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Frontiers in Immunology|October 10, 2017
Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 DeficiencyCarsten Speckmann, Sushree Sangita Sahoo, Marta Rizzi, et al.
Cell Reports|April 15, 2023
AKT activity orchestrates marginal zone B cell development in mice and humansEva-Maria Cox, Mohamed El-Behi, Stefanie Ries, et al.
Frontiers in Immunology|May 17, 2017
Clinical and Molecular Heterogeneity of RTEL1 DeficiencyCarsten Speckmann, Sushree Sangita Sahoo, Marta Rizzi, et al.
Clinical Immunology (Orlando, Fla.)|August 27, 2013
X-linked inhibitor of apoptosis (XIAP) deficiency: the spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosisC Speckmann, K Lehmberg, M H Albert, et al.
American Heart Journal|November 2, 2025
Routine versus selective protamine administration to reduce bleeding after TAVI: Rationale and design of the POPular ACE TAVI trialDaniël C Overduin, Dirk Jan van Ginkel, Christophe Dubois, et al.
The Journal of Allergy and Clinical Immunology|October 4, 2023
Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndromeOlivier Pellé, Solange Moreno, Myriam Ricarda Lorenz, et al.
The Plant Journal : for Cell and Molecular Biology|April 23, 2018
The Physcomitrella patens gene atlas project: large-scale RNA-seq based expression dataPierre-François Perroud, Fabian B Haas, Manuel Hiss, et al.
The Journal of Allergy and Clinical Immunology|December 26, 2025
Somatic STAT5B<sup>N642H</sup> mutations shape variable immune landscapes resulting in heterogenous immune diseasesSarah Grün, Anne Rensing-Ehl, Tobias Suske, et al.
Science Advances|July 1, 2021
Gene-rich UV sex chromosomes harbor conserved regulators of sexual developmentSarah B Carey, Jerry Jenkins, John T Lovell, et al.
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