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Jonathan Shillingford, Ph.D.Project Scientist Contact Information
Phone: (805) 893-4725
Molecular, Cellular, and Developmental Biology |
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Area of general research interest:Function of polycystin-1, the polycystic kidney disease gene product. Professional education and positions held:
Awards and Fellowships
Memberships in professional societiesScience Advisory Board member PublicationsShillingford JM, Murcia NS, Larson CH, Low SH, Hedgepeth R, Brown N,
Flask CA, Novick AC, Goldfarb DA, Kramer-Zucker A, Walz G, Piontek KB,
Germino GG, Weimbs T (2006) Cases, S., Zhou, P., Shillingford, J.M., Wiseman, B.S., Fish, J.D., Angle, C.S., Hennighausen, L., Werb, Z. and Farese, Jr., R.V. (2004). Development of the mammary gland requires DGAT1 expression in stromal and epithelial tissues. Development. Accepted. Long, W., Wagner, K.U., Lloyd, K.C.K., Binart, N., Shillingford, J.M., Hennighausen, L. and Jones, F. (2003). Conditional deletion of Erbb4 in the mammary gland identifies ErbB4 as an obligate mediator of Stat5 activation and epithelial functional differentiation. Development, 130, 5257-5268. Bierie, B., Nozawa, M., Renou, J.-P., Shillingford, J.M., Morgan, F., Oka, T., Taketo, M.M., Cardiff, R.D., Miyoshi, K., Wagner, K-U., Robinson, G.W. and Hennighausen, L. (2003). Activation of beta-catenin in prostate epithelium induces hyperplasias and squamous transdifferentiation. Oncogene 22:3875-3877. Shillingford, J.M., Miyoshi, K., Robinson, G.W., Bierie, B., Cao, Y., Karin, M. and Hennighausen, L.(2003). Proteotyping of mammary tissue from transgenic and gene knockout mice with immunohistochemical markers. A tool to define developmental lesions. J. Histochem. Cytochem. 51:555-565. Shillingford, J.M., Miyoshi, K., Flagella, M., Shull, G.E. and Hennighausen, L. (2002). Mouse mammary epithelial cells express the Na-K-Cl cotransporter, NKCC1: characterization, localization, and involvement in ductal development and morphogenesis. Mol. Endocrinol. 16:1309-1321. Shillingford, J.M., Miyoshi, K., Robinson, G.W., Grimm, S.L., Rosen, J.M., Neubauer, H., Pfeffer, K. and Hennighausen, L. (2002). Jak2 is an essential tyrosine kinase involved in pregnancy-mediated development of mammary secretory epithelium. Mol. Endocrinol. 16:563-570. Miyoshi, K., Shillingford, J.M., Le Provost, F., Gounari, F., Bronson, R., von Boehmer, H., Taketo, M.M., Cardiff, R.D., Hennighausen, L. and Khazaie, K. (2002). Activation of beta-catenin signaling in differentiated mammary secretory cells induces transdifferentiation into epidermis and squamous metaplasias. Proc. Natl. Acad. Sci. 99:219-224. Walton, K.D., Wagner, K.U., Rucker, E.B. 3rd, Shillingford, J.M., Miyoshi, K. and Hennighausen, L. (2001). Conditional deletion of the bcl-x gene from mouse mammary epithelium results in accelerated apoptosis during involution but does not compromise cell function during lactation. Mech. Dev. 109:281-293. Miyoshi, K., Shillingford, J.M., Smith, G.H., Grimm, S.L., Wagner, K.U., Oka, T., Rosen, J.M., Robinson, G.W. and Hennighausen, L. (2001). Signal transducer and activator of transcription (Stat) 5 controls the proliferation and differentiation of mammary alveolar epithelium. J. Cell. Biol. 155:531-542. Shillingford, J.M. and Hennighausen, L. (2001). Experimental mouse genetics -- answering fundamental questions about mammary gland biology. Trends Endocrinol. Metab. 12:402-408. Review. |
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