Imrie H - Search Results

1

Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease.

Vaidya B, Imrie H, Geatch DR, Perros P, Ball SG, Baylis PH, Carr D, Hurel SJ, James RA, Kelly WF, Kemp EH, Young ET, Weetman AP, Kendall-Taylor P, Pearce SH. Vaidya B, et al. Among authors: imrie h. J Clin Endocrinol Metab. 2000 Feb;85(2):688-91. doi: 10.1210/jcem.85.2.6369. J Clin Endocrinol Metab. 2000. PMID: 10690877

2

Mutational analysis of the thyrotropin receptor gene in sporadic and familial feline thyrotoxicosis.

Pearce SH, Foster DJ, Imrie H, Myerscough N, Beckett GJ, Thoday KL, Kendall-Taylor P. Pearce SH, et al. Among authors: imrie h. Thyroid. 1997 Dec;7(6):923-7. doi: 10.1089/thy.1997.7.923. Thyroid. 1997. PMID: 9459639

3

A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1.

Pearce SH, Cheetham T, Imrie H, Vaidya B, Barnes ND, Bilous RW, Carr D, Meeran K, Shaw NJ, Smith CS, Toft AD, Williams G, Kendall-Taylor P. Pearce SH, et al. Among authors: imrie h. Am J Hum Genet. 1998 Dec;63(6):1675-84. doi: 10.1086/302145. Am J Hum Genet. 1998. PMID: 9837820 Free PMC article.

4

A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients.

Kemp EH, Ajjan RA, Husebye ES, Peterson P, Uibo R, Imrie H, Pearce SH, Watson PF, Weetman AP. Kemp EH, et al. Among authors: imrie h. Clin Endocrinol (Oxf). 1998 Nov;49(5):609-13. doi: 10.1046/j.1365-2265.1998.00579.x. Clin Endocrinol (Oxf). 1998. PMID: 10197076

5

The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus.

Vaidya B, Imrie H, Perros P, Young ET, Kelly WF, Carr D, Large DM, Toft AD, McCarthy MI, Kendall-Taylor P, Pearce SH. Vaidya B, et al. Among authors: imrie h. Hum Mol Genet. 1999 Jul;8(7):1195-9. doi: 10.1093/hmg/8.7.1195. Hum Mol Genet. 1999. PMID: 10369864

6

Cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism confers susceptibility to thyroid associated orbitopathy.

Vaidya B, Imrie H, Perros P, Dickinson J, McCarthy MI, Kendall-Taylor P, Pearce SH. Vaidya B, et al. Among authors: imrie h. Lancet. 1999 Aug 28;354(9180):743-4. doi: 10.1016/S0140-6736(99)01465-8. Lancet. 1999. PMID: 10475192

7

Further evidence for a susceptibility locus on chromosome 20q13.11 in families with dominant transmission of Graves disease.

Pearce SH, Vaidya B, Imrie H, Perros P, Kelly WF, Toft AD, McCarthy MI, Young ET, Kendall-Taylor P. Pearce SH, et al. Among authors: imrie h. Am J Hum Genet. 1999 Nov;65(5):1462-5. doi: 10.1086/302610. Am J Hum Genet. 1999. PMID: 10521315 Free PMC article. No abstract available.

8

Evidence for a new Graves disease susceptibility locus at chromosome 18q21.

Vaidya B, Imrie H, Perros P, Young ET, Kelly WF, Carr D, Large DM, Toft AD, Kendall-Taylor P, Pearce SH. Vaidya B, et al. Among authors: imrie h. Am J Hum Genet. 2000 May;66(5):1710-4. doi: 10.1086/302908. Epub 2000 Apr 3. Am J Hum Genet. 2000. PMID: 10762555 Free PMC article.

9

Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population.

Imrie H, Vaidya B, Perros P, Kelly WF, Toft AD, Young ET, Kendall-Taylor P, Pearce SH. Imrie H, et al. J Clin Endocrinol Metab. 2001 Feb;86(2):626-30. doi: 10.1210/jcem.86.2.7191. J Clin Endocrinol Metab. 2001. PMID: 11158020

10

CTLA4 gene and Graves' disease: association of Graves' disease with the CTLA4 exon 1 and intron 1 polymorphisms, but not with the promoter polymorphism.

Vaidya B, Oakes EJ, Imrie H, Dickinson AJ, Perros P, Kendall-Taylor P, Pearce SH. Vaidya B, et al. Among authors: imrie h. Clin Endocrinol (Oxf). 2003 Jun;58(6):732-5. doi: 10.1046/j.1365-2265.2003.01778.x. Clin Endocrinol (Oxf). 2003. PMID: 12780750

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