Francoise Muscatelli

UPMC Univ Paris 6, France 
"Francoise Muscatelli"
Mean distance: (not calculated yet)


Sign in to add mentor
Michel Fontes grad student 1992 UPMC Univ Paris 6
 (Cartographie de la region xq11-q21 humaine; approche du mecanisme d'inactivation du chromosome x)
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Vaidyanathan R, Schaller F, Muscatelli F, et al. (2020) Colocalization of Oxtr with Prader-Willi Syndrome transcripts in the trigeminal ganglion of neonatal mice. Human Molecular Genetics
Zanella S, Tauber M, Muscatelli F. (2009) Breathing deficits of the Prader-Willi syndrome. Respiratory Physiology & Neurobiology. 168: 119-24
Andrieu D, Meziane H, Marly F, et al. (2006) Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death. Bmc Developmental Biology. 6: 56
Le Meur E, Watrin F, Landers M, et al. (2005) Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region. Developmental Biology. 286: 587-600
Landers M, Bancescu DL, Le Meur E, et al. (2004) Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn. Nucleic Acids Research. 32: 3480-92
Runte M, Faerber C, Lich C, et al. (2001) Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15 European Journal of Human Genetics. 9: 519-526
Muscatelli F, Abrous DN, Massacrier A, et al. (2000) Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome. Human Molecular Genetics. 9: 3101-10
Boccaccio I, Glatt-Deeley H, Watrin F, et al. (1999) The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. Human Molecular Genetics. 8: 2497-505
Jay P, Rougeulle C, Massacrier A, et al. (1997) The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nature Genetics. 17: 357-61
Watrin F, Roëckel N, Lacroix L, et al. (1997) The Mouse Necdin Gene Is Expressed from the Paternal Allele Only and Lies in the 7C Region of the Mouse Chromosome 7, a Region of Conserved Synteny to the Human Prader-Willi Syndrome Region European Journal of Human Genetics. 5: 324-332
See more...