Deladoëy J - Search Results

1

Effect of different growth hormone (GH) mutants on the regulation of GH-receptor gene transcription in a human hepatoma cell line.

Deladoëy J, Gex G, Vuissoz JM, Strasburger CJ, Wajnrajch MP, Mullis PE. Deladoëy J, et al. Eur J Endocrinol. 2002 Apr;146(4):573-81. doi: 10.1530/eje.0.1460573. Eur J Endocrinol. 2002. PMID: 11916628

2

New GH-1 gene mutations: expanding the spectrum of causes of isolated growth hormone deficiency.

Mullis PE, Deladoëy J, Dannies PS. Mullis PE, et al. Among authors: deladoey j. J Pediatr Endocrinol Metab. 2002 Dec;15 Suppl 5:1301-10. J Pediatr Endocrinol Metab. 2002. PMID: 12510984 Review.

3

Isolated autosomal dominant growth hormone deficiency: an evolving pituitary deficit? A multicenter follow-up study.

Mullis PE, Robinson IC, Salemi S, Eblé A, Besson A, Vuissoz JM, Deladoey J, Simon D, Czernichow P, Binder G. Mullis PE, et al. Among authors: deladoey j. J Clin Endocrinol Metab. 2005 Apr;90(4):2089-96. doi: 10.1210/jc.2004-1280. Epub 2005 Jan 25. J Clin Endocrinol Metab. 2005. PMID: 15671105

4

Short stature caused by a biologically inactive mutant growth hormone (GH-C53S).

Besson A, Salemi S, Deladoëy J, Vuissoz JM, Eblé A, Bidlingmaier M, Bürgi S, Honegger U, Flück C, Mullis PE. Besson A, et al. Among authors: deladoey j. J Clin Endocrinol Metab. 2005 May;90(5):2493-9. doi: 10.1210/jc.2004-1838. Epub 2005 Feb 15. J Clin Endocrinol Metab. 2005. PMID: 15713716

5

Isolated autosomal dominant growth hormone deficiency: stimulating mutant GH-1 gene expression drives GH-1 splice-site selection, cell proliferation, and apoptosis.

Salemi S, Yousefi S, Lochmatter D, Eblé A, Deladoëy J, Robinson IC, Simon HU, Mullis PE. Salemi S, et al. Among authors: deladoey j. Endocrinology. 2007 Jan;148(1):45-53. doi: 10.1210/en.2006-0772. Epub 2006 Oct 12. Endocrinology. 2007. PMID: 17038549

6

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: deladoey j. J Endocrinol. 2000 May;165(2):313-20. doi: 10.1677/joe.0.1650313. J Endocrinol. 2000. PMID: 10810295

7

Autosomal dominant GH deficiency due to an Arg183His GH-1 gene mutation: clinical and molecular evidence of impaired regulated GH secretion.

Deladoëy J, Stocker P, Mullis PE. Deladoëy J, et al. J Clin Endocrinol Metab. 2001 Aug;86(8):3941-7. doi: 10.1210/jcem.86.8.7723. J Clin Endocrinol Metab. 2001. PMID: 11502836

8

Molecular and cellular basis of isolated dominant-negative growth hormone deficiency, IGHD type II: insights on the secretory pathway of peptide hormones.

Mullis PE, Deladoëy J, Dannies PS. Mullis PE, et al. Among authors: deladoey j. Horm Res. 2002;58(2):53-66. doi: 10.1159/000064663. Horm Res. 2002. PMID: 12207163 Review.

9

Congenital secondary hypothyroidism due to a mutation C105Vfs114X thyrotropin-beta mutation: genetic study of five unrelated families from Switzerland and Argentina.

Deladoëy J, Vuissoz JM, Domené HM, Malik N, Gruneiro-Papendieck L, Chiesa A, Heinrich JJ, Mullis PE. Deladoëy J, et al. Thyroid. 2003 Jun;13(6):553-9. doi: 10.1089/105072503322238818. Thyroid. 2003. PMID: 12930599

10

Impact of del32-71-GH (exon 3 skipped GH) on intracellular GH distribution, secretion and cell viability: a quantitative confocal microscopy analysis.

Salemi S, Yousefi S, Eblé A, Deladoëy J, Mullis PE. Salemi S, et al. Among authors: deladoey j. Horm Res. 2006;65(3):132-41. doi: 10.1159/000091607. Epub 2006 Feb 17. Horm Res. 2006. PMID: 16491012

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

66 results

Search Page

Filters