivo expansion of cells expressing acquired CSF3R mutations in patients with severe congenital neutropenia.
    Germeshausen M, Welte K, Ballmaier M.
    Blood; 2009 Jan 15; 113(3):668-70. PubMed ID: 19020310
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  • 12. Effect of the unfolded protein response and oxidative stress on mutagenesis in CSF3R: a model for evolution of severe congenital neutropenia to myelodysplastic syndrome/acute myeloid leukemia.
    Sapra A, Jaksik R, Mehta H, Biesiadny S, Kimmel M, Corey SJ.
    Mutagenesis; 2020 Dec 01; 35(5):381-389. PubMed ID: 33511998
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  • 13. A congenital CSF3R mutation in chronic neutropenia reveals a vital role for a cytokine receptor extracellular hinge motif in the response to granulocyte colony-stimulating factor.
    Feyen J, Ernst MPT, van der Velden VHJ, Valk PJM, Broeders L, Touw IP, Raaijmakers MHGP.
    Pediatr Blood Cancer; 2023 Apr 01; 70(4):e30039. PubMed ID: 36316822
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  • 14. Prevalence of a new auto-activating colony stimulating factor 3 receptor mutation (CSF3R-T595I) in acute myeloid leukemia and severe congenital neutropenia.
    Beekman R, Valkhof M, van Strien P, Valk PJ, Touw IP.
    Haematologica; 2013 May 01; 98(5):e62-3. PubMed ID: 23508011
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  • 16. Incidence of CSF3R mutations in severe congenital neutropenia and relevance for leukemogenesis: Results of a long-term survey.
    Germeshausen M, Ballmaier M, Welte K.
    Blood; 2007 Jan 01; 109(1):93-9. PubMed ID: 16985178
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  • 17. Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis.
    Skokowa J, Steinemann D, Katsman-Kuipers JE, Zeidler C, Klimenkova O, Klimiankou M, Unalan M, Kandabarau S, Makaryan V, Beekman R, Behrens K, Stocking C, Obenauer J, Schnittger S, Kohlmann A, Valkhof MG, Hoogenboezem R, Göhring G, Reinhardt D, Schlegelberger B, Stanulla M, Vandenberghe P, Donadieu J, Zwaan CM, Touw IP, van den Heuvel-Eibrink MM, Dale DC, Welte K.
    Blood; 2014 Apr 03; 123(14):2229-37. PubMed ID: 24523240
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  • 19. Prevalence and impact of colony stimulating factor 3 receptor (CSF3R) mutations among Egyptian acute myeloid leukemia patients.
    Aref S, El-Ghonemy M, Abouzeid T, El-Sabbagh A, El-Baiomy M.
    Leuk Res; 2014 Jun 03; 38(6):722-5. PubMed ID: 24746896
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  • 20. GM-CSF treatment is not effective in congenital neutropenia patients due to its inability to activate NAMPT signaling.
    Koch C, Samareh B, Morishima T, Mir P, Kanz L, Zeidler C, Skokowa J, Welte K.
    Ann Hematol; 2017 Mar 03; 96(3):345-353. PubMed ID: 27966038
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