219 related articles for article (PubMed ID: 29572239)
1. Identification of novel
Connelly JA; Mody RJ; Wu YM; Robinson DR; Lonigro RJ; Vats P; Rabban E; Anderson B; Walkovich K
Cold Spring Harb Mol Case Stud; 2018 Apr; 4(2):. PubMed ID: 29572239
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [Gene Mutation and Acute Leukemia Transformation of Severe Congenital Neutropenia- Review].
Chi ZH; Zhu P
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Oct; 25(5):1580-1584. PubMed ID: 29070147
[TBL] [Abstract][Full Text] [Related]
4. H2AFY is a novel fusion partner of MECOM in acute myeloid leukemia.
Han Q; Lu J; Wang J; Ye J; Jiang X; Chen H; Liu C; Chen L; Lin T; Chen S; Sun M; Gao F
Cancer Genet; 2018 Apr; 222-223():9-12. PubMed ID: 29666008
[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. Impaired myelopoiesis in congenital neutropenia: insights into clonal and malignant hematopoiesis.
Warren JT; Link DC
Hematology Am Soc Hematol Educ Program; 2021 Dec; 2021(1):514-520. PubMed ID: 34889405
[TBL] [Abstract][Full Text] [Related]
7. Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia.
Beekman R; Valkhof MG; Sanders MA; van Strien PM; Haanstra JR; Broeders L; Geertsma-Kleinekoort WM; Veerman AJ; Valk PJ; Verhaak RG; Löwenberg B; Touw IP
Blood; 2012 May; 119(22):5071-7. PubMed ID: 22371884
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Malignant Transformation Involving
Olofsen PA; Fatrai S; van Strien PMH; Obenauer JC; de Looper HWJ; Hoogenboezem RM; Erpelinck-Verschueren CAJ; Vermeulen MPWM; Roovers O; Haferlach T; Jansen JH; Ghazvini M; Bindels EMJ; Schneider RK; de Pater EM; Touw IP
Cell Rep Med; 2020 Aug; 1(5):100074. PubMed ID: 33205068
[TBL] [Abstract][Full Text] [Related]
10. Mechanisms of leukemic transformation in congenital neutropenia.
Link DC
Curr Opin Hematol; 2019 Jan; 26(1):34-40. PubMed ID: 30431463
[TBL] [Abstract][Full Text] [Related]
11. 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]
12.
Olofsen PA; Touw IP
Mol Cells; 2020 Feb; 43(2):139-144. PubMed ID: 32041395
[TBL] [Abstract][Full Text] [Related]
13. Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia.
Link DC; Kunter G; Kasai Y; Zhao Y; Miner T; McLellan MD; Ries RE; Kapur D; Nagarajan R; Dale DC; Bolyard AA; Boxer LA; Welte K; Zeidler C; Donadieu J; Bellanné-Chantelot C; Vardiman JW; Caligiuri MA; Bloomfield CD; DiPersio JF; Tomasson MH; Graubert TA; Westervelt P; Watson M; Shannon W; Baty J; Mardis ER; Wilson RK; Ley TJ
Blood; 2007 Sep; 110(5):1648-55. PubMed ID: 17494858
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Truncated CSF3 receptors induce pro-inflammatory responses in severe congenital neutropenia.
Olofsen PA; Bosch DA; de Looper HWJ; van Strien PMH; Hoogenboezem RM; Roovers O; van der Velden VHJ; Bindels EMJ; De Pater EM; Touw IP
Br J Haematol; 2023 Jan; 200(1):79-86. PubMed ID: 36168923
[TBL] [Abstract][Full Text] [Related]
16. MLL-rearranged acute myeloid leukemia: Influence of the genetic partner in allo-HSCT response and prognostic factor of MLL 3' region mRNA expression.
Burillo-Sanz S; Morales-Camacho RM; Caballero-Velázquez T; Carrillo E; Sánchez J; Pérez-López O; Pérez de Soto I; González Campos J; Prats-Martín C; Bernal R; Vargas MT
Eur J Haematol; 2018 May; 100(5):436-443. PubMed ID: 29384595
[TBL] [Abstract][Full Text] [Related]
17. NUP98-HOXA9 bearing therapy-related myeloid neoplasm involves myeloid-committed cell and induces HOXA5, EVI1, FLT3, and MEIS1 expression.
Burillo-Sanz S; Morales-Camacho RM; Caballero-Velázquez T; Vargas MT; García-Lozano JR; Falantes JF; Prats-Martín C; Bernal R; Pérez-Simón JA
Int J Lab Hematol; 2016 Feb; 38(1):64-71. PubMed ID: 26418229
[TBL] [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. Mutation, drift and selection in single-driver hematologic malignancy: Example of secondary myelodysplastic syndrome following treatment of inherited neutropenia.
Wojdyla T; Mehta H; Glaubach T; Bertolusso R; Iwanaszko M; Braun R; Corey SJ; Kimmel M
PLoS Comput Biol; 2019 Jan; 15(1):e1006664. PubMed ID: 30615612
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
