Search Results - "Solomon, Lauren A"

  • Showing 1 - 19 results of 19
Refine Results
  1. 1

    Activation of Th2 cells downregulates CRTh2 through an NFAT1 mediated mechanism by MacLean Scott, Emily, Solomon, Lauren A, Davidson, Courtney, Storie, Jessica, Palikhe, Nami Shrestha, Cameron, Lisa

    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. 2

    PU.1 Regulates Ig Light Chain Transcription and Rearrangement in Pre-B Cells during B Cell Development by Batista, Carolina R, Li, Stephen K H, Xu, Li S, Solomon, Lauren A, DeKoter, Rodney P

    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. 3

    Comparative efficacy of glucocorticoid receptor agonists on Th2 cell function and attenuation by progesterone by Luchak, Alexander, Solomon, Lauren A, Kanagalingam, Tharsan, Vijeyakumaran, Meerah, Rowe, Brian H, Cameron, Lisa

    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. 4

    Genome-wide comparison of PU.1 and Spi-B binding sites in a mouse B lymphoma cell line by Solomon, Lauren A, Li, Stephen K H, Piskorz, Jan, Xu, Li S, DeKoter, Rodney P

    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. 5

    Identification of a negative regulatory role for spi-C in the murine B cell lineage by Li, Stephen K H, Solomon, Lauren A, Fulkerson, Patricia C, DeKoter, Rodney P

    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. 6
  7. 7

    Loss of ATRX in chondrocytes has minimal effects on skeletal development by Solomon, Lauren A, Li, Jennifer R, Bérubé, Nathalie G, Beier, Frank

    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. 8

    Loss of ATRX does not confer susceptibility to osteoarthritis by Solomon, Lauren A, Russell, Bailey A, Makar, David, Bérubé, Nathalie G, Beier, Frank

    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. 9

    Transcriptional regulators of chondrocyte hypertrophy by Solomon, Lauren A., Bérubé, Nathalie G., Beier, Frank

    “…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. 10

    A role for ATP Citrate Lyase in cell cycle regulation during myeloid differentiation by Rhee, Jess, Solomon, Lauren A., DeKoter, Rodney P.

    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. 11

    Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span by Watson, L Ashley, Solomon, Lauren A, Li, Jennifer Ruizhe, Jiang, Yan, Edwards, Matthew, Shin-ya, Kazuo, Beier, Frank, Bérubé, Nathalie G

    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. 12

    Lenalidomide modulates gene expression in human ABC-DLBCL cells by regulating IKAROS interaction with an intronic control region of SPIB by Solomon, Lauren A., Batista, Carolina R., DeKoter, Rodney P.

    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. 13

    Coordination of Myeloid Differentiation with Reduced Cell Cycle Progression by PU.1 Induction of MicroRNAs Targeting Cell Cycle Regulators and Lipid Anabolism by Solomon, Lauren A., Podder, Shreya, He, Jessica, Jackson-Chornenki, Nicholas L., Gibson, Kristen, Ziliotto, Rachel G., Rhee, Jess, DeKoter, Rodney P.

    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. 14

    The effect of maternal protein restriction during perinatal life on the inflammatory response in pediatric rats by Veldhuizen, Ruud A W, Baer, Brandon, McCaig, Lynda A, Solomon, Lauren A, Cameron, Lisa, Hardy, Daniel B

    “…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. 15

    Targeted loss of the ATR-X syndrome protein in the limb mesenchyme of mice causes brachydactyly by Solomon, Lauren A, Russell, Bailey A, Watson, L Ashley, Beier, Frank, Bérubé, Nathalie G

    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. 16

    PU.1 opposes IL-7-dependent proliferation of developing B cells with involvement of the direct target gene bruton tyrosine kinase by Christie, Darah A, Xu, Li S, Turkistany, Shereen A, Solomon, Lauren A, Li, Stephen K H, Yim, Edmund, Welch, Ian, Bell, Gillian I, Hess, David A, DeKoter, Rodney P

    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. 17

    Nfkb1 Activation by the E26 Transformation-Specific Transcription Factors PU.1 and Spi-B Promotes Toll-Like Receptor-Mediated Splenic B Cell Proliferation by Li, Stephen K. H., Abbas, Ali K., Solomon, Lauren A., Groux, Gaëlle M. N., DeKoter, Rodney P.

    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. 18

    Abstract 2098: Genome-wide comparison of PU.1 and Spi-B binding sites in a mouse B lymphoma cell line by Solomon, Lauren A., Li, Stephen K.h., Piskorz, Jan, Xu, Li S., DeKoter, Rodney P.

    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. 19

    The Chromatin Remodeling Protein ATRX in Development and Maintenance of Mouse Skeletal Tissues by Solomon, Lauren A

    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