(Q33403530)

26 July 2017

title

Activating CBL mutations are associated with a distinct MDS/MPN phenotype (English)

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26 July 2017

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Andreas Hochhaus

11

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Torsten Haferlach

9

object named as

Torsten Haferlach

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26 July 2017

7

Georgia Metzgeroth

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5

Susanne Schnittger

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1

Juliana Schwaab

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3

Philipp Erben

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12

Wolf-Karsten Hofmann

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26 July 2017

Thomas Ernst

2

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26 July 2017

Jenny Rinke

4

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Philipp Ströbel

6

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26 July 2017

Max Mossner

8

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Nicholas C P Cross

10

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Andreas Reiter

13

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publication date

10 August 2012

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26 July 2017

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26 July 2017

volume

91

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26 July 2017

issue

11

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26 July 2017

page(s)

1713-1720

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Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms

26 July 2017

cites work

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https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Mutations of e3 ubiquitin ligase cbl family members constitute a novel common pathogenic lesion in myeloid malignancies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Myeloproliferative neoplasms: molecular pathophysiology, essential clinical understanding, and treatment strategies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Mutations in CBL occur frequently in juvenile myelomonocytic leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Recent advances in the pathogenesis and treatment of juvenile myelomonocytic leukaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

CBL exon 8/9 mutants activate the FLT3 pathway and cluster in core binding factor/11q deletion acute myeloid leukemia/myelodysplastic syndrome subtypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

The Cbl family proteins: ring leaders in regulation of cell signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Beyond the RING: CBL proteins as multivalent adapters

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

The Cbl interactome and its functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Differential regulation of EGF receptor internalization and degradation by multiubiquitination within the kinase domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Alix facilitates the interaction between c-Cbl and platelet-derived growth factor beta-receptor and thereby modulates receptor down-regulation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Gene expression profiling for diagnosis and therapy in acute leukaemia and other haematologic malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

JAK2V617F-positive polycythemia vera and Philadelphia chromosome-positive chronic myeloid leukemia: one patient with two distinct myeloproliferative disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

E3 ligase-defective Cbl mutants lead to a generalized mastocytosis and myeloproliferative disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

A high occurrence of acquisition and/or expansion of C-CBL mutant clones in the progression of high-risk myelodysplastic syndrome to acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

JAK2-V617F mutation in a patient with Philadelphia-chromosome-positive chronic myeloid leukaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00277-012-1521-3

10.1007/S00277-012-1521-3

21 January 2018

Identifiers

DOI

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26 July 2017

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