Muir A - Search Results

1

Novel TSHbeta subunit gene mutation causing congenital central hypothyroidism in a newborn male.

Morales AE, Shi JD, Wang CY, She JX, Muir A. Morales AE, et al. Among authors: muir a. J Pediatr Endocrinol Metab. 2004 Mar;17(3):355-9. doi: 10.1515/jpem.2004.17.3.355. J Pediatr Endocrinol Metab. 2004. PMID: 15112912

2

Autoantibody epitope mapping of the 21-hydroxylase antigen in autoimmune Addison's disease.

Song YH, Connor EL, Muir A, She JX, Zorovich B, Derovanesian D, Maclaren N. Song YH, et al. Among authors: muir a. J Clin Endocrinol Metab. 1994 May;78(5):1108-12. doi: 10.1210/jcem.78.5.7513715. J Clin Endocrinol Metab. 1994. PMID: 7513715

3

Although DR3-DQB1*0201 may be associated with multiple component diseases of the autoimmune polyglandular syndromes, the human leukocyte antigen DR4-DQB1*0302 haplotype is implicated only in beta-cell autoimmunity.

Huang W, Connor E, Rosa TD, Muir A, Schatz D, Silverstein J, Crockett S, She JX, Maclaren NK. Huang W, et al. Among authors: muir a. J Clin Endocrinol Metab. 1996 Jul;81(7):2559-63. doi: 10.1210/jcem.81.7.8675578. J Clin Endocrinol Metab. 1996. PMID: 8675578

4

IL4 and IL4Ralpha genes are not linked or associated with type 1 diabetes.

Reimsnider SK, Eckenrode SE, Marron MP, Muir A, She JX. Reimsnider SK, et al. Among authors: muir a. Pediatr Res. 2000 Feb;47(2):246-9. doi: 10.1203/00006450-200002000-00016. Pediatr Res. 2000. PMID: 10674354

5

Preservation of C-peptide secretion in subjects at high risk of developing type 1 diabetes mellitus--a new surrogate measure of non-progression?

Schatz D, Cuthbertson D, Atkinson M, Salzler MC, Winter W, Muir A, Silverstein J, Cook R, Maclaren N, She JX, Greenbaum C, Krischer J. Schatz D, et al. Among authors: muir a. Pediatr Diabetes. 2004 Jun;5(2):72-9. doi: 10.1111/j.1399-543X.2004.00047.x. Pediatr Diabetes. 2004. PMID: 15189492 Clinical Trial.

6

Advances in the genetics and immunology of autoimmune polyglandular syndrome II/III and their clinical applications.

Muir A, She JX. Muir A, et al. Ann Med Interne (Paris). 1999 Jun;150(4):301-12. Ann Med Interne (Paris). 1999. PMID: 10519018 Review. No abstract available.

7

Affected-sib-pair mapping of a novel susceptibility gene to insulin-dependent diabetes mellitus (IDDM8) on chromosome 6q25-q27.

Luo DF, Bui MM, Muir A, Maclaren NK, Thomson G, She JX. Luo DF, et al. Among authors: muir a. Am J Hum Genet. 1995 Oct;57(4):911-9. Am J Hum Genet. 1995. PMID: 7573053 Free PMC article.

8

The IDDMK(1,2)22 retrovirus is not detectable in either mRNA or genomic DNA from patients with type 1 diabetes.

Muir A, Ruan QG, Marron MP, She JX. Muir A, et al. Diabetes. 1999 Jan;48(1):219-22. doi: 10.2337/diabetes.48.1.219. Diabetes. 1999. PMID: 9892248

9

Association of LMP2 and LMP7 genes within the major histocompatibility complex with insulin-dependent diabetes mellitus: population and family studies.

Deng GY, Muir A, Maclaren NK, She JX. Deng GY, et al. Among authors: muir a. Am J Hum Genet. 1995 Feb;56(2):528-34. Am J Hum Genet. 1995. PMID: 7847389 Free PMC article.

10

Additive susceptibility to insulin-dependent diabetes conferred by HLA-DQB1 and insulin genes.

She JX, Bui MM, Tian XH, Muir A, Wakeland EK, Zorovich B, Zhang LP, Liu MC, Thomson G, Maclaren NK. She JX, et al. Among authors: muir a. Autoimmunity. 1994;18(3):195-203. doi: 10.3109/08916939409007996. Autoimmunity. 1994. PMID: 7858104 Free article.

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