BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

224 related articles for article (PubMed ID: 30028820)

  • 1. 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; 41(3):e190-e192. PubMed ID: 30028820
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.
    Yılmaz Karapınar D; Patıroğlu T; Metin A; Çalışkan Ü; Celkan T; Yılmaz B; Karakaş Z; Karapınar TH; Akıncı B; Özkınay F; Onay H; Yeşilipek MA; Akar HH; Tüysüz G; Tokgöz H; Özdemir GN; Aslan Kıykım A; Karaman S; Kılınç Y; Oymak Y; Küpesiz A; Olcay L; Keskin Yıldırım Z; Aydoğan G; Gökçe M; İleri T; Aral YZ; Bay A; Atabay B; Kaya Z; Söker M; Özdemir Karadaş N; Özbek U; Özsait Selçuk B; Özdemir HH; Uygun V; Tezcan Karasu G; Yılmaz Ş
    Pediatr Blood Cancer; 2019 Oct; 66(10):e27923. PubMed ID: 31321910
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Management of a Patient With Congenital Biallelic CSF3R Mutation With GM-CSF.
    Yilmaz Karapinar D; Özdemir HH; Akinci B; Yaşar AŞ; Siviş ZÖ; Onay H; Özkinay F
    J Pediatr Hematol Oncol; 2020 Apr; 42(3):e164-e166. PubMed ID: 30499904
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Role of CSF3R mutations in the pathomechanism of congenital neutropenia and secondary acute myeloid leukemia.
    Klimiankou M; Mellor-Heineke S; Zeidler C; Welte K; Skokowa J
    Ann N Y Acad Sci; 2016 Apr; 1370(1):119-25. PubMed ID: 27270496
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ultra-Sensitive
    Klimiankou M; Uenalan M; Kandabarau S; Nustede R; Steiert I; Mellor-Heineke S; Zeidler C; Skokowa J; Welte K
    Front Immunol; 2019; 10():116. PubMed ID: 30891028
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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; 123(14):2229-37. PubMed ID: 24523240
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 35(5):381-389. PubMed ID: 33511998
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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; 70(4):e30039. PubMed ID: 36316822
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Truncated Granulocyte Colony-stimulating Factor Receptor (G-CSFR) Inhibits Apoptosis Induced by Neutrophil Elastase G185R Mutant: IMPLICATION FOR UNDERSTANDING CSF3R GENE MUTATIONS IN SEVERE CONGENITAL NEUTROPENIA.
    Qiu Y; Zhang Y; Hu N; Dong F
    J Biol Chem; 2017 Feb; 292(8):3496-3505. PubMed ID: 28073911
    [TBL] [Abstract][Full Text] [Related]  

  • 12. In vivo expansion of cells expressing acquired CSF3R mutations in patients with severe congenital neutropenia.
    Germeshausen M; Welte K; Ballmaier M
    Blood; 2009 Jan; 113(3):668-70. PubMed ID: 19020310
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 109(1):93-9. PubMed ID: 16985178
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 7():44455. PubMed ID: 28281657
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A zebrafish model for HAX1-associated congenital neutropenia.
    Doll L; Aghaallaei N; Dick AM; Welte K; Skokowa J; Bajoghli B
    Haematologica; 2021 May; 106(5):1311-1320. PubMed ID: 32327498
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 38(6):722-5. PubMed ID: 24746896
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 98(5):e62-3. PubMed ID: 23508011
    [No Abstract]   [Full Text] [Related]  

  • 18. Cooperating, congenital neutropenia-associated Csf3r and Runx1 mutations activate pro-inflammatory signaling and inhibit myeloid differentiation of mouse HSPCs.
    Ritter M; Klimiankou M; Klimenkova O; Schambach A; Hoffmann D; Schmidt A; Kanz L; Link DC; Welte K; Skokowa J
    Ann Hematol; 2020 Oct; 99(10):2329-2338. PubMed ID: 32821971
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. HAX1 mutation positive children presenting with haemophagocytic lymphohistiocytosis.
    Karapınar TH; Yılmaz Karapinar D; Oymak Y; Ay Y; Demirağ B; Aykut A; Onay H; Hazan F; Aydınok Y; Özkınay F; Vergin C
    Br J Haematol; 2017 May; 177(4):597-600. PubMed ID: 28169428
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.