Briet C - Search Results

1

Mutations causing acrodysostosis-2 facilitate activation of phosphodiesterase 4D3.

Briet C, Pereda A, Le Stunff C, Motte E, de Dios Garcia-Diaz J, de Nanclares GP, Dumaz N, Silve C. Briet C, et al. Hum Mol Genet. 2017 Oct 15;26(20):3883-3894. doi: 10.1093/hmg/ddx271. Hum Mol Genet. 2017. PMID: 29016851

2

Phase 3 Trial of Crinecerfont in Adult Congenital Adrenal Hyperplasia.

Auchus RJ, Hamidi O, Pivonello R, Bancos I, Russo G, Witchel SF, Isidori AM, Rodien P, Srirangalingam U, Kiefer FW, Falhammar H, Merke DP, Reisch N, Sarafoglou K, Cutler GB Jr, Sturgeon J, Roberts E, Lin VH, Chan JL, Farber RH; CAHtalyst Adult Trial Investigators. Auchus RJ, et al. N Engl J Med. 2024 Aug 8;391(6):504-514. doi: 10.1056/NEJMoa2404656. Epub 2024 Jun 1. N Engl J Med. 2024. PMID: 38828955 Free PMC article. Clinical Trial.

3

Knock-In of the Recurrent R368X Mutation of PRKAR1A that Represses cAMP-Dependent Protein Kinase A Activation: A Model of Type 1 Acrodysostosis.

Le Stunff C, Tilotta F, Sadoine J, Le Denmat D, Briet C, Motte E, Clauser E, Bougnères P, Chaussain C, Silve C. Le Stunff C, et al. Among authors: briet c. J Bone Miner Res. 2017 Feb;32(2):333-346. doi: 10.1002/jbmr.2987. Epub 2016 Oct 24. J Bone Miner Res. 2017. PMID: 27589370 Free article.

4

Modulation of signaling through GPCR-cAMP-PKA pathways by PDE4 depends on stimulus intensity: Possible implications for the pathogenesis of acrodysostosis without hormone resistance.

Motte E, Le Stunff C, Briet C, Dumaz N, Silve C. Motte E, et al. Among authors: briet c. Mol Cell Endocrinol. 2017 Feb 15;442:1-11. doi: 10.1016/j.mce.2016.11.026. Epub 2016 Nov 28. Mol Cell Endocrinol. 2017. PMID: 27908835

5

TRα Mutations in Human.

Briet C, Bouhours-Nouet N, Illouz F, Prunier-Mirebeau D, Rodien P. Briet C, et al. Methods Mol Biol. 2018;1801:241-245. doi: 10.1007/978-1-4939-7902-8_19. Methods Mol Biol. 2018. PMID: 29892829 Review.

6

Thyrotropin receptor, still much to be learned from the patients.

Briet C, Suteau-Courant V, Munier M, Rodien P. Briet C, et al. Best Pract Res Clin Endocrinol Metab. 2018 Apr;32(2):155-164. doi: 10.1016/j.beem.2018.03.002. Epub 2018 Mar 22. Best Pract Res Clin Endocrinol Metab. 2018. PMID: 29678283 Review.

7

New case of bilateral pheochromocytomas involving the homozygous TMEM127 mutation.

Laboureau S, Guichet A, Duriez T, Veyrat-Durebex C, Bouzamondo N, Briet C, Mirebeau-Prunier D. Laboureau S, et al. Among authors: briet c. Clin Genet. 2018 Aug;94(2):278-279. doi: 10.1111/cge.13361. Epub 2018 May 11. Clin Genet. 2018. PMID: 29749617 No abstract available.

8

Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paraganglioma.

Ben Aim L, Pigny P, Castro-Vega LJ, Buffet A, Amar L, Bertherat J, Drui D, Guilhem I, Baudin E, Lussey-Lepoutre C, Corsini C, Chabrier G, Briet C, Faivre L, Cardot-Bauters C, Favier J, Gimenez-Roqueplo AP, Burnichon N. Ben Aim L, et al. Among authors: briet c. J Med Genet. 2019 Aug;56(8):513-520. doi: 10.1136/jmedgenet-2018-105714. Epub 2019 Mar 15. J Med Genet. 2019. PMID: 30877234

9

Sex Bias in Differentiated Thyroid Cancer.

Suteau V, Munier M, Briet C, Rodien P. Suteau V, et al. Among authors: briet c. Int J Mol Sci. 2021 Nov 30;22(23):12992. doi: 10.3390/ijms222312992. Int J Mol Sci. 2021. PMID: 34884794 Free PMC article. Review.

10

Bariatric surgery in adolescents with severe obesity: Review and state of the art in France.

Coutant R, Bouhours-Nouet N, Donzeau A, Fauchard M, Decrequy A, Malka J, Riquin E, Beaumesnil M, Sallé A, Briet C, Topart P, Schmitt F. Coutant R, et al. Among authors: briet c. Ann Endocrinol (Paris). 2017 Oct;78(5):462-468. doi: 10.1016/j.ando.2017.03.002. Epub 2017 Sep 1. Ann Endocrinol (Paris). 2017. PMID: 28870706 Review.

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