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Items: 1 to 20 of 158

1.

B-lymphoblastic leukemia/lymphoma associated with t(8;13)(p11;q12)/ ZMYM2 (ZNF198)-FGFR1 : rare case and review of the literature.

Trimaldi J, Carballido EM, Bowers JW, Anguiano AL, Zhang ZJ, Shah BD, Bruno S, List AF, Moscinski LC, Grady T, Agosti SJ, Kang L, Zhang L.

Acta Haematol. 2013;130(3):127-34. doi: 10.1159/000347030. Epub 2013 Apr 16. Review.

PMID:
23594707
2.

Myeloid and lymphoid neoplasm with abnormalities of FGFR1 presenting with trilineage blasts and RUNX1 rearrangement: a case report and review of literature.

Kumar KR, Chen W, Koduru PR, Luu HS.

Am J Clin Pathol. 2015 May;143(5):738-48. doi: 10.1309/AJCPUD6W1JLQQMNA. Review.

3.

A rare case report of 8p11 myeloid and lymphoid neoplasm with FGFR1 abnormality in a young adult.

Shaaban H, Dabu J, Al-Rabi K, Gauchan D, Guron G.

Ann Hematol. 2013 Jan;92(2):285-6. doi: 10.1007/s00277-012-1562-7. Epub 2012 Sep 2. No abstract available.

PMID:
22941307
4.

Molecular monitoring of 8p11 myeloproliferative syndrome in an infant.

Zhang WW, Habeebu S, Sheehan AM, Naeem R, Hernandez VS, Dreyer ZE, López-Terrada D.

J Pediatr Hematol Oncol. 2009 Nov;31(11):879-83. doi: 10.1097/MPH.0b013e3181b83fd0.

PMID:
19829149
5.

Biphenotypic hematologic malignancy: a case report of the 8p11 myeloproliferative syndrome in a child.

Chen X, Zhang Y, Li Y, Lei P, Zhai Y, Liu L.

J Pediatr Hematol Oncol. 2010 Aug;32(6):501-3. doi: 10.1097/MPH.0b013e3181e413fa.

PMID:
20562652
6.
7.

FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome.

Xiao S, Nalabolu SR, Aster JC, Ma J, Abruzzo L, Jaffe ES, Stone R, Weissman SM, Hudson TJ, Fletcher JA.

Nat Genet. 1998 Jan;18(1):84-7.

PMID:
9425908
8.

[Clinical pathological features of the 8p11 myeloproliferative syndrome].

Yan Z, Yang B, Wang QS, Wang LL, Han XP, Ren F, Yu L.

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2010 Oct;18(5):1321-6. Chinese.

PMID:
21129285
9.

Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome.

Reiter A, Sohal J, Kulkarni S, Chase A, Macdonald DH, Aguiar RC, Gonçalves C, Hernandez JM, Jennings BA, Goldman JM, Cross NC.

Blood. 1998 Sep 1;92(5):1735-42.

10.

Identification of four new translocations involving FGFR1 in myeloid disorders.

Sohal J, Chase A, Mould S, Corcoran M, Oscier D, Iqbal S, Parker S, Welborn J, Harris RI, Martinelli G, Montefusco V, Sinclair P, Wilkins BS, van den Berg H, Vanstraelen D, Goldman JM, Cross NC.

Genes Chromosomes Cancer. 2001 Oct;32(2):155-63.

PMID:
11550283
11.

8p11 myeloproliferative syndrome: a review.

Jackson CC, Medeiros LJ, Miranda RN.

Hum Pathol. 2010 Apr;41(4):461-76. doi: 10.1016/j.humpath.2009.11.003. Review.

PMID:
20226962
12.

Acute myeloid leukemia associated with FGFR1 abnormalities.

Lee H, Kim M, Lim J, Kim Y, Han K, Cho BS, Kim HJ.

Int J Hematol. 2013 Jun;97(6):808-12. doi: 10.1007/s12185-013-1337-5. Epub 2013 Apr 23. Review.

PMID:
23609419
13.

A case of therapy-related acute lymphoblastic leukemia with t(11;19)(q23;p13.3) and MLL/MLLT1 gene rearrangement.

Yoo BJ, Nam MH, Sung HJ, Lim CS, Lee CK, Cho YJ, Lee KN, Yoon SY.

Korean J Lab Med. 2011 Jan;31(1):13-7. doi: 10.3343/kjlm.2011.31.1.13.

14.

8p11 myeloproliferative syndrome preceded by t(8;9)(p11;q33), CEP110/FGFR1 fusion transcript: morphologic, molecular, and cytogenetic characterization of myeloid neoplasms associated with eosinophilia and FGFR1 abnormality.

Park TS, Song J, Kim JS, Yang WI, Song S, Kim SJ, Suh B, Choi JR.

Cancer Genet Cytogenet. 2008 Mar;181(2):93-9. doi: 10.1016/j.cancergencyto.2007.11.011. Erratum in: Cancer Genet Cytogenet. 2008 May;183(1):82.

PMID:
18295660
15.

14-3-3 Integrates prosurvival signals mediated by the AKT and MAPK pathways in ZNF198-FGFR1-transformed hematopoietic cells.

Dong S, Kang S, Gu TL, Kardar S, Fu H, Lonial S, Khoury HJ, Khuri F, Chen J.

Blood. 2007 Jul 1;110(1):360-9. Epub 2007 Mar 27.

16.

Molecular identification of a TPR-FGFR1 fusion transcript in an adult with myeloproliferative neoplasm, T-lymphoblastic lymphoma, and a t(1;8)(q25;p11.2).

Kim SY, Kim JE, Park S, Kim HK.

Cancer Genet. 2014 Jun;207(6):258-62. doi: 10.1016/j.cancergen.2014.05.011. Epub 2014 Jun 7.

PMID:
25037443
17.

B-cell acute lymphoblastic leukemia as evolution of a 8p11 myeloproliferative syndrome with t(8;22)(p11;q11) and BCR-FGFR1 fusion gene.

Baldazzi C, Iacobucci I, Luatti S, Ottaviani E, Marzocchi G, Paolini S, Stacchini M, Papayannidis C, Gamberini C, Martinelli G, Baccarani M, Testoni N.

Leuk Res. 2010 Oct;34(10):e282-5. doi: 10.1016/j.leukres.2010.05.009. Epub 2010 Jun 9. No abstract available.

PMID:
20594995
18.

t(8;22)/BCR-FGFR1 myeloproliferative disorder presenting as B-acute lymphoblastic leukemia: report of a case treated with sorafenib and review of the literature.

Wakim JJ, Tirado CA, Chen W, Collins R.

Leuk Res. 2011 Sep;35(9):e151-3. doi: 10.1016/j.leukres.2011.05.013. Epub 2011 May 31. Review. No abstract available.

PMID:
21628071
19.

Distinct stem cell myeloproliferative/T lymphoma syndromes induced by ZNF198-FGFR1 and BCR-FGFR1 fusion genes from 8p11 translocations.

Roumiantsev S, Krause DS, Neumann CA, Dimitri CA, Asiedu F, Cross NC, Van Etten RA.

Cancer Cell. 2004 Mar;5(3):287-98.

20.

Clonal evolution of 8p11 stem cell syndrome in a 14-year-old Chinese boy: a review of literature of t(8;13) associated myeloproliferative diseases.

Wong WS, Cheng KC, Lau KM, Chan NP, Shing MM, Cheng SH, Chik KW, Li CK, Ng MH.

Leuk Res. 2007 Feb;31(2):235-8. Epub 2006 Jun 13.

PMID:
16777224
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