Eblé A - Search Results

1

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

2

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

3

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

4

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

5

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

6

Effect of different serum concentrations of growth hormone-binding protein (GHBP) on the regulation of GH receptor/GHBP gene transcription in a human hepatoma cell line.

Mullis PE, Eblé A, Wagner JK, Holl RW, Silbergeld A, Laron Z. Mullis PE, et al. Among authors: eble a. Horm Res. 1997;47(2):73-80. doi: 10.1159/000185435. Horm Res. 1997. PMID: 9030971

7

Regulation of human growth hormone receptor gene transcription by human growth hormone binding protein.

Mullis PE, Wagner JK, Eblé A, Nuoffer JM, Postel-Vinay MC. Mullis PE, et al. Among authors: eble a. Mol Cell Endocrinol. 1997 Jul 4;131(1):89-96. doi: 10.1016/s0303-7207(97)00096-8. Mol Cell Endocrinol. 1997. PMID: 9256367

8

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

9

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

10

Regulation of human growth hormone receptor gene transcription by triiodothyronine (T3).

Mullis PE, Eblé A, Marti U, Bürgi U, Postel-Vinay MC. Mullis PE, et al. Among authors: eble a. Mol Cell Endocrinol. 1999 Jan 25;147(1-2):17-25. doi: 10.1016/s0303-7207(98)00232-9. Mol Cell Endocrinol. 1999. PMID: 10195688

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