de Roux N - Search Results

1

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

2

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

3

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.

4

Estrogen Receptor α Inactivation in 2 Sisters: Different Phenotypic Severities for the Same Pathogenic Variant.

Delcour C, Khawaja N, Gonzalez-Duque S, Lebon S, Talbi A, Drira L, Chevenne D, Ajlouni K, de Roux N. Delcour C, et al. Among authors: de roux n. J Clin Endocrinol Metab. 2022 May 17;107(6):e2553-e2562. doi: 10.1210/clinem/dgac065. J Clin Endocrinol Metab. 2022. PMID: 35134944

5

An inactivating mutation within the first extracellular loop of the thyrotropin receptor impedes normal posttranslational maturation of the extracellular domain.

Sura-Trueba S, Aumas C, Carre A, Durif S, Leger J, Polak M, de Roux N. Sura-Trueba S, et al. Among authors: de roux n. Endocrinology. 2009 Feb;150(2):1043-50. doi: 10.1210/en.2008-1145. Epub 2008 Oct 16. Endocrinology. 2009. PMID: 18927215

6

Negative fetal FSH/LH regulation in late pregnancy is associated with declined kisspeptin/KISS1R expression in the tuberal hypothalamus.

Guimiot F, Chevrier L, Dreux S, Chevenne D, Caraty A, Delezoide AL, de Roux N. Guimiot F, et al. Among authors: de roux n. J Clin Endocrinol Metab. 2012 Dec;97(12):E2221-9. doi: 10.1210/jc.2012-2078. Epub 2012 Sep 26. J Clin Endocrinol Metab. 2012. PMID: 23015653

7

GnRH receptor and GPR54 inactivation in isolated gonadotropic deficiency.

de Roux N. de Roux N. Best Pract Res Clin Endocrinol Metab. 2006 Dec;20(4):515-28. doi: 10.1016/j.beem.2006.10.005. Best Pract Res Clin Endocrinol Metab. 2006. PMID: 17161329 Review.

8

PRR repeats in the intracellular domain of KISS1R are important for its export to cell membrane.

Chevrier L, de Brevern A, Hernandez E, Leprince J, Vaudry H, Guedj AM, de Roux N. Chevrier L, et al. Among authors: de roux n, de brevern a. Mol Endocrinol. 2013 Jun;27(6):1004-14. doi: 10.1210/me.2012-1386. Epub 2013 Apr 22. Mol Endocrinol. 2013. PMID: 23608644 Free PMC article.

9

Somatostatin receptors type 2 and 5 expression and localization during human pituitary development.

Peineau S, Guimiot F, Csaba Z, Jacquier S, Fafouri A, Schwendimann L, de Roux N, Schulz S, Gressens P, Auvin S, Dournaud P. Peineau S, et al. Among authors: de roux n. Endocrinology. 2014 Jan;155(1):33-9. doi: 10.1210/en.2013-1683. Epub 2013 Dec 20. Endocrinology. 2014. PMID: 24189142

10

Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations.

Ramos HE, Carré A, Chevrier L, Szinnai G, Tron E, Cerqueira TL, Léger J, Cabrol S, Puel O, Queinnec C, De Roux N, Guillot L, Castanet M, Polak M. Ramos HE, et al. Among authors: de roux n. Eur J Endocrinol. 2014 Oct;171(4):499-507. doi: 10.1530/EJE-13-1006. Eur J Endocrinol. 2014. PMID: 25214233

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