Search Results - "Lorenz, Myriam R."
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1
Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome
Published in Haematologica (Roma) (01-02-2017)Get full text
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2
Long-term robustness of a T-cell system emerging from somatic rescue of a genetic block in T-cell development
Published in EBioMedicine (01-09-2020)“…The potential of a single progenitor cell to establish and maintain long-term protective T-cell immunity in humans is unknown. For genetic disorders disabling…”
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3
Sequential decisions on FAS sequencing guided by biomarkers in patients with lymphoproliferation and autoimmune cytopenia
Published in Haematologica (Roma) (01-12-2013)“…Clinical and genetic heterogeneity renders confirmation or exclusion of autoimmune lymphoproliferative syndrome difficult. To re-evaluate and improve the…”
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4
Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency
Published in Blood (01-10-2015)“…Omenn syndrome (OS) is a severe immunodeficiency associated with erythroderma, lymphoproliferation, elevated IgE, and hyperactive oligoclonal T cells. A…”
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5
A novel thymoma-associated immunodeficiency with increased naive T cells and reduced CD247 expression
Published in The Journal of immunology (1950) (01-04-2015)“…The mechanisms underlying thymoma-associated immunodeficiency are largely unknown, and the significance of increased blood γδ Τ cells often remains elusive. In…”
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6
CD57 identifies T cells with functional senescence before terminal differentiation and relative telomere shortening in patients with activated PI3 kinase delta syndrome
Published in Immunology and cell biology (01-11-2018)“…Premature T‐cell immunosenescence with CD57+ CD8+ T‐cell accumulation has been linked to immunodeficiency and autoimmunity in primary immunodeficiencies…”
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7
Patients with T+/low NK+ IL‐2 receptor γ chain deficiency have differentially‐impaired cytokine signaling resulting in severe combined immunodeficiency
Published in European journal of immunology (01-10-2014)“…X‐linked severe combined immunodeficiency (X‐SCID) leads to a T−NK−B+ immunophenotype and is caused by mutations in the gene encoding the IL‐2 receptor γ‐chain…”
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8
Cellular Uptake Behavior of Unfunctionalized and Functionalized PBCA Particles Prepared in a Miniemulsion
Published in Macromolecular bioscience (09-07-2007)“…Fluorescent dye labeled unfunctionalized and functionalized poly(n‐butylcyanoacrylate) nanoparticles were prepared using a miniemulsion technique. Amino acid…”
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Synthesis of Fluorescent Polyisoprene Nanoparticles and their Uptake into Various Cells
Published in Macromolecular bioscience (11-08-2008)“…Fluorescent polyisoprene nanoparticles were synthesized by the miniemulsion technique as marker particles for cells. The uptake of the non‐functionalized…”
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10
Autophagy and ATP-induced anti-apoptosis in antigen presenting cells (APC) follows the cytokine storm in patients after major trauma
Published in Journal of cell communication and signaling (01-06-2011)“…Severe trauma and the systemic inflammatory response syndrome (SIRS) occur as a result of a cytokine storm which is in part due to ATP released from damaged…”
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11
CD 57 identifies T cells with functional senescence before terminal differentiation and relative telomere shortening in patients with activated PI 3 kinase delta syndrome
Published in Immunology and cell biology (01-11-2018)“…Premature T‐cell immunosenescence with CD 57 + CD 8 + T‐cell accumulation has been linked to immunodeficiency and autoimmunity in primary immunodeficiencies…”
Get full text
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12
Patients with T super(+/low) NK super(+) IL-2 receptor gamma chain deficiency have differentially-impaired cytokine signaling resulting in severe combined immunodeficiency
Published in European journal of immunology (01-10-2014)“…X-linked severe combined immunodeficiency (X-SCID) leads to a T super(-)NK super(-)B super(+) immunophenotype and is caused by mutations in the gene encoding…”
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13
Patients with T+/low NK+ IL-2 receptor [gamma] chain deficiency have differentially-impaired cytokine signaling resulting in severe combined immunodeficiency
Published in European journal of immunology (01-10-2014)“…X-linked severe combined immunodeficiency (X-SCID) leads to a T-NK-B+ immunophenotype and is caused by mutations in the gene encoding the IL-2 receptor…”
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Journal Article