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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 4
1992 2
1994 6
1995 10
1996 14
1997 12
1998 9
1999 7
2000 7
2001 11
2002 8
2003 11
2004 5
2005 14
2006 15
2007 14
2008 19
2009 15
2010 21
2011 23
2012 21
2013 24
2014 23
2015 23
2016 21
2017 21
2018 28
2019 9
2020 0
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353 results
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Page 1
MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia.
Germeshausen M, Ancliff P, Estrada J, Metzler M, Ponstingl E, Rütschle H, Schwabe D, Scott RH, Unal S, Wawer A, Zeller B, Ballmaier M. Germeshausen M, et al. Blood Adv. 2018 Mar 27;2(6):586-596. doi: 10.1182/bloodadvances.2018016501. Blood Adv. 2018. PMID: 29540340 Free PMC article.
Deciphering the complexities of MECOM rearrangement-driven chromosomal aberrations.
Tang Z, Tang G, Hu S, Patel KP, Yin CC, Wang W, Lin P, Toruner GA, Ok CY, Gu J, Lu X, Khoury JD, Medeiros LJ. Tang Z, et al. Cancer Genet. 2019 Apr;233-234:21-31. doi: 10.1016/j.cancergen.2019.03.002. Epub 2019 Mar 11. Cancer Genet. 2019. PMID: 31109591
Hereditary thrombocytopenias: a growing list of disorders.
Noris P, Pecci A. Noris P, et al. Hematology Am Soc Hematol Educ Program. 2017 Dec 8;2017(1):385-399. doi: 10.1182/asheducation-2017.1.385. Hematology Am Soc Hematol Educ Program. 2017. PMID: 29222283 Free PMC article. Review.
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. Han Q, et al. Cancer Genet. 2018 Apr;222-223:9-12. doi: 10.1016/j.cancergen.2018.01.004. Epub 2018 Feb 17. Cancer Genet. 2018. PMID: 29666008 Free article.
The creatine kinase pathway is a metabolic vulnerability in EVI1-positive acute myeloid leukemia.
Fenouille N, Bassil CF, Ben-Sahra I, Benajiba L, Alexe G, Ramos A, Pikman Y, Conway AS, Burgess MR, Li Q, Luciano F, Auberger P, Galinsky I, DeAngelo DJ, Stone RM, Zhang Y, Perkins AS, Shannon K, Hemann MT, Puissant A, Stegmaier K. Fenouille N, et al. Nat Med. 2017 Mar;23(3):301-313. doi: 10.1038/nm.4283. Epub 2017 Feb 13. Nat Med. 2017. PMID: 28191887 Free PMC article.
Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm.
Capela de Matos RR, Othman MAK, Ferreira GM, Costa ES, Melo JB, Carreira IM, de Souza MT, Lopes BA, Emerenciano M, Land MGP, Liehr T, Ribeiro RC, Silva MLM. Capela de Matos RR, et al. Cancer Genet. 2018 Feb;221:25-30. doi: 10.1016/j.cancergen.2017.12.002. Epub 2017 Dec 19. Cancer Genet. 2018. PMID: 29405993 Free article.
Identification of novel MECOM gene fusion and personalized therapeutic targets through integrative clinical sequencing in secondary acute myeloid leukemia in a patient with severe congenital neutropenia: a case report and literature review.
Connelly JA, Mody RJ, Wu YM, Robinson DR, Lonigro RJ, Vats P, Rabban E, Anderson B, Walkovich K. Connelly JA, et al. Cold Spring Harb Mol Case Stud. 2018 Apr 2;4(2):a002204. doi: 10.1101/mcs.a002204. Print 2018 Apr. Cold Spring Harb Mol Case Stud. 2018. PMID: 29572239 Free PMC article. Review.
Complex chromosomal rearrangements leading to MECOM overexpression are recurrent in myeloid malignancies with various 3q abnormalities.
Baldazzi C, Luatti S, Zuffa E, Papayannidis C, Ottaviani E, Marzocchi G, Ameli G, Bardi MA, Bonaldi L, Paolini R, Gurrieri C, Rigolin GM, Cuneo A, Martinelli G, Cavo M, Testoni N. Baldazzi C, et al. Genes Chromosomes Cancer. 2016 Apr;55(4):375-88. doi: 10.1002/gcc.22341. Epub 2016 Jan 27. Genes Chromosomes Cancer. 2016. PMID: 26815134
A single oncogenic enhancer rearrangement causes concomitant EVI1 and GATA2 deregulation in leukemia.
Gröschel S, Sanders MA, Hoogenboezem R, de Wit E, Bouwman BAM, Erpelinck C, van der Velden VHJ, Havermans M, Avellino R, van Lom K, Rombouts EJ, van Duin M, Döhner K, Beverloo HB, Bradner JE, Döhner H, Löwenberg B, Valk PJM, Bindels EMJ, de Laat W, Delwel R. Gröschel S, et al. Cell. 2014 Apr 10;157(2):369-381. doi: 10.1016/j.cell.2014.02.019. Epub 2014 Apr 3. Cell. 2014. PMID: 24703711 Free article.
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