标题
The evolution of cellular deficiency in GATA2 mutation
作者
关键词
-
出版物
BLOOD
Volume 123, Issue 6, Pages 863-874
出版商
American Society of Hematology
发表日期
2013-12-18
DOI
10.1182/blood-2013-07-517151
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56bright subset
- (2013) E. M. Mace et al. BLOOD
- NK cell responses to cytomegalovirus infection lead to stable imprints in the human KIR repertoire and involve activating KIRs
- (2013) V. Beziat et al. BLOOD
- Clinical and biological implications of driver mutations in myelodysplastic syndromes
- (2013) E. Papaemmanuil et al. BLOOD
- GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome
- (2013) A. P. Hsu et al. BLOOD
- Dendritic cell homeostasis is maintained by nonhematopoietic and T-cell-produced Flt3-ligand in steady state and during immune responses
- (2013) Yasuyuki Saito et al. EUROPEAN JOURNAL OF IMMUNOLOGY
- Highly variable clinical manifestations in a large family with a novel GATA2 mutation
- (2013) P G N J Mutsaers et al. LEUKEMIA
- The inverted CD4/CD8 ratio and associated parameters in 66-year-old individuals: the Swedish HEXA immune study
- (2012) J. Strindhall et al. AGE
- CD8 T cells express randomly selected KIRs with distinct specificities compared with NK cells
- (2012) N. K. Bjorkstrom 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
- GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia
- (2012) Hiroyuki Ishida et al. EUROPEAN JOURNAL OF PEDIATRICS
- 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
- Cytometry by Time-of-Flight Shows Combinatorial Cytokine Expression and Virus-Specific Cell Niches within a Continuum of CD8+ T Cell Phenotypes
- (2012) Evan W. Newell et al. IMMUNITY
- Conditional Gata2 inactivation results in HSC loss and lymphatic mispatterning
- (2012) Kim-Chew Lim et al. JOURNAL OF CLINICAL INVESTIGATION
- Cis-element mutated in GATA2-dependent immunodeficiency governs hematopoiesis and vascular integrity
- (2012) Kirby D. Johnson et al. JOURNAL OF CLINICAL INVESTIGATION
- Preventing preterm births: analysis of trends and potential reductions with interventions in 39 countries with very high human development index
- (2012) Hannah H Chang et al. LANCET
- 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
- Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency
- (2011) R. E. Dickinson 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
- Myelodysplasia in autosomal dominant and sporadic monocytopenia immunodeficiency syndrome: diagnostic features and clinical implications
- (2011) K. R. Calvo et al. HAEMATOLOGICA
- The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency
- (2011) Venetia Bigley et al. JOURNAL OF EXPERIMENTAL MEDICINE
- CD56brightCD16+ NK Cells: A Functional Intermediate Stage of NK Cell Differentiation
- (2011) V. Beziat et al. JOURNAL OF IMMUNOLOGY
- 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
- Poor prognosis in familial acute myeloid leukaemia with combined biallelic CEBPA mutations and downstream events affecting the ATM, FLT3 and CDX2 genes
- (2010) Catherine L. Carmichael et al. BRITISH JOURNAL OF HAEMATOLOGY
- Antimicrobial activity of mucosal-associated invariant T cells
- (2010) Lionel Le Bourhis et al. NATURE IMMUNOLOGY
- Age-Related Trends in Pediatric B-Cell Subsets
- (2010) Eline T. Luning Prak et al. PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
- NK Cell Terminal Differentiation: Correlated Stepwise Decrease of NKG2A and Acquisition of KIRs
- (2010) Vivien Béziat et al. PLoS One
- Autosomal dominant and sporadic monocytopenia with susceptibility to mycobacteria, fungi, papillomaviruses, and myelodysplasia
- (2009) D. C. Vinh et al. BLOOD
- Differential cytokine/chemokines and KL-6 profiles in patients with different forms of tuberculosis
- (2009) Joel Fleury Djoba Siawaya et al. CYTOKINE
- Feedback control of regulatory T cell homeostasis by dendritic cells in vivo
- (2009) Guillaume Darrasse-Jèze et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Hematopoiesis is not clonal in healthy elderly women
- (2008) S. I. Swierczek et al. BLOOD
- Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy
- (2008) C. J. Owen et al. BLOOD
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started