Absence of a simple code: how transcription factors read the genome
Transcription factors (TFs) influence cell fate by interpreting the regulatory DNA within a
genome. TFs recognize DNA in a specific manner; the mechanisms underlying this …
genome. TFs recognize DNA in a specific manner; the mechanisms underlying this …
The GATA factor revolution in hematology
KR Katsumura, EH Bresnick… - Blood, The Journal …, 2017 - ashpublications.org
The discovery of the GATA binding protein (GATA factor) transcription factor family
revolutionized hematology. Studies of GATA proteins have yielded vital contributions to our …
revolutionized hematology. Studies of GATA proteins have yielded vital contributions to our …
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 …
disease. We investigated 426 children and adolescents with primary myelodysplastic …
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 …
and mycobacterial infections; dendritic cell, monocyte, B, and natural killer (NK) lymphoid …
Single-cell transcriptomic analysis identifies an immune-prone population in erythroid precursors during human ontogenesis
C Xu, J He, H Wang, Y Zhang, J Wu, L Zhao, Y Li… - Nature …, 2022 - nature.com
Nonimmune cells can have immunomodulatory roles that contribute to healthy development.
However, the molecular and cellular mechanisms underlying the immunomodulatory …
However, the molecular and cellular mechanisms underlying the immunomodulatory …
GATA2 is required for lymphatic vessel valve development and maintenance
J Kazenwadel, KL Betterman… - The Journal of …, 2015 - Am Soc Clin Investig
Heterozygous germline mutations in the zinc finger transcription factor GATA2 have recently
been shown to underlie a range of clinical phenotypes, including Emberger syndrome, a …
been shown to underlie a range of clinical phenotypes, including Emberger syndrome, a …
Gata2 is required for HSC generation and survival
E de Pater, P Kaimakis, CS Vink, T Yokomizo… - Journal of Experimental …, 2013 - rupress.org
Knowledge of the key transcription factors that drive hematopoietic stem cell (HSC)
generation is of particular importance for current hematopoietic regenerative approaches …
generation is of particular importance for current hematopoietic regenerative approaches …
Decreased serum selenium levels of COVID-19 patients in comparison with healthy individuals
O Younesian, B Khodabakhshi, N Abdolahi… - Biological trace element …, 2021 - Springer
Abstract Background Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) is
the cause of the COVID-19 pandemic and is the cause of increased mortality, especially …
the cause of the COVID-19 pandemic and is the cause of increased mortality, especially …
GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome
AP Hsu, KD Johnson, EL Falcone… - Blood, The Journal …, 2013 - ashpublications.org
Previous reports of GATA2 mutations have focused on the coding region of the gene or full
gene deletions. We recently identified 2 patients with novel insertion/deletion mutations …
gene deletions. We recently identified 2 patients with novel insertion/deletion mutations …
The GATA2 transcriptional network is requisite for RAS oncogene-driven non-small cell lung cancer
MS Kumar, DC Hancock, M Molina-Arcas, M Steckel… - Cell, 2012 - cell.com
Non-small cell lung cancer (NSCLC) is the most frequent cause of cancer deaths worldwide;
nearly half contain mutations in the receptor tyrosine kinase/RAS pathway. Here we show …
nearly half contain mutations in the receptor tyrosine kinase/RAS pathway. Here we show …