Dodé C - Search Results

1

Biased signaling through G-protein-coupled PROKR2 receptors harboring missense mutations.

Sbai O, Monnier C, Dodé C, Pin JP, Hardelin JP, Rondard P. Sbai O, et al. Among authors: dode c. FASEB J. 2014 Aug;28(8):3734-44. doi: 10.1096/fj.13-243402. Epub 2014 May 15. FASEB J. 2014. PMID: 24830383

2

PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity.

Monnier C, Dodé C, Fabre L, Teixeira L, Labesse G, Pin JP, Hardelin JP, Rondard P. Monnier C, et al. Among authors: dode c. Hum Mol Genet. 2009 Jan 1;18(1):75-81. doi: 10.1093/hmg/ddn318. Epub 2008 Sep 29. Hum Mol Genet. 2009. PMID: 18826963 Free PMC article.

3

PROK2/PROKR2 Signaling and Kallmann Syndrome.

Dodé C, Rondard P. Dodé C, et al. Front Endocrinol (Lausanne). 2013 Apr 12;4:19. doi: 10.3389/fendo.2013.00019. eCollection 2013. Front Endocrinol (Lausanne). 2013. PMID: 23596439 Free PMC article.

4

[Kallmann De Morsier syndrome: FGF-signaling insufficiency?].

Dodé C, Hardelin JP. Dodé C, et al. Med Sci (Paris). 2004 Aug-Sep;20(8-9):793-8. doi: 10.1051/medsci/2004208-9793. Med Sci (Paris). 2004. PMID: 15361347 Free article. Review. French.

5

Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.

Dodé C, Teixeira L, Levilliers J, Fouveaut C, Bouchard P, Kottler ML, Lespinasse J, Lienhardt-Roussie A, Mathieu M, Moerman A, Morgan G, Murat A, Toublanc JE, Wolczynski S, Delpech M, Petit C, Young J, Hardelin JP. Dodé C, et al. PLoS Genet. 2006 Oct 20;2(10):e175. doi: 10.1371/journal.pgen.0020175. Epub 2006 Sep 1. PLoS Genet. 2006. PMID: 17054399 Free PMC article.

6

Kallmann syndrome.

Dodé C, Hardelin JP. Dodé C, et al. Eur J Hum Genet. 2009 Feb;17(2):139-46. doi: 10.1038/ejhg.2008.206. Epub 2008 Nov 5. Eur J Hum Genet. 2009. PMID: 18985070 Free PMC article.

7

Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients.

Sarfati J, Fouveaut C, Leroy C, Jeanpierre M, Hardelin JP, Dodé C. Sarfati J, et al. Among authors: dode c. Eur J Endocrinol. 2013 Oct 21;169(6):805-9. doi: 10.1530/EJE-13-0419. Print 2013 Dec. Eur J Endocrinol. 2013. PMID: 24031091

8

Defective signaling through plexin-A1 compromises the development of the peripheral olfactory system and neuroendocrine reproductive axis in mice.

Marcos S, Monnier C, Rovira X, Fouveaut C, Pitteloud N, Ango F, Dodé C, Hardelin JP. Marcos S, et al. Among authors: dode c. Hum Mol Genet. 2017 Jun 1;26(11):2006-2017. doi: 10.1093/hmg/ddx080. Hum Mol Genet. 2017. PMID: 28334861

9

Kallmann syndrome: fibroblast growth factor signaling insufficiency?

Dodé C, Hardelin JP. Dodé C, et al. J Mol Med (Berl). 2004 Nov;82(11):725-34. doi: 10.1007/s00109-004-0571-y. Epub 2004 Sep 8. J Mol Med (Berl). 2004. PMID: 15365636 Review.

10

Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome.

Leroy C, Fouveaut C, Leclercq S, Jacquemont S, Boullay HD, Lespinasse J, Delpech M, Dupont JM, Hardelin JP, Dodé C. Leroy C, et al. Among authors: dode c. Eur J Hum Genet. 2008 Jul;16(7):865-8. doi: 10.1038/ejhg.2008.15. Epub 2008 Feb 20. Eur J Hum Genet. 2008. PMID: 18285834

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