Epidemiology of acute myeloid leukemia: Recent progress and enduring challenges

RM Shallis, R Wang, A Davidoff, X Ma, AM Zeidan - Blood reviews, 2019 - Elsevier
Acute myeloid leukemia (AML) is a malignant disorder of the bone marrow which is
characterized by the clonal expansion and differentiation arrest of myeloid progenitor cells …

Natural killer cell deficiency

JS Orange - Journal of Allergy and Clinical Immunology, 2013 - Elsevier
Natural killer (NK) cells are part of the innate immune defense against infection and cancer
and are especially useful in combating certain viral pathogens. The utility of NK cells in …

X-linked recessive TLR7 deficiency in~ 1% of men under 60 years old with life-threatening COVID-19

T Asano, B Boisson, F Onodi, D Matuozzo… - Science …, 2021 - science.org
Autosomal inborn errors of type I IFN immunity and autoantibodies against these cytokines
underlie at least 10% of critical COVID-19 pneumonia cases. We report very rare …

Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents

MW Wlodarski, S Hirabayashi, V Pastor… - Blood, The Journal …, 2016 - ashpublications.org
Germline GATA2 mutations cause cellular deficiencies with high propensity for myeloid
disease. We investigated 426 children and adolescents with primary myelodysplastic …

Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency

MJ Ciancanelli, SXL Huang, P Luthra, H Garner, Y Itan… - Science, 2015 - science.org
Severe influenza disease strikes otherwise healthy children and remains unexplained. We
report compound heterozygous null mutations in IRF7, which encodes the transcription …

GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity

MA Spinner, LA Sanchez, AP Hsu… - Blood, The Journal …, 2014 - ashpublications.org
Haploinsufficiency of the hematopoietic transcription factor GATA2 underlies monocytopenia
and mycobacterial infections; dendritic cell, monocyte, B, and natural killer (NK) lymphoid …

The genetic basis of myelodysplasia and its clinical relevance

M Cazzola, MG Della Porta… - Blood, The Journal of the …, 2013 - ashpublications.org
Myelodysplasia is a diagnostic feature of myelodysplastic syndromes (MDSs) but is also
found in other myeloid neoplasms. Its molecular basis has been recently elucidated by …

Severe influenza pneumonitis in children with inherited TLR3 deficiency

HK Lim, SXL Huang, J Chen, G Kerner… - Journal of Experimental …, 2019 - rupress.org
Autosomal recessive IRF7 and IRF9 deficiencies impair type I and III IFN immunity and
underlie severe influenza pneumonitis. We report three unrelated children with influenza A …

Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency

N Hernandez, I Melki, H Jing, T Habib… - Journal of Experimental …, 2018 - rupress.org
Life-threatening pulmonary influenza can be caused by inborn errors of type I and III IFN
immunity. We report a 5-yr-old child with severe pulmonary influenza at 2 yr. She is …

The genomic landscape of juvenile myelomonocytic leukemia

E Stieglitz, AN Taylor-Weiner, TY Chang, LC Gelston… - Nature …, 2015 - nature.com
Juvenile myelomonocytic leukemia (JMML) is a myeloproliferative neoplasm (MPN) of
childhood with a poor prognosis. Mutations in NF1, NRAS, KRAS, PTPN11 or CBL occur in …