Strachan T - Search Results

1

Localisation of a gene for Darier's disease.

Bashir R, Munro CS, Mason S, Stephenson A, Rees JL, Strachan T. Bashir R, et al. Among authors: strachan t. Hum Mol Genet. 1993 Nov;2(11):1937-9. doi: 10.1093/hmg/2.11.1937. Hum Mol Genet. 1993. PMID: 7506604 No abstract available.

2

Hailey-Hailey disease: molecular and clinical characterization of novel mutations in the ATP2C1 gene.

Dobson-Stone C, Fairclough R, Dunne E, Brown J, Dissanayake M, Munro CS, Strachan T, Burge S, Sudbrak R, Monaco AP, Hovnanian A. Dobson-Stone C, et al. Among authors: strachan t. J Invest Dermatol. 2002 Feb;118(2):338-43. doi: 10.1046/j.0022-202x.2001.01675.x. J Invest Dermatol. 2002. PMID: 11841554

3

A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3.

Tonkin ET, Smith M, Eichhorn P, Jones S, Imamwerdi B, Lindsay S, Jackson M, Wang TJ, Ireland M, Burn J, Krantz ID, Carr P, Strachan T. Tonkin ET, et al. Among authors: strachan t. Hum Genet. 2004 Jul;115(2):139-48. doi: 10.1007/s00439-004-1134-6. Epub 2004 May 27. Hum Genet. 2004. PMID: 15168106 Free PMC article.

4

Expression analyses and interaction with the anaphase promoting complex protein Apc2 suggest a role for inversin in primary cilia and involvement in the cell cycle.

Morgan D, Eley L, Sayer J, Strachan T, Yates LM, Craighead AS, Goodship JA. Morgan D, et al. Among authors: strachan t. Hum Mol Genet. 2002 Dec 15;11(26):3345-50. doi: 10.1093/hmg/11.26.3345. Hum Mol Genet. 2002. PMID: 12471060

5

Identification and characterisation of novel mammalian homologues of Drosophila polyhomeoticpermits new insights into relationships between members of the polyhomeotic family.

Tonkin E, Hagan DM, Li W, Strachan T. Tonkin E, et al. Among authors: strachan t. Hum Genet. 2002 Oct;111(4-5):435-42. doi: 10.1007/s00439-002-0814-3. Epub 2002 Aug 21. Hum Genet. 2002. PMID: 12384788

6

The left-right determinant inversin has highly conserved ankyrin repeat and IQ domains and interacts with calmodulin.

Morgan D, Goodship J, Essner JJ, Vogan KJ, Turnpenny L, Yost HJ, Tabin CJ, Strachan T. Morgan D, et al. Among authors: strachan t. Hum Genet. 2002 Apr;110(4):377-84. doi: 10.1007/s00439-002-0696-4. Epub 2002 Mar 2. Hum Genet. 2002. PMID: 11941489

7

Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.

Braybrook C, Lisgo S, Doudney K, Henderson D, Marçano AC, Strachan T, Patton MA, Villard L, Moore GE, Stanier P, Lindsay S. Braybrook C, et al. Among authors: strachan t. Hum Mol Genet. 2002 Oct 15;11(22):2793-804. doi: 10.1093/hmg/11.22.2793. Hum Mol Genet. 2002. PMID: 12374769

8

Cornelia de Lange Syndrome and the link between chromosomal function, DNA repair and developmental gene regulation.

Strachan T. Strachan T. Curr Opin Genet Dev. 2005 Jun;15(3):258-64. doi: 10.1016/j.gde.2005.04.005. Curr Opin Genet Dev. 2005. PMID: 15917200 Review.

9

Breakpoint position on 17q identifies the most aggressive neuroblastoma tumors.

Łastowska M, Cotterill S, Bown N, Cullinane C, Variend S, Lunec J, Strachan T, Pearson AD, Jackson MS. Łastowska M, et al. Among authors: strachan t. Genes Chromosomes Cancer. 2002 Aug;34(4):428-36. doi: 10.1002/gcc.10089. Genes Chromosomes Cancer. 2002. PMID: 12112532

10

NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome.

Tonkin ET, Wang TJ, Lisgo S, Bamshad MJ, Strachan T. Tonkin ET, et al. Among authors: strachan t. Nat Genet. 2004 Jun;36(6):636-41. doi: 10.1038/ng1363. Epub 2004 May 16. Nat Genet. 2004. PMID: 15146185

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