References
- Cox D. R., Burmeister M., Price E. R., Kim S., Myers R. M. Radiation hybrid mapping: a somatic cell genetic method for constructing high resolution maps of mammalian chromosomes. Science 1990; 250: 245–250, Stanford Human Genome Center: http://shgc-www.stan-ford.edu/
- Goto S., Nagahiro S., Ushio Y., Hirano A. Calcineurin, a calcium / calmodulin-regulated protein phosphatase, in mammalian neuroendocrine cells and neoplasms. Neurosci. Lett 1992; 143: 51–54
- Guerini D., Krinks M. H., Sikela J. M., Hahn W. E., Klee C. B. Isolation and sequence of a cDNA clone for human calcineurin B, the Ca2+-binding subunit of the Ca2+/calmodulin-stimulated protein phosphatase. DNA 1989; 8: 675–682
- Hurley D. M., Accili D., Stratakis C. A., Karl M., Vamvakopoulos N., Rorer E., Constantine K., Taylor S. I., Chrousos G. P. Point mutation causing a single amino acid substitution in the hormone binding domain of the glucocorticoid receptor in familial glucocorticoid resistance. J. Clin. Invest. 1991; 87: 680–686
- Kirschner L. S., Taymans S., Vottero A., Lin J.-P., Stratakis C. A. Genetic and radiation hybrid map of the Carney complex (CNC) locus; construction of a yeast artificial chromosome (YAC)-based physical map. Washington, DC 1997, Biomedicine -97, 1997
- Klee C. B., Draetta G., Hubbard M. Calcineurin (review). Adv. Enzymol. Relat. Areas Mol Biol 1987; 61: 149–200
- Lin M. J., Parsia S. S., Papolos D. F., Lachman H. M. Highly polymorphic sequence variation in calcineurin B coding region (PPP3R1). Hum. Mol. Genet 1994; 3: 520
- Mukai H., Chang C. D., Tanaka H., Ito A., Kuno T., Tanaka C. cDNA cloning of a novel testis-specific calcineurin B-like protein. Biochem. Biophys. Res. Commun 1991; 188: 265–271
- Sanger F., Nicklen S., Couson A. R. DNA sequencing with chainterminating inhibitors. Proc. Natl. Acad. Sci. USA 1977; 74: 5463–5467
- Spurr N. K., Bashir R., Bushby K., Cox S., Cox A., Hildebrandt F., Hill N., Kao F.-T., Krois L., Marzella R., Miller N., Nothwang H. G., Rocchi M., Sarfarazi M., Stratakis C. A., Wallgren-Petterson C., Naylor S. Report of the fourth international workshop on human chromosome 2 mapping. Cytogenet. Cell Genet 1996; 73: 255–273
- Stratakis C. A., Carney J. A., Lin J.-P., Papanicolaou D. P., Karl M., Kastner D. L., Pras E., Chrousos G. P. Carney complex, a familial multiple neoplasia and lentiginosis syndrome: Analysis of 11 kindreds and linkage to the short arm of chromosome 2. J. Clin. Invest 1996; 97: 599–607
- Stratakis C. A., Jenkins R. B., Pras E., Mitsiades C. S., Raff S., Stalboerger P. G., Tsigos C., Carney J. A., Chrousos G. P. Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex). J. Clin. Endocrinol. Metab 1996; 81: 3607–3614
- Stratakis C. A., Orban Z., Burns A. L., Vottero A., Mitsiades C. S., Marx S. J., Abbassi V., Chrousos G. P. Dideoxyfingerprinring (ddF) analysis of the type X collagen gene (COL10A1) and identification of a novel mutation (S671P) in a kindred with Schmid metaphyseal chondrodysplasia. Biochem. Mol. Med 1996; 59: 112–117
- Wang M. G., Yi H., Guerini D., Klee C. B., McBride O. W. Calcineurin A alpha (PPP3CA), calcineurin A beta (PPP3CB) and calcineurin B (PPP3R1) are located on human chromosomes 4, 10q21-q22 and 2pl6-pl5 respectively. Cytogenet. Cell Genet 1996; 72: 236–241