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Human Immunology|May 13, 1999
Contributions of CD4+, CD8+, and CD4+CD8+ T cells to skewing within the peripheral T cell receptor beta chain repertoire of healthy macaquesJ R Currier, K S Stevenson, P J Kehn, et al.
Genes and Immunity|December 4, 2009
rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotypeA K Steck, E E Baschal, J M Jasinski, et al.
Immunogenetics|January 1, 1985
Localization of C4 genes within the HLA complex by molecular genotypingM A Robinson, M C Carroll, A H Johnson, et al.
Veterinary Journal (London, England : 1997)|June 28, 2015
AICAR administration affects glucose metabolism by upregulating the novel glucose transporter, GLUT8, in equine skeletal muscleM A de Laat, M A Robinson, K J Gruntmeir, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1997
CAND3: a ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 11q23.1X Chen, L Yang, N Udar, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 13, 2016
CAND3: A ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 1lq23.1X Chen, L Yang, N Udar, et al.
Drugs|January 1, 1976
Clinical and haemodynamic effects of minoxidil in refractory hypertensionR Zacest, D B Frewin, M A Robinson, et al.
Journal of Veterinary Pharmacology and Therapeutics|May 29, 2012
Pharmacokinetics of dexamethasone following intra-articular, intravenous, intramuscular, and oral administration in horses and its effects on endogenous hydrocortisoneL R Soma, C E Uboh, Y Liu, et al.
Cell Death & Disease|March 22, 2014
Homozygous mutation of MTPAP causes cellular radiosensitivity and persistent DNA double-strand breaksN T Martin, K Nakamura, U Paila, et al.
American Journal of Human Genetics|June 23, 1998
Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotypeK M Cerosaletti, E Lange, H M Stringham, et al.
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