de Roux N - Search Results

1

Haploinsufficiency of Dmxl2, encoding a synaptic protein, causes infertility associated with a loss of GnRH neurons in mouse.

Tata B, Huijbregts L, Jacquier S, Csaba Z, Genin E, Meyer V, Leka S, Dupont J, Charles P, Chevenne D, Carel JC, Léger J, de Roux N. Tata B, et al. Among authors: de roux n. PLoS Biol. 2014 Sep 23;12(9):e1001952. doi: 10.1371/journal.pbio.1001952. eCollection 2014 Sep. PLoS Biol. 2014. PMID: 25248098 Free PMC article.

2

Rabconnectin-3α is required for the morphological maturation of GnRH neurons and kisspeptin responsiveness.

Tata BK, Harbulot C, Csaba Z, Peineau S, Jacquier S, de Roux N. Tata BK, et al. Among authors: de roux n. Sci Rep. 2017 Feb 17;7:42463. doi: 10.1038/srep42463. Sci Rep. 2017. PMID: 28209974 Free PMC article.

3

DLK1 is a somato-dendritic protein expressed in hypothalamic arginine-vasopressin and oxytocin neurons.

Villanueva C, Jacquier S, de Roux N. Villanueva C, et al. Among authors: de roux n. PLoS One. 2012;7(4):e36134. doi: 10.1371/journal.pone.0036134. Epub 2012 Apr 26. PLoS One. 2012. PMID: 22563444 Free PMC article.

4

[Congenital hypogonadotropic hypogonadism].

Roze C, Touraine P, Leger J, de Roux N. Roze C, et al. Among authors: de roux n. Ann Endocrinol (Paris). 2009 Mar;70(1):2-13. doi: 10.1016/j.ando.2008.06.005. Epub 2009 Feb 5. Ann Endocrinol (Paris). 2009. PMID: 19200533 French.

5

Pituitary-thyroid feedback in a patient with a sporadic activating thyrotropin (TSH) receptor mutation: implication that thyroid-secreted factors other than thyroid hormones contribute to serum TSH levels.

Gelwane G, de Roux N, Chevenne D, Carel JC, Léger J. Gelwane G, et al. Among authors: de roux n. J Clin Endocrinol Metab. 2009 Aug;94(8):2787-91. doi: 10.1210/jc.2008-2524. Epub 2009 May 19. J Clin Endocrinol Metab. 2009. PMID: 19454581

6

DNA polymorphisms of the KiSS1 3' untranslated region interfere with the folding of a G-rich sequence into G-quadruplex.

Huijbregts L, Roze C, Bonafe G, Houang M, Le Bouc Y, Carel JC, Leger J, Alberti P, de Roux N. Huijbregts L, et al. Among authors: de roux n. Mol Cell Endocrinol. 2012 Apr 4;351(2):239-48. doi: 10.1016/j.mce.2011.12.014. Epub 2011 Dec 30. Mol Cell Endocrinol. 2012. PMID: 22230814

7

KISS1 is down-regulated by 17beta-estradiol in MDA-MB-231 cells through a nonclassical mechanism and loss of ribonucleic acid polymerase II binding at the proximal promoter.

Huijbregts L, de Roux N. Huijbregts L, et al. Among authors: de roux n. Endocrinology. 2010 Aug;151(8):3764-72. doi: 10.1210/en.2010-0260. Epub 2010 Jun 9. Endocrinology. 2010. PMID: 20534720

8

Congenital Hypogonadotropic Hypogonadism: A Trait Shared by Several Complex Neurodevelopmental Disorders.

de Roux N, Carel JC, Léger J. de Roux N, et al. Endocr Dev. 2016;29:72-86. doi: 10.1159/000438875. Epub 2015 Dec 17. Endocr Dev. 2016. PMID: 26680573 Review.

9

Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations.

Villanueva C, Jacobson-Dickman E, Xu C, Manouvrier S, Dwyer AA, Sykiotis GP, Beenken A, Liu Y, Tommiska J, Hu Y, Tiosano D, Gerard M, Leger J, Drouin-Garraud V, Lefebvre H, Polak M, Carel JC, Phan-Hug F, Hauschild M, Plummer L, Rey JP, Raivio T, Bouloux P, Sidis Y, Mohammadi M, de Roux N, Pitteloud N. Villanueva C, et al. Among authors: de roux n. Genet Med. 2015 Aug;17(8):651-9. doi: 10.1038/gim.2014.166. Epub 2014 Nov 13. Genet Med. 2015. PMID: 25394172 Free PMC article.

10

Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54.

de Roux N, Genin E, Carel JC, Matsuda F, Chaussain JL, Milgrom E. de Roux N, et al. Proc Natl Acad Sci U S A. 2003 Sep 16;100(19):10972-6. doi: 10.1073/pnas.1834399100. Epub 2003 Aug 27. Proc Natl Acad Sci U S A. 2003. PMID: 12944565 Free PMC article.

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