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Annals of the Rheumatic Diseases|August 7, 2021
Humoral and T-cell responses to SARS-CoV-2 vaccination in patients receiving immunosuppressionMaria Prendecki, Candice Clarke, Helena Edwards, et al.Plos One|April 26, 2016
A Recurrent Germline Mutation in the 5'UTR of the Androgen Receptor Causes Complete Androgen Insensitivity by Activating Aberrant uORF TranslationNadine C Hornig, Carine de Beaufort, Friederike Denzer, et al.The Journal of Clinical Endocrinology and Metabolism|June 11, 2019
Reduced Androgen Receptor Expression in Genital Skin Fibroblasts From Patients With 45,X/46,XY MosaicismNadine C Hornig, Jeta Demiri, Pascal Rodens, et al.Journal of Cell Science|July 30, 2024
Reprogramming macrophages with R848-loaded artificial protocells to modulate skin and skeletal wound healingPaco López-Cuevas, Tiah C L Oates, Qiao Tong, et al.Frontiers in Cell and Developmental Biology|August 12, 2021
The Action of Reproductive Fluids and Contained Steroids, Prostaglandins, and Zn2+ on CatSper Ca2+ Channels in Human SpermJanice K Jeschke, Cristina Biagioni, Tobias Schierling, et al.Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|April 4, 2025
Diagnosis and treatment of radiation induced pneumonitis in patients with lung cancer: An ESTRO clinical practice guidelineDirk De Ruysscher, Els Wauters, Verena Jendrossek, et al.Blood|April 4, 2002
A humanized non-FcR-binding anti-CD3 antibody, visilizumab, for treatment of steroid-refractory acute graft-versus-host diseasePaul A Carpenter, Frederick R Appelbaum, Lawrence Corey, et al.The Lancet. Diabetes & Endocrinology|August 5, 2018
Oestrogen versus androgen in hormone-replacement therapy for complete androgen insensitivity syndrome: a multicentre, randomised, double-dummy, double-blind crossover trialWiebke Birnbaum, Louise Marshall, Ralf Werner, et al.Neuroendocrinology|January 16, 2023
A Prospective Analysis of the Metyrapone Short Test Using Targeted and Untargeted MetabolomicsAnna Katharina Seoudy, Kristina Schlicht, Alexandra Kulle, et al.European Journal of Endocrinology|February 19, 2013
Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1Maik Welzel, Leyla Akin, Anja Büscher, et al.Pageof 85