4.7 Review

Mutations in ASXL1 are associated with poor prognosis across the spectrum of malignant myeloid diseases

Related references

Note: Only part of the references are listed.
Letter Hematology

ASXL1 mutations in primary and secondary myelofibrosis

Clara Ricci et al.

BRITISH JOURNAL OF HAEMATOLOGY (2012)

Article Hematology

Acquired mutations in ASXL1 in acute myeloid leukemia: prevalence and prognostic value

Marta Pratcorona et al.

HAEMATOLOGICA-THE HEMATOLOGY JOURNAL (2012)

Article Multidisciplinary Sciences

The genetic basis of early T-cell precursor acute lymphoblastic leukaemia

Jinghui Zhang et al.

NATURE (2012)

Article Hematology

EZH2 mutational status predicts poor survival in myelofibrosis

Paola Guglielmelli et al.

BLOOD (2011)

Article Oncology

Prognostic Significance of ASXL1 Mutations in Patients With Myelodysplastic Syndromes

Felicitas Thol et al.

JOURNAL OF CLINICAL ONCOLOGY (2011)

Article Genetics & Heredity

De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome

Alexander Hoischen et al.

NATURE GENETICS (2011)

Article Medicine, General & Internal

Clinical Effect of Point Mutations in Myelodysplastic Syndromes

Rafael Bejar et al.

NEW ENGLAND JOURNAL OF MEDICINE (2011)

Article Hematology

ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia

Veronique Gelsi-Boyer et al.

BRITISH JOURNAL OF HAEMATOLOGY (2010)

Article Biochemistry & Molecular Biology

ASXL1 Represses Retinoic Acid Receptor-mediated Transcription through Associating with HP1 and LSD1

Sang-Wang Lee et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2010)

Article Oncology

Spectrum of mutations in RARS-T patients includes TET2 and ASXL1 mutations

Hadrian Szpurka et al.

LEUKEMIA RESEARCH (2010)

Article Multidisciplinary Sciences

Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB

Johanna C. Scheuermann et al.

NATURE (2010)

Article Genetics & Heredity

Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes

Gorica Nikoloski et al.

NATURE GENETICS (2010)

Article Genetics & Heredity

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

Thomas Ernst et al.

NATURE GENETICS (2010)

Article Hematology

Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia

Veronique Gelsi-Boyer et al.

BRITISH JOURNAL OF HAEMATOLOGY (2009)

Letter Oncology

Mutations of ASXL1 gene in myeloproliferative neoplasms

N. Carbuccia et al.

LEUKEMIA (2009)

Article Multidisciplinary Sciences

JAK2 phosphorylates histone H3Y41 and excludes HP1α from chromatin

Mark A. Dawson et al.

NATURE (2009)

Article Biochemistry & Molecular Biology

Additional sex comb-like 1 (ASXL1), in cooperation with SRC-1, acts as a ligand-dependent coactivator for retinoic acid receptor

Yang-Sook Cho et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2006)