Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia

Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia

Podrobná bibliografie
Hlavní autoři:	Fernandez-Mercado, M, Pellagatti, A, Perry, J, Fernandez-Santamaria, C, Calasanz, M, Larrayoz, M, Odero, MD, Killick, S, Wainscoat, J, Boultwood, J
Médium:	Conference item
Vydáno:	2010

Podobné jednotky

Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.
Autor: Boultwood, J, a další
Vydáno: (2010)

Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia
Autor: Boultwood, J, a další
Vydáno: (2009)

Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia
Autor: Pellagatti, A, a další
Vydáno: (2014)

Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia.
Autor: Pellagatti, A, a další
Vydáno: (2014)

High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression.
Autor: Boultwood, J, a další
Vydáno: (2010)

High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression
Autor: Boultwood, J, a další
Vydáno: (2010)

Mutation patterns of 16 genes in primary and secondary acute myeloid leukemia (AML) with normal cytogenetics
Autor: Fernandez-Mercado, M, a další
Vydáno: (2012)

Mutated ASXL1 and number of somatic mutations as possible indicators of progression to chronic myelomonocytic leukemia of myelodysplastic syndromes with single or multilineage dysplasia
Autor: Ana Valencia-Martinez, a další
Vydáno: (2017-09-01)

Oncogenic gene expression and epigenetic remodeling of cis-regulatory elements in ASXL1-mutant chronic myelomonocytic leukemia
Autor: Moritz Binder, a další
Vydáno: (2022-03-01)

TET2 mutations are associated with specific 5-methylcytosine and 5-hydroxymethylcytosine profiles in patients with chronic myelomonocytic leukemia
Autor: Pérez, C, a další
Vydáno: (2012)

Mutation patterns of 16 genes in primary and secondary acute myeloid leukemia (AML) with normal cytogenetics.
Autor: Marta Fernandez-Mercado, a další
Vydáno: (2012-01-01)

Mutations in PTPN11 are rare in adult myelodysplastic syndromes and acute myeloid leukemia.
Autor: Watkins, F, a další
Vydáno: (2004)

Spliceosomal gene mutations are frequent events in the diverse mutational spectrum of chronic myelomonocytic leukemia but largely absent in juvenile myelomonocytic leukemia
Autor: Sarah Abu Kar, a další
Vydáno: (2013-01-01)

Silencing of ASXL1 impairs the granulomonocytic lineage potential of human CD34+ progenitor cells
Autor: Davies, C, a další
Vydáno: (2013)

Silencing of ASXL1 impairs the granulomonocytic lineage potential of human CD34⁺ progenitor cells.
Autor: Davies, C, a další
Vydáno: (2013)

Decitabine/Cedazuridine in the Management of Myelodysplastic Syndrome and Chronic Myelomonocytic Leukemia in Canada
Autor: John Paul Yun, a další
Vydáno: (2023-08-01)

Treatment and outcomes for chronic myelomonocytic leukemia compared to myelodysplastic syndromes in older adults
Autor: Dan P. Zandberg, a další
Vydáno: (2013-04-01)

P709: H2AK119UB IN THE TRANSCRIPTIONAL REGULATION OF PATIENTS WITH ASXL1-MUTANT CHRONIC MYELOMONOCYTIC LEUKEMIA
Autor: Moritz Binder, a další
Vydáno: (2023-08-01)

Gene expression profiling in the myelodysplastic syndromes.
Autor: Pellagatti, A, a další
Vydáno: (2005)

Acute Myeloid Leukemia with Co-mutated ASXL1 and SRSF2 Exhibits Monocytic Differentiation and has a Mutational Profile Overlapping with Chronic Myelomonocytic Leukemia
Autor: Steven M. Johnson, a další
Vydáno: (2019-10-01)

Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.
Autor: Fernandez-Mercado, M, a další
Vydáno: (2013)

Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression
Autor: Fernandez-Mercado, M, a další
Vydáno: (2013)

TET2 mutations are associated with specific 5-methylcytosine and 5-hydroxymethylcytosine profiles in patients with chronic myelomonocytic leukemia.
Autor: Cristina Pérez, a další
Vydáno: (2012-01-01)

PB2022: ELTROMBOPAG IN MYELODYSPLASTIC SYNDROME AND CHRONIC MYELOMONOCYTIC LEUKEMIA: A SINGLE-CENTER EXPERIENCE
Autor: Amaia Lopez Peña, a další
Vydáno: (2023-08-01)

Cytogenetic risk stratification in chronic myelomonocytic leukemia
Autor: Esperanza Such, a další
Vydáno: (2011-03-01)

<i>ASXL1/TET2</i> genotype-based risk stratification outperforms <i>ASXL1</i> mutational impact and is independent of mutant variant allele fractions in chronic myelomonocytic leukemia
Autor: Clifford M. Csizmar, a další
Vydáno: (2024-06-01)

Gene Expression Profiling of CD34(+) Cells in Patients with Myelodysplastic Syndromes
Autor: Pellagatti, A, a další
Vydáno: (2008)

The prognostic value of the interaction between ASXL1 and TET2 gene mutations in patients with chronic myelomonocytic leukemia: a meta-analysis
Autor: Wenxia Zhao, a další
Vydáno: (2022-12-01)

Prognosis and risk factors for ASXL1 mutations in patients with newly diagnosed acute myeloid leukemia and myelodysplastic syndrome
Autor: Liqing Yang, a další
Vydáno: (2024-01-01)

Clinical spectrum, outcome and management of immune thrombocytopenia associated with myelodysplastic syndromes and chronic myelomonocytic leukemia
Autor: Vincent Jachiet, a další
Vydáno: (2021-02-01)

Molecular similarity between myelodysplastic form of chronic myelomonocytic leukemia and refractory anemia with ring sideroblasts
Autor: Véronique Gelsi-Boyer, a další
Vydáno: (2013-04-01)

TET2 gene mutation is a frequent and adverse event in chronic myelomonocytic leukemia
Autor: Olivier Kosmider, a další
Vydáno: (2009-12-01)

Genome profiling of chronic myelomonocytic leukemia: frequent alterations of <it>RAS </it>and <it>RUNX1 </it>genes
Autor: Olschwang Sylviane, a další
Vydáno: (2008-10-01)

Prognostic significance of SETBP1 mutations in myelodysplastic syndromes, chronic myelomonocytic leukemia, and chronic neutrophilic leukemia: A meta-analysis.
Autor: Li-Hong Shou, a další
Vydáno: (2017-01-01)

Azacitidine Treatment in Patients with Myelodysplastic Syndrome, Chronic Myelomonocytic Leukemia Type 2 and Acute Myeloid Leukemia According to their Cytogenetic Findings
Autor: Nikolova D., a další
Vydáno: (2021-10-01)

Targeted re-sequencing analysis of 25 genes commonly mutated in myeloid disorders in del(5q) myelodysplastic syndromes.
Autor: Fernandez-Mercado, M, a další
Vydáno: (2013)

Clonality in the myelodysplastic syndromes.
Autor: Boultwood, J, a další
Vydáno: (2001)

Molecular basis of juvenile myelomonocytic leukemia
Autor: Andrica C.H. de Vries, a další
Vydáno: (2010-02-01)

Deregulated Gene Expression Pathways in Myelodysplastic Syndrome Hematopoietic Stem Cells
Autor: Pellagatti, A, a další
Vydáno: (2009)

Case Report: ASXL1, RUNX1, and IDH1 mutation in tyrosine kinase-independent resistant chronic myeloid leukemia progressing to chronic myelomonocytic leukemia-like accelerated phase
Autor: Emmanuella Oyogoa, a další
Vydáno: (2023-09-01)