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Ingrid Müller-Fleckenstein

Researcher at University of Erlangen-Nuremberg

Publications -  27
Citations -  2416

Ingrid Müller-Fleckenstein is an academic researcher from University of Erlangen-Nuremberg. The author has contributed to research in topics: T cell & Gammaherpesvirinae. The author has an hindex of 20, co-authored 27 publications receiving 2201 citations. Previous affiliations of Ingrid Müller-Fleckenstein include Harvard University.

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Transformation to continuous growth of primary human T lymphocytes by human T-cell leukemia virus type I X-region genes transduced by a herpesvirus saimiri vector

TL;DR: These experiments demonstrate that the X region encodes the functions of HTLV-I that immortalize a distinct subpopulation of human T cells and demonstrate the utility of the H. saimiri vector for the transduction of heterologous genes intohuman T cells.
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Revisiting Human IL-12Rβ1 Deficiency: A Survey of 141 Patients From 30 Countries

Ludovic de Beaucoudrey, +127 more
- 01 Nov 2010 - 
TL;DR: An international survey of 141 patients from 102 kindreds in 30 countries found that IL-12R&bgr;1 deficiency has higher clinical penetrance, broader susceptibility to infections, and less favorable outcome than previously thought.
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Stable growth transformation of human T lymphocytes by herpesvirus saimiri.

TL;DR: It is reported that infection of human blood lymphocytes and thymocytes with strains of subgroup C, in contrast to viruses of the other subgroups, yields continuously proliferating T-cell lines with the phenotype of mature CD4- or CD8-positive cells.
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Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

Alexandra Y. Kreins, +70 more
TL;DR: The identification and immunological characterization of a group of TYK2-deficient patients is reported and they are described as having at least some of the hallmarks of central giant cell apoptosis.
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Atypical X-Linked Severe Combined Immunodeficiency Due to Possible Spontaneous Reversion of the Genetic Defect in T Cells

TL;DR: X-linked severe combined immunodeficiency is a recessive hereditary disease characterized by severe and persistent infections starting in the first months of life and associated with diarrhea and failure to thrive.