Placental Iodothyronine Deiodinase Expression in Normal and Growth-Restricted Human Pregnancies
Chan, S, Kachilele, S, Hobbs, E, Bulmer, J. N, Boelaert, K, McCabe, C. J, Driver, P. M, Bradwell, A. R, Kester, M, Visser, T. J, Franklyn, J. A, Kilby, M. D
Published in The journal of clinical endocrinology and metabolism (01.09.2003)
Published in The journal of clinical endocrinology and metabolism (01.09.2003)
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A potential role for PTTG/securin in the developing human fetal brain
Boelaert, K, Tannahill, L A, Bulmer, J N, Kachilele, S, Chan, S Y, Kim, D, Gittoes, N J L, Franklyn, J A, Kilby, M D, McCabe, C J
Published in The FASEB journal (01.09.2003)
Published in The FASEB journal (01.09.2003)
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Dysregulation of iodothyronine deiodinase enzyme expression and function in human pituitary tumours
Tannahill, L. A., Visser, T. J., McCabe, C. J., Kachilele, S., Boelaert, K., Sheppard, M. C., Franklyn, J. A., Gittoes, N. J. L.
Published in Clinical endocrinology (Oxford) (01.06.2002)
Published in Clinical endocrinology (Oxford) (01.06.2002)
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Early expression of thyroid hormone deiodinases and receptors in human fetal cerebral cortex
Chan, Shiao, Kachilele, Stivelia, McCabe, Chris J, Tannahill, Lesley A, Boelaert, Kristien, Gittoes, Neil J, Visser, Theo J, Franklyn, Jayne A, Kilby, Mark D
Published in Brain research. Developmental brain research (20.10.2002)
Published in Brain research. Developmental brain research (20.10.2002)
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Dysregulation of iodothyronine deiosinase enzyme expression and function in human pituitary tumours
Tannahill, L S, Visser, T J, McCabe, C J, Kachilele, S
Published in Clinical endocrinology (Oxford) (01.06.2002)
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Published in Clinical endocrinology (Oxford) (01.06.2002)
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Mutations in the human sterol delta7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome
Wassif, C A, Maslen, C, Kachilele-Linjewile, S, Lin, D, Linck, L M, Connor, W E, Steiner, R D, Porter, F D
Published in American journal of human genetics (01.07.1998)
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Published in American journal of human genetics (01.07.1998)
Journal Article
Mutations in the human sterol Δ7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome
WASSIF, C. A, MASLEN, C, KACHILELE-LINJEWILE, S, LIN, D, LINCK, L. M, CONNOR, W. E, STEINER, R. D, PORTER, F. D
Published in American journal of human genetics (01.07.1998)
Published in American journal of human genetics (01.07.1998)
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