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Items: 1 to 20 of 122

1.

A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: a review.

Macdonald D, Aguiar RC, Mason PJ, Goldman JM, Cross NC.

Leukemia. 1995 Oct;9(10):1628-30. Review.

PMID:
7564500
2.

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
3.

Characterization of a t(8;13)(p11;q11-12) in an atypical myeloproliferative disorder.

Smedley D, Somers G, Venter D, Chow CW, Cooper C, Shipley J.

Genes Chromosomes Cancer. 1998 Jan;21(1):70-3.

PMID:
9443043
4.

t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12.

Chaffanet M, Popovici C, Leroux D, Jacrot M, Adélaïde J, Dastugue N, Grégoire MJ, Hagemeijer A, Lafage-Pochitaloff M, Birnbaum D, Pébusque MJ.

Oncogene. 1998 Feb 19;16(7):945-9.

5.

Myeloproliferative disorders with t(8;9)(p12;q33): a case report and review of the literature.

Hu S, He Y, Zhu X, Li J, He H.

Pediatr Hematol Oncol. 2011 Mar;28(2):140-6. doi: 10.3109/08880018.2010.528170. Epub 2011 Jan 8. Review.

PMID:
21214407
6.

Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL.

Fioretos T, Panagopoulos I, Lassen C, Swedin A, Billström R, Isaksson M, Strömbeck B, Olofsson T, Mitelman F, Johansson B.

Genes Chromosomes Cancer. 2001 Dec;32(4):302-10.

PMID:
11746971
7.

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
8.

Four new recurring translocations in non-Hodgkin lymphoma.

Levine EG, Arthur DC, Machnicki J, Frizzera G, Hurd D, Peterson B, Gajl-Peczalska KJ, Bloomfield CD.

Blood. 1989 Oct;74(5):1796-800.

9.

Chronic myelomonocytic leukaemia with t(8;9)(p11;q34) in childhood: an example of the 8p11 myeloproliferative disorder?

Nakayama H, Inamitsu T, Ohga S, Kai T, Suda M, Matsuzaki A, Ueda K.

Br J Haematol. 1996 Mar;92(3):692-5.

PMID:
8616038
10.

New reciprocal translocation t(6;10) (q27;q11) associated with idiopathic myelofibrosis and eosinophilia.

Cox MC, Panetta P, Venditti A, Abruzzese E, Del Poeta G, Cantonetti M, Amadori S.

Leuk Res. 2001 Apr;25(4):349-51.

PMID:
11248333
11.

The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1.

Macdonald D, Reiter A, Cross NC.

Acta Haematol. 2002;107(2):101-7. Review.

PMID:
11919391
12.

A novel t(1;8)(q25;p11.2) translocation associated with 8p11 myeloproliferative syndrome.

Yoshida C, Takeuchi M, Sadahira Y.

Br J Haematol. 2012 Jan;156(2):271-3. doi: 10.1111/j.1365-2141.2011.08839.x. Epub 2011 Aug 18. No abstract available.

PMID:
21848523
13.

A fourth case of 8p11 myeloproliferative disorder transforming to B-lineage acute lymphoblastic leukaemia. A case report.

JabbarAl-Obaidi M, Rymes N, White P, Pomfret M, Smith H, Starczynski J, Johnson R.

Acta Haematol. 2002;107(2):98-100. Review.

PMID:
11919390
14.

Chromosome 8p11.2 translocations: prevalence, FISH analysis for FGFR1 and MYST3, and clinicopathologic correlates in a consecutive cohort of 13 cases from a single institution.

Patnaik MM, Gangat N, Knudson RA, Keefe JG, Hanson CA, Pardanani A, Ketterling RP, Tefferi A.

Am J Hematol. 2010 Apr;85(4):238-42. doi: 10.1002/ajh.21631.

15.

[The 8p11 myeloproliferative syndrome].

Reither A, Hehlmann R, Goldman JM, Cross NC.

Med Klin (Munich). 1999 Apr 15;94(4):207-10. Review. German.

PMID:
10373756
17.
18.

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
19.

The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1.

Popovici C, Zhang B, Grégoire MJ, Jonveaux P, Lafage-Pochitaloff M, Birnbaum D, Pébusque MJ.

Blood. 1999 Feb 15;93(4):1381-9.

20.

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

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