Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literature
Published 2014 View Full Article
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Title
Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literature
Authors
Keywords
GATA2, Familial acute myeloid leukemia-myelodysplastic syndrome
Journal
Journal of Hematology & Oncology
Volume 7, Issue 1, Pages 36
Publisher
Springer Nature
Online
2014-04-22
DOI
10.1186/1756-8722-7-36
References
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Note: Only part of the references are listed.- CEBPAdouble-mutated acute myeloid leukaemia harbours concomitant molecular mutations in 76·8% of cases withTET2andGATA2alterations impacting prognosis
- (2013) Vera Grossmann et al. BRITISH JOURNAL OF HAEMATOLOGY
- Acquired ASXL1 mutations are common in patients with inherited GATA2 mutations and correlate with myeloid transformation
- (2013) R. R. West et al. HAEMATOLOGICA
- High GATA2 expression is a poor prognostic marker in pediatric acute myeloid leukemia
- (2012) M. Luesink et al. BLOOD
- High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia
- (2012) M. Pasquet et al. BLOOD
- Marked genetic heterogeneity in familial myelodysplasia/acute myeloid leukaemia
- (2012) Harriet Holme et al. BRITISH JOURNAL OF HAEMATOLOGY
- Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival
- (2012) C. Bodor et al. HAEMATOLOGICA
- GATA2 mutations are frequent in intermediate-risk karyotype AML with biallelic CEBPA mutations and are associated with favorable prognosis
- (2012) A Fasan et al. LEUKEMIA
- Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature
- (2011) J. Kazenwadel et al. BLOOD
- Successful allogeneic hematopoietic stem cell transplantation for GATA2 deficiency
- (2011) J. Cuellar-Rodriguez et al. BLOOD
- Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome
- (2011) A. P. Hsu et al. BLOOD
- Familial Aggregation of Acute Myeloid Leukemia and Myelodysplastic Syndromes
- (2011) Lynn R. Goldin et al. JOURNAL OF CLINICAL ONCOLOGY
- The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency
- (2011) Venetia Bigley et al. JOURNAL OF EXPERIMENTAL MEDICINE
- GATA2 mutations lead to MDS and AML
- (2011) R. Katherine Hyde et al. NATURE GENETICS
- Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
- (2011) Pia Ostergaard et al. NATURE GENETICS
- Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
- (2011) Christopher N Hahn et al. NATURE GENETICS
- Emberger syndrome-Primary lymphedema with myelodysplasia: Report of seven new cases
- (2010) Sahar Mansour et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Autosomal dominant and sporadic monocytopenia with susceptibility to mycobacteria, fungi, papillomaviruses, and myelodysplasia
- (2009) D. C. Vinh et al. BLOOD
- Gain-of-function mutation of GATA-2 in acute myeloid transformation of chronic myeloid leukemia
- (2008) S.-J. Zhang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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