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The Journal of Clinical Investigation|March 1, 1995
Missense mutation in exon 7 of the common gamma chain gene causes a moderate form of X-linked combined immunodeficiencyF C Schmalstieg, W J Leonard, M Noguchi, et al.Current Oncology (Toronto, Ont.)|June 4, 2020
Treatment of non-small-cell lung cancer after progression on nivolumab or pembrolizumabA T Freeman, M Lesperance, E S Wai, et al.The Journal of Clinical Investigation|November 1, 1990
A novel X-linked combined immunodeficiency diseaseE G Brooks, F C Schmalstieg, D P Wirt, et al.Osteoarthritis and Cartilage|April 28, 2019
Characterization of synovial fluid metabolomic phenotypes of cartilage morphological changes associated with osteoarthritisA K Carlson, R A Rawle, C W Wallace, et al.Molecular and Cellular Biology|July 13, 2000
Mutations in conserved regions of the predicted RAG2 kelch repeats block initiation of V(D)J recombination and result in primary immunodeficienciesC A Gomez, L M Ptaszek, A Villa, et al.Gastroenterology|March 13, 1998
Lymphocytes in the human gastric mucosa during Helicobacter pylori have a T helper cell 1 phenotypeK B Bamford, X Fan, S E Crowe, et al.Blood|January 3, 2001
V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentationsA Villa, C Sobacchi, L D Notarangelo, et al.Pageof 3