Bole-Feysot C - Search Results

1

Prolactin (PRL) and its receptor: actions, signal transduction pathways and phenotypes observed in PRL receptor knockout mice.

Bole-Feysot C, Goffin V, Edery M, Binart N, Kelly PA. Bole-Feysot C, et al. Endocr Rev. 1998 Jun;19(3):225-68. doi: 10.1210/edrv.19.3.0334. Endocr Rev. 1998. PMID: 9626554 Review.

2

Regulation of prolactin receptor mRNA expression in peripheral lymphocytes in rats in response to changes in serum concentrations of prolactin.

Di Carlo R, Bole-Feysot C, Gualillo O, Meli R, Nagano M, Kelly PA. Di Carlo R, et al. Endocrinology. 1995 Oct;136(10):4713-6. doi: 10.1210/endo.136.10.7664695. Endocrinology. 1995. PMID: 7664695

3

In vivo study of prolactin (PRL) intracellular signalling during lactogenesis in the rat: JAK/STAT pathway is activated by PRL in the mammary gland but not in the liver.

Jahn GA, Daniel N, Jolivet G, Belair L, Bole-Feysot C, Kelly PA, Djiane J. Jahn GA, et al. Biol Reprod. 1997 Oct;57(4):894-900. doi: 10.1095/biolreprod57.4.894. Biol Reprod. 1997. PMID: 9314595

4

Prolactin: a hormone at the crossroads of neuroimmunoendocrinology.

Goffin V, Bouchard B, Ormandy CJ, Weimann E, Ferrag F, Touraine P, Bole-Feysot C, Maaskant RA, Clement-Lacroix P, Edery M, Binart N, Kelly PA. Goffin V, et al. Ann N Y Acad Sci. 1998 May 1;840:498-509. doi: 10.1111/j.1749-6632.1998.tb09588.x. Ann N Y Acad Sci. 1998. PMID: 9629276 Review.

5

From the molecular biology of prolactin and its receptor to the lessons learned from knockout mice models.

Goffin V, Binart N, Clément-Lacroix P, Bouchard B, Bole-Feysot C, Edery M, Lucas BK, Touraine P, Pezet A, Maaskant R, Pichard C, Helloco C, Baran N, Favre H, Bernichtein S, Allamando A, Ormandy C, Kelly PA. Goffin V, et al. Genet Anal. 1999 Nov;15(3-5):189-201. doi: 10.1016/s1050-3862(99)00025-x. Genet Anal. 1999. PMID: 10596761 Review.

6

Analysis of prolactin-modulated gene expression profiles during the Nb2 cell cycle using differential screening techniques.

Bole-Feysot C, Perret E, Roustan P, Bouchard B, Kelly PA. Bole-Feysot C, et al. Genome Biol. 2000;1(4):RESEARCH0008. doi: 10.1186/gb-2000-1-4-research0008. Epub 2000 Oct 16. Genome Biol. 2000. PMID: 11178248 Free PMC article.

7

A rare castration-resistant progenitor cell population is highly enriched in Pten-null prostate tumours.

Sackmann Sala L, Boutillon F, Menara G, De Goyon-Pélard A, Leprévost M, Codzamanian J, Lister N, Pencik J, Clark A, Cagnard N, Bole-Feysot C, Moriggl R, Risbridger GP, Taylor RA, Kenner L, Guidotti JE, Goffin V. Sackmann Sala L, et al. J Pathol. 2017 Sep;243(1):51-64. doi: 10.1002/path.4924. Epub 2017 Jul 28. J Pathol. 2017. PMID: 28603917

8

Abnormal Wnt and PI3Kinase signaling in the malformed intestine of lama5 deficient mice.

Ritié L, Spenlé C, Lacroute J, Bolcato-Bellemin AL, Lefebvre O, Bole-Feysot C, Jost B, Klein A, Arnold C, Kedinger M, Bagnard D, Orend G, Simon-Assmann P. Ritié L, et al. PLoS One. 2012;7(5):e37710. doi: 10.1371/journal.pone.0037710. Epub 2012 May 30. PLoS One. 2012. PMID: 22666383 Free PMC article.

9

TCTN3 mutations cause Mohr-Majewski syndrome.

Thomas S, Legendre M, Saunier S, Bessières B, Alby C, Bonnière M, Toutain A, Loeuillet L, Szymanska K, Jossic F, Gaillard D, Yacoubi MT, Mougou-Zerelli S, David A, Barthez MA, Ville Y, Bole-Feysot C, Nitschke P, Lyonnet S, Munnich A, Johnson CA, Encha-Razavi F, Cormier-Daire V, Thauvin-Robinet C, Vekemans M, Attié-Bitach T. Thomas S, et al. Am J Hum Genet. 2012 Aug 10;91(2):372-8. doi: 10.1016/j.ajhg.2012.06.017. Am J Hum Genet. 2012. PMID: 22883145 Free PMC article.

10

Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears.

Gordon CT, Petit F, Kroisel PM, Jakobsen L, Zechi-Ceide RM, Oufadem M, Bole-Feysot C, Pruvost S, Masson C, Tores F, Hieu T, Nitschké P, Lindholm P, Pellerin P, Guion-Almeida ML, Kokitsu-Nakata NM, Vendramini-Pittoli S, Munnich A, Lyonnet S, Holder-Espinasse M, Amiel J. Gordon CT, et al. Am J Hum Genet. 2013 Dec 5;93(6):1118-25. doi: 10.1016/j.ajhg.2013.10.023. Epub 2013 Nov 21. Am J Hum Genet. 2013. PMID: 24268655 Free PMC article.

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