In: Personal and Ubiquitous Computing, 2015, vol. 19, no. 2, p. 335-353
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In: Cell Stress and Chaperones, 2015, vol. 20, no. 2, p. 391-395
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In: Biomedical Microdevices, 2015, vol. 17, no. 5, p. 1-9
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In: Seminars in Immunopathology, 2015, vol. 37, no. 5, p. 519-528
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In: Bulletin of Earthquake Engineering, 2015, vol. 13, no. 12, p. 3553-3596
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In: Clinical Oral Investigations, 2015, vol. 19, no. 2, p. 385-399
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In: Journal of Inherited Metabolic Disease, 2015, vol. 38, no. 5, p. 957-967
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In: International Journal of Molecular Sciences, 2020, vol. 21, no. 21, p. 8403
Androgen insensitivity syndrome (AIS), manifesting incomplete virilization in 46,XY individuals, is caused mostly by androgen receptor (AR) gene mutations. Therefore, a search for AR mutations is a routine approach in AIS diagnosis. However, some AIS patients lack AR mutations, which complicates the diagnosis. Here, we describe a patient suffering from partial androgen insensitivity syndrome...
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In: Frontiers in Bioengineering and Biotechnology, 2020, vol. 8, p. -
A large number of prevalent lung diseases is associated with tissue inflammation. Clinically, corticosteroid therapies are applied systemically or via inhalation for the treatment of lung inflammation, and a number of novel therapies are being developed that require preclinical testing. In alveoli, macrophages and dendritic cells play a key role in initiating and diminishing pro-inflammatory...
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In: Nature communications, 2017, vol. 8, p. 1600
We have previously reported the molecular signature of murine pathogenic TH17 cells that induce experimental autoimmune encephalomyelitis (EAE) in animals. Here we show that human peripheral blood IFN-γ+IL-17+ (TH1/17) and IFN-γ−IL-17+ (TH17) CD4+ T cells display distinct transcriptional profiles in high-throughput transcription analyses. Compared to TH17 cells, TH1/17 cells have gene...
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