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.
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| 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. |
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| Authors: | Meggendorfer, M1, Bacher, U1, Alpermann, T1, Haferlach, C1, Kern, W1, Gambacorti-Passerini, C2, Haferlach, T1, Schnittger, S1 |
| Source: | Leukemia (08876924). Sep2013, Vol. 27 Issue 9, p1852-1860. 9p. 2 Diagrams, 3 Charts, 1 Graph. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 90063810 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: 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. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Meggendorfer%2C+M%22">Meggendorfer, M</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Bacher%2C+U%22">Bacher, U</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Alpermann%2C+T%22">Alpermann, T</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Haferlach%2C+C%22">Haferlach, C</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Kern%2C+W%22">Kern, W</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Gambacorti-Passerini%2C+C%22">Gambacorti-Passerini, C</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Haferlach%2C+T%22">Haferlach, T</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Schnittger%2C+S%22">Schnittger, S</searchLink><relatesTo>1</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Leukemia+%2808876924%29%22">Leukemia (08876924)</searchLink>. Sep2013, Vol. 27 Issue 9, p1852-1860. 9p. 2 Diagrams, 3 Charts, 1 Graph. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=90063810 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/leu.2013.133 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 9 StartPage: 1852 Titles: – TitleFull: 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. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Meggendorfer, M – PersonEntity: Name: NameFull: Bacher, U – PersonEntity: Name: NameFull: Alpermann, T – PersonEntity: Name: NameFull: Haferlach, C – PersonEntity: Name: NameFull: Kern, W – PersonEntity: Name: NameFull: Gambacorti-Passerini, C – PersonEntity: Name: NameFull: Haferlach, T – PersonEntity: Name: NameFull: Schnittger, S IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 09 Text: Sep2013 Type: published Y: 2013 Identifiers: – Type: issn-print Value: 08876924 Numbering: – Type: volume Value: 27 – Type: issue Value: 9 Titles: – TitleFull: Leukemia (08876924) Type: main |
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