Clark AJ - Search Results

1

Familial glucocorticoid deficiency: New genes and mechanisms.

Meimaridou E, Hughes CR, Kowalczyk J, Guasti L, Chapple JP, King PJ, Chan LF, Clark AJ, Metherell LA. Meimaridou E, et al. Among authors: clark aj. Mol Cell Endocrinol. 2013 May 22;371(1-2):195-200. doi: 10.1016/j.mce.2012.12.010. Epub 2012 Dec 29. Mol Cell Endocrinol. 2013. PMID: 23279877 Review.

2

Adrenocorticotropin receptor gene mutations in familial glucocorticoid deficiency: relationships with clinical features in four families.

Weber A, Toppari J, Harvey RD, Klann RC, Shaw NJ, Ricker AT, Näntö-Salonen K, Bevan JS, Clark AJ. Weber A, et al. Among authors: clark aj. J Clin Endocrinol Metab. 1995 Jan;80(1):65-71. doi: 10.1210/jcem.80.1.7829641. J Clin Endocrinol Metab. 1995. PMID: 7829641

3

Mutations of the ACTH receptor gene are only one cause of familial glucocorticoid deficiency.

Weber A, Clark AJ. Weber A, et al. Among authors: clark aj. Hum Mol Genet. 1994 Apr;3(4):585-8. doi: 10.1093/hmg/3.4.585. Hum Mol Genet. 1994. PMID: 8069303

4

Familial glucocorticoid deficiency: one syndrome, but more than one gene.

Clark AJ, Cammas FM, Watt A, Kapas S, Weber A. Clark AJ, et al. J Mol Med (Berl). 1997 Jun;75(6):394-9. doi: 10.1007/s001090050124. J Mol Med (Berl). 1997. PMID: 9231879 Review.

5

Analysis of the first exon of the murine ACTH receptor gene.

King PJ, Clark AJ. King PJ, et al. Among authors: clark aj. Endocr Res. 1998 Aug-Nov;24(3-4):397-402. doi: 10.3109/07435809809032621. Endocr Res. 1998. PMID: 9888513

6

DNA methylation and silencing of gene expression.

Newell-Price J, Clark AJ, King P. Newell-Price J, et al. Among authors: clark aj. Trends Endocrinol Metab. 2000 May-Jun;11(4):142-8. doi: 10.1016/s1043-2760(00)00248-4. Trends Endocrinol Metab. 2000. PMID: 10754536 Review.

7

Tall stature in familial glucocorticoid deficiency.

Elias LL, Huebner A, Metherell LA, Canas A, Warne GL, Bitti ML, Cianfarani S, Clayton PE, Savage MO, Clark AJ. Elias LL, et al. Among authors: clark aj. Clin Endocrinol (Oxf). 2000 Oct;53(4):423-30. doi: 10.1046/j.1365-2265.2000.01122.x. Clin Endocrinol (Oxf). 2000. PMID: 11012566

8

The CpG island promoter of the human proopiomelanocortin gene is methylated in nonexpressing normal tissue and tumors and represses expression.

Newell-Price J, King P, Clark AJ. Newell-Price J, et al. Among authors: clark aj. Mol Endocrinol. 2001 Feb;15(2):338-48. doi: 10.1210/mend.15.2.0599. Mol Endocrinol. 2001. PMID: 11158338

9

The molecular pathogenesis of ACTH insensitivity syndromes.

Clark AJ, Metherell L, Swords FM, Elias LL. Clark AJ, et al. Ann Endocrinol (Paris). 2001 Apr;62(2):207-11. Ann Endocrinol (Paris). 2001. PMID: 11353896 Review.

10

Pseudoexon activation as a novel mechanism for disease resulting in atypical growth-hormone insensitivity.

Metherell LA, Akker SA, Munroe PB, Rose SJ, Caulfield M, Savage MO, Chew SL, Clark AJ. Metherell LA, et al. Among authors: clark aj. Am J Hum Genet. 2001 Sep;69(3):641-6. doi: 10.1086/323266. Epub 2001 Jul 20. Am J Hum Genet. 2001. PMID: 11468686 Free PMC article.

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