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M T Pirro

Showing results (1-10 of 6) with videos related to

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Molecular and Cellular Biology|March 25, 2000
Multiple ras downstream pathways mediate functional repression of the homeobox gene product TTF-1C Missero, M T Pirro, R Di Lauro
The Journal of Biological Chemistry|July 5, 2001
The DNA glycosylase T:G mismatch-specific thymine DNA glycosylase represses thyroid transcription factor-1-activated transcriptionC Missero, M T Pirro, S Simeone, et al.
Thyroid : Official Journal of the American Thyroid Association|December 1, 1995
Thyroperoxidase microsatellite polymorphism in thyroid diseasesM T Pirro, V De Filippis, A Di Cerbo, et al.
Metabolism: Clinical and Experimental|August 1, 1996
Nonfunctioning adenomas of the pituitaryA Liuzzi, V Tassi, M T Pirro, et al.
Journal of Molecular Endocrinology|December 1, 1995
A thyroid hormone receptor beta gene polymorphism associated with Graves' diseaseV Tassi, L Scarnecchia, A Di Cerbo, et al.
Nature Genetics|May 20, 1998
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesisP E Macchia, P Lapi, H Krude, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Molecular and Cellular Biology|March 25, 2000
Multiple ras downstream pathways mediate functional repression of the homeobox gene product TTF-1C Missero, M T Pirro, R Di Lauro
The Journal of Biological Chemistry|July 5, 2001
The DNA glycosylase T:G mismatch-specific thymine DNA glycosylase represses thyroid transcription factor-1-activated transcriptionC Missero, M T Pirro, S Simeone, et al.
Thyroid : Official Journal of the American Thyroid Association|December 1, 1995
Thyroperoxidase microsatellite polymorphism in thyroid diseasesM T Pirro, V De Filippis, A Di Cerbo, et al.
Metabolism: Clinical and Experimental|August 1, 1996
Nonfunctioning adenomas of the pituitaryA Liuzzi, V Tassi, M T Pirro, et al.
Journal of Molecular Endocrinology|December 1, 1995
A thyroid hormone receptor beta gene polymorphism associated with Graves' diseaseV Tassi, L Scarnecchia, A Di Cerbo, et al.
Nature Genetics|May 20, 1998
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesisP E Macchia, P Lapi, H Krude, et al.
Pageof 1