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Journal of Medical Genetics|September 1, 1990
Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunctionS J Charles, A T Moore, J R Yates, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1986
Protein sequencing by tandem mass spectrometryD F Hunt, J R Yates, J Shabanowitz, et al.Journal of Medical Genetics|October 1, 1994
Chimaerism shown by cytogenetics and DNA polymorphism analysisA J Green, D E Barton, P Jenks, et al.Protein Science : a Publication of the Protein Society|April 16, 1998
High throughput protein characterization by automated reverse-phase chromatography/electrospray tandem mass spectrometryA Ducret, I Van Oostveen, J K Eng, et al.Journal of Medical Genetics|December 24, 1998
Mutations in the TSC1 gene account for a minority of patients with tuberous sclerosisJ B Ali, T Sepp, S Ward, et al.Nucleic Acids Research|February 13, 2001
A novel multiple affinity purification tag and its use in identification of proteins associated with a cyclin-CDK complexS Honey, B L Schneider, D M Schieltz, et al.Protein Science : a Publication of the Protein Society|July 1, 1992
Complete enzymatic deglycosylation of native sex steroid-binding protein (SBP or SHBG) of human and rabbit plasma: effect on the steroid-binding activityP H Petra, P R Griffin, J R Yates, et al.Genomics|July 15, 1994
A new human gene (DXS1357E) with ubiquitous expression, located in Xq28 adjacent to the adrenoleukodystrophy geneJ Mosser, C O Sarde, S Vicaire, et al.Immunogenetics|January 1, 1982
Monoclonal antibodies as a tool for phylogenetic studies of major histocompatibility antigens and beta 2-microglobulinJ L Teillaud, D Crevat, P Chardon, et al.Acta Radiologica (Stockholm, Sweden : 1987)|May 1, 1993
Acute electrolyte disturbances in coronary sinus during left coronary arteriography in manK Hayakawa, M Mitsumori, H Uwatoko, et al.Pageof 27