Molecular effects of novel mutations in Hesx1/HESX1 associated with human pituitary disorders.

Autor: Brickman, J M, Clements, M, Tyrell, R, McNay, D, Woods, K, Warner, J, Stewart, A, Beddington, R S, Dattani, M

Publikováno v: Development; December 2001, Vol. 128 Issue: 24 p5189-99, 11p

Interactions of a Rel protein with its inhibitor.

Autor: Lehming, N, McGuire, S, Brickman, J M, Ptashne, M

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America; October 1995, Vol. 92 Issue: 22 p10242-10246, 5p

HESX1: A novel gene implicated in a familial form of septo-optic dysplasia

Autor: Dattani, M. T., Juan Pedro Martinez-Barbera, Thomas, P. Q., Brickman, J. M., Gupta, R., Wales, J. K. H., Hindmarsh, P. C., Beddington, R. S. P., Robinson, I. C. A. F.

Publikováno v: Scopus-Elsevier

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Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia.

Autor: Thomas PQ; Gene Discovery Unit, The Murdoch Children's Research Institute, Royal Children's Hospital, Flemington Road, Parkville, Melbourne, Vic. 3052, Australia. thomasp@cryptic.rch.unimelb.edu.au, Dattani MT, Brickman JM, McNay D, Warne G, Zacharin M, Cameron F, Hurst J, Woods K, Dunger D, Stanhope R, Forrest S, Robinson IC, Beddington RS

Publikováno v: Human molecular genetics [Hum Mol Genet] 2001 Jan 01; Vol. 10 (1), pp. 39-45.