Author Palomo, Laura
Collado, Rosa
Solé, Francesc
García, Olga
Luño, Elisa
Larráyoz, María J.
Calasanz, María J.
Mallo, Mar
Pérez‐Oteyza, Jaime
Agirre, Xabier
Blazquez, Beatriz
Cervera, José
Arenillas, Leonor
Lumbreras, Eva
Patiño‐García, Ana
Valiente, Alberto
Adema, Vera
Hernández‐Rivas, Jesús M.
Buño, Ismael
Álvarez, Sara
Martinez‐Laperche, Carolina
Vallespí, María T.
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Issue 1
Keywords SETBP1
i(q10)
TP53
myelodysplastic syndromes
Language English
LinkModel DirectLink
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PublicationDate October 2015
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PublicationPlace England
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PublicationTitle British journal of haematology
PublicationTitleAlternate Br J Haematol
PublicationYear 2015
References 2009
2008
2012; 120
2013; 163
2013; 27
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2012; 30
References_xml – volume: 27
  start-page: 1852
  year: 2013
  end-page: 1860
  article-title: SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations
  publication-title: Leukemia
– volume: 45
  start-page: 18
  year: 2013
  end-page: 24
  article-title: Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
  publication-title: Nature Genetics
– volume: 115
  start-page: 615
  year: 2010
  end-page: 625
  article-title: SETBP1 overexpression is a novel leukemogenic mechanism that predicts adverse outcome in elderly patients with acute myeloid leukemia
  publication-title: Blood
– year: 2009
– volume: 30
  start-page: 820
  year: 2012
  end-page: 829
  article-title: New comprehensive cytogenetic scoring system for primary myelodysplastic syndromes (MDS) and oligoblastic acute myeloid leukemia after MDS derived from an international database merge
  publication-title: Journal of Clinical Oncology
– volume: 120
  start-page: 2454
  year: 2012
  end-page: 2465
  article-title: Revised international prognostic scoring system for myelodysplastic syndromes
  publication-title: Blood
– volume: 45
  start-page: 942
  year: 2013
  end-page: 946
  article-title: Somatic SETBP1 mutations in myeloid malignancies
  publication-title: Nature Genetics
– start-page: 87
  year: 2008
  end-page: 107
– volume: 163
  start-page: 235
  year: 2013
  end-page: 239
  article-title: Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression
  publication-title: British Journal of Haematology
– volume: 118
  start-page: 2879
  year: 2012
  end-page: 2888
  article-title: 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
  publication-title: Cancer
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StartPage 137
SubjectTerms Adult
Aged
Aged, 80 and over
Carrier Proteins - genetics
Chromosomes, Human, Pair 17 - genetics
Female
Humans
i(q10)
Male
Middle Aged
Mutation
myelodysplastic syndromes
Myelodysplastic Syndromes - genetics
Nuclear Proteins - genetics
SETBP1
TP53
Tumor Suppressor Protein p53 - genetics
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Title Correlation of myelodysplastic syndromes with i(17)(q10) and TP53 and SETBP1 mutations
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