Search Results - "Solomon, Lauren A"
-
1
Activation of Th2 cells downregulates CRTh2 through an NFAT1 mediated mechanism
Published in PloS one (03-07-2018)“…CRTh2 (encoded by PTGDR2) is a G-protein coupled receptor expressed by Th2 cells as well as eosinophils, basophils and innate lymphoid cells (ILC)2s…”
Get full text
Journal Article -
2
PU.1 Regulates Ig Light Chain Transcription and Rearrangement in Pre-B Cells during B Cell Development
Published in The Journal of immunology (1950) (15-02-2017)“…B cell development and Ig rearrangement are governed by cell type- and developmental stage-specific transcription factors. PU.1 and Spi-B are…”
Get full text
Journal Article -
3
Comparative efficacy of glucocorticoid receptor agonists on Th2 cell function and attenuation by progesterone
Published in BMC immunology (19-10-2020)“…Abstract Background Corticosteroids (CS)s suppress cytokine production and induce apoptosis of inflammatory cells. Prednisone and dexamethasone are oral CSs…”
Get full text
Journal Article -
4
Genome-wide comparison of PU.1 and Spi-B binding sites in a mouse B lymphoma cell line
Published in BMC genomics (14-02-2015)“…Spi-B and PU.1 are highly related members of the E26-transformation-specific (ETS) family of transcription factors that have similar, but not identical, roles…”
Get full text
Journal Article -
5
Identification of a negative regulatory role for spi-C in the murine B cell lineage
Published in The Journal of immunology (1950) (15-04-2015)“…Spi-C is an E26 transformation-specific family transcription factor that is highly related to PU.1 and Spi-B. Spi-C is expressed in developing B cells, but its…”
Get full text
Journal Article -
6
Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span
Published in The Journal of clinical investigation (01-05-2013)Get full text
Journal Article -
7
Loss of ATRX in chondrocytes has minimal effects on skeletal development
Published in PloS one (23-09-2009)“…Mutations in the human ATRX gene cause developmental defects, including skeletal deformities and dwarfism. ATRX encodes a chromatin remodeling protein, however…”
Get full text
Journal Article -
8
Loss of ATRX does not confer susceptibility to osteoarthritis
Published in PloS one (30-12-2013)“…The chromatin remodelling protein ATRX is associated with the rare genetic disorder ATR-X syndrome. This syndrome includes developmental delay, cognitive…”
Get full text
Journal Article -
9
Transcriptional regulators of chondrocyte hypertrophy
Published in Birth defects research. Part C. Embryo today (01-06-2008)“…Coordinated transition from proliferation to terminal differentiation and hypertrophy of growth plate chondrocytes is required for normal growth of…”
Get full text
Journal Article -
10
A role for ATP Citrate Lyase in cell cycle regulation during myeloid differentiation
Published in Blood cells, molecules, & diseases (01-05-2019)“…Differentiation of myeloid progenitor cells into macrophages is accompanied by increased PU.1 concentration and increasing cell cycle length, culminating in…”
Get full text
Journal Article -
11
Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span
Published in The Journal of clinical investigation (01-05-2013)“…Human ATRX mutations are associated with cognitive deficits, developmental abnormalities, and cancer. We show that the Atrx-null embryonic mouse brain…”
Get full text
Journal Article -
12
Lenalidomide modulates gene expression in human ABC-DLBCL cells by regulating IKAROS interaction with an intronic control region of SPIB
Published in Experimental hematology (01-12-2017)“…•Lenalidomide's mechanism of action in activated B-cell diffuse large B-cell lymphoma (ABC-DLBCL) is not understood.•SPIB is transcriptionally downregulated by…”
Get full text
Journal Article -
13
Coordination of Myeloid Differentiation with Reduced Cell Cycle Progression by PU.1 Induction of MicroRNAs Targeting Cell Cycle Regulators and Lipid Anabolism
Published in Molecular and cellular biology (01-05-2017)“…During macrophage development, myeloid progenitor cells undergo terminal differentiation coordinated with reduced cell cycle progression. Differentiation of…”
Get full text
Journal Article -
14
The effect of maternal protein restriction during perinatal life on the inflammatory response in pediatric rats
Published in Canadian journal of physiology and pharmacology (01-05-2021)“…Fetal growth restriction can affect health outcomes in postnatal life. This study tested the hypothesis that the response to an inflammatory pulmonary insult…”
Get more information
Journal Article -
15
Targeted loss of the ATR-X syndrome protein in the limb mesenchyme of mice causes brachydactyly
Published in Human molecular genetics (15-12-2013)“…ATR-X syndrome is a rare genetic disorder caused by mutations in the ATRX gene. Affected individuals are cognitively impaired and display a variety of…”
Get full text
Journal Article -
16
PU.1 opposes IL-7-dependent proliferation of developing B cells with involvement of the direct target gene bruton tyrosine kinase
Published in The Journal of immunology (1950) (15-01-2015)“…Deletion of genes encoding the E26 transformation-specific transcription factors PU.1 and Spi-B in B cells (CD19-CreΔPB mice) leads to impaired B cell…”
Get full text
Journal Article -
17
Nfkb1 Activation by the E26 Transformation-Specific Transcription Factors PU.1 and Spi-B Promotes Toll-Like Receptor-Mediated Splenic B Cell Proliferation
Published in Molecular and cellular biology (01-05-2015)“…Generation of antibodies against T-independent and T-dependent antigens requires Toll-like receptor (TLR) engagement on B cells for efficient responses…”
Get full text
Journal Article -
18
Abstract 2098: Genome-wide comparison of PU.1 and Spi-B binding sites in a mouse B lymphoma cell line
Published in Cancer research (Chicago, Ill.) (01-08-2015)“…Abstract Background. The E26-transformation-specific (ETS) transcription factor Spi-B is required for the survival of Activated B Cell-type Diffuse Large B…”
Get full text
Journal Article -
19
The Chromatin Remodeling Protein ATRX in Development and Maintenance of Mouse Skeletal Tissues
Published 01-01-2013“…Alpha-thalassemia X-linked mental retardation (ATR-X) syndrome is a rare genetic disorder associated with severe developmental delay, mental retardation and…”
Get full text
Dissertation