Clark AJ - Search Results

1

Phenotypic characteristics of familial glucocorticoid deficiency (FGD) type 1 and 2.

Chung TT, Chan LF, Metherell LA, Clark AJ. Chung TT, et al. Among authors: clark aj. Clin Endocrinol (Oxf). 2010 May;72(5):589-94. doi: 10.1111/j.1365-2265.2009.03663.x. Epub 2009 Jun 24. Clin Endocrinol (Oxf). 2010. PMID: 19558534 Free PMC article.

2

Defective glucocorticoid regulation of proopiomelanocortin gene expression and peptide secretion in a small cell lung cancer cell line.

Clark AJ, Stewart MF, Lavender PM, Farrell W, Crosby SR, Rees LH, White A. Clark AJ, et al. J Clin Endocrinol Metab. 1990 Feb;70(2):485-90. doi: 10.1210/jcem-70-2-485. J Clin Endocrinol Metab. 1990. PMID: 1967615

3

The molecular pathology of pituitary hormone deficiency and resistance.

Woods KA, Weber A, Clark AJ. Woods KA, et al. Among authors: clark aj. Baillieres Clin Endocrinol Metab. 1995 Jul;9(3):453-87. doi: 10.1016/s0950-351x(95)80536-2. Baillieres Clin Endocrinol Metab. 1995. PMID: 7575328 Review.

4

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

5

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

6

Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor.

Clark AJ, McLoughlin L, Grossman A. Clark AJ, et al. Lancet. 1993 Feb 20;341(8843):461-2. doi: 10.1016/0140-6736(93)90208-x. Lancet. 1993. PMID: 8094489

7

Functional characterization of the cloned human ACTH receptor: impaired responsiveness of a mutant receptor in familial glucocorticoid deficiency.

Weber A, Kapas S, Hinson J, Grant DB, Grossman A, Clark AJ. Weber A, et al. Among authors: clark aj. Biochem Biophys Res Commun. 1993 Nov 30;197(1):172-8. doi: 10.1006/bbrc.1993.2456. Biochem Biophys Res Commun. 1993. PMID: 8250922

8

A homozygous splice site mutation affecting the intracellular domain of the growth hormone (GH) receptor resulting in Laron syndrome with elevated GH-binding protein.

Woods KA, Fraser NC, Postel-Vinay MC, Savage MO, Clark AJ. Woods KA, et al. Among authors: clark aj. J Clin Endocrinol Metab. 1996 May;81(5):1686-90. doi: 10.1210/jcem.81.5.8626815. J Clin Endocrinol Metab. 1996. PMID: 8626815

9

Diminished adrenal androgen secretion in familial glucocorticoid deficiency implicates a significant role for ACTH in the induction of adrenarche.

Weber A, Clark AJ, Perry LA, Honour JW, Savage MO. Weber A, et al. Among authors: clark aj. Clin Endocrinol (Oxf). 1997 Apr;46(4):431-7. doi: 10.1046/j.1365-2265.1997.1580969.x. Clin Endocrinol (Oxf). 1997. PMID: 9196605

10

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.

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