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A novel putative receptor protein tyrosine kinase of the met family.
Ronsin C, Muscatelli F, Mattei MG, Breathnach R. Ronsin C, et al. Among authors: muscatelli f. Oncogene. 1993 May;8(5):1195-202. Oncogene. 1993. PMID: 8386824
Mouse 5-hydroxytryptamine5A and 5-hydroxytryptamine5B receptors define a new family of serotonin receptors: cloning, functional expression, and chromosomal localization.
Matthes H, Boschert U, Amlaiky N, Grailhe R, Plassat JL, Muscatelli F, Mattei MG, Hen R. Matthes H, et al. Among authors: muscatelli f. Mol Pharmacol. 1993 Mar;43(3):313-9. Mol Pharmacol. 1993. PMID: 8450829
A male with two contiguous inactivation centers on a single X chromosome: study of X inactivation and XIST expression.
Muscatelli F, Lena D, Mettei MG, Fontes M. Muscatelli F, et al. Hum Mol Genet. 1992 May;1(2):115-9. doi: 10.1093/hmg/1.2.115. Hum Mol Genet. 1992. PMID: 1301147
Isolation of new probes from Xq12-->q13: an example of the screening of reference libraries with Alu-PCR products from radiation hybrids.
Muscatelli F, Monaco AP, Goodfellow PN, Hors-Cayla MC, Lehrach H, Fontes M. Muscatelli F, et al. Cytogenet Cell Genet. 1992;61(2):109-13. doi: 10.1159/000133383. Cytogenet Cell Genet. 1992. PMID: 1395715
BMX, a novel nonreceptor tyrosine kinase gene of the BTK/ITK/TEC/TXK family located in chromosome Xp22.2.
Tamagnone L, Lahtinen I, Mustonen T, Virtaneva K, Francis F, Muscatelli F, Alitalo R, Smith CI, Larsson C, Alitalo K. Tamagnone L, et al. Among authors: muscatelli f. Oncogene. 1994 Dec;9(12):3683-8. Oncogene. 1994. PMID: 7970727
Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndrome.
Moncla A, Piras L, Arbex OF, Muscatelli F, Mattei MG, Mattei JF, Fontes M. Moncla A, et al. Among authors: muscatelli f. Hum Genet. 1993 Feb;90(6):657-60. doi: 10.1007/BF00202487. Hum Genet. 1993. PMID: 8444473
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region.
Jay P, Rougeulle C, Massacrier A, Moncla A, Mattei MG, Malzac P, Roëckel N, Taviaux S, Lefranc JL, Cau P, Berta P, Lalande M, Muscatelli F. Jay P, et al. Among authors: muscatelli f. Nat Genet. 1997 Nov;17(3):357-61. doi: 10.1038/ng1197-357. Nat Genet. 1997. PMID: 9354807
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.
Watrin F, Roëckel N, Lacroix L, Mignon C, Mattei MG, Disteche C, Muscatelli F. Watrin F, et al. Among authors: muscatelli f. Eur J Hum Genet. 1997 Sep-Oct;5(5):324-32. Eur J Hum Genet. 1997. PMID: 9412790
The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region.
Boccaccio I, Glatt-Deeley H, Watrin F, Roëckel N, Lalande M, Muscatelli F. Boccaccio I, et al. Among authors: muscatelli f. Hum Mol Genet. 1999 Dec;8(13):2497-505. doi: 10.1093/hmg/8.13.2497. Hum Mol Genet. 1999. PMID: 10556298
Homologous chromosomal locations of the four genes for inter-alpha-inhibitor and pre-alpha-inhibitor family in human and mouse: assignment of the ancestral gene for the lipocalin superfamily.
Salier JP, Simon D, Rouet P, Raguenez G, Muscatelli F, Gebhard W, Guenet JL, Mattei MG. Salier JP, et al. Among authors: muscatelli f. Genomics. 1992 Sep;14(1):83-8. doi: 10.1016/s0888-7543(05)80287-3. Genomics. 1992. PMID: 1385302
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