Causes and consequences of gray matter heterotopia
F Watrin, JB Manent, C Cardoso… - CNS neuroscience & …, 2015 - Wiley Online Library
The objective of this article is to review the pathophysiological bases of gray matter
heterotopia and to appreciate their involvement in brain cortical development and functional …
heterotopia and to appreciate their involvement in brain cortical development and functional …
[PDF][PDF] Anti-müllerian hormone and freemartinism: inhibition of germ cell development and induction of seminiferous cord-like structures in rat fetal ovaries exposed in …
B Vigier, F Watrin, S Magre, D Tran… - Reproduction …, 1988 - rnd.edpsciences.org
In 13 and 14-day old fetal rat ovaries maintained 3 to 10 days in organ culture, purified bovine
anti-Mullerian hormone (AMH)(1.5 to 3 pg/ml) induced a characteristic freemartin effect. …
anti-Mullerian hormone (AMH)(1.5 to 3 pg/ml) induced a characteristic freemartin effect. …
H19 acts as a trans regulator of the imprinted gene network controlling growth in mice
…, MA Ripoche, A Le Digarcher, F Watrin… - …, 2009 - journals.biologists.com
The imprinted H19 gene produces a non-coding RNA of unknown function. Mice lacking
H19 show an overgrowth phenotype, due to a cis effect of the H19 locus on the adjacent Igf2 …
H19 show an overgrowth phenotype, due to a cis effect of the H19 locus on the adjacent Igf2 …
A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene
F Schaller, F Watrin, R Sturny… - Human molecular …, 2010 - academic.oup.com
… ) in surviving mutants of our Magel2 KO model (F. Muscatelli, personal communication). This
… Dierich for her help in KO mouse line, Dr F. Michel for his help in microscopy and the use of …
… Dierich for her help in KO mouse line, Dr F. Michel for his help in microscopy and the use of …
The Human Magel2 Gene and Its Mouse Homologue Are Paternally Expressed and Mapped to the Prader-Willi Region
I Boccaccio, H Glatt-Deeley, F Watrin… - Human molecular …, 1999 - academic.oup.com
… in F 1 mice derived from matings between M.spretus males and C57Bl6 females andinN 2
mice derived from matings between F … the M.spretus allele from their F 1 mother and a paternal …
mice derived from matings between F … the M.spretus allele from their F 1 mother and a paternal …
Deletion of the mouse T-cell receptor beta gene enhancer blocks alphabeta T-cell development.
G Bouvier, F Watrin, M Naspetti… - Proceedings of the …, 1996 - National Acad Sciences
… In addition, staining with anti-CD4 and CD8 mAbs were lower in intensity in AE,8-f- animals
as compared with wild-type controls, most probably because of the developmental arrest in …
as compared with wild-type controls, most probably because of the developmental arrest in …
Purified bovine AMH induces a characteristic freemartin effect in fetal rat prospective ovaries exposed to it in vitro
B Vigier, F Watrin, S Magre, D Tran, N Josso - Development, 1987 - journals.biologists.com
To determine whether anti-Müllerian hormone (AMH) is responsible for the gonadal lesions
observed in bovine genetic females united by placental anastomoses to male twins (…
observed in bovine genetic females united by placental anastomoses to male twins (…
[HTML][HTML] Selective suppression of excessive GluN2C expression rescues early epilepsy in a tuberous sclerosis murine model
…, NA Goriounova, E Buhler, F Watrin… - Nature …, 2014 - nature.com
Tuberous sclerosis complex (TSC), caused by dominant mutations in either TSC1 or TSC2
tumour suppressor genes is characterized by the presence of brain malformations, the …
tumour suppressor genes is characterized by the presence of brain malformations, the …
TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway
A Falace, E Buhler, M Fadda, F Watrin… - Proceedings of the …, 2014 - National Acad Sciences
… (F) Quantification of GFP cells in cortical upper layers (II–IV) and the cortical deep layers (V–VI)
and expressed as a percentage of the total number of transfected cells (n = 7 for each …
and expressed as a percentage of the total number of transfected cells (n = 7 for each …
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene
Periventricular nodular heterotopia is caused by defective neuronal migration that results in
heterotopic neuronal nodules lining the lateral ventricles. Mutations in filamin A (FLNA) or …
heterotopic neuronal nodules lining the lateral ventricles. Mutations in filamin A (FLNA) or …