Strachan T - Search Results

1

Identification of a novel family of human endogenous retroviruses and characterization of one family member, HERV-K(C4), located in the complement C4 gene cluster.

Tassabehji M, Strachan T, Anderson M, Campbell RD, Collier S, Lako M. Tassabehji M, et al. Among authors: strachan t. Nucleic Acids Res. 1994 Dec 11;22(24):5211-7. doi: 10.1093/nar/22.24.5211. Nucleic Acids Res. 1994. PMID: 7816608 Free PMC article.

2

A method for specific amplification and PCR sequencing of individual members of multigene families: application to the study of steroid 21-hydroxylase deficiency.

Collier S, Tassabehji M, Strachan T. Collier S, et al. Among authors: strachan t. PCR Methods Appl. 1992 Feb;1(3):181-6. doi: 10.1101/gr.1.3.181. PCR Methods Appl. 1992. PMID: 1472941 Free article.

3

Characterization of an expressible nonclassical class I HLA gene.

Pook MA, Woodcock V, Tassabehji M, Campbell RD, Summers CW, Taylor M, Strachan T. Pook MA, et al. Among authors: strachan t. Hum Immunol. 1991 Oct;32(2):102-9. doi: 10.1016/0198-8859(91)90106-j. Hum Immunol. 1991. PMID: 1744000

4

Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency.

Sinnott P, Collier S, Costigan C, Dyer PA, Harris R, Strachan T. Sinnott P, et al. Among authors: strachan t. Proc Natl Acad Sci U S A. 1990 Mar;87(6):2107-11. doi: 10.1073/pnas.87.6.2107. Proc Natl Acad Sci U S A. 1990. PMID: 2315306 Free PMC article.

5

Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes.

Collier S, Sinnott PJ, Dyer PA, Price DA, Harris R, Strachan T. Collier S, et al. Among authors: strachan t. EMBO J. 1989 May;8(5):1393-402. doi: 10.1002/j.1460-2075.1989.tb03520.x. EMBO J. 1989. PMID: 2788573 Free PMC article.

6

A de novo pathological point mutation at the 21-hydroxylase locus: implications for gene conversion in the human genome.

Collier S, Tassabehji M, Sinnott P, Strachan T. Collier S, et al. Among authors: strachan t. Nat Genet. 1993 Mar;3(3):260-5. doi: 10.1038/ng0393-260. Nat Genet. 1993. PMID: 8485582

7

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene.

Tassabehji M, Read AP, Newton VE, Harris R, Balling R, Gruss P, Strachan T. Tassabehji M, et al. Among authors: strachan t. Nature. 1992 Feb 13;355(6361):635-6. doi: 10.1038/355635a0. Nature. 1992. PMID: 1347148

8

Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome.

Tassabehji M, Strachan T, Sharland M, Colley A, Donnai D, Harris R, Thakker N. Tassabehji M, et al. Among authors: strachan t. Am J Hum Genet. 1993 Jul;53(1):90-5. Am J Hum Genet. 1993. PMID: 8317503 Free PMC article.

9

Isolation and characterization of WNT8B, a novel human Wnt gene that maps to 10q24.

Lako M, Strachan T, Curtis AR, Lindsay S. Lako M, et al. Among authors: strachan t. Genomics. 1996 Jul 15;35(2):386-8. doi: 10.1006/geno.1996.0374. Genomics. 1996. PMID: 8661156

10

Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lung.

Lako M, Strachan T, Bullen P, Wilson DI, Robson SC, Lindsay S. Lako M, et al. Among authors: strachan t. Gene. 1998 Sep 28;219(1-2):101-10. doi: 10.1016/s0378-1119(98)00393-x. Gene. 1998. PMID: 9757009

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