Clark AJ - Search Results

1

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

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

An alternatively spliced human insulin-like growth factor-I transcript with hepatic tissue expression that diverts away from the mitogenic IBE1 peptide.

Chew SL, Lavender P, Clark AJ, Ross RJ. Chew SL, et al. Among authors: clark aj. Endocrinology. 1995 May;136(5):1939-44. doi: 10.1210/endo.136.5.7720641. Endocrinology. 1995. PMID: 7720641

5

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

6

Absence of mutations in the MEN2A region of the ret proto-oncogene in non-MEN 2A phaeochromocytomas.

Chew SL, Lavender P, Jain A, Weber A, Ross RJ, Wass JA, Besser GM, Clark AJ. Chew SL, et al. Among authors: clark aj. Clin Endocrinol (Oxf). 1995 Jan;42(1):17-21. doi: 10.1111/j.1365-2265.1995.tb02593.x. Clin Endocrinol (Oxf). 1995. PMID: 7889627

7

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

8

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

9

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

10

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

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