Myelodysplastic syndrome due to somatic GATA1 mutation.

Myelodysplastic syndrome due to somatic GATA1 mutation.

Podrobná bibliografie
Hlavní autoři:	Freson, K, Vyas, P, Thys, C, Wittevrongel, C, De Vos, R, Van Geet, C
Médium:	Conference item
Vydáno:	2004

Podobné jednotky

A Myelodysplastic Syndrome Associated with a Clonal GATA1 Mutation.
Autor: Freson, K, a další
Vydáno: (2008)

PLATELET DYSFUNCTION AND MDS FEATURES DUE TO NOVEL SOMATIC GATA1 MUTATION
Autor: Freson, K, a další
Vydáno: (2010)

The transcription factor GATA1 regulates NBEAL2 expression through a long-distance enhancer
Autor: Anouck Wijgaerts, a další
Vydáno: (2017-04-01)

Somatic mutations in children with GATA2-associated myelodysplastic syndrome who lack other features of GATA2 deficiency
Autor: Kevin E. Fisher, a další
Vydáno: (2017-02-01)

GATA1 gene variants associated with thrombocytopenia and anemia
Autor: Kathleen Freson, a další
Vydáno: (2017-10-01)

GATA1 and cooperating mutations in myeloid leukaemia of Down syndrome
Autor: Garnett, C, a další
Vydáno: (2019)

GATA2 and secondary mutations in familial myelodysplastic syndromes and pediatric myeloid malignancies
Autor: Xinan Wang, a další
Vydáno: (2015-10-01)

Defective nuclear localization of Hsp70 is associated with dyserythropoiesis and GATA-1 cleavage in myelodysplastic syndromes.
Autor: Frisan, E, a další
Vydáno: (2012)

Can somatic GATA2 mutation mimic germ line GATA2 mutation?
Autor: Mallika Sekhar, a další
Vydáno: (2018-04-01)

Analysis of GATA-1 mutations in chronic myeloid leukaemia.
Autor: Halsey, C, a další
Vydáno: (2006)

Severe TMD/AMKL with GATA1 mutation in a stillborn fetus with Down syndrome.
Autor: Heald, B, a další
Vydáno: (2007)

PB1916: SOMATIC MUTATIONS ASSOCIATED WITH MYELODYSPLASTIC SYNDROME IN RUSSIAN PATIENTS
Autor: A. Kohno, a další
Vydáno: (2022-06-01)

GATA1 Mutation In Transient Leukemia (TL) and Myeloid Leukemia of Down Syndrome
Autor: Reinhardt, K, a další
Vydáno: (2010)

GATA1 Mutation In Transient Leukemia (TL) and Myeloid Leukemia of Down Syndrome
Autor: Reinhardt, K, a další
Vydáno: (2010)

Natural history of GATA-1 mutations in Down syndrome.
Autor: Ahmed, M, a další
Vydáno: (2003)

GATA1 mutational analysis in chronic myeloid leukaemia.
Autor: Halsey, C, a další
Vydáno: (2007)

Natural history of GATA1 mutations in Down syndrome.
Autor: Ahmed, M, a další
Vydáno: (2004)

Analysis of GATA1 mutations in Down syndrome transient myeloproliferative disorder and myeloid leukemia.
Autor: Alford, K, a další
Vydáno: (2011)

Somatic Mutations in Myelodysplastic Syndrome Patients in the Context of Allogeneic Stem Cell Transplantation
Autor: Olga Blau, a další
Vydáno: (2016-11-01)

CONTRIBUTION OF SOMATIC MUTATIONS IN THE RISK STRATIFICATION OF MYELODYSPLASTIC NEOPLASMS
Autor: FK Marques, a další
Vydáno: (2023-10-01)

Are somatic mutations predictive of response to erythropoiesis stimulating agents in lower risk myelodysplastic syndromes?
Autor: Olivier Kosmider, a další
Vydáno: (2016-07-01)

Two novel somatic mutations of the ATRX gene in female patients with acquired alpha thalassemia of myelodysplastic syndrome (ATMDS).
Autor: Haas, P, a další
Vydáno: (2006)

GATA1 mutation analysis demonstrates two distinct primary leukemias in a child with down syndrome; implications for leukemogenesis.
Autor: Hellebostad, M, a další
Vydáno: (2005)

Somatic mutations of calreticulin in myeloproliferative neoplasms and myelodysplastic/myeloproliferative neoplasms
Autor: Luca Malcovati, a další
Vydáno: (2014-11-01)

Inappropriately low hepcidin levels in patients with myelodysplastic syndrome carrying a somatic mutation of SF3B1
Autor: Ilaria Ambaglio, a další
Vydáno: (2013-03-01)

Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation
Autor: Abdulhay, N, a další
Vydáno: (2019)

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)

Transcriptional regulation of GATA1
Autor: Drissen, R, a další
Vydáno: (2007)

GATA1-mediated megakaryocyte differentiation and growth control can be uncoupled and mapped to different domains in GATA1
Autor: Kuhl, C, a další
Vydáno: (2005)

Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms.
Autor: Malcovati, L, a další
Vydáno: (2011)

Outcomes and effect of somatic mutations after erythropoiesis stimulating agents in patients with lower-risk myelodysplastic syndromes
Autor: Juan Carlos Caballero, a další
Vydáno: (2024-01-01)

Somatic mutations and DNA methylation identify a subgroup of poor prognosis within lower‐risk myelodysplastic syndromes
Autor: David Rombaut, a další
Vydáno: (2025-01-01)

Clinical and biological implications of driver mutations in myelodysplastic syndromes.
Autor: Papaemmanuil, E, a další
Vydáno: (2013)

Collaborating constitutive and somatic genetic events in myeloid malignancies: ASXL1 mutations in patients with germline GATA2 mutations
Autor: Jean-Baptiste Micol, a další
Vydáno: (2014-02-01)

Deletion of the major GATA1 enhancer HS 1 does not affect eosinophil GATA1 expression and eosinophil differentiation.
Autor: Guyot, B, a další
Vydáno: (2004)

GATA1-mediated megakaryocyte differentiation and growth control can be uncoupled and mapped to different domains in GATA1.
Autor: Kuhl, C, a další
Vydáno: (2005)

Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome
Autor: Michaela Nováková, a další
Vydáno: (2016-06-01)

Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia
Autor: Steensma, D, a další
Vydáno: (2004)

Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia.
Autor: Steensma, D, a další
Vydáno: (2005)

Abnormalities in the myeloid progenitor compartment in Down syndrome fetal liver precede acquisition of GATA1 mutations.
Autor: Tunstall-Pedoe, O, a další
Vydáno: (2008)