Eblé A - Search Results

1

Isolated growth hormone (GH) deficiency type IA associated with a 45-kilobase gene deletion within the human GH gene cluster.

Akinci A, Kanaka C, Eblé A, Akar N, Vidinlisan S, Mullis PE. Akinci A, et al. Among authors: eble a. J Clin Endocrinol Metab. 1992 Aug;75(2):437-41. doi: 10.1210/jcem.75.2.1322425. J Clin Endocrinol Metab. 1992. PMID: 1322425

2

Prevalence of human growth hormone-1 gene deletions among patients with isolated growth hormone deficiency from different populations.

Mullis PE, Akinci A, Kanaka C, Eblé A, Brook CG. Mullis PE, et al. Among authors: eble a. Pediatr Res. 1992 May;31(5):532-4. doi: 10.1203/00006450-199205000-00026. Pediatr Res. 1992. PMID: 1603635

3

Regulation of human growth hormone-binding protein production by human growth hormone in a hepatoma cell line.

Mullis PE, Holl RW, Lund T, Eblé A, Brickell PM. Mullis PE, et al. Among authors: eble a. Mol Cell Endocrinol. 1995 Jun;111(2):181-90. doi: 10.1016/0303-7207(95)03567-q. Mol Cell Endocrinol. 1995. PMID: 7556880

4

Isolated growth hormone deficiency: testing the little mouse hypothesis in man and exclusion of mutations within the extracellular domain of the growth hormone-releasing hormone receptor.

Cao Y, Wagner JK, Hindmarsh PC, Eblé A, Mullis PE. Cao Y, et al. Among authors: eble a. Pediatr Res. 1995 Dec;38(6):962-6. doi: 10.1203/00006450-199512000-00022. Pediatr Res. 1995. PMID: 8618801

5

Allelic variations in the human growth hormone-1 gene promoter of growth hormone-deficient patients and normal controls.

Wagner JK, Eblé A, Cogan JD, Prince MA, Phillips JA 3rd, Mullis PE. Wagner JK, et al. Among authors: eble a. Eur J Endocrinol. 1997 Nov;137(5):474-81. doi: 10.1530/eje.0.1370474. Eur J Endocrinol. 1997. PMID: 9405026

6

Prevalence of human GH-1 gene alterations in patients with isolated growth hormone deficiency.

Wagner JK, Eblé A, Hindmarsh PC, Mullis PE. Wagner JK, et al. Among authors: eble a. Pediatr Res. 1998 Jan;43(1):105-10. doi: 10.1203/00006450-199801000-00016. Pediatr Res. 1998. PMID: 9432120

7

Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C).

Flück C, Deladoey J, Rutishauser K, Eblé A, Marti U, Wu W, Mullis PE. Flück C, et al. Among authors: eble a. J Clin Endocrinol Metab. 1998 Oct;83(10):3727-34. doi: 10.1210/jcem.83.10.5172. J Clin Endocrinol Metab. 1998. PMID: 9768691

8

"Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency.

Deladoëy J, Flück C, Büyükgebiz A, Kuhlmann BV, Eblé A, Hindmarsh PC, Wu W, Mullis PE. Deladoëy J, et al. Among authors: eble a. J Clin Endocrinol Metab. 1999 May;84(5):1645-50. doi: 10.1210/jcem.84.5.5681. J Clin Endocrinol Metab. 1999. PMID: 10323394

9

Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line.

Nuoffer JM, Flück C, Deladoëy J, Eblé A, Dattani MT, Mullis PE. Nuoffer JM, et al. Among authors: eble a. J Endocrinol. 2000 May;165(2):313-20. doi: 10.1677/joe.0.1650313. J Endocrinol. 2000. PMID: 10810295

10

Isolated GH deficiency type II: knockdown of the harmful Delta3GH recovers wt-GH secretion in rat tumor pituitary cells.

Lochmatter D, Strom M, Eblé A, Petkovic V, Flück CE, Bidlingmaier M, Robinson IC, Mullis PE. Lochmatter D, et al. Among authors: eble a. Endocrinology. 2010 Sep;151(9):4400-9. doi: 10.1210/en.2010-0196. Epub 2010 Jun 30. Endocrinology. 2010. PMID: 20591972

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