John Routes
Affiliations: | Microbiology and Molecular Genetics | Medical College of Wisconsin, Milwaukee, WI, United States |
Area:
Immunology, Cell Biology, OncologyGoogle:
"John Routes"
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Publications
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| Tallar M, Routes J. (2020) Omenn Syndrome Identified by Newborn Screening. Clinics in Perinatology. 47: 77-86 |
| Bausch-Jurken MT, Hintermeyer M, Woodliff J, et al. (2019) Damaging BTK Variant Demonstrated by Carrier, Allele-Specific BTK Expression in B Cells and Monocytes. Journal of Clinical Immunology |
| Routes J, Verbsky J. (2018) Newborn Screening for Severe Combined Immunodeficiency. Current Allergy and Asthma Reports. 18: 34 |
| Gallagher J, Adams J, Hintermeyer M, et al. (2016) X-linked Hyper IgM Syndrome Presenting as Pulmonary Alveolar Proteinosis. Journal of Clinical Immunology |
| Korrer MJ, Zhang Y, Routes JM. (2016) Correction: Possible Role of Arginase-1 in Concomitant Tumor Immunity. Plos One. 11: e0153122 |
| Korrer MJ, Routes JM. (2015) Adenovirus serotype 5 E1A expressing tumor cells elicit a tumor-specific CD8+ T cell response independent of NKG2D. Results in Immunology. 5: 1-5 |
| Kwan A, Abraham RS, Currier R, et al. (2014) Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States. Jama. 312: 729-38 |
| Routes J, Abinun M, Al-Herz W, et al. (2014) ICON: the early diagnosis of congenital immunodeficiencies. Journal of Clinical Immunology. 34: 398-424 |
| Korrer MJ, Routes JM. (2014) Possible role of arginase-1 in concomitant tumor immunity. Plos One. 9: e91370 |
| Accetta D, Syverson G, Bonacci B, et al. (2011) Human phagocyte defect caused by a Rac2 mutation detected by means of neonatal screening for T-cell lymphopenia. The Journal of Allergy and Clinical Immunology. 127: 535-538.e1-2 |