SAMHD1 is recurrently mutated in T-cell prolymphocytic leukemia

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2044-5385

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: SAMHD1 is recurrently mutated in T-cell prolymphocytic leukemia ; volume:8 ; number:1 ; day:19 ; month:1 ; year:2018 ; pages:1-16 ; date:1.2018
Blood cancer journal ; 8, Heft 1 (19.1.2018), 1-16, 1.2018

Creator: Johansson, Patricia

Contributor: Klein-Hitpass, Ludger
Choidas, Axel
Habenberger, Peter
Mahboubi, Bijan
Kim, Baek
Bergmann, Anke
Scholtysik, René
Brauser, Martina
Lollies, Anna
Siebert, Reiner
Zenz, Thorsten
Dührsen, Ulrich
Küppers, Ralf
Dürig, Jan
SpringerLink (Online service)

DOI: 10.1038/s41408-017-0036-5

URN: urn:nbn:de:1111-2018041115361

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 30.01.20252025, 2:22 PM CET

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Associated

Johansson, Patricia
Klein-Hitpass, Ludger
Choidas, Axel
Habenberger, Peter
Mahboubi, Bijan
Kim, Baek
Bergmann, Anke
Scholtysik, René
Brauser, Martina
Lollies, Anna
Siebert, Reiner
Zenz, Thorsten
Dührsen, Ulrich
Küppers, Ralf
Dürig, Jan
SpringerLink (Online service)

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SAMHD1 is recurrently mutated in T-cell prolymphocytic leukemia

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Other Objects (12)

Genetic alterations in chronic lymphocytic leukemia and plasma cell neoplasms – a practical guide to WHO HAEM5

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Appraisal of current technologies for the study of genetic alterations in hematologic malignancies with a focus on chromosome analysis and structural variants

Genetic alterations in the classification of tumors of the haematopoietic system: From guiding diagnosis to instructing treatment in leukaemias and lymphomas

Genetic alterations in mature B- and T-cell lymphomas – a practical guide to WHO-HAEM5

DNA methylation profile of a hepatosplenic gamma/delta T-cell lymphoma patient associated with response to interferon-α therapy

SWI/SNF-Komplex-assoziierte Tumordispositions-Syndrome

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T‐cell prolymphocytic leukemia is associated with deregulation of oncogenic microRNAs on transcriptional and epigenetic level

Exploration of whole genome and transcriptome sequencing data lacks evidence for oncogenic viral elements to drive the pathogenesis of T-cell prolymphocytic leukemia

Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B cell lymphomas

Genetic alterations in chronic lymphocytic leukemia and plasma cell neoplasms – a practical guide to WHO HAEM5

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Seltene Tumordispositionssyndrome

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Genetic alterations in the classification of tumors of the haematopoietic system: From guiding diagnosis to instructing treatment in leukaemias and lymphomas

Genetic alterations in mature B- and T-cell lymphomas – a practical guide to WHO-HAEM5

DNA methylation profile of a hepatosplenic gamma/delta T-cell lymphoma patient associated with response to interferon-α therapy

SWI/SNF-Komplex-assoziierte Tumordispositions-Syndrome

Overview on WHO-HAEM5 and the diagnostic relevance of genetic alterations for the classification

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Overview on WHO-HAEM5 and the diagnostic relevance of genetic alterations for the classification

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