Robinson IC - Search Results

1

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

Thomas PQ, 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. Thomas PQ, et al. Among authors: robinson ic. Hum Mol Genet. 2001 Jan 1;10(1):39-45. doi: 10.1093/hmg/10.1.39. Hum Mol Genet. 2001. PMID: 11136712

2

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse.

Dattani MT, Martinez-Barbera JP, Thomas PQ, Brickman JM, Gupta R, Mårtensson IL, Toresson H, Fox M, Wales JK, Hindmarsh PC, Krauss S, Beddington RS, Robinson IC. Dattani MT, et al. Among authors: robinson ic. Nat Genet. 1998 Jun;19(2):125-33. doi: 10.1038/477. Nat Genet. 1998. PMID: 9620767

3

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

Dattani MT, Martinez-Barbera JP, Thomas PQ, Brickman JM, Gupta R, Wales JK, Hindmarsh PC, Beddington RS, Robinson IC. Dattani MT, et al. Among authors: robinson ic. Acta Paediatr Suppl. 1999 Dec;88(433):49-54. doi: 10.1111/j.1651-2227.1999.tb14403.x. Acta Paediatr Suppl. 1999. PMID: 10626545 Review.

4

Molecular genetics of septo-optic dysplasia.

Dattani ML, Martinez-Barbera J, Thomas PQ, Brickman JM, Gupta R, Wales JK, Hindmarsh PC, Beddington RS, Robinson IC. Dattani ML, et al. Among authors: robinson ic. Horm Res. 2000;53 Suppl 1:26-33. doi: 10.1159/000053201. Horm Res. 2000. PMID: 10895039 Review.

5

Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism.

Woods KS, Cundall M, Turton J, Rizotti K, Mehta A, Palmer R, Wong J, Chong WK, Al-Zyoud M, El-Ali M, Otonkoski T, Martinez-Barbera JP, Thomas PQ, Robinson IC, Lovell-Badge R, Woodward KJ, Dattani MT. Woods KS, et al. Among authors: robinson ic. Am J Hum Genet. 2005 May;76(5):833-49. doi: 10.1086/430134. Epub 2005 Mar 30. Am J Hum Genet. 2005. PMID: 15800844 Free PMC article.

6

HESX1 and Septo-Optic Dysplasia.

Dattani MT, Robinson IC. Dattani MT, et al. Among authors: robinson ic. Rev Endocr Metab Disord. 2002 Dec;3(4):289-300. doi: 10.1023/a:1020945406356. Rev Endocr Metab Disord. 2002. PMID: 12424431 Review. No abstract available.

7

The molecular basis for developmental disorders of the pituitary gland in man.

Dattani MT, Robinson IC. Dattani MT, et al. Among authors: robinson ic. Clin Genet. 2000 May;57(5):337-46. doi: 10.1034/j.1399-0004.2000.570503.x. Clin Genet. 2000. PMID: 10852367 Review.

8

Genetic regulation of pituitary gland development in human and mouse.

Kelberman D, Rizzoti K, Lovell-Badge R, Robinson IC, Dattani MT. Kelberman D, et al. Among authors: robinson ic. Endocr Rev. 2009 Dec;30(7):790-829. doi: 10.1210/er.2009-0008. Epub 2009 Oct 16. Endocr Rev. 2009. PMID: 19837867 Free PMC article. Review.

9

SOX3 is required during the formation of the hypothalamo-pituitary axis.

Rizzoti K, Brunelli S, Carmignac D, Thomas PQ, Robinson IC, Lovell-Badge R. Rizzoti K, et al. Among authors: robinson ic. Nat Genet. 2004 Mar;36(3):247-55. doi: 10.1038/ng1309. Epub 2004 Feb 15. Nat Genet. 2004. PMID: 14981518

10

Evolution of gonadotropin deficiency in a patient with type II autosomal dominant GH deficiency.

Turton JP, Buchanan CR, Robinson IC, Aylwin SJ, Dattani MT. Turton JP, et al. Among authors: robinson ic. Eur J Endocrinol. 2006 Dec;155(6):793-9. doi: 10.1530/eje.1.02293. Eur J Endocrinol. 2006. PMID: 17132747

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