Francoise Muscatelli
Affiliations: | UPMC Univ Paris 6, France |
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Parents
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) | ||||
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| 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 |