Literature DB >> 25932448

A novel case of extreme thrombocytosis in acute myeloid leukemia associated with isochromosome 17q and copy neutral loss of heterozygosity.

Eunkyoung You1, Sun Young Cho2, John Jeongseok Yang2, Hee Joo Lee2, Woo-In Lee2, Juhie Lee3, Kyung Sam Cho4, Eun Hae Cho5, Tae Sung Park2.   

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Year:  2015        PMID： 25932448      PMCID： PMC4390708          DOI： 10.3343/alm.2015.35.3.366

Source DB:  PubMed          Journal:  Ann Lab Med        ISSN： 2234-3806            Impact factor:   3.464


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  8 in total

1.  The localization of the human myeloperoxidase gene is in close proximity to the translocation breakpoint in acute promyelocytic leukemia.

Authors:  K S Chang; W Schroeder; M J Siciliano; L H Thompson; K McCredie; M Beran; E J Freireich; J C Liang; J M Trujillo; S A Stass
Journal:  Leukemia       Date:  1987-05       Impact factor: 11.528

2.  Localization of the human G-CSF gene to the region of a breakpoint in the translocation typical of acute promyelocytic leukemia.

Authors:  R N Simmers; J Smith; M F Shannon; G Wong; A F Lopez; E Baker; G R Sutherland; M A Vadas
Journal:  Hum Genet       Date:  1988-02       Impact factor: 4.132

3.  Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53.

Authors:  Rashmi Kanagal-Shamanna; Carlos E Bueso-Ramos; Bedia Barkoh; Gary Lu; Sa Wang; Guillermo Garcia-Manero; Saroj Vadhan-Raj; Daniela Hoehn; L Jeffrey Medeiros; C Cameron Yin
Journal:  Cancer       Date:  2011-10-28       Impact factor: 6.860

4.  Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations.

Authors:  T Fioretos; B Strömbeck; T Sandberg; B Johansson; R Billström; A Borg; P G Nilsson; H Van Den Berghe; A Hagemeijer; F Mitelman; M Höglund
Journal:  Blood       Date:  1999-07-01       Impact factor: 22.113

5.  Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis.

Authors:  Andres Jerez; Yuka Sugimoto; Hideki Makishima; Amit Verma; Anna M Jankowska; Bartlomiej Przychodzen; Valeria Visconte; Ramon V Tiu; Christine L O'Keefe; Azim M Mohamedali; Austin G Kulasekararaj; Andrea Pellagatti; Kathy McGraw; Hideki Muramatsu; Alison R Moliterno; Mikkael A Sekeres; Michael A McDevitt; Seiji Kojima; Alan List; Jacqueline Boultwood; Ghulam J Mufti; Jaroslaw P Maciejewski
Journal:  Blood       Date:  2012-05-02       Impact factor: 22.113

Review 6.  Acute myeloid leukemia associated with t(1;3)(p36;q21) and extreme thrombocytosis: a clinical study with literature review.

Authors:  Gayoung Lim; Min Jin Kim; Seung Hwan Oh; Sun Young Cho; Hee Joo Lee; Jin-Tae Suh; Juhie Lee; Woo-In Lee; Kyung Sam Cho; Tae Sung Park
Journal:  Cancer Genet Cytogenet       Date:  2010-12

7.  GCSF gene is expressed but not rearranged in a patient with isochromosome 17q positive acute nonlymphocytic leukemia.

Authors:  W Fiedler; H J Weh; S Hegewisch-Becker; D K Hossfeld
Journal:  Cancer Genet Cytogenet       Date:  1993-07-01

Review 8.  Isochromosomes in neoplasia.

Authors:  F Mertens; B Johansson; F Mitelman
Journal:  Genes Chromosomes Cancer       Date:  1994-08       Impact factor: 5.006
  8 in total
  1 in total

1.  Isochromosome 17q in Chronic Lymphocytic Leukemia.

Authors:  Eyad Alhourani; Martina Rincic; Joana B Melo; Isabel M Carreira; Anita Glaser; Beate Pohle; Cordula Schlie; Thomas Liehr
Journal:  Leuk Res Treatment       Date:  2015-11-30
  1 in total

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