D. Smith

发表

A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC.

B. Ponder, M. Zvelebil, C. Healey, 1995, Oncogene.

RET activation by germline MEN2A and MEN2B mutations.

M. Borrello, C. Eng, M. Pierotti, 1995, Oncogene.

First continuous human pheochromocytoma cell line: KNA Biological, cytogenetic and molecular characterization of KNA cells

B. Ponder, T. Henn, B. Niederle, 1998, Journal of neurocytology.

Multiple mRNA isoforms of the human RET proto-oncogene generated by alternate splicing.

B. Ponder, C. Healey, L. Mulligan, 1995, Oncogene.

LIP1, a cytoplasmic protein functionally linked to the Peutz-Jeghers syndrome kinase LKB1.

A. Ashworth, J. Spicer, S. Rayter, 2001, Human molecular genetics.

Apparent Opitz BBBG syndrome with a partial duplication of 5p.

W. T. Bass, A. Brothman, L. Leichtman, 1991, American journal of medical genetics.

The mouse Peutz-Jeghers syndrome gene Lkb1 encodes a nuclear protein kinase.

A. Ashworth, J. Spicer, S. Swift, 1999, Human molecular genetics.

Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.

C. Healey, L. Mulligan, C. Eng, 1994, Human molecular genetics.

Expression of multiple endocrine neoplasia 2B RET in neuroblastoma cells alters cell adhesion in vitro, enhances metastatic behavior in vivo, and activates Jun kinase.

B. Ponder, J. Hancock, A. Peaston, 1997, Cancer research.

The MEN II syndromes and the role of the ret proto-oncogene.

B. Ponder, Darrin P. Smith, D. Smith, 1996, Advances in cancer research.

LETTERS TO THE EDITOR Detection of a familial cryptic translocation by fluorescent in situ hybridisation

B. Say, D. Smith, M. Floyd, 2004 .