Search Results - "Kachilele, S."

Placental Iodothyronine Deiodinase Expression in Normal and Growth-Restricted Human Pregnancies by 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.

“…We have described the expression of specific iodothyronine deiodinase mRNAs (using quantitative RT-PCR) and activities in normal human placentas throughout…”
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A potential role for PTTG/securin in the developing human fetal brain by 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.

“…ABSTRACT Human securin, known also as PTTG, has established oncogenic and cell cycle regulatory functions. PTTG/securin transforms cells in vitro, inhibits…”
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Dysregulation of iodothyronine deiodinase enzyme expression and function in human pituitary tumours by Tannahill, L. A., Visser, T. J., McCabe, C. J., Kachilele, S., Boelaert, K., Sheppard, M. C., Franklyn, J. A., Gittoes, N. J. L.

“…Summary objective Thyroid hormones (THs) perform essential roles in pituitary function. They regulate anterior pituitary hormone secretion and are also key…”
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Effects of temporary cooling, and of different explantation and storage conditions, on the subsequent development of post-implantation rat embryos in vitro by Kachilele, S G, New, D A

“…Rat embryos explanted at head fold stage were stored under various levels of hypothermia prior to culture. The storage media were Hanks' Balanced Salt Solution…”
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Early expression of thyroid hormone deiodinases and receptors in human fetal cerebral cortex by Chan, Shiao, Kachilele, Stivelia, McCabe, Chris J, Tannahill, Lesley A, Boelaert, Kristien, Gittoes, Neil J, Visser, Theo J, Franklyn, Jayne A, Kilby, Mark D

“…Thyroid hormones are known to be important for optimal development of the human central nervous system. Classically, maternal thyroid hormones have not been…”
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Dysregulation of iodothyronine deiosinase enzyme expression and function in human pituitary tumours by Tannahill, L S, Visser, T J, McCabe, C J, Kachilele, S

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Mutations in the human sterol delta7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome by Wassif, C A, Maslen, C, Kachilele-Linjewile, S, Lin, D, Linck, L M, Connor, W E, Steiner, R D, Porter, F D

“…The Smith-Lemli-Opitz syndrome (SLOS; also known as "RSH syndrome" [MIM 270400]) is an autosomal recessive multiple malformation syndrome due to a defect in…”
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Mutations in the human sterol Δ7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome by WASSIF, C. A, MASLEN, C, KACHILELE-LINJEWILE, S, LIN, D, LINCK, L. M, CONNOR, W. E, STEINER, R. D, PORTER, F. D

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