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Journal of Immunological Methods|October 4, 1988
Characterization of a method using viable human target cells as the solid phase in a cell concentration fluorescence immunoassay (CCFIA) for screening of monoclonal antibodies and hybridoma supernatantsB Avner, B P Avner, B Gaydos, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 12, 1999
Physical mapping of the autoimmune disease susceptibility locus, Bphs: co-localization with a cluster of genes from the TNF receptor superfamily on mouse chromosome 6N D Meeker, A N Stafford, J K Lunceford, et al.
Genomics|June 22, 2000
Sequence-ready BAC contig, physical, and transcriptional map of a 2-Mb region overlapping the mouse chromosome 6 host-resistance locus Cmv1C Depatie, S H Lee, A Stafford, et al.
Cancer Immunology, Immunotherapy : CII|January 1, 1989
Immunohistochemical phenotyping of human solid tumors with monoclonal antibodies in devising biotherapeutic strategiesS K Liao, C Meranda, B P Avner, et al.
Genome Research|July 21, 1999
Linkage disequilibrium and physical mapping of Pas1 in miceG Manenti, A Stafford, L De Gregorio, et al.
Cytogenetic and Genome Research|April 1, 2006
A SAGE approach to identifying novel trans-acting factors involved in the X inactivation processA Bourdet, C Ciaudo, L Zakin, et al.
Genomics|April 1, 1988
Conservation and reorganization of loci on the mammalian X chromosome: a molecular framework for the identification of homologous subchromosomal regions in man and mouseL C Amar, L Dandolo, A Hanauer, et al.
Journal of Neuroscience Research|March 4, 2000
Functional properties, developmental regulation, and chromosomal localization of murine connexin36, a gap-junctional protein expressed preferentially in retina and brainM R Al-Ubaidi, T W White, H Ripps, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1990
Minisatellite linkage maps in the mouse by cross-hybridization with human probes containing tandem repeatsC Julier, B de Gouyon, M Georges, et al.
Clinical Genetics|September 29, 2009
Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression burstsF Molinari, A Kaminska, G Fiermonte, et al.
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